Qatar Medical Journal - 1 - Extracorporeal Life Support Organisation of the South and West Asia Chapter 2017 Conference Proceedings, February 2017

Extracorporeal Life Support (ECLS) is saving an increasing number of lives worldwide,¹ so it is a great pleasure to welcome for the first time in Qatar the South and West Asia Chapter (SWAC) of the Extracorporeal Life Support Organisation (ELSO). The conference organizing and scientific committees have worked tirelessly under the leadership of Dr Ibrahim Fawzy Hassan (2017 Conference Chair) to make ELSO SWAC 2017 an enriching event that will help progress ECLS in the region. For this special occasion, the SWAC ELSO 2017 submission editorial team (AAH, AS, GA, CC, TM) is pleased to have been able to publish all accepted abstracts in this special issue of the Qatar Medical Journal (QMJ) as a legacy of everyone's efforts and commitment to contribute to saving lives. The vast majority of the abstracts are invited contributions from selected clinicians who are bringing specific knowledge and expertise to the conference and to the pre-conference workshops. The submissions received as part of the call for abstracts are presented at the end of this QMJ issue and been presented either as short oral or poster presentations during the conference. All submissions have been subjected to a rigorous peer review process involving a team of reviewers with a range of subject expertise and to whom we are grateful. Overall, this QMJ special issue represents the scientific contributions from over 150 authors from 17 countries.

The spread of the safe practice of ECLS, especially with regard to severe respiratory failure (SRF), relies on effective team training and education of the clinicians. To that effect, this year's theme is “Bringing ECMO Simulation to Life” and is directly reflected in the series of simulation-based pre-conference workshops which include:

  ‐ Adult respiratory ECMO ‐ Adult cardiac ECMO ‐ Neonatal and pediatric ECMO ‐ Percutaneous cannulation ECMO ‐ ECMO transport

We hope that the experiences regarding simulation technology^2–4 and educational approaches⁵ shared within the abstracts will benefit everyone. We believe that ECMO-specific simulation plays a vital role in safely implementing this crucial but complex lifesaving treatment modality in the medical community.^6,7

The first successful clinical use of ECMO (Extracorporeal Membrane Oxygenation) was seen in the 1970s followed by encouraging results in clinical trials in neonatal population in the 1980s. ECMO became a standard of care for management of post-operative cardiac failure in major pediatric heart centers in the 1990s. The use of ECMO as a modality of care in adult ICU was initially faced with multiple challenges until H1N1 flu pandemic in 2008–2009 which, along with major improvement in devices, led to a rapid increase in its use for cases of acute respiratory distress syndrome (ARDS). Currently, ECMO is used for severe heart and lung failure in all ages.⁸

After being almost abandoned, veno-venous (VV) ECMO, commonly known as “respiratory” ECMO gained a new and strong legitimacy among ARDS therapies. Indeed, whether among neonatal, pediatric, or adult cases, the number of respiratory ECLS runs has increased over the last decade and has the best patient survival rate of all ECLS strategies.⁹ Every year, new centers start their program with the best aspirations of saving lives and share information about their journey.^10–14 As VV ECMO is becoming the gold standard therapy as a bridge to many options (e.g. recovery, diagnosis, decision, transplant), it is nearly becoming unacceptable to die from an acute SRF. The abstracts presented in this conference show that teams use VV ECMO for increasingly diverse clinical indications such as pulmonary embolism (PE), septic shock, trauma, and HIV,^15–20 far from the formerly accepted indications. The positive outcomes sometimes achieved are encouraging and support the idea of researching new ECMO applications as a rescue therapy.

Nurses are an integral part and essential to the VV ECMO management team. Daily nursing care of ECMO patients is an area of research for improving VV ECMO management.²¹ Finally, the historical imperative need to anticoagulate all patients on VV ECMO becomes actually nuanced and better assessed by many centers depending on the clinical situation if the risk of bleeding is high.^20,22,23 This allows the possibility of initiating ECMO on patients who have a contraindication to anticoagulation.²⁴ It seems VV ECMO continues to successfully shape its own future.

Another form of ECLS therapy is cardiac or veno-arterial (VA) ECMO for which indications are also diverse. Established indications include post-cardiotomy and as a bridge to recovery or to mechanical support. Provision of VA ECMO for cardiac arrest survivors and as part of cardio-pulmonary resuscitation (E-CPR) is gaining popularity worldwide.²⁵ The results of this novel resuscitation strategy remain to be established. Enthusiasts advocate E-CPR for out-of-hospital cardiac arrest, while others provide E-CPR in the Emergency Department.^26,27 Most probably, we will learn along the way how to better select patients and who are the most likely to benefit from E-CPR. Another huge area for development is ECMO in the cardiac catheterization laboratory.^25,28,29 Interventional cardiology and minimally invasive cardiac procedures have revolutionized the care of cardiac patients. Initiation of VA ECMO prior to, during, or after PCI is likely to increase with more complex patients and higher expectations of the public. Cardiac ECMO management poses several challenges. Echocardiography is particularly useful, may reveal new or worsening pathology, and can help tailor management strategies.³⁰ Distension of left ventricle during VA ECMO is problematic and needs special consideration.³¹ Another potential complication of VA ECMO is Harlequin syndrome.³²

Although the VA mode still remains the primary mode of ECMO support in neonates, a steady rise in the use of the VV mode has been witnessed in the recent times.^33–35 The physiological principles of management on ECMO are well established; however, improvement in ongoing care is attributed to the advanced research in the field of ECMO.^8,36 Controversies and important questions still exist in certain aspects of care like best agent and tool to monitor anticoagulation,²² prognostication and long-term outcome,³³ and modality to provide renal support therapy. Criteria for ECMO in neonates with congenital diaphragmatic hernia still remain an inexact science.³⁷ Owing to significant improvements in neonatal clinical care and innovation of novel therapies for the primary diseases, ECMO is finding its way in previously unexplored indications and in clinical situations considered as absolute contraindication in the past. In 2008–2012, the ELSO registry documented that 178 patients with malignancy received ECLS, which equates to 1% and a doubling of utilization compared with that reported previously. This is attributable to the significant improvement in five-year survival (>80%) for childhood cancers.³⁸

A particular aspect, underrepresented in the literature, research, and training, is mobile ECMO. ECMO patients represent the extreme of pathophysiology and moving them adds increased risk, and hence requires meticulous planning, competent personnel, checklists, and attention to details to ensure patient safety. ECMO is often located in specialized regional centers, thus necessitating moving patients.^39,40 As yet, no consensus exists on optimal team composition, and specific roles vary considerably between centers. Whatever the configuration, the mobile ECMO team should have the necessary skills and competency to safely initiate, maintain, and trouble shoot any ECMO or clinical emergency.¹² They should be self-sufficient and ensure adequate supply of all ECMO-specific equipment and have adequately trained personnel, appropriate vehicles, equipment, and medication.^41,42 Incorporating the Ambulance Service professionals into the team to provide seamless team dynamics during retrieval may significantly contribute to improving mobile ECMO safety. Intensive or Critical Care Paramedics (CCPs) can play a logistics and safety role, allowing other members of the team to focus on their specific duties. CCPs are experienced in advanced airway, ventilation, and advanced cardiovascular life support (ACLS) skills, providing the team with additional skills in the event of an emergency.⁴³ One of the key aspects in preventing patient safety issues and minimizing risks of harm during the transportation of an ECMO patient is to develop a well-prepared multiprofessional team. Mobile ECMO simulation can play a very important role in developing not only core skills but also enhance general team dynamics^5,6 (Figure 1).Figure 1.  ECMO team taking part in a truly interprofessional simulation-based training activity with the purpose-designed ICU ambulance and ECMO stretcher (picture courtesy of Hamad Medical Corporation).

Of increasingly recognized importance to improve the quality of care and improve patient outcome is the involvement of other allied healthcare professionals into the ECMO team such as physiotherapists and perfusionist.^44,45 They complement the key role played by the critical care nursing staff who have acquired expert knowledge and skills and become ECMO nurse specialists who can integrate the operation of the ECMO machine, ventilatory requirements, and patient's medical management.^21,46,47 They fulfill an increasing number of responsibilities in the multiprofessional team.

Each ECMO center needs to create their own program-specific indications, team structure and composition, and management strategies, including clear exit plan after taking into consideration the available resources, and ethical, religious, and cultural aspects of their specific environment.⁴⁸ We hope that this new collection of articles and abstracts will contribute to the advancement of ECLS therapies worldwide and development of expert teams who safely acquire the required skills and knowledge using various simulation modalities.

Introduction: The aim of the program was to establish a severe respiratory failure (SRF) service with mobile extracorporeal membrane oxygenation (ECMO) retrieval capability throughout Qatar. This was achieved through the collaboration of various Hamad Medical Corporation (HMC) entities (critical care, cardiothoracic surgery, vascular surgery, and ambulance services). The service was commissioned by the Ministry of Public Health in October 2013 in response to the emerging MERS-Corona outbreak and its associated high mortality. After extensive team building and training, the service treated its first patient in June 2014. The key result has been an improvement in survival rate from 19 to 68%. The service is ranked among the best in the Extracorporeal Life Support Organization (ELSO) outcomes benchmark of worldwide SRF services. The provision of the highest quality care to patients with high predicted mortality has given a new hope in improving clinical outcomes and their reintegration into community. Background: In 2013, a novel virus (MERS Corona virus) was identified in Saudi Arabia, with subsequent cases in other gulf states including Qatar.¹ The MERS virus was associated with rapid onset of severe respiratory and renal failure, resulting in a very high mortality rate (>50%) in the early days of the infection.² The need to establish a SRF center with mobile ECMO retrieval capabilities was identified by the HMC senior leadership in order to anticipate and proactively deal with the situation. The program became a matter of utmost importance due to the inevitable social, political, and geographical factors, which united the people of the GCC. Strategically speaking, regulating the travel norms or bringing in a quarantine on travelers arriving from the countries affected by the MERS Corona virus were not a feasible alternative.³ Furthermore, the high mortality rate, failure of conventional ICU care, and the high cost of transporting and hospitalizing these patients in other countries with advanced respiratory support capability highlighted the need for the development of a severe respiratory failure and extracorporeal membrane oxygenation (SRF-ECMO) service program in Qatar. Evidence: The value of a SRF-ECMO service had previously been demonstrated during the international outbreak of H1N1 virus, when survival of patients with significant respiratory failure would have been left to chance or luck if no such advanced program had been in place. The SRF-ECMO services were achieving global survival rates of 60–70% in patients with otherwise very high mortality rates.⁴ Additionally, treatment of SRF in the SRF-ECMO Center decreased mortality rates.⁵ The vision of the leadership in promoting interdepartmental collaboration along with the support from the management at various levels was the highlight in the development of this program which now is recognized internationally for its clinical excellence and well known for its best practices, teaching, and mentorship programs. Program implementation and team training: The idea of a SRF-ECMO service in the State of Qatar had to be planned immaculately due to the fact that this was the first project of its kind in the country and there is always a sense of anticipation and enigma surrounding such a cutting-edge technology being made available with the help of the government itself. As a result of various fruitful deliberations, a steering committee was created which identified all the potential services that would be involved in the program along with the identification of the potential stakeholders in its successful implementation. The Guys and St Thomas (GSTT) Hospital team in London (UK) was identified as the potential partner for the implementation of the SRF-ECMO in Qatar and hence an official mission consisting of leaders from various services involved went on a field visit to get a firsthand experience about the program. Various discussions with the GSTT team took place in order to understand the processes and the actual difficulties they faced when they started their own SRF-ECMO service.

The clinical leaders realized that the only way this project could succeed – taking into consideration the relative inexperience of the team involved with regards to ECMO – was to provide hands-on experience to all HMC staff involved so they could become a fully functional and highly efficient team, which worked according to the best current evidence-based practices. The HMC senior leadership left no page unturned in the training of the team members, which is exemplified by the various international courses and workshops they were supported to attend to master the art of ECMO. Members of the team attended:

  ■ ECMO simulation course at GSTT ■ Cadaveric ECMO course in Charité Hospital (Berlin) ■ Residential hands-on training in London

In addition, selected stakeholders spent a short period of time at GSTT to observe their service and obtain more technical information to effectively set up the program. This investment was highly fruitful in the sense that various members of the team which included physicians, nurses, perfusionists, respiratory therapists, pharmacists, physiotherapist, nutritionists, critical care paramedics, and educators were able to take part and bring the knowledge and skills back in Qatar for the benefit of a whole region.

The training was intended to provide each member with the whole repertoire of knowledge so as to help in the smooth gelling and functioning of the team, which could produce optimum results within the minimal timeframe and with the resources then available.

The physicians were provided with all the resources to master the relevant knowledge in quality and research, and were given the best training for cannulation. They were also provided with the knowledge of the anticipated problems that could arise during the procedure and during the retrieval and transport of ECMO patients. The most important part of the documentation and guidelines were mastered by the very skillful team that included consultants, specialists, and fellows from the MICU.

The nurses in the team, who form an integral part in the success of the procedure and process, were trained as ECMO specialist nurses with the responsibility of ensuring that all were functioning well with the help of checklists, protocols, and guidelines. They also have an important role in training other nurses in the MICU about the techniques and processes involved in this complex lifesaving procedure. They were also provided with the Sheikh Khalifa Medical City (SKMC, Abu Dhabi) nurses training program to further enhance their clinical skills.

The respiratory specialists in the team were given training in pre-ECMO management and positive end expiratory pressure (PEEP) optimization along with the other important procedures like positioning in ECMO, recruitment maneuvers, and ventilation in ECMO.

The perfusionists were given training in all the technical aspects of the circuit and its interaction with the patient throughout the various phases of ECMO.

The pharmacists were trained with all the potential drug interactions in the ECMO patient interface and were given the responsibility of reviewing all the protocols for the drugs used by the GSTT team.

The physiotherapists were given training in the positioning of the patient (which can be tricky especially when they are prone) and were given the all-important jobs of resuming mobilization and exercise training of the patients while still on ECMO. Further, they were given special training in chest physiotherapy in patients who were on ECMO, which can be very challenging, given the technology involved.

The nutritionists in the team were responsible for the total parenteral nutrition (TPN) and the interactions with the circuits. They further were given training in enteral feeding in ECMO, which reduces the complications and the morbidity in patients who undergo successful decannulation.

The Critical Care Paramedics play an essential role in the mobile retrieval capabilities of the program, including the road map plan for activation and deployment of the team. In our case, they had crucial input into the design of the ECMO and ambulance trolley.

The educator integrated all the knowledge and skills to maintain the competency of the team, from simple water drills all the way to advanced simulation-based competency assessment. Up-to-date cases: The first patient was admitted to the SRF-ECMO service in May 2014 with H1N1 pneumonia and successfully discharged from the hospital after 3 weeks of ECMO therapy. Since then, the SRF-ECMO service has treated 50 patients with a survival rate of 66% in total. Of these patients, 25% were trauma cases. Additionally, the SRF-ECMO service has also started its retrieval arm, moving patients from other hospitals in Qatar to the SRF-ECMO Center following cannulation and placing the patient on ECMO, 11 retrievals have been undertaken with one patient dying before transport. Additionally, two patients have been transferred with ECMO to the Heart Hospital for Cardiothoracic Surgery (severe PE and thoracic trauma with bronchial tear) and one patient has been successfully repatriated on ECMO to India using our own aeromedical ECMO transfer team. Summary: The Qatar SRF-ECMO program is one of the few programs worldwide that operates to the highest level and has been developed in less than 6 months. This has only been possible thanks to the enormous support of the leadership, dedication of the multidisciplinary team, and the partnership with an experienced center such as Guy's and St Thomas’ NHS Foundation Trust.

Introduction: The H1N1 epidemic in 2009 caused a significant increase in the utilization of respiratory extracorporeal membrane oxygenation (ECMO) therapy for severe respiratory failure (SRF) patients who failed to improve following conventional ventilation therapy. Its use was linked to a high patient survival rate (more than 70%) reported from Australian and New Zealand¹ as well as Canadian ECMO² registries. It eventually led to the CESAR randomized controlled trial³ that clearly showed mortality benefits for adult patients with, potentially reversible, severe respiratory failure who were treated in ECMO centers. In that study, more than 63% of the referred patients survived and 75% of them received ECMO therapy, whereas in the conventional treatment arm, the survival rate was only 47%.

The significant change in the outcome, compared with old data, is related to several factors, such as advances in ECMO technologies, the use of veno-venous (VV) ECMO instead of veno-arterial (VA) ECMO, advances in the tubing and the membrane that are currently used, better understanding of lung and patient management during ECMO therapy, and early deployment of the rescue therapy.

In this review, we are going to discuss the physiology of oxygenation and the overall management strategy on ECMO during early course of active inflammation, all the way through to weaning during the healing phase of the lung injury. O2 is a perfusion-limited gas: This means that O2 depends not only on its ability to diffuse through the membrane, which is 25 times less than CO2, but also on perfusion capacity of the area being oxygenated. To explain that in a simple way, we will assume that O2 is a gas that cannot swim in the blood, and if it is left alone it will sink and cause free radical injury. It needs a carrier, such as the hemoglobin, and flow, which is the cardiac output or ECMO flow to push that carrier. If the transport capability of the blood is saturated, additional oxygen will be left out and will not be transported to the rest of the body. The perfusion limitation concept is very important to understand the shunt physiology. For example, if a patient with complete consolidation of both lungs has a cardiac output of 10 L/min and is on a 5 L/min ECMO flow, only 50% of the patient cardiac output is getting exposed to the gas exchange area and 50% is shunting through the diseased lung. When they mix together, 50% of the blood will be de-oxygenated, which will cause severe persistent hypoxemia. To solve this problem, we either recruit more lung units or decrease the overall patient cardiac output to decrease the intrapulmonary shunt. Adding more oxygen to either disease obstructed alveoli or the ECMO membrane will not solve the problem.⁴Carbon dioxide is a diffusion-limited gas: CO2 does not have the same problem as oxygen. It can ride on the hemoglobin, the albumin, and can also swim in the CO2–HCO3 buffer. The only limitation of CO2 is the flow of fresh air, whether it is minute ventilation or ECMO sweep gas flow, and this is related to the very low concentration of CO2 in room air and its ability to diffuse through the membrane 25 times more than oxygen. CO2 clearance on ECMO can be controlled by increasing the sweep gas flow. The difference between membrane lung and artificial membrane: Despite the significant advances in technologies, the artificial lung development remains in its infancy and far from complete for various reasons:

The total surface area of a normal human lung is about 70 m², whereas the best artificial lung membrane has a maximum equivalent of 4 m². The thickness of a normal human lung is about 0.5 μm, whereas an artificial membrane is 300 times thicker, with an average thickness of 150 μm. Important factors affecting the diffusion and the uptake of oxygen are:

  A– The red blood cell (RBC) transient time, which is 0.4–1 second in a normal lung and much shorter in the artificial membrane lung. B– The way that RBC cross the normal capillary is almost one cell at the time, compared with the membrane lung capillary where red blood cells cross in clusters. For all the above reasons, the maximum oxygen transfer capability of the artificial membrane (400–600 mL O2/min) is much less than the normal human lung (>2000 mL O2/min).

The focuses in this phase are:

  1– Maximizing ECMO flow as the patient depends almost 100% on the ECMO for oxygenation to maximize O2 delivery; 2– Resting the lung and switching the focus of ventilation from enhancing lung recruitment to preventing the de-recruitment of whatever is left of the lung tissue. 3– Full patient rest to decrease O2 consumption, which will also decrease the cardiac output appropriately and hence decrease intra-pulmonary shunt. This is usually achieved by sedation, paralysis, temperature control, and sometimes adding beta blockade. 4– Optimizing the native lung function by early diagnosis and treatment of the underlying condition, negative fluid balance if tolerated by the ECMO flow and secretion mobilization usually with bronchoscopies rather than just physiotherapy, as the patient is usually deeply sedated.

The focuses in this phase are:

  1– Starting to wean ECMO flow and sweep gas flow to allow the stimulation of the native lung. 2– Focusing on lung recruitment and diaphragmatic muscle dysfunction prevention using various ventilation modes such as neutrally adjusted ventilatory assist (NAVA), pressure support ventilation (PSV), and others, and also early extubation on ECMO is warranted. 3– Weaning of all sedatives and paralytics, management of delirium, and most importantly, aggressive physiotherapy on ECMO. 4– Continuing to optimize native lung function with aggressive chest physiotherapy; however, fluid strategy could be liberal at this stage to facilitate sedation weaning without affecting the ECMO flow.

Later in the course, as discussed earlier, the goal is to wean sedation and paralysis, and to ensure spontaneous ventilation to decrease the risk of ventilator-induced diaphragmatic muscle dysfunction. During this period, the access insufficiency occurrence might increase and controlling the access will be by fluid boluses in the expense of weaning the sedatives and paralytics. Summary: The use of respiratory ECMO has been continuously increasing for SRF patients globally. Despite significant advances in technologies, the artificial membrane lung still has significant limitations in comparison to the normal human lung. Given that oxygen is a perfusion-limited gas, maximizing the ECMO flow to match the patient's cardiac output is essential to overcome the membrane limitation.

The management strategy during an ECMO run is different from the early inflammatory course to the late recovery course, not only on the diseased lung, but also on the entire body system, and this has to be considered during therapy on VV ECMO. Fluid management in particular has to be carefully evaluated using different tools such as ECHO-guided assessment for volume responsiveness.

Introduction: Extracorporeal membrane oxygenation (ECMO) is an adaptation of conventional cardiopulmonary bypass techniques used for long-term support of respiratory and/or cardiac function. It provides physiologic cardiopulmonary support for patients with acute, reversible cardiac or respiratory failure. The term “extracorporeal life support” (ECLS) was proposed to describe prolonged but temporary (1–30 days) support of heart or lung function using mechanical devices. Technically, ECMO terminology is used for modalities that provide pulmonary support system involving oxygenation and carbon dioxide removal, and ECLS is used for both cardiac and pulmonary support systems, but these terminologies are still used interchangeably.^1,2

Over the past 30 years, due to significant advances in the understanding of physiology, improvement in clinical care, innovation of novel therapies for primary diseases, and technological advances, there have been major changes in indications, cannulation, duration of treatment, and outcome for the children being treated with ECMO. Patient selection remains key to a successful outcome since ECMO is a supportive therapy utilized while waiting for a reversible condition to resolve through other treatment strategies.

According to the registry report of the Extracorporeal Life Support Organization (ELSO), over 78,000 cases have been reported until July 2016. Of these cases, 29,153 are newborn infants with respiratory failure, 74% of which survived to hospital discharge; 18,153 of them are patients managed with ECMO for severe respiratory failure in the pediatric (7,552) and adult (10,601) age groups with survival to a hospital discharge rate of 58% in each group. All other cases relate to cardiac support in neonates, children, and adults with rates of survival to hospital discharge ranging between 40 and 50%.³History: Bubble oxygenators, used in early cardiopulmonary bypass systems, were characterized by a direct interface between blood and gas. However, significant hemolysis caused by these oxygenators limited prolonged exposure.⁴ Long-term support was made possible by the development and introduction of membrane oxygenators, which physically separated the blood and gas phases and thus minimized the problem of hemolysis.⁵ In 1972, the first successful use of prolonged cardiopulmonary bypass was reported by J. Donald Hill.⁶ The patient was supported for 3 days with venoarterial extracorporeal bypass support for a ruptured aorta following a motorcycle accident. Neonatal evidence: In 1976, Bartlett et al.¹ reported on baby Esperanza, the first successful neonatal ECMO survivor. She was supported for 3 days on ECMO for respiratory failure secondary to meconium aspiration. Dr Bartlett led the first prospective randomized, controlled trial (RCT) that evaluated neonatal respiratory ECMO against conventional management, which was conducted at the University of Michigan in 1985.⁷ This study was published to demonstrate the benefit of ECMO by comparing cases in which all patients supported with ECMO survived, while conventionally treated patients died. The study faced much criticism. This led to a second larger study by Dr Pearl O'Rourke at Boston Children's Hospital in 1989. Of 10 patients who were conventionally supported, only 6 survived, whereas of 29 patients who were supported with ECMO, 28 survived.⁸ In 1996, the UK Collaborative ECMO Trial Group published a 55-center conventionally designed RCT. Neonates with PPHN were randomized to either stay in their referral center for standard therapy or be transferred to a regional ECMO center. Survival was found to be higher in those receiving ECMO than in those who did not receive it (60% vs. 40%). Follow-up at 1 year showed a significantly lower death rate or severe disability in the ECMO group.⁹ A Cochrane review (2008) by Mugford and colleagues evaluated four trials by comparing ECMO and conventional management for neonatal respiratory failure. Increased survival to hospital discharge with ECMO support was demonstrated by all the four studies when compared with conventional therapeutic strategies. Of a total of 244 infants, 77% survived in the ECMO group whereas only 44% survived in the conventionally managed group.¹⁰ Bartlett et al.¹¹ attributed the success of ECMO in newborns to the fact that the lungs require only a short time for recovery in neonates with respiratory failure. The data from the prospective randomized controlled trial from the UK showed rigorous evidence of the cost-effectiveness of neonatal ECMO during childhood.¹²Pediatric evidence: In the 1980s, the benefit of ECMO for pediatric patients was subject to discussion in the medical community.^13,14 Concerns were raised about the application of the new, expensive, and potentially dangerous technology in children in whom pulmonary injury could be due to widely unknown mechanisms. To gain further acceptance of ECMO in children, performance of a RCT was considered mandatory. However, this approach was postponed due to ethical considerations. In 1996, Green et al.¹⁵ published the results of a retrospective multicenter cohort analysis in 331 pediatric patients. Evaluation of factors associated with survival was done with a multivariate logistic regression analysis. ECMO was found to be associated with a reduction in mortality. An additional matched-pairs analysis revealed 74% survival in the ECMO group (n = 29) and 53% in the non-ECMO group (n = 53) (P < 0.01).

In the review of ECMO utilization in neonatal and pediatric respiratory failure between 2002 and 2012, survival was found to be consistent at 57%, despite increasing comorbidities. However, for patients without comorbidities, survival increased from 57 to 72% over the study period. Children supported with ECMO for status asthmaticus, aspiration pneumonia, and respiratory syncytial virus pneumonia had higher survival rates (between 70 and 83%). Poor prognostic indicators included patient age between 10 and 18 years, hepatic or renal failure, evidence of immune dysfunction, and diagnosis of fungal pneumonia, pertussis, or ARDS secondary to sepsis.¹⁶

For children with severe cardiac failure, ECMO is used to provide temporary circulatory support for patients with potentially reversible disease or as a bridge to decision, either device or transplant. In a prospective multicenter study involving 17 pediatric cardiac centers, children who underwent implantation of the pediatric Ventricular Assist Device (VAD) as a bridge to transplantation were compared with a historical control group of children who received circulatory support with ECMO. Significantly higher survival rates were associated with VAD when compared with ECMO (88–92% vs. 75–67%). However, VAD use is not without complications, with the most common ones being bleeding, infection, stroke, and hypertension. This makes balancing when (or if) to institute the support even more challenging.¹⁷

The way forward: With the success of less-invasive respiratory support measures, the demographics of pediatric ECMO patients will continue to change with increasing numbers of support for patients with cardiac dysfunction and less for those with respiratory failure.^18–20 Improving results will encompass highly complex patients, and those with single-ventricle physiology will not be denied support and, in fact, will contribute a large percentage of ECMO patients.²¹ Smaller and more efficient cannulas²² are increasingly available for effective and rapid peripheral cannulation,^23,24 and can potentially trigger an upsurge in ECMO-CPR in children.^18,25

Remarkable advancement in pumps, oxygenators, and heparin coating of artificial surfaces has resulted in higher biocompatibility and lower rates of complications. Furthermore, improvements in monitoring anti-coagulation and control of bleeding²⁴ through the development of rapid and accurate point-of-care devices will make ECMO safer for children. A key factor leading to complications in small bodies is the exposure to large volumes of fluids. Experimental miniature pumps that diminish priming volumes and circumvent hemodilution could eventually provide a solution.²⁶

Upcoming generation of centrifugal pumps using magnetic levitation appears to improve end-organ recovery where supported patients show a trend toward better hospital survival and significantly higher late survival.²⁷ It is essential that future ECMO devices should make support much simpler, safer, and to a great extent automatic, while decreasing the need for anticoagulation. ICU nurses rather than ECMO specialists should manage the system, reducing the cost while maintaining ease and safety.^20,28 Continued education with the help of regulated training of all participants and use of simulation should be part of in-service activities within each institution committed to advance the service.

Pediatric cardiac transplantation will hopefully be available in the Gulf area, but is not currently a treatment strategy. Technological advances in implantable centrifugal and axial flow pumps have yet to be miniaturized for suitable use in infants and neonates, which is proven difficult until now.²⁹ On the flip side, significant advances to provide successful ECMO support for weeks or months have been achieved.¹⁹ Reduction in sedative use and keeping patients more awake,¹⁹ together with improvement in ventilator support to the point of extubation, could potentially lead to ambulatory ECMO. It could therefore potentially evolve into a definitive component of mechanical heart failure therapy in this region.

Data and registry need to be widespread and garnered from multicenter experiences to provide understanding to the quality of life after ECMO in children. It could also guide us to develop criteria for the use of ECMO as a resuscitative tool in cardiac arrest,¹⁹ and provide an answer to the controversial relationship between volume and outcome, and whether service regionalization would deliver the promise of improved results. Conclusion: ECMO is used as a standard of care for neonates and children with severe cardiac and pulmonary dysfunction refractory to conventional management. A lot of wisdom has been gained through research and experience with a resultant change in practice in the field of neonatal and pediatric ECMO over the past three decades with many promising advances awaiting support with robust evidence.

Introduction: The provision of an effective extracorporeal membrane oxygenation (ECMO) service requires a dedicated unit with sufficient caseload and access to specialised resources.¹ Moving unstable patients, with refractory respiratory failure on conventional mechanical ventilation, to the specialised centre for ECMO poses great risk to the patient.^1,2 Therefore, there is a need to have mobile ECMO capabilities with specialised retrieval teams, capable of initiating ECMO in the referral hospital and safely transporting the patient to the ECMO centre. Transport of patients on ECMO has been demonstrated to be safe, if undertaken by well-trained teams^2–7 providing seamless care.⁸ However, most studies pay little attention to the role of the ambulance service within the ECMO team.

The ideal configuration of the team has yet to be demonstrated, with different regions using different models.² The ELSO guidelines recommend, beside the ECMO specialist and cannulating physician, a transport nurse or respiratory therapist to provide ongoing critical care to the patient.⁹ This recommendation presupposes a model where nurses are routinely involved in interfacility transport of patients. It further ignores the role of ambulance service staff, who potentially play an integral role in the movement of the patient. This model is by no means universal, and certainly not the case in Qatar, hence the decision to include Critical Care Paramedics (CCP) as an integral part of the Qatar ECMO team, in service of safe ECMO patient transport. Multidisciplinary team dynamics in patient transport: As with the management of the ECMO patient within the ICU unit, the success of each retrieval and transport depends as much on team dynamics as on the technical skills of the individual specialities represented in the team.¹⁰

Due to the specialised nature of ECMO, the retrieval team cannot rely on the referring hospital having all the required equipment. Thus, the team needs to be self-sufficient and the team members interdependent on each other. Prior to activation of the team, each speciality is responsible for ensuring their specific retrieval equipment has been checked and sealed in readiness for the next retrieval. As part of this process, the ECMO retrieval team developed a set of checklists for each of the equipment sets (checked weekly) and a master retrieval checklist to be used by the CCP on activation of the team. The use of checklists ensures that all equipment boxes, required for cannulation and patient care, are loaded into the transport vehicles.⁹

The design of the retrieval service vehicle and High Acuity Patient Transport Trolley has factored in the principle of redundancy, realising that the patient on ECMO has limited physiological reserve if equipment, power or oxygen supply failure should occur. The close working relationship between the ECMO director and the Ambulance Service staff has helped develop a platform and system that provides redundancy and limits the requirement for the ECMO team to have to carry additional backup equipment.

Once at the referring hospital, each member of the team has preassigned roles. The ECMO physician takes lead on assessment of the patient, deciding on the eligibility for ECMO. The decision to initiate ECMO requires consent from the family to begin. During that time, the rest of the team begin the process of identifying additional resources within the hospital. The ECMO specialist nurse begins assessing the needs of the patient prior to movement. Once consent is obtained, the team can begin the process of preparing the patient for transfer to theatre (unless the decision has been made to cannulate in the ICU) and to prepare the operating theatre for cannulation. Delegating the role of patient safety and logistics to the CCP frees up the need for the lead physician to multitask, thus being able to concentrate on the task of patient assessment, reducing the risk of error and co-ordinating the requirements for cannulation of the patient at the receiving hospital. The CCP also plays a support role for the ECMO nurse specialist in preparing the patient for transfer to the theatre (infusions, monitoring and ventilation), and becomes lead for the safe movement of the patient from the unit to the theatre, and later to the ambulance. Each step in the patient preparation and movement is confirmed as per the safety checklist to ensure nothing is missed, and the risk of accidental dislodgment of invasive lines or ET tube is minimised. Having a dedicated safety person allows other team members to concentrate on their primary task. Background:Building the Ambulance Service–Medical Intensive Care Unit relationship: Following the outbreak of MERS coronavirus, the leadership of HMC made a decision to develop a severe respiratory failure (SRF) service, including the implementation of an ECMO programme, as none existed in the country or the region. This service would be based at Hamad General Hospital in Doha. A centralised model of care would be used, thus requiring the establishment of an ECMO retrieval service.

The project development was tasked to the MICU Director, who also held the Deputy Medical Directorship of the Ambulance Service. This relationship had previously led to the Ambulance Service and the Medical Intensive Care Unit co-developing a multidisciplinary, simulation-based training programme in preparation for the launching of a High-Acuity Adult Retrieval Programme. This model paired MICU intensivists with Critical Care and Ambulance Paramedics on a purpose-built Mobile Intensive Care Ambulance, with the CCP as team leader. Based on the success of this programme, it was decided to include a small group of experienced CCPs in the ECMO training programme, which was initiated in November 2013. The envisaged role of the CCPs was to undertake the logistic lead and patient and team safety role on ECMO retrieval development.

As part of the initial training programme, two of the CCPs were included in the team that were sent for training with an established ECMO service in the UK. Their role was to get insight into the logistical requirements and evolution of ECMO retrieval and then become the project leads for the development of the Ambulance Service's capacity to support a seamless ECMO retrieval service. The ECMO retrieval team: In Qatar, the ECMO retrieval team is made up of either two ECMO specialists or an ECMO specialist and a MICU consultant, with an ECMO specialist nurse, perfusionist and respiratory therapist. In addition, the team has a CCP as an integral member of the team, with a central role in logistics and safety. The CCP helps link the decision-making and execution of patient movement and transport to any additional resources within the Ambulance Service that may be required and adds additional clinical capacity to the retrieval team.

In many countries, Critical Care or Intensive Care Paramedics play a central role in the interfacility transport of critically ill or injured patients, either by ground or air ambulance. Advanced Life Support Paramedics receive additional training in Critical Care Transport and Aeromedical Medicine, and then, work in multidisciplinary teams geared to the safe transport of high acuity patients, either by ground or by air. These Critical Care Teams may be composed of two CCPs, or a CCP working with a Critical Care Nurse or Physician.

CCPs develop their skills of leadership, required for working in high-stress environments, through their training and through experience working in complex and austere clinical environments. In many of the countries mentioned above, paramedics are required to gain experience in the emergency setting, before being permitted to transfer into Critical Care Transport teams. This model ensures that the CCP/ICP is not only competent in Advanced Life Support skills but has had time to master the complexity of assessing and managing critical patients, patient advocacy and professional engagement with other healthcare professionals.

Qatar recruits its CCPs from Australia, Canada, New Zealand, USA and South Africa. All these countries have established Critical Care Transport programmes through tertiary-based paramedic education (Associate Degrees or Degrees). CCPs, within the Ambulance Service in Qatar, are able to provide advanced airway interventions (rapid sequence induction and intubation), use multimodal mechanical ventilation and provide advanced cardiovascular life support – including infusion devices, inotropes, external pacing and mechanical chest compression devices. In addition, the group of CCPs selected to be part of the ECMO programme all had more than 10 years of clinical experience and were trained and experienced in aeromedical work.

Being familiar with the equipment and systems of the Ambulance Service, the competencies of interfacility patient transport and having been trained with the MICU multidisciplinary team in the process of ECMO, allowed them a unique ability to take on a lead role in the logistics process and patient safety roles and provide an additional resource for the provision of airway care, ventilation or advanced cardiac life support.

From late 2014 to date, the Qatar ECMO team have undertaken 13 retrievals, including one international transport from Qatar to India, without any adverse incidents. The strong relationship between the ECMO team and the Ambulance Service has facilitated the development of a safe and effective retrieval service. Future plans to include the initiation of ECMO transport simulations to ensure maintenance of skills and develop team dynamics with new staff being added to the Service.

In the USA, trauma represents the leading cause of death between the ages of 1 and 46 years and contributed to 192,000 deaths in 2014.¹ Major trauma is also responsible for significant disabilities and increased hospital length of stay (LOS), and represents a huge financial burden. Acute respiratory failure (ARF) is multifactorial in trauma patients with diverse underlying pathophysiological mechanisms. In a blunt thoracic injury, all the chest compartments can be affected and are directly responsible for mortality of 20–25%.² Two main mechanisms contribute to pulmonary injury; the first mechanism is a direct trauma leading to contusion, intra-alveolar hemorrhage, and aspiration pneumonia. Some of the mechanical injuries to the chest (pneumothorax, hemothorax, airways injury) are reversible by various interventions (pleural drains, surgical airway repair, etc.). The second mechanism is an indirect immunological lung injury, which may result from extrapulmonary trauma and/or the required management of trauma patients (massive transfusion, fluid overload, ventilator lung induced injury, etc.) leading to acute respiratory distress syndrome (ARDS). Extracorporeal membrane oxygenation (ECMO) is an attractive therapy in ARF. In 1972, the first successful use of ECMO was in a 24-year-old polytrauma patient who developed a “shock lung syndrome”.³ However, subsequent results in the next two to three decades were disappointing. The H1N1 influenza epidemic with a high number of young patients with severe respiratory failure led to resurgence of ECMO use. ECMO has been successfully used in severe ARDS secondary to the influenza A (H1N1) epidemic in 2009 with acceptable outcomes. A large multicenter trial (CESAR trial) in the UK showed that referral and transfer of patients to severe respiratory failure centers with ECMO capabilities reduced mortality in severe ARDS patients.⁴ Despite these encouraging results and use of ECMO worldwide for severe ARDS, use of ECMO in trauma patient is poorly studied. Severe ARF requiring mechanical ventilation (MV) in trauma patients is associated with high mortality and increased hospital LOS. In patients with severe impaired gas exchange despite optimized MV, ECMO is proposed to avoid injurious lung ventilation. It is prudent to start ECMO at an earlier stage to avoid irreversible MV-induced pulmonary injury in these cases. In severe thoracic trauma cases requiring lung resection or progressive lung fibrosis with severely limited reserve, ECMO may prove to be the main therapy as a bridge to lung transplant. The heterogeneity and complexity of trauma patients make ECMO use challenging in trauma cases with uncertain benefit/risk balance and multidisciplinary decision-making becomes extremely important on a case-by-case basis. Among trauma patients with ARF, those with a traumatic brain injury represent a specific group as their prognosis is mainly dependent on neurological recovery. These patients may require earlier ECMO support compared with non-brain-injured patients, to prevent secondary neurological injury from severe hypoxemia, hypercapnic acidosis, and worsening cerebral edema from fluid overload. Indeed, the combination of gas exchange alteration from respiratory failure and intracerebral pathology leads to a difficult challenge in ventilatory management of these patients. The usual dilemma of lung-protective versus neuroprotective ventilation creates contradictory goals. A high PEEP strategy, permissive hypercapnia, and permissive hypoxemia are well-accepted strategies for ARDS management, but may lead to secondary neurological insult in brain-injured patients. Munoz-Bendix and colleagues showed in their study that intracerebral pressure can be decreased by the PaCO2 control with ECMO support in trauma patients, which is a major goal of neuroprotective ventilation in these patients.⁵ ECMO in brain-injured patient is an attractive option as it allows the combination of neuroprotective and lung-protective ventilator strategies at the same time. The goal of ECMO is to support the patients who have good functional prognosis from their neurological injury. Unfortunately, this prognostication is not easy in brain-injured patients at the time when they are in need of ECMO. Better prognostic predictors in brain-injured patients may help the healthcare teams to improve the selection of patients who will benefit from ECMO.

ECMO use is limited in trauma patients, particularly those with traumatic brain injury, complicated pelvic fractures, or major vascular injuries in view of fear of serious bleeding during systemic anticoagulation. However, with improved ECMO circuit technology (newer pump systems, reduced circuit area, newer biocompatible circuit material, heparin coating etc.), and a relatively high blood flow during veno-venous (VV) ECMO, thrombotic complications during heparin-free ECMO runs are relatively uncommon. In the literature, there are many reports of prolonged heparin-free ECMO use in patients with trauma as well as other pathologies with high risk of bleeding complications with excellent outcomes and no serious thrombotic complications.^6–9 Recently, a systematic review of the literature with an aggregated total of 215 trauma patients showed an overall survival to discharge ranging from 50 to 79%;¹⁰ however, this work suffered from various limitations. All studies included were retrospective and included a maximum of five patients per year per center. Most of the studies with a high number of patients were performed over many years making definitive conclusions difficult to formulate as the ECMO management and techniques and ICU approaches have evolved over the years. An interesting cohort study using data from two American centers compared 76 trauma patients on MV and 26 who required VV extracorporeal life support (ECLS).¹¹ There were no differences between the two groups regarding ventilator days, intensive care unit LOS, and hospital LOS. However, when ECLS patients were severity matched to patients on MV, a better survival was demonstrated in the ECLS group. These are very encouraging results, but there were multiple limitations, and lot of questions remained unanswered. Further studies are needed to define the appropriate time to initiate ECMO, proper patient selection, and outcome data beyond survival to hospital discharge, including functional and psychosocial outcomes, particularly in brain-injured patients. The holy grail of ECMO use in trauma patients is the optimal timing to initiate this therapy. ECMO is a complex treatment modality, which involves a multiprofessional team of clinicians, and financial and physical resources for its optimal implementation. The use of ECMO in inappropriate patient at an inappropriate time may lead to poor outcomes with wastage of precious healthcare resources. Unfortunately, several large ECMO centers do not have a level 3 trauma center and, at the same time, multiple trauma centers do not have any ECMO service. Therefore, studies from centers with combined trauma and ECMO services are really needed to demonstrate their complementary positive impact on the care of trauma patients. Trauma patients should be considered as a genuine group to benefit from ECMO support. Beside the encouragement of centers to publish their individual experiences, a multidisciplinary task force under the aegis of ELSO may be a reasonable approach to conduct studies to answer the unresolved questions of ECMO use in trauma patients. A reasonable first phase towards this goal would be to create a specific registry for interested centers with experience in trauma care as well as ECMO capabilities. The management of these patients is complex and needs a multidisciplinary team approach with experience of trauma teams as well as intensivists and an ECMO team with a reasonable patient volume. The specific pathways created by collaboration of ECMO specialists, perfusionists, intensivists, emergency room physicians, trauma surgeons, and interventional radiologists will lead to improved patient care as well as valuable data to optimize the care of these patients in the future. The time has come not to deny the lifesaving ECMO therapy to trauma patient based on our perceived notions and prejudices. Indeed, the decision to start ECMO in trauma patients is not easy and straightforward and needs input from multidisciplinary team members but should be considered for each patient on an individual basis and may lead to very satisfying outcome in these mostly young patients. The need for more data and more outcome-based well-designed studies are needed to better define the role of ECMO in the care of trauma patients. The ECMO community should work in harmony to achieve this goal. The future of ECMO in trauma patients may prove to be bright after all.

“Bringing ECMO simulation to life”: The main theme of the 4th Annual Conference of the Extracorporeal Life Support Organisation – South and West Asia Chapter (ELSO-SWAC), “Bringing ECMO Simulation to Life”, is meant to emphasise the growing role of simulation in healthcare and medical education at large and in the highly specialised and complex field of extracorporeal life support (ECLS), and in particular for extracorporeal membrane oxygenation (ECMO). Application of ECMO simulation to improve team response to ECMO emergencies was first described in 2006.¹ In the last decade, several authors have described the development, utility, and advantages of simulation-based training for ECMO. In this editorial, we will discuss the role of and evidence supporting the use of simulation-based education in ECMO. ECMO is a complex intervention: The first point to consider when it comes to ECMO is the complexity, time critical, and inter-disciplinary nature of the intervention. Typically, ECMO is considered for the most sick and physiologically deranged patient, sometimes as a last resort rescue measure. Time pressure, the patient critical condition, the potential rapid deterioration, and the uncertainty interact within the critical care environment to make decision-making, planning, and execution quite challenging for the less experienced members of the clinical team. This relates to the domains of team and crisis resource management in which there is a complex interplay of human and environmental factors involved.² Appropriate training programmes of the required technical and non-technical skills for ECMO are lacking.^3,4 In addition, ECMO is relatively new to many centres and/or countries, and this novelty brings with it a general lack of experience regarding such therapy and the fear of the unknown. Simulation can help relieve staff anxiety and introduce ECMO in a safe, less intimidating learning environment.^3,4 Ideally, all aspects of ECMO patient care can be progressively introduced to the staff being trained through the use of various simulation modalities to promote better understanding and deep learning regarding the initiation of an ECMO run and ongoing ECMO patient care. Simulation can expedite preparedness for crisis: On 11 June 2009, the World Health Organisation (WHO) declared a global H1N1 pandemic only two months after the influenza outbreak in Mexico and USA. This allowed very little time for governments and organisations to prepare.⁴ A 2010 European taskforce for the intensive care unit (ICU) triage of influenza epidemic or mass disaster recommended commencing training of clinicians as early as possible with demonstration followed by practice under supervision.⁵ In line with these recommendations, a 3-day ECMO-based simulation training was established to provide a large number of clinicians with the technical, behavioural, and cognitive ECMO skills in anticipation of the H1N1 pandemic. The programme enabled some ICUs with no previous ECMO experience to care for patients on ECMO.⁴ Although it was probably the product of an expedited process of rapidly setting up a custom simulation programme, as opposed to adopting a more structured approach involving step-by-step development and validation through piloting,⁶ the anticipated outcome was still deemed beneficial to justify the rapid process. The European Taskforce's recommendation demonstrated the importance given to this educational approach in such a critical time as clinicians had to commit to 3 days of training to master life-saving skills and it was widely rolled out. What can ECMO simulation provide?: Traditional ECMO training and education focused on didactic lectures, water drills, and animal laboratory.⁷ This mostly passive learning approach is suboptimum for adult learning as adults tend to prefer developing knowledge and understanding using problem-solving, as it encourages active leaning, sharing of knowledge, and acquisition of experience.⁸ It calls upon “learners” to develop and use critical thinking skills, not only during the simulation-based experience, but also during the “review” phase, which corresponds to the debriefing of the simulation. This phase is usually in the form of a facilitated discussion, which helps learners further explore the event they partook in, clarify doubts, and develop their knowledge.⁹ It is not always without difficulty, but it is a crucial learning phase to understand the thought process behind learners' actions and it allows to deepen their learning.¹⁰

ECMO is a unique patient management and therapeutic strategy that requires a diverse set of technical, practical, cognitive, as well as behavioural and other non-technical skills. Initiation and maintenance of ECMO requires ongoing interprofessional interactions, which may sometimes occur in high-intensity situations such as a circuit emergency, which usually requires a coordinated and synchronised response from the various team members. Akin to high-risk industries, poor communication, inadequate leadership, and a dysfunctional team can cause significant harm.¹¹ The remedy adopted by high-risk industries, such as aviation, military, and the nuclear power plants, is regular simulation-based training for the employees, even if incidents are relatively rare, to ensure adequate readiness in the event of a potential crisis.¹² The work by Brum et al.³ shows that a one-day multi-professional ECMO simulation course significantly improved staff confidence of ECMO management and enhanced behavioural skills. In another report, ECMO simulation improved thoracic surgery residents' skills in the management of post-cardiotomy ECMO crisis.¹³ Management of patients on ECMO mandates high level of communication skills and team work, and rapid decision-making and actions. Simulation-based ECMO training provides an ideal platform to develop and maintain such skills. It enhances team response to crisis and permits rehearsal of less common and atypical life-threatening emergencies.^3,11 Simulation allows practice and acquisition of procedural skills in a safe environment,¹¹ and these can be initially practised in isolation and individually, prior to being embedded into more complex scenarios tackled as part of a multiprofessional team. In addition, team building, decision sharing, and execution are improved via simulation-based ECMO training, which enhances patient safety and minimises errors in response to an ECMO crisis.^3,11 The level of complexity and fidelity or realism adopted needs to match the intended types of learning objective and the level of experience of the participants.¹⁴ Beyond learners' educational and experiential benefits, simulation presents great opportunities with regard to systems' testing, environment orientation, as well as protocols and guidelines development. An application of particular interest is “in-situ” simulation, which engages the clinical team in their actual work environment,¹⁵ and hence with their own equipment with which they should already be familiar. Running in-situ simulations in particular is very useful to test the implementation of new services and identify potential risks and actual omissions of critical safety components.^16,17 Putting clinical teams in various simulated normal and emergency situations within their own context allows for observation of their actions and challenges they face in relation to the procedure, equipment availability or familiarity, or physical environment configuration. The immediate next phase is to engage them in a debriefing that will help identify potential as well as actual system or environmental issues, and assist in developing appropriate solutions. Organising in-situ simulation can however be challenging, especially in an operational clinical environment where real patients who might be critically ill are also present.¹⁸ In the case of ECMO patient care-related in-situ simulation, it is the ideal setting to train a team to respond to a patient or circuit emergency, as it will test their ability to act appropriately and test the availability of the resources required to deal with an emergency circuit change or pump failure for example. A facility that has limited regular exposure to ECMO patients should be recommended to impose more regular in-situ simulations to ensure the clinical team and equipment are always ready to deal with any aspect of ECMO, right from the cannulation phase (wherever it may take place) and ability to bring together all required resources, performing an emergency circuit change, right through to weaning off a patient from ECMO. Conclusion: There is a universal growing interest in various aspects and applications of simulation-based training. Simulation for the initiation and maintenance of ECMO provides several advantages over traditional passive learning approaches. ECMO simulation improves technical skills such as cannulation as well as non-technical skills that include, among others, effective communication, team working, decision making, and leadership skills. Appropriately designed simulation-based and educational ECMO interventions can alleviate staff anxiety with regard to new technology and equipment, and boost confidence in relation to crisis management. In future, advances in simulation technology will allow for increased realism and higher fidelity, and subsequently further enhance the clinical team learning experience.

Extracorporeal life support (ECLS) is the prototype example of translational research. It began in laboratory studies to design, test, and characterize devices for prolonged extracorporeal circulation in the 1960s. The first clinical cases of ECLS for heart and lung failure were in the 1970s. These cases were met with skepticism, but the results in neonatal respiratory failure were encouraging. In the early 1980s, two centers conducted randomized trials in neonates, which demonstrated much higher survival with ECLS, and the term extracorporeal membrane oxygenation (ECMO) was coined. By 1986, there were 18 neonatal ECMO centers and data on 700 cases. These centers formed a consortium (The Extracorporeal Life Support Organization: ELSO) to maintain the registry, define guidelines and techniques, provide education, and hold an annual meeting.

In the 1990s, these centers expanded indications to older children with lung and heart failure. ECMO management for post-operative cardiac failure became standard in major pediatric heart centers. A multi-center randomized trial in the UK demonstrated a major survival advantage to ECMO in neonates. A few centers continued to evaluate and improve ECMO and extracorporeal CO2 removal (ECCOR) in adults with 50–60% survival in uncontrolled case series. At the ELSO meeting in 1999, a group met to plan a randomized trial in adult respiratory failure (ARDS). That study was carried out in the UK from 2002 to 2006 (the CESAR trial) using the same study design as the neonatal trial. The results were similar to the neonatal trial but adult intensivists were still skeptical, arguing that the single ECMO center in Leicester was just better at respiratory care than the other non-ECMO centers.

During all this time, we used modified pumps, oxygenators, and other equipment designed for cardiac surgery. A new medical profession of “ECMO specialist” developed to manage the ECMO system and patient. The number of specialists determined the number of ECMO cases that could be treated. Around 2008, a few companies made major improvements in these devices and manufactured specific ECMO machines. These machines were much safer, simpler, and reliable than the early ECMO equipment, and patients could be managed for weeks, primarily by the bedside ICU nurse with support from the specialist. This new equipment came along at the same time as the H1N1 flu pandemic of 2008–2009. ECMO was remarkably successful in saving the sickest patients, and adult intensivists scrambled to learn the technology. This was born out by two matched-pairs trials. ECMO for ARDS (acute respiratory disease syndrome) grew rapidly in adult intensive care units (ICU). The use of awake ambulatory ECMO as a bridge to lung transplantation has been expanded to all ECMO patients, in fact, to all ICU patients.¹

Currently, ECMO is used for severe heart and lung failure in all ages. Research is focused on improving anticoagulation and devices, defining indications, and new applications like septic shock, ECPR for cardiac arrest, and EDCD to salvage organs for transplantation. Laboratory research has continued as clinical practice proceeded, and it currently includes an artificial placenta for very premature infants and four versions of implantable, wearable lungs for chronic support.²

The South and West Asia Chapter of Extracorporeal Life Support Organisation (SWAC ELSO) was established in the year 2013 with the combined efforts of senior members from the ELSO and the ECMO society of India.¹ It was established with the idea of improving the awareness and practice of ECMO in this part of the world. I am pleased to see the growth of the organisation in the next couple of years. This region is representative of the member countries from the SAARC (South Asian Association for Regional Cooperation) and Gulf region. In 2016, South Africa joined the chapter.

The population of the SWAC ELSO region is 2.56 billion, which is one-third of the world's population.² South Asia, West Asia and Africa are unique with respect to the challenges offered to the healthcare delivery. There are wide variations in the economic potential of the countries. Healthcare inequalities do exist. ECMO is an intervention which is likely to bring the patient back to life in reversible cases of cardiorespiratory failure, when it is initiated at the right time. It does not come free of cost. Optimisation of the healthcare cost remains a priority. More efforts need to be put in this direction of developing a cost-effective model of ECMO.

Though I appreciate the way ECLS is provided in much of the developed world, there must be innovative ways to practice the science with the same principles in the resource-limited countries. Quality is very important and must be maintained. Collectively, similar-minded individuals with entrepreneurship should be able to develop a model of ECMO for resource-limited parts of the world. Infection is a main deterrent in achieving the optimal results globally.³ By adopting antibiotic stewardship principles and self-governance, infection can be brought under control. We do not need new antibiotics to achieve this goal.

The indications for ECMO have been varying in this part of the world. Though ARDS (adult respiratory distress syndrome) secondary to viral and bacterial pneumonias remains the predominant cause⁴ to seek support from ECMO, myocarditis due to scorpion stings, snake bites, supporting patients post poisoning like organo-phosphorous poisoning, celphos poisoning and exposure to various other poisons are some of the other examples. ARDS secondary to malaria, tuberculosis and other newer varieties of viral pneumonias (SARS, H1NI, H5N1, Dengue, etc.) offers exciting opportunities for application of this life-saving modality. Controlling drug-resistant infections is a major challenge and a priority. There are other challenges like lack of ideal transport facilities to cover long distances effectively. Cardiac ECMO as extended cardiopulmonary bypass is practised much more widely than respiratory ECMO.

The past has seen the development and standardisation of ECMO. We have been seeing the implications for solving the healthcare needs of mankind using ECLS (extracorporeal life support). With united efforts and mutual co-operation, we should make progress and help each other in unleashing the obstacles preventing the growth potential of ECLS. Life is a God-given gift. Let us join hands and save more lives. Let us show the unity in diversity.

The clarion call for setting up a Qatar adult extracorporeal membrane oxygenation (ECMO) program came during the MERS-CoV outbreak in the Arabian Peninsula region.¹ This carried a high mortality rate in those presenting with severe respiratory failure, and recent data from the “CESAR Trial” showed that treatment in a severe respiratory failure center with ECMO capabilities improved severe respiratory failure (SRF) patient survival.²

Owing to the regional novelty of the program, potential partners of external well-established ECMO programs were sought. The model of care hinged on medical versus surgical ECMO delivery. The balance tipped in favor of a medical model in view of the prevailing nature of the pandemic outbreak at the time. There is plenty of evidence demonstrating that the intensivist-led ECMO cannulation model is safe.³ The commissioning body also favored the notion of a severe respiratory failure outreach and retrieval service, delivered round-the-clock with the provision of on-site cannulation for ECMO and transportation thereafter.^4,5 In early 2013, an ECMO partnership with a UK-based academic healthcare system was established with the view to train and initially mirror the UK-based ECMO program with subsequent tailoring and localization to fit the local need in Qatar. Team members were chosen locally, who were physicians, nurses, perfusionists, respiratory therapists, nutritionists, pharmacists, physiotherapists, and critical care paramedics.⁶ These underwent ECMO (VV modality) simulation and hands-on training in London as well as cadaveric cannulation training in Berlin, Germany. After extensive training abroad, the team members returned to Qatar where further training through simulation was carried out.⁷ This was supervised and signed off by the UK-based ECMO center. In April 2014, the first case qualifying for ECMO due to severe respiratory failure was treated at the Hamad Medical Corporation (HMC) ECMO center. Through the rest of 2014, the center was treating one patient per month. The survival rate was 100%. The first ECMO retrieval occurred in October 2014. This was carried with no recorded incidents. The year 2015 saw ECMO team size expansion and consolidation through in-house simulation courses and the HMC ECMO center joining ELSO. By the end of 2015, the center had treated 25 patients with a recorded survival rate of 70%. The year 2016 witnessed the introduction of VA ECMO modality, and the first aeromedical ECMO transfer occurred in June that year. Towards the end of 2016, the center began an ECMO fellowship program and registered its participation in multicenter ECMO trials. By the end of 2016, the center had carried out 50 runs of ECMO, with 10 patients dying while on ECMO (20% mortality). The ECMO patient survival to ICU discharge was 70% and to hospital survival was 68%. The future direction of the HMC ECMO program is to play a role of an adult regional center of excellence with not only land,⁸ but also aeromedical transport capability, and to consolidate on ECMO education and training, through simulation courses, for both static and transport modalities.⁷ Other future directions are, through local partnership, build on pediatric and cardiac ECMO, to introduce neonatal ECMO programs.

Rationale: Transport of critically ill patients on extracorporeal membrane oxygenation (ECMO) can be challenging; however, this has been demonstrated to be safe and feasible if undertaken by adequately trained teams,^1–3 with appropriate equipment and a platform that can accommodate the team and allows full access to the patient.

The ECMO retrieval service is a key component of the severe respiratory failure (SRF-ECMO) program. The Hamad Medical Corporation (HMC) stakeholders realized the need for this “mobile” program as core to the ECMO program, given the geographical location of the hospital facilities and the complexity of the ECMO program.

The development of mobile ECMO is built on the established multidisciplinary Safe High Acuity Adult Retrieval Program (SHAARP) partnership between the HMC Ambulance Service and Medical Intensive Care Unit (MICU). The service operates on a Hub and Spoke model, whereby patients requiring ECMO are transferred to the MICU ECMO Centre at Hamad General Hospital (HGH). The major factor that influenced the initiation of the mobile ECMO program was the need for a secure and competent transport system to the only Adult ECMO Centre in Qatar with the necessary infrastructure and expertise to handle such complex cases. Mobile ECMO team: The need for a multidisciplinary, team-based approach to ECMO retrieval and transport was realized early due to the fact that the transport of these high acuity cases needed dedicated expertise. Our team model in Qatar is composed of two ECMO consultants, an ECMO nurse, a perfusionist, a respiratory therapist, and a critical care paramedic from the Ambulance Service, and is also supported by two ambulance paramedics (driver and attendant).

Transport of ECMO patients is a low volume high-risk event and hence there is a need for a specialized team. All team members received training and participated in retrievals in the UK on mobile ECMO. There is an ongoing training program,⁴ covering emergencies and techniques for safe movement of patients. The team dedication has resulted in the program being a success. To date, 13 retrievals have been successfully carried out including one intercontinental air-transfer, all without adverse outcomes. Mobile ECMO logistics: The mobile ECMO platform and trolley were custom designed. There was a recognition that a mobile SRF-ECMO service may require the team to transport a patient on ECMO, or to first stabilize on current therapy and then transport the patient to the acute care hospital to perform cannulation at a later time; if required.

As such, the adult Intensive Care Trolleys have been designed to provide ergonomic, safe, and comfortable transportation of high dependency intensive care patients, either on ECMO or on standard intensive care therapy. It is configured to meet the specific needs of the clinical team and designed to accommodate a wide range of medical apparatus. This stretcher carries all the basic intensive care monitoring accoutrements and is suited for pre-hospital, and inter- and intra-hospital transit care. The stretcher can hold a transport ventilator, monitor, infusion pumps, oxygen cylinders, a medication bag, and a miscellaneous pack. The mobile intensive care unit can safely accommodate the whole five-person team and specialized equipment in an appropriate working environment, with 360-degree access to the patient and equipment, in addition to the two paramedic crew driving the vehicle.

Quality and patient safety are core elements of a successful extracorporeal membrane oxygenation (ECMO) program. Patient survival, patient safety, and quality of life were the main considerations when establishing an ECMO service in Qatar, with the alternatives being death from refractory hypoxemia or permanent lung fibrosis and reduced quality of life as a result of harmful ventilation. The program strives to achieve these goals through a systematic, evidence-based, and structured program that does not use shortcuts, and integrates and provides high quality of care to improve survival rates among critically ill patients.

There is strong clinical evidence supporting the use of ECMO as a lifesaving procedure in critical patients, as it provides a viable alternative for patients with certain conditions that previously had high mortality rates.¹ This leads us to define one of our objectives as improving our patients' outcome, while avoiding needless harm through the introduction of this service. Our objective was to establish an evidence-based but locally relevant structure for an ECMO center of excellence in the region, learning from other centers' experiences through strategic partnerships.² The development involved an appropriately structured and staged education and training program for our staff to develop the required knowledge and skills and understanding the challenges associated with ECMO. We defined each team members' functions, roles, and responsibilities and established effective communication processes, thus inculcating a change to a collaborative culture of multi-professional teamwork. To ensure the best delivery of the service, we have ongoing support from experienced regional centers with high patient volumes, and focused and trained multidisciplinary teams, helping to positively impact patient outcomes in complex cases.

To ensure the maintenance of quality, our center believes that collecting accurate ECMO data in a timely manner is essential to track the progress, improve the logistics, report the metrics, and link them to international registries for benchmarking, sharing experience, and evaluating our performance. We use debriefing sessions, demonstrated as an effective reflective tool in simulation-based education,³ in our program's different daily activities to enhance the culture of our multidisciplinary teamwork. The success and program outcome is made and measured here, as everyone is accountable and contributes to analyzing the available data of our patients. The team reviews the structure, processes, and outcome using the quality tools of plan–do–study–act, root-cause analysis, process mapping, etc. Clear tasks and assignments are distributed and SMART goals are set.⁴ Crisis Resource Management (CRM) is another valuable component in developing and maintaining a quality service in the ECMO program, and empowerment of the team to ensure expectations are met through effective communication, involvement, skill enhancement, professional development, recredentialing, and setting the standards.⁵ Our center invests in developing and running simulation-based workshops and training sessions that provide additional learning opportunities beyond the traditional quality improvement tools.⁶

In conclusion, it needs a persistent effort to maintain a quality ECMO program, with clear objectives, quality standards, ongoing training, and good communication as important elements for success.

Introduction: Acute severe respiratory failure poses a major treatment challenge which stubbornly carries high mortality and morbidity rates. Here, we review PaO2/FiO2 (PF) ratio and disease severity, and discuss protective lung ventilation and the rescue therapies, and when to use what? PF ratio alone is not sufficient to determine disease severity: A recent study by Villar and colleagues demonstrated that only 38% of patients who were classified as severe acute respiratory disease syndrome (ARDS) patients based on the PF ratio met the actual severe ARDS criteria after a standardized ventilator setting. In a recent trial conducted by Caironi¹ and colleagues, alteration in the positive end-expiratory pressure (PEEP) level affected the PF ratio and disease severity. Using the PF ratio alone as the major determinant for disease severity will increase the risk of selecting the wrong therapy for the patient. Protective lung ventilation: Between 1998 and 2000, two prospective randomized controlled trials (RCT's) showed that lower tidal volumes (VT) decrease mortality compared with higher VT.^2,3 Retrospectively, plateau pressure (pPlat) <  32 cmH2O was the major difference between survival and non-survival, hence VT 4–6 mL/kg of predicted body weight (PBW) and pPlat <  30 cmH2O became the standard of care.

Several papers challenged the pPlat value of 30; in 2005, Hager⁴ and colleagues could not identify a safe upper limit for plateau pressures in patients with ARDS. Moreover, VT reduction would have improved the outcome, even in patients who already had pPlat <  30 cmH2O. More recently, Amato⁵ and colleagues demonstrated that driving pressure was the ventilation variable that best stratified risk independently of concomitant variations in PEEP and plateau pressure. This was supported by another retrospective study on ECMO patients by Serpa et al.⁶ That opened the question: “What is protective lung ventilation?” Rescue therapies: The two proven rescue therapies to date are: “Prone Position” and “ECMO”.

Prone Position enhances lung recruitment in a potentially recruitable lung by various mechanisms, releasing the diaphragm, decreasing the effect of heart and lung weight and shape on lung tissue, decreasing the lung compression by the abdomen, and releasing the lower lobes, which improves gas exchange and decreases mortality in severe ARDS patients.

ECMO provides extracorporeal gas exchange with no effect on lung recruitment. It affords lung rest and works well for the non-recruitable lung. It has been shown to improve survival for certain groups of patients in high-performance ECMO centers.⁷

It is important to note that the delay in utilizing such rescue therapies worsen the outcome. Discussion: PF ratio combined with standardized ventilator setting is superior to PF ratio alone to determine disease severity. This is essential to determine the correct therapy for the right patient. Lung protective ventilation strategy remains the corner stone for decreasing morbidity and mortality in ARDS patients. However, the lung protective concept may require to be tailored to disease severity; pPlat of 30 cmH2O might be safe for a patient with moderate ARDS but may be deleterious in the severe ARDS patient. Moreover, the driving pressure as the safety guard needs to be explored in more RCTs. Clear definition of “Failure of conventional ventilation” needs to be agreed upon and a clear pathway for trial of prone ventilation versus directly initiating ECMO therapy needs to be defined.

The extracorporeal membrane oxygenation (ECMO) cannulae can be safely inserted into the jugular and femoral regions using a percutaneous dilation technique or by open surgical cannulation. Percutaneous dilation that avoids skin cutting can achieve a tight seal between skin, vessels and cannulae. This avoids bleeding associated with surgical dissection and limits tissue damage. Surgical dissection is also associated with additional risks of wound breakdown and seroma formation in critically ill patients (particularly those requiring long-term immunosuppression). Non-surgical cannulation also offers the advantage of avoiding the need for additional patient transfer to the operating theatre. Moreover, it has been safely performed in a variety of settings, without affecting surgical workflow. Percutaneous cannulation can be performed by a broad range of hospital medical specialists and obviates the need for surgical attendance in time critical settings. Non-surgical cannulation for both veno-arterial and veno-venous ECMO is well established in many experienced ECMO centres and is an entrenched practice.^1,2

Risks associated with “blind” percutaneous cannulation can be greatly reduced with the use of real-time vascular ultrasound, which is now commonplace in modern intensive care and anaesthetic settings. In conjunction with real-time echocardiography, complete visualisation of guide-wire and cannula insertion is possible. Other radiological support can also increase the safety of percutaneous insertion.

Technical training and skill acquisition is required for safe percutaneous cannulation with ultrasound. It should not be performed by those without training and credentialing. Direct visualisation of the vessel does not remove the risks of serious complications from ECMO cannulation.

Utility of ultrasound in ECMO cannulation include:

• Anatomical assessment of the target vessel and cannulation planning. This includes the detection of intravascular thrombosis prior to cannulation as well as the detection of peripheral vascular disease;

• Real-time needle localisation facilitates accurate needle insertion, which reduces the risks of inadvertent sapheno-femoral junction venous cannulation and inadvertent profunda femoris artery injury (femoral artery cannulation), and ultrasound assessment of guidewire placement allows confirmation of position prior to dilation;

• Optimal siting of venous cannulae tips;

• Detection and avoidance of cardiac abnormalities – particularly involving the right atrium such as Chiari network or prominent, remnant eustachian and thebesian valves which can have an impact on correct siting of access cannulae.

Surgical cannulation is required for subclavian arterial return ECMO configurations and central ECMO configurations. Central cannulation should not be used unless adequate support cannot be achieved by peripheral cannulation due to the very high rates of bleeding and serious complications.

Surgical repair is also standardly required for vascular repair following the removal of an arterial ECMO cannula.

Ideally patients should have access to timely ECMO support and should have their configuration modified to best meet their needs when required. Thus, access to timely non-surgical cannulation and recourse to surgical cannulation for specific needs is the optimal model of care.

Temporary mechanical cardiopulmonary support may be used intraoperatively to facilitate cardiac surgery. Over the past decade, this intervention has been extended for prolonged use in the intensive care unit (ICU) as extracorporeal membrane oxygenation (ECMO).¹

Two types of ECMO exist in clinical practice: veno-arterial (VA) and veno-venous (VV). VV ECMO provides support to the pulmonary system by extracting blood from the right atrium, oxygenating it and returning it to the right atrium, where the patient remains dependent on their own circulation. In VA ECMO, blood is extracted from the right atrium and returned to the arterial system, bypassing the heart and lungs, which provides both respiratory and hemodynamic support.²

Patients who require ECMO support receive anticoagulation with heparin³ before the cannulas are inserted, either in the right jugular area or in the left/right femoral area(s). In VV ECMO, blood is drained from the venous cannula placed typically in the inferior vena cava (IVC), and returned through a cannula with its tip at close proximity of the right atrium, either through the femoral vein or through the right internal jugular vein. In VA ECMO, blood is drained from the IVC and returned through right femoral artery or the aorta to the systemic cannulation.²

ECMO support is initiated when the patient is connected to the ECMO circuit. The deoxygenated blood will be withdrawn from the patient through the access line under negative pressure (usually created by a centrifugal pump) entering the oxygenator (artificial lung membrane), where gas exchange occurs. Blood is then returned back to the patient through the return line.⁴ Oxygenated Flow on ECMO machine is controlled across the hollow fiber membrane. The blood flows outside of the fibers and the gas flows through the fibers in a counter current flow pattern. The non-direct contact between blood and gas reduces blood trauma. The gas exchange occurs through diffusion due to the concentration gradient between O2 and CO2. Oxygenated blood is then returned back to the patient through the return line.⁴

Pressures within an ECMO circuit are highly important and need to be understood (access, pre-membrane, and post-membrane pressures) to quickly identify potential issues. The transmembrane pressure (TMP) is the difference between the pre- and post-membrane pressures. The TMP baseline should be monitored when ECMO is initiated and be compared with the TMP trend during the ECMO run, as it reflects the function of the circuit membrane. The membrane acts as the blood oxygenator and should be regularly checked for clots.

The patient oxygen saturation, temperature, hemoglobin, sedation, preload, and afterload will be continuously monitored. FiO2 and sweep gas flow is adjusted according to pre- and post-membrane blood gases.

Anticoagulation is sustained while the patient is on ECMO and it is monitored through the activated clotting time (ACT). ACT of 180–210 seconds or APTT of 35–45 seconds are accepted.³ The use of Bioline coating on the internal circuit surfaces improves biocompatibility of extracorporeal circulation system devices: oxygenators, cannulas, connectors, centrifugal pumps, and tubes by mimicking human tissue.

It is highly important to understand the possible complications that may occur while patients are on ECMO, whether it is patient related (bleeding, thromboembolism, etc.) or ECMO circuit related.¹ Therefore, all safety devices within an ECMO machine and circuit should be connected properly, functioning well, and checked continuously until the patient is weaned from ECMO.⁴

The use of venovenous extracorporeal membrane oxygenation (VV-ECMO) for severe acute respiratory failure (ARF) has considerably increased worldwide. Therefore, extracorporeal membrane oxygenation (ECMO) teams called for practical guidelines with clear objectives on how to manage ECMO on daily basis.¹ All classical topics of intensive care management have been put in perspective with the use of ECMO, opening multiple areas of research. Good teamwork is the central pillar of any ECMO program.

After starting an ECMO run, the medical team has to deal with a triangle including the patient, the ECMO machine, and their interaction. This unique interdependence makes the management challenging, as any change occurring on one side (patient or ECMO) will affect the other side. The priority is to diagnose and treat the cause of ARF. Bronchoscopy showed a reasonable safety for diagnostic yield and clearing airways. The optimization of the oxygen delivery is primordial within the acute period and is represented by matching the ECMO flow and the cardiac output, maintaining an adapted level of hemoglobin, and decreasing causes of high oxygen consumption.² The management of volume status is essential for keeping a precise balance between the patient and the machine.

Echocardiography is an essential tool that provides much information before cannulation on hemodynamic, access insufficiency once the patient is on ECMO, initial cannula positioning or readjustment, and finally tolerance to ECMO weaning before and after decannulation.³

Once ECMO provides adequate oxygenation delivery for the patient, the different parameters of mechanical ventilation have to be readjusted with an actual trend to decrease most of them: FiO2 (25%), inspiratory pressure (10 cm H2O), and respiratory rate (10 cycles/min) that results in ultra-protective lung ventilation with an expected tidal volume in a range of 1–3 ml/kg.⁴ More than knowing the “best” positive end expiratory pressure, a low driving pressure less than 1 cm H2O has to be targeted.⁵ This is to ensure that the lungs can rest and recover over time. The exact duration required to reach these settings to allow an improvement on oxygenation is unpredictable. The weaning process is challenging as the gas exchange function improvement and the lung compliance recovery are sometimes not concomitant. It requires daily monitoring to allow early extubation while on ECMO. The anticoagulation has to be balanced not only to avoid any clots in the circuit when just connected, but also to avoid any bleeding.

Analgesia and sedation are important for the initial oxygen consumption after cannulation and have to be minimized from the second day to the third day. The goal is for the patient to receive sufficient oxygenation without pain. Depending on their tolerance, patients will sometimes be awake while on ECMO. Then, an active physiotherapy (PT) program including mobilization, sitting on the edge of the bed, standing up, and walking should follow the passive PT started from the first day on ECMO. Acute renal failure is common during ECMO and should be prevented and treated with renal replacement therapy. Many other points including nutritional support and nosocomial infection prevention are specifically integrated in the patient management.

In summary, the management strategies on VV-ECMO are complex and require to master critical care and ECMO knowledge combined with a strong collaborative multidisciplinary environment. The goal is to wean patients from ECMO as soon as clinical parameters permit it while avoiding ECMO-related complications.

Introduction: Echocardiography (ECHO) plays a fundamental role in the management of patients supported with extracorporeal membrane oxygenation (ECMO).¹ It is particularly useful for the detection of cardiac complications that may arise during ECMO. It helps in many ways during the ECMO run, as presented in Table 1.

ECHO helps to identify or exclude new reversible pathology, which could be the actual cause of patient hemodynamic deterioration (cardiac tamponade/undiagnosed valvular lesions and left ventricular (LV) dysfunction), thus avoiding the need for ECMO support. It also helps to provide information about contraindications, for example aortic dissection. Identification of significant aortic regurgitation (AR) is a relative contraindication in veno-arterial (VA) ECMO, in which the LV afterload is increased, leading to a further increase in AR. It also provides information on aortic atherosclerosis, thus guiding the intensivist in deciding the cannulation sites (central versus peripheral) or the technique (surgical versus percutaneous). ECHO also helps to evaluate the right heart morphology for any structural abnormality, which could impede the positioning of venous cannula for veno-venous (VV) ECMO or VA ECMO. ECHO aids in diagnosing complications during ECMO: The diagnosis of upper limb hyperperfusion relies heavily on clinical features, with imaging utilized more to determine etiology. Transthoracic echocardiography (TTE) may add incremental value to the diagnosis of arterial upper limb hyperperfusion during ECMO support with an axillary artery, and it can be easily and quickly performed at the bedside.²

ECHO has a crucial role during ECMO cannulation as it guides the correct placement of the ECMO cannulas. TTE may not have the adequate spatial resolution to guide ECMO cannulation, and therefore transesophageal echocardiography (TEE) is essential. There should be a direct communication between the operator and the echocardiologist as to the site of the indented cannula insertion. For example, in VV ECMO, when one cannula is used for access and another to return the blood, the position of the access cannula tip is in the proximal inferior vena cava (IVC), just before the entry into the right atrium (RA). On the other hand, the optimal position for the return cannula is in the mid-RA, but well clear from the interatrial septum and the tricuspid valve. This can be determined with ECHO.

ECHO is critical in the detection and management of specific complications that may arise during ECMO support. Because TTE has limited spatial resolution, TEE is usually used to detect these complications. ECHO enables rapid assessment of cannula positioning, cardiac filling, cardiac function, and evidence of chamber compression from tamponade. The detection of cardiac tamponade and the assessment of the significance of pericardial effusion or collection can be difficult in patients supported with ECMO as the heart is in a partially bypassed state.

Complications in any part of the ECMO circuit can be well seen on ECHO as well as thrombosis on 2D or 3D ECHO. Conclusion: ECHO is mandatory during the initiation of ECMO, cannula insertion, hemodynamic monitoring, and detection of complications during weaning.

Extracorporeal membrane oxygenation (ECMO) is used to support patients with hypoxemia due to severe respiratory failure. Hypoxemia can persist during ECMO as a result of reduction in mechanical ventilatory support as part of a lung protective strategy, following which gas exchange provided by the native lungs is reduced or absent. If tissue oxygen delivery is maintained, mild to moderate hypoxemia will be well tolerated, but if tissue hypoxia develops, then the cause of hypoxemia must be addressed and corrected.

Patterns of hypoxemia are dependent on the mode of ECMO support. During veno-venous support for respiratory failure, hypoxemia is global, with all tissues receiving hypoxemic blood. When femoral veno-arterial support is used in the presence of respiratory failure, then differential hypoxemia can result, with hypoxemia limited to the upper part of the body. The approach to hypoxemia is dependent on whether veno-venous (VV) or veno-arterial (VA) ECMO is used.

Adequate oxygen saturation on VV ECMO requires adequate hemoglobin, a membrane lung operating below its rated flow, low recirculation, and extracorporeal circuit flow that captures most of the cardiac output. The approach to hypoxemia during VV ECMO includes addressing each of these. Identifying and limiting recirculation will improve effective extracorporeal flow. Anemia has two detrimental effects. First, it limits oxygen transfer through the membrane lung. Second, it increases oxygen extraction resulting in low mixed venous oxygen saturation that increases the effective venous admixture with circuit blood. Transfusion to near normal levels will help improve oxygen saturation. Increasing effective extracorporeal flow to capture at least 60% of the cardiac output is necessary.¹ If the extracorporeal flow fraction is less than 60% due to an increased cardiac output, then reducing cardiac output through reducing exogenous catecholamines, use of beta blockade,² or hypothermia³ will help improve the extracorporeal flow fraction. Hypothermia has the added benefit of reducing oxygen consumption and therefore improving mixed venous saturation. A final option is to leverage the native lungs, such as through prone positioning, as long as lung protective strategies can be maintained.⁴

Oxygen saturation on femoral VA ECMO is typically normal (>90%). The upper part of the body is provided with blood from the left ventricle that has been saturated by normally functioning lungs. The lower part of the body is provided with fully saturated blood from the extracorporeal circuit. The two circulations meet at some point in the aorta that depends on the relative magnitude of flow rate in these two circulations. If there is pulmonary dysfunction, then the blood ejected by the left ventricle will be hypoxemic, and tissues perfused proximal to the mixing point will be perfused with hypoxemic blood, while the lower body will have a normal saturation. Management of this differential hypoxemia is through improvement of pulmonary gas exchange if possible, increasing extracorporeal flow to decrease pulmonary blood flow, or conversion of VA ECMO to VVA (hybrid veno-arterial and veno-venous).

The prone position has been used successfully for many years to improve oxygenation in patients who require mechanical ventilatory support for management of acute respiratory distress syndrome (ARDS). Proning improves oxygenation by optimizing lung recruitment and ventilation–perfusion matching. The following improved outcomes have been shown: when the prone position is used for moderate to severe ARDS; when used in combination with protective lung ventilation; and when the duration of the proning session is >16 h.¹ However, proning is not without contraindications and complications.² There are only two absolute contraindications to proning, which are suspected raised intracranial pressure and spinal instability. Some high-risk relative contraindications that may preclude proning include: recent sternotomy, facial surgery, and severe haemodynamic instability. Other relative contraindications include an open abdomen, pregnancy, and multiple traumas with unstable fractures. Respiratory ECMO is not a contraindication to proning. The risk of proning needs to be weighed against the potential lifesaving benefits of proning. The Extracorporeal Life Support Organisation (ELSO) guidelines for adult respiratory failure recommend the consideration of introducing prone positioning therapy to patients receiving ECMO, if there is posterior consolidation of the lung fields with some lung fields open anteriorly. The guidelines recommend exercising caution to prevent the dislodgement of the ECMO cannulas.³ Expert nursing care can prevent most complications occurring. Complications associated with the mechanics of proning include transient desaturation, haemodynamic instability, accidental extubation, and central lines displacement. Other complications that can occur during proning include the development of pressure ulcers, vomiting, the need for increased sedation ±  paralysis, nerve damage, and bleeding from ECMO cannula sites. To reduce the risk of potential complications, trained critical care staff, strict protocols, and procedures for the implementation of proning, including the mechanics of the proning procedure itself together with the care of the patient and circuit whilst the patient is proned, must be implemented. An experienced team of critical care staff who routinely use this intervention and who are familiar with the procedure are required to facilitate the mechanics of the proning process and the ongoing management of the patient to ensure the safety of both the patient and the ECMO circuit. There is no standard method for moving a patient from supine to the prone position. Most centres that prone adult patients use a “double sheet rolling” technique, whereby the patient is securely wrapped between two sheets and then manually turned from the supine to prone position through careful team coordination.³ Commercially available beds are also available which can initiate, maintain, and facilitate prone positioning. The recommended minimum number of staff required to safely prone an adult patient are five members of staff, six if the patient is on ECMO (four to prone, one to manage the airway, and one to manage the ECMO circuit), although ideally there should be seven members of the team, eight if the patient is on ECMO (six to prone, one to manage the airway, and one to manage the ECMO circuit) (local guidance GSTT).

Introduction: Extracorporeal circulation has been around for more than half a century, but many questions remain regarding how to best achieve anticoagulation in a patient on extracorporeal membrane oxygenation (ECMO). Although unfractionated heparin is the predominant agent used for cardiopulmonary bypass, the amount required and how best to monitor its effects are still unresolved. Extracorporeal circulation is associated with the activation of clotting cascade upon contact with a foreign surface of the ECMO circuit; therefore, heparin or a heparin-bonded circuit is used for anticoagulation. Objectives: To describe commonly used tests to monitor anticoagulation status and ways to maintain a clot-free circuit with least damage to circulating platelets. Methods: A literature search was conducted on PubMed for articles published in peer-reviewed medical journals in English in the past 10 years. Results: Various evidence-based facts emerged. Upon initiation of ECMO flow, there is a strong inflammatory response almost similar to systemic inflammatory response syndrome (SIRS) with the release of various cytokine mediators such as interleukins and tumor necrosis factor as well as a trigger to arachidonic acid metabolism with the release of prostaglandins and destruction of platelets.¹ Monitoring of anticoagulation status requires close monitoring of activated clotting times (ACTs), a close watch of platelet count, looking for evidence of heparin-induced thrombocytopenia (HIT), and finally, greater use of thromboelastogram (TEG) for precise analysis of coagulation status (Figs. 1 and 2). The ECMO circuit needs to be physically monitored (lines, pump head, oxygenator) for any clots as well as the values of the pre- and post-membrane pressures to detect clots in the membrane oxygenator. In view of a higher duration of ECMO run when compared with cardiopulmonary bypass, it is particularly challenging to achieve an optimal anticoagulation keeping in mind inflammation, disseminated intravascular coagulation, as well as side effects such as HIT.² Treatment of bleeding/clotting emergencies involves early detection and use of anticoagulation reversal agents with or without transfusion of blood or blood products with full round-the-clock support by blood bank. Although heparin-coated circuits have been safely used for extracorporeal lung assist with little or no systemic anticoagulation,³ prospective studies are clearly needed to determine whether this approach is advantageous, and it would seem appropriate to develop heparin coating for silicone-based membrane oxygenators.Figure 1.  TEG report on clot characteristics (http://marylandccproject.org/core-content/utility-teg-blood-component-therapy/).

Figure 2.  Interpretation of thromboelastogram.⁴

Conclusion: Various tests are available to monitor the anticoagulation status of a patient on ECMO with bedside availability. It is important to perform physical inspection of the ECMO circuit as well as to monitor pre- and post-membrane pressures frequently, in order to detect clots in the circuit, and to further regulate heparin therapy. Activated clotting time (ACT) by far remains the most commonly used monitoring tool at most ECMO centers.

Bleeding is a common complication in patients undergoing extracorporeal membrane oxygenation (ECMO) management.¹ It requires immediate management to achieve hemostasis, replace blood, and compensate volume loss. Refractory hemorrhage can be lethal and can lead to massive transfusions with all their known complications. Refractory bleeding and massive transfusions in ECMO patients are associated with high mortality even after decannulation. Management of bleeding in ECMO patients requires thorough evaluation with multi-disciplinary approach that addresses surgical causes of bleeding, correction of coagulopathy, and the balanced use of anticoagulation factors to prevent circuit clotting, avoid excessive bleeding, and replace different blood products as needed. Adjusting anticoagulants and the use of fresh frozen plasma (FFP) with correction of thrombocytopenia can control common bleeding events. Management of refractory hemorrhage may require exploration for surgical bleeding and administration of platelets, packed red blood cells (pRBCs), cryoprecipitate, anti-fibrinolytics, and selective coagulation factors. In some cases, however, the bleeding is diffuse and cannot be controlled surgically. The use of activated factor VII (rFVIIa) at different described doses for patients on ECMO with refractory bleeding has been tried.^2,3 There are many reports indicating successful use with live-saving outcome.³ Unfortunately, there are also some conflicting results with the use of rFVIIa regarding failure to control bleeding or the risk of intravascular thrombosis or circuit clotting. Furthermore, there are reports about catastrophic outcome or fatal thrombosis when rFVIIa was used in ECMO cases.⁴ Therefore, the medication is currently recommended as off-label prescription. It should be used with extreme caution with clear patient/family awareness about potential complications. The recommended doses are not established and range from 24 to 174 μg/kg.² Some centers will administer lower doses of rFVIIa (25–50 μg/kg) and, if more than one dose is required, it is not administered more often than every 2–4 hours. Some centers recommended the use of prothrombin complex concentrate (PCC), which contains unactivated factors II, VII, IX, and X, and therefore, potentially have less risk of thrombosis. To correct a prolonged prothrombin time (PT) and activated partial thromboplastin time (APTT) during ECMO run in patients with active bleeding, PCC 25-50 international units/kg can be administered.⁵

In summary, bleeding during ECMO remains a serious problem, which increases mortality risk. rFVIIa has been used successfully but with awareness of the risk of thrombosis. Clinical trials comparing alternative anticoagulation regiments are needed to determine efficacy, dosing, and safety of rFVIIa in patients suffering from refractory bleeding while on ECMO. Unfortunately, until such evidence is available, the ECMO care team is left with few evidence-based interventions to prevent and treat serious bleeding.

This presentation will discuss the use of rFVIIa in ECMO patients with focus on its benefits in controlling refractory bleeding, and the risk of thrombosis and circuit clotting associated with it. The discussion will include suggestions for recommended doses, how to monitor for thrombosis, and the potential risk/benefit of using rFVIIa in the management of life-threatening bleeding in patients on ECMO.

The application of veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is becoming an increasingly frequent procedure in emergency medicine.¹ Correct appraisal of clinical conditions and patient selection are critical not only in terms of expected outcome, but also in terms of adequate temporary support configuration, optimization of resources, and organization of daily hospital activities, since inappropriate implant may remarkably impact all these aspects.

According to recent analysis of ECMO use in the USA,¹ VA-ECMO was most commonly applied in post-cardiac surgery candidates, however with a constant decline for the period from 2007 to 2011. Indeed, from 57% of the total ECMO cases, post-cardiotomy VA-ECMO went to 38%, but with a significant rise in cases of cardio-pulmonary failure (from 3.9 to 11.1%).¹ This situation is certainly further changing during the last 5 years as VA-ECMO in cardiogenic shock and cardiac arrest is becoming more popular. Cardiac arrest: Patient selection in this setting is rather variable. However, potential cardiac etiology (acute myocardial infarction – AMI) represents almost 50% of the causes, and witnessed cardiac arrest, immediate cardio-pulmonary resuscitation (CPR) by bystanders, adequate CPR (possibly with mechanical cardiac massage devices), and not prolonged time from cardiac arrest to ECMO application ( < 60 min) represent positive predictors in the setting of extracorporeal cardio-pulmonary resuscitation (ECPR).² Recent publications have shown that ECPR might achieve respectful outcome also in elderly patients.^3,4,5 Therefore, age should not disqualify potential candidates. Absence of severe acidosis and still acceptable end-tidal CO2 may represent additional elements for patient selection in this setting. Post-cardiotomy: ECMO results in this setting appear rather unsatisfactory with in-hospital survival below 30%.⁵ Prompt initiation of ECMO and avoiding unnecessary prolonged cardio-pulmonary bypass and metabolic as well as coagulation derangement are among the most relevant key factors. The absence of severe cardiac or co-morbidities prior to surgery and the expected temporary impairment of the cardio-respiratory systems represent additional indications for post-cardiotomy ECMO. Cardiogenic shock: This setting represents the most expanding field of ECMO application. Indications may derive from refractoriness of cardio-circulatory impairment to conventional therapies (drug and IABP). Moreover, in this setting, advanced age and severe co-morbidities may represent relative contraindications. Furthermore, in this field, the potential for cardiac recovery or the possibility to bridge the patient to other treatments, if recovery is considered unlikely, represents indication for ECMO use. Respiratory distress: VA-ECMO is generally indicated if right ventricular dysfunction is present or develops, and if VV-ECMO does not provide sufficient peripheral oxygenation. In the last case, hybrid configuration (VVA or VAV) might be more suitable and advisable. Uncommon indications: Sepsis, trauma (most often treated with VV-ECMO), fulminant myocarditis, Tako-Tsubo, or complicated interventional procedures (TAVI, PCI, balloon valvuloplasty) represent areas in which ECMO is increasingly applied.^6,7 Despite wider use in these settings, more clinical evidences are still needed to conclusively define patient selection criteria and ultimate benefits. Finally, a developing indication might be prophylactic VA-ECMO in critically ill patients undergoing either cardiac surgery or interventional cardiological procedures. In these patients, in whom post-procedural severely complicated course is expected, timely and pre-crash support may help to provide a smooth peri-procedural period. Short-time controlled support of cardio-circulatory system and peripheral organ perfusion, with avoidance of metabolic and hemodynamic derangement, may also affect emergency VA-ECMO implant should patient deterioration occur, and allow a better complicated patient management with better final outcome.

Veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is increasingly applied for the treatment of cardiogenic shock despite its high complication rate.¹ The lack of left ventricular unloading is one of the serious problems associated with the poor outcome of VA-ECMO. Therefore, hemodynamic management during VA-ECMO should address the higher afterload caused by the retrograde blood flow and the consequent left ventricular distension. In fact, the blood stasis can result in ventricle or pulmonary thrombosis. Moreover, a high end-diastolic pressure can cause pulmonary venous congestion and lung injury, as well as subendocardial malperfusion and consequently impair recovery.

Possible strategies to unload the left ventricle include inotropic support or intra-aortic balloon pump implantation, as described in 135 cases by Gass and colleagues.² Surgical left ventricle venting can be performed with the cannulation of the left atrium or the left ventricle although this strategy is highly invasive. Blade atrial septostomy or atrial septostomy and placement of a venting cannula are also described.^3,4

Our group recently described a new strategy employing Impella on top of VA-ECMO in a large series of patients, compared with VA-ECMO only.⁵ Impella device is a small heart pump that pulls blood from the left ventricle through an inlet area near the tip and expels blood from the catheter into the ascending aorta. The device was inserted percutaneously through the femoral artery into the ascending aorta, via the aortic valve into the left ventricle. In compliance with the Declaration of Helsinki and in agreement with Italian and German data protection laws, we retrospectively collected data on patients with severe refractory cardiogenic shock from two tertiary critical care referral centers and enrolled 157 patients (January 2013 to April 2015): 123 received VA-ECMO support and 34 had concomitant treatment with VA-ECMO and Impella implanted simultaneously. The decision for an additional implantation of Impella was undertaken as the attending physician recognized signs of echocardiographic, radiological, and clinical signs of impaired left ventricle unloading or left ventricle stasis (stone heart, pulmonary edema, impending clotting on the left ventricle, significant aortic regurgitation). Impella was left running at P8 speed in order to produce a forward flow of 2.0 L without complications. A propensity-matching analysis was performed in a 2:1 ratio, resulting in 42 patients undergoing VA-ECMO alone (control group) compared with 21 patients treated with VA-ECMO and Impella. Patients in the VA-ECMO and Impella group had significantly lower hospital mortality (47% vs. 80%, P <  0.001) and a higher rate of successful bridging to either recovery or further therapy (68% vs. 28%, P <  0.001) compared with VA-ECMO patients. Other results are presented in Table 1.

In conclusion, among different strategies to unload the left ventricle during VA-ECMO, Impella can be considered a feasible option. Nevertheless, randomized studies are warranted to validate this strategy.

The use of mechanical circulatory assistance remains controversial during refractory septic shock in adults.¹ However, a profound myocardial dysfunction can occur during bacterial septic shock.^2–4 In this context, extracorporeal membrane oxygenation (ECMO) is highly effective as salvage therapy for children with refractory septic shock.^5,6 We reported the largest cohort of adults who received VA-ECMO for refractory cardiovascular dysfunction in the context of severe bacterial septic shock.⁵ Despite multiorgan failure at ECMO initiation and simplified acute physiology score (SAPS) 3-predicted mortality of 79%, >70% of these patients survived with complete recovery of cardiac function. The hemodynamic profile we describe herein (low cardiac index, elevated filling pressure, profound myocardial depression, and elevated systemic vascular resistance) is certainly a rare entity in the spectrum of septic shock, which resembles that of the classic paradigm of cardiogenic shock. In this setting, the infusion of very high catecholamine doses used to increase cardiac output and maintain perfusion before ECMO initiation might have contributed to the vicious circle that led to vasoconstriction and refractory cardiovascular failure. Considering the reversibility of myocardial depression associated with septic shock,^7,8, we hypothesized that ECMO could help salvage these dying patients by restoring adequate perfusion to vital organs to reverse multiple organ failures and by buying time to achieve infection control by antibiotics. Indeed, all our survivors could be explanted without recourse to cardiac transplantation or switching to another cardiac assist device, and all recovered with a normal myocardial function within a few weeks. These results seem to be far better than those obtained with ECMO for cardiogenic shock, with reported survival rates around 40%, that required cardiac transplantation or switching to a LV (left ventricular) assist device for about 10% of the survivors.⁹ Considering these promising results, ECMO might be considered a valuable therapeutic option for patients with refractory cardiovascular dysfunction in the context of septic shock, although more data and larger patient cohorts are needed to confirm the findings presented herein. Ethical statement: In accordance with the ethical standards of our hospital's institutional review board, the Committee for the Protection of Human Subjects, informed consent for demographic, physiologic, and hospital-outcome data analyses was not obtained because this observational study did not modify existing diagnostic or therapeutic strategies. Survivors gave oral consent to participate in the telephone interview, conducted by the same investigator, who asked the questions in the questionnaire in the same order.

Background: Mortality of patients on extracorporeal membrane oxygenation (ECMO) remains high. Diagnosis of infection during extracorporeal life support (ECLS) is still challenging, and prevention strategies vary widely from center to center.^1–3 These facts led us to analyze the occurrence rate, site, and organism in our ECLS patients in order to implement infection control measures to reduce the incidence of infections during ECLS.⁴

Our objective was to analyze our Extracorporeal Life Support Organization (ELSO) registry center data specifically focused on incidence of infection, typical microorganisms, time of manifestation, and site of cultures in the settings of tertiary pediatric cardiac intensive care unit mainly utilizing transthoracic cannulation and VA-ECMO, and compare with the ELSO database.¹Methods: We conducted a retrospective study analyzing 25 neonatal and pediatric ECMO cases in relation to infection from January 2014 to December 2015, in comparison to the ELSO database age and modality specific data. We obtained ethical approval from our institution. We examined the prevalence of infection, the time of the first positive cultures, the site of the positive cultures, and the underlying microorganisms and compared with ELSO data whenever feasible. Results: There is no specific data on the incidence of infection in the ELSO database with open chest/transthoracic cannulation; our incidence was 0.44. The Candida species was the highest offending organism (24% vs. ELSO 12% concerning the entire ECMO population), followed by Klebsiella 20%, E. coli 16%, and Pseudomonas 12%. The first positive culture was taken on the 8th day of ECMO (median). By site, the highest prevalence of infection is as follows: ventilator-associated pneumonia (VAP), 41%, followed by bloodstream infection (BSI), 22%, and then catheter-associated urinary tract infection (CAUTI), 12%. Conclusions: The highest prevalence of Candida infections is most probably due to the combined antibiotic and steroid therapy for patients with capillary leak syndrome. This may prompt that routine antifungal prophylaxis can be added after 1 week of ECMO for this patient group. Alternatively, the early detection with fungal polymerase chain reaction (PCR) assay should be evaluated.⁵ The high occurrence of VAP may indicate the need of reinforcing enteral feeding, oral decontamination protocol along with VAP bundle, and investigation of alternative source of contamination. As Gram-negative Enterobacteriaceae and Pseudomonas were in second line as typical multidrug-resistant (MDR) organisms, those should be covered whenever a need for empiric antibiotic therapy arises.

Veno-arterial extracorporeal membrane oxygenation (ECMO) has been used successfully for several years in refractory cardiogenic shock. Of note, the survival rate is markedly affected by the underlying patient condition, and especially their capacity to recover. Combes et al.¹ demonstrated a short- and a long-term survival rate (11 months of median follow-up time) of, respectively, 42 and 36% in a large series of patients with cardiogenic shock of various origins, including fulminant myocarditis (30%), post-cardiotomy (24%), post-myocardial infarction (15%), and shock after heart transplantation (15%). In that study,¹ implantation during cardiopulmonary resuscitation (CPR) was associated with a marked increase in the risk of death (OR 20.68 (1.09–392.03)).

As the probability of achieving return to spontaneous circulation (ROSC) decreases rapidly when the duration of cardiopulmonary resuscitation CPR exceeds 10 min and dramatically after 30 min,² some clinicians questioned whether ECMO could also be used to restore flow in patients not responding to classical resuscitation procedures. Data of ECMO for out-of-hospital cardiac arrest (OHCA) or extracorporeal CPR (ECPR) are scarce and conflicting. Several case reports and small series suggested some benefits but these were subject to publication bias. The first large study of 51 patients with OHCA showed a very low survival rate, with only two survivors.³ Recently, some other teams reported more favorable outcomes. In 42 patients with OHCA, Kagawa et al.⁴ reported a 30-day survival of 24%, with a favorable neurological outcome of 21% in the group of OHCA patients who received intra-arrest percutaneous coronary intervention (PCI). One of the explanations for the variability of the results is the duration from cardiac arrest to ECMO initiation. Leguen et al.³ reported a 4% of survival with a time to ECMO of 120 min, while studies with more favorable outcomes reported a shorter time to ECMO (40 min [25–51]) in the trial by Kagawa et al.,⁴ and systematic implementation of intra-arrest PCI. Indeed, the difference in outcome between in-hospital and OHCA results depends more on the duration of cardiac arrest than on the location of the cardiac arrest itself.

Importantly, all series mentioned that selection of candidates for ECPR seems to be crucial, especially in the setting of OHCA: witnessed cardiac arrest, with a no-flow period < 5 min, whenever possible bystander CPR or a very rapid response team, a pre-hospital care policy prompting to alert a specialized hospital with an ECMO team, and rapid transport after initiation of CPR (scoop and run strategy). In addition, good quality CPR should be provided from the start up to the initiation of ECMO flow.^5,6

In conclusion, when used, all efforts should be made to minimize the time from cardiac arrest to ECMO flow, as the latter is a critical determinant of outcome. Organ donation might be considered in patients with poor neurological outcomes, but experiencing full recovery of organ function.

Aim: Refractory cardiogenic shock (CS) complicates 5–7% of cases with ST-elevation myocardial infarction (STEMI), and is a leading cause of hospital death after myocardial infarction.¹

CS complicating acute myocardial infarction (AMI) continues to have a high mortality of 40–50% despite early revascularization and adjunctive therapies.² Extracorporeal membrane oxygenation (ECMO) technology has advanced significantly and is readily available at the bedside. This is a viable option for short-term support in the setting of acute cardiac ischemia. According to the 2003 USA National Registry of cardiopulmonary resuscitation (CPR), in-hospital cardiac arrest has a poor prognosis with an overall survival to hospital discharge rate of 17% with conventional CPR.³ One of the most common causes of cardiac arrest is ventricular fibrillation (VF) secondary to ischemia, which carries an improved prognosis if successfully defibrillated, with the rate of survival to hospital discharge being 34%.³ In cases with refractory ischemic VF, definitive therapy with percutaneous coronary intervention (PCI) may not be possible without anoxic brain injury secondary to hemodynamic collapse. CPR was introduced in the 1960s as a lifesaving method in patients with cardiac arrest.³ To supplement CPR in select patients, ECMO is used successfully for witnessed in-hospital cardiac arrest.³ In the setting of an AMI, bridging to a revascularization procedure is important in improving neurological outcome and overall survival. We report the profile and the outcome of patients in refractory VF resistant to defibrillation on ECMO support. Subsequent to revascularization, the patient's cardiac rhythm converted back to sinus rhythm with a single defibrillation shock with excellent neurological recovery. Methods: Since January 2014, we have been reviewing patients who had suffered from progressive severe refractory CS post STEMI undergoing emergency PCI on percutaneous veno-arterial (VA)-ECMO support. Results: For 11 male patients (mean age 50 ± 18 years), the mean duration of support was 7 ± 4 days. Of these patients, 9 (81%) were weaned successfully from ECMO. However, two patients on ECMO support died: one due to massive gastrointestinal bleeding and the other due to septic shock. Three other patients also died; one due to occluded stent on third day post-ECMO removal, one due to intracranial hemorrhage on second day post-ECMO removal, and one due to septic shock on fourth day post-ECMO removal. The 30-day survival was 54% (6/11 patients) without any neurological deficit. Conclusion: VA-ECMO has shown to be an option to bridge patients in CS and/or refractory VF to allow for a successful revascularization procedure and ultimately good neurological and survival outcome.

Background: Extracorporeal cardiopulmonary resuscitation (ECPR) is the rapid deployment of extracorporeal membrane oxygenation (ECMO) – or cardiopulmonary bypass – to provide immediate cardiovascular support for patients who have cardiac arrest unresponsive to conventional cardiopulmonary resuscitation (CPR) measures.

There is improved survival with isolated cardiac lesions.¹ Cardiac disease (adjusted for confounding factors) was associated with improved survival when compared with non-cardiac diseases (odds ratio 6.3, 2.01–19.80).²

Conventional CPR versus ECPR has a lower survival to discharge 8.2–22% and about 6–11% for critically ill patients. The survival of out-of-hospital cardiac arrest is less than 3%.³ The long-term survival is 53% with ECPR versus 17% with conventional CPR.⁴ ECPR in witnessed in-hospital cardiac arrest in areas of advanced life support system and effective CPR with single organ dysfunction with minimum time elapse in logistics like ECPR in cath lab is associated with much better patient outcome and revival to hospital discharge. Methods: Procedural support for angioplasty, arrhythmia ablation, pulmonary embolectomy, and bypass surgery are few examples of crash down situations, which are better managed with ECPR. A cath lab is the best place for application of ECMO in a short time. The equipment consists of the ECMO circuit with a centrifugal pump, hollow fiber oxygenator, heat exchanger, back up battery, 3/8 inch venous quick prime tubing, arterial tubing, and percutaneous arterial and venous cannulas. This is a study of 16 cases of ECPR done in a cath lab for witnessed adult cardiac arrests. The decision to initiate ECPR was done in 5 min with circuit priming within 20 min, and simultaneous cannulation performed in 15 min by another team. Results: Overall, 16 patients with cardiac disease over a period of 3 years were included in this study. The age group varied from 35 to 70 years. There were 12 males and 4 females. Six patients had poor left ventricle (LV) with heart failure, who were undergoing bypass surgery. Seven patients had acute myocardial infarction (MI) with cardiac arrest, who were considered for primary angioplasty (PAMI). Two patients had malignant arrhythmias (post-viral) and one patient had pulmonary embolism. There was 8/16 (50%) survival at least 24 h after ECMO decannulation and 5/16 (33%) survival to hospital discharge. Two patients could not be weaned off ECMO support. The most common cause of death was ischemic brain injury. All the survivors had favorable neurological outcome. Two patients had CPR of 60 min prior to ECPR. Pre-arrest factors associated with non-survival were persistent hypotension and renal insufficiency. Conclusions: ECPR promotes survival with ECMO application. Pre-ECMO quality of resuscitation will influence success percentage. Functional outcomes in survivors were reasonable with few derangements, particularly neurological impairments. All procedures were uncomplicated following ECMO application.

Acute myocardial infarction is a common cause of cardiogenic shock (approximately 75% of all patients) and out-of-hospital cardiac arrest (approximately 70% of survivors).¹ Mechanical hemodynamic support is employed prior to coronary revascularization (pre-percutaneous coronary intervention (PCI)), during or after PCI.² Revascularization procedure is characterized by a transient interruption of coronary blood flow (due to repetitive contrast dye injections, balloon inflations, atherectomy passes, and stent manipulations) resulting in a negative inotropic effect. Percutaneous left ventricular assist device implantation (Impella and TandemHeart), and intra-aortic balloon pump implantation have been described as strategies to avoid the worsening of cardiac function during PCI in the literature, especially in high-risk patients. The USpella registry has shown that pre-PCI implantation of IMPELLA 2.5 significantly improves survival of cardiogenic shock patients (Figure 1).³

Cardiac arrest is a recognized complication in the cath lab during percutaneous procedures, such as valve interventions, left auricle closure, and vascular interventions in addition to PCI. Extracorporeal cardiopulmonary resuscitation (ECPR) in terms of VA-ECMO plays a role in rescue therapy for cardiac arrest⁴ with a better outcome, when compared with conventional cardiopulmonary resuscitation (CPR), when CPR is failing.⁵ However, the technical and logistical possibility to implement ECPR in the cath lab is challenging. First, to deal with an emergency strategy out of intensive care and operative theater. In this context, trained personnel and dedicated sets of instruments and drugs could play a role. Second, the fluoroscope limits the free access to the patient. Moreover, percutaneous VA-ECMO cannulation requires a complex approach as the vascular accesses have been violated in most cases during the procedure. On the other hand, the presence of a multidisciplinary team has to be considered as an important resource.

In conclusion, an adequate cardiac support during cath lab procedures should be planned whenever possible to avoid emergencies especially in high-risk patients. Training and local protocols should be provided to overcome the procedural difficulties of ECPR.

The rapid institution of veno-arterial extracorporeal membrane oxygenation (VA ECMO) support for patients with prolonged, recurrent cardiac arrest (CA) complicated by severe shock and cases of refractory arrhythmia without return of spontaneous circulation (ROSC) is now termed ECMO-CPR (E-CPR). The use of E-CPR is increasing and there are reported benefits for both out-of-hospital and in-hospital patient populations. Recently, this service has been provided by staff from the hospital Emergency Department. It is likely that the best model of service provision for E-CPR depends on local factors.

Currently, there is no unifying or accepted definition for E-CPR¹ and many case series reports include both patients with and without ROSC^2,3. From analyses of outcomes from cardiac arrest data (without the use of ECMO), the likelihood of recovery from prolonged CA beyond 20 min is negligible for both in- and out-of-hospital populations, and this seems to be a reasonable threshold for the classification of ECMO-CPR.

There is a strong correlation in case series between the CPR time and the survival from ECMO with long-term survival without neurological injury becoming rare if CPR has extended beyond 60 min.

The SAVE-J study is the best evidence for the use of E-CPR for out-of-hospital cardiac arrests. This large prospective (non-randomized) cohort study showed that good neurological outcome at 6 months occurred in 12.3% of patients who received E-CPR and in 1.5% of patients who did not have access to ECMO following prolonged CA.² Propensity studies of retrospective case series suggest that neurological injury (but not survival) may be improved by the use of E-CPR in the in-hospital setting⁴. Attempts to delineate risk prediction algorithms for in-hospital cardiac arrest have consistently identified advanced age and an initial cardiac arrest rhythm other than ventricular tachycardia (VT) or ventricular fibrillation (VF) as highly predictive of poor outcome.

E-CPR should be predominately used for younger patients with VT/VF arrests, where there is access to early coronary investigation and intervention and the time to ECMO can be less than one hour.⁵ While temperature control is vital in the first 36 h following cardiac arrest, hypothermia is no longer considered beneficial. Partial pressure of oxygen and carbon dioxide may have effects on neurological outcome following cardiac arrest, but more investigation is currently underway. E-cpr Is Not The Same As “Fast” Va Ecmo: The technical skills, equipment preparedness, staffing, and staff training required for an E-CPR program are different from those required for non-CA ECMO initiation. An E-CPR program should work in concert with medical emergency teams that provide early patient assessment for deteriorating patients.

Cardiac arrest is a common problem, both in the in-hospital environment and in the out-of-hospital environment with an estimated incidence of over 300,000–400,000 cases of out-of-hospital cardiac arrests every year in the USA. Globally, the outcome of cardiac arrest remains poor, particularly with respect to neurological outcomes.¹ It is estimated that approximately 10–11% of patients with cardiac arrest survive to hospital discharge. Approximately 8–9% of patients survive to a good neurological outcome with a cerebral performance class of 1 to 2 (surviving to living at home with no or minimal support for activities of daily life). Survival is more likely if cardiac arrest has been witnessed by bystanders and cardiopulmonary resuscitation (CPR) has been commenced immediately. Survival is also more likely if the cause of cardiac arrest is ventricular arrhythmia, either ventricular fibrillation or ventricular tachycardia, and if early defibrillation is available. Given the poor outcomes from cardiac arrest, there has been a growing interest in using novel approaches to try and improve the outcomes, particularly the neurologically intact outcomes from cardiac arrest. One of the potential therapeutic modalities which has arisen in the last decade has been the use of extracorporeal membrane oxygenation (ECMO) for patients with cardiac arrest (E-CPR).² Although there have been a number of retrospective and prospective uncontrolled studies, or for some studies propensity matched with a current or historical control, observational studies have demonstrated potential benefits associated with ECMO.³ Currently, there are no randomized trials in the literature, although there are at least two trials currently being undertaken. Furthermore, at present, there is no widely accepted pathway for patients which provides recovery from cardiac arrest, commencement of E-CPR, management of the cardiovascular system and targeted therapy designed to protect the brain. E-CPR continues to pose significant challenges in patient management, both in its implementation and in the management of patients following cardiac arrest and resuscitation.^2,4 The management of patients is likely to be substantially different with E-CPR compared with conventional approaches, particularly following cardiac arrest. In particular, the management of the cardiac function is different in patients with retrograde aortic blood flow, and the ideal management of the brain, including mean arterial pressure, cerebral perfusion pressure, ideal targets for carbon dioxide and arterial oxygen content, has yet to be defined. Another key challenge is neurological prognostication and diagnosis of brain stem death, which is more challenging on ECMO.⁴ An additional area that requires careful consideration is temperature management, given the results of recent trials exploring the outcomes for patients managed with hypothermia compared with normothermia.⁵ The relevant literature will be covered and an approach to the management of the post-arrest patient, particularly with respect to considerations on ECMO, will be discussed.

Since its development in the early 1990s, extracorporeal membrane oxygenation (ECMO) has become a standard therapy for a wide variety of respiratory and cardiac problems in neonates. Traditionally, the preferred method of access and support has been using a venous inflow, with arterial outflow methodology (venoarterial or VA ECMO), bypassing the cardiac circulation.¹ Ongoing improvements in catheter configuration have made the use of a dual lumen catheter, with venous inflow from above and below the atrium and directed outflow of oxygenated blood into the right atrium, possible in the majority of neonates (venovenous or VV ECMO).^2,3 The advantages of VV ECMO include improved physiology with preservation of pulsatile blood flow, reduced cardiac stun, delivery of oxygenated blood to the pulmonary circulation, maintenance of normal cerebral perfusion, and reduced risk of emboli. However, only 30% of infants are supported using VV methodology, while up to 80% are potential candidates.¹ The reasons cited for choosing VA ECMO are patient size, instability, and the need for ongoing pressor support. Although these are concerns, none, except for patient size, are absolute indications for VA support. With appropriate cannulation methods, and verification of catheter position and function, the majority of neonates can be supported using VV ECMO. This article reviews the practical considerations for using VV ECMO in neonates. Patient selection is based on diagnosis and size. Almost all respiratory, septic, and most cardiac indications can be supported with VV ECMO if the patient weighs more than 2500 g. The two main catheter types differ in size and configuration; both have been shown to be efficient when properly placed. Catheter positioning during cannulation should be confirmed with an echocardiogram for flow and mixing, and a radiograph for positioning. The Avalon catheter must have an echocardiogram for placement and has a higher reported incidence of complications.⁴ Typically, a secondary venous inflow catheter is required, either as a cephalad jugular or as a femoral line. Medical management during a VV ECMO run commonly requires pressor management; however, this is also associated with a more stable perfusion profile. There are no other changes in management required; anti-coagulation requirements and decannulation are simpler with the VV ECMO methodology. Overall, outcomes (survival and neurological status) in all major disease classes are better with VV ECMO; however, controversy exists as to whether this is due to the therapy, or a selection bias in choosing candidates.¹ In summary, with appropriate preparation of the team and selection of catheter sizes, the majority of neonates can be supported with VV ECMO. This offers the potential for improvement in survival, and reduced incidence of neurological injury. These long-term outcomes should be the primary consideration in the choice of cannulation technique.

Introduction: Strategy during extracorporeal membrane oxygenation (ECMO) support is guided by available outcome data. Boundaries limiting selection of cases are shifting with advances in ECMO technology, conventional support, and destination therapies. Evolution: Neonatal respiratory ECMO numbers continue to decline due to improved conventional therapies, whereas infants historically excluded from ECMO (for example, ex-premature infants with O2-dependent chronic lung disease and severe RSV) are now successfully supported. ECMO for bridging of children to lung transplant is now established.¹ Advances are also being made in mobile ECMO,² long duration of ECMO support, and ECMO while wide awake. Initiation: Flow requirements and patient or vessel size govern cannula choice. Percutaneous cannulation of vessels with ultrasound guidance is described in all sizes of children, including small infants.³ Serial imaging and ECHO control are needed for optimisation of cannula position and orientation. Transoesophageal ECHO is preferable to transthoracic where available. Reconfiguration of the circuit may prove necessary in some cases and is better done early in the run.⁴Troubleshooting: Protocol and bundle adherence are the keys to preventing complications. Detection requires vigilance and rigorous checks along with comprehensive handover and tight teamwork. Management is about appropriate escalation and pathway utilisation. Simulation is an essential component of staff training and a powerful tool for reinforcing these points.⁵Lung recovery: ECMO can be considered the ultimate in “lung rest” techniques. Enhancing lung recovery during the rest provided by ECMO is mainly achieved by attention to fluid balance, pulmonary toilet, and adoption of ventilator rest settings. Bronchoscopy is also particularly useful in this context.⁶ Other therapies such as prone position, steroid use, surfactant, perfluorocarbon,⁷ and even individual lung ventilation² have a role in selected cases. De-cannulation: Patience can be needed when timing the end to VV ECMO support. Removing the sweep gas from the oxygenator can be done simply without having to wean ECMO flow. In more difficult situations, 12–24 h trial off can be used. Radiological lung clearance, improving lung compliance, reduction of sweep gas requirements, and oxygen challenges are all informative in the run up to a decision to trial off. Lung biopsy⁸ or genetic test results are useful when recovery is absent to help establish futility. Earlier de-cannulation can be indicated in the setting of an intractable or severe complication. Summary: Strategy for management of VV ECMO support is evolving with improvements in ECMO techniques and advances in supporting therapies. A proactive, rigorous but flexible approach to individual cases can deliver excellence.

For neonates, veno-arterial (VA) extracorporeal membrane oxygenation (ECMO) support is still commonly used for respiratory as well as for cardiac or combined failure. However, in the pediatric population, veno-venous (VV) ECMO is establishing itself as the standard mode of support for respiratory failure.¹

The need for ECMO in neonatal respiratory support has declined over the past years following introduction of alternative options. Conversely, a significant increase in VA ECMO for cardiac support has been identified (see Figure 1). The present article aims to describe the various indications for VA ECMO in the neonatal population.

Although the majority of cardiac runs for neonates still relates to congenital heart defects, widening experience and indications, such as myocarditis, sepsis, poisoning (reversible), or extracorporeal cardiopulmonary resuscitation (ECPR), have led to an increased use of VA ECMO in neonates and children.

For congenital heart defects, special considerations must be made, especially for ECMO in the context of single ventricle (SV) physiology:³ the balancing between pulmonary and systemic circulation remains crucial whether a Blalock–Taussig shunt or a Sano shunt is used. For the second and third stages of single ventricular palliation, cannulation strategies must be adapted to the underlying anatomy on a case-to-case basis.

Myocarditis due to various reasons can be supported successfully with VA ECMO, which constitutes the ultimate endpoint of the myocarditis management algorithm. Timely deployment before irreversible multi-organ damage has occurred is crucial. Further attention must be paid that myocardium can be quite stunned and left ventricular decompression is mandatory to allow adequate myocardial recovery.⁴

Sepsis has become an indication if conventional management fails,⁵ as reflected in the algorithm published by the Surviving Sepsis Campaign in 2012, which recommends starting ECMO in refractory shock.

Case reports with successful support of heart and lung function until recovery for various poisonings or during cath lab interventions have been published.⁶

ECPR with the deployment of extracorporeal life support (ECLS) during resuscitation has been mentioned in the PALS guideline since 2010 as class II recommendation. As could be expected, outcomes for survival and neurological deficits are related to centers’ experience and resuscitation time prior to ECLS installment.⁷

VA support remains common in neonates and children placed on extracorporeal membrane oxygenation (ECMO) for respiratory, cardiac or combined dysfunction.¹ Providing adequate ECMO flow to reverse tissue oxygen debt is imperative in the first few hours of ECMO. Several studies outline the poor outcome which results if lactic acidosis and pH do not improve after institution of ECMO. Following serial lactate, urine output, and other signs of organ perfusion are vital aspects of care.

For infants and children, the common route for adequate vessel size is use of the right internal jugular vein and right common carotid artery. Some centers also utilize a venous drainage cannula placed retrograde up the internal jugular vein to the level just below the jugular bulb to augment venous drainage. Whether this also reduces risk for venous congestion in the brain is unknown. Older children (usually at least 15 kg or 2–3 years old) may be supported via the femoral vessels (vein and artery) or a combination of cervical and femoral routes. There is some evidence to suggest that use of the carotid artery is associated with more risk for neurologic abnormalities such as seizures or intracranial infarction. For patients cannulated via the femoral vessels, care must be taken to avoid distal venous congestion in the extremity, which can lead to compartment syndrome. Similarly, distal lack of arterial perfusion can lead to ischemia and need for amputation in severe cases. Placement of a distal cannula which is then Y-ed into the arterial return from the ECMO circuit can provide perfusion to the limb. Neurovascular integrity of the lower extremities is important to prevent injury.²

Veno-arterial ECMO increases left ventricular afterload. This can result in sudden and severe left ventricle failure, leading to pulmonary edema or hemorrhage from back-up into the left atrium and pulmonary venous hypertension. Transmural ischemia from left ventricular distention can also occur. While afterload reduction or low-dose vasoactives to improve ventricular performance and maintain left ventricular output can be effective, some patients will require decompression of the left side of the heart. This can be done via a balloon septostomy across the atrial septum (allowing left atrial blood to then be drained into the right atrium and removed with the venous drainage cannula), by placement of a direct venting cannula into the left atrium, left ventricle, or pulmonary vein and then Y-ing this into the venous side of the ECMO circuit.³ Following left ventricle performance with ECHO and maintaining a pulse pressure of at least 10 mmHG following ECMO initiation are important aspects of VA care. For weaning during VA ECMO, decompression efforts must be ceased to allow adequate filling of the left ventricle. For post-cardiotomy patients placed on VA ECMO, early cardiac catheterization to identify correctible residual lesions should be performed. Failure to recover heart function within the first week of ECMO is associated with high mortality and discussion of listing for heart transplant or discontinuation should occur as appropriate.⁴

Extracorporeal membrane oxygenation (ECMO) is a commonly used form of mechanical circulatory support in children with congenital or acquired heart disease, and cardiac failure refractory to conventional medical treatments.¹ The cardiac output is partially or completely provided by the ECMO machine. To assess how much support is needed at any given time, a constant balance of oxygen delivery and oxygen consumption is required. Permanent monitoring of flow, hemoglobin, arterial, and mixed venous saturations are key elements to provide the needed understanding and continuous guidance of body requirements, aiming at controlling and maintaining optimal management of the ECMO patient.

Although ECMO is lifesaving in many circumstances, it bares challenges and certain risks of complications. Despite bioline-coated circuits, anticoagulation is required. Measurement of activated clotting time (ACT) and activated partial thromboplastin time (APTT) are both used to guide anticoagulation, but it is unclear which method is the best, and constant monitoring of the hemoglobin level allows the early detection of internal and external bleeding.² For children, sedation and analgesia, most often in combination with paralysis, is unavoidable for a smooth ECMO run. On the other hand, with such treatment on board, it is almost impossible to assess the neurological status of the patient on ECMO. Different monitoring tools, such as cerebral near infrared spectroscopy (NIRS) and serial brain ultrasound studies, are used to estimate brain integrity and function, but further research is needed to show which methods are the most practical and useful to achieve a favorable outcome.³ Nutrition in critically ill children is known to be crucial but debated how to achieve as the gut perfusion can be impaired and therefore the risk of necrotizing enterocolitis (NEC) is increased. It is discussed if somatic perfusion by NIRS monitoring can help to avoid NEC.⁴ The kidney function is often impaired in these critically ill children and careful monitoring of kidney function and urine output leads the decision when to start which type of renal replacement therapy for renal clearance and/or fluid removal. Techniques available include peritoneal dialysis or continuous renal replacement therapy (CRRT) incorporated with the ECMO circuit. Medication dosing is under discussion in many centers as the circulatory volume is higher than normal. Adjustment of medication dosing could consequently be of great importance. Close monitoring of medications where toxic levels can be reached is crucial to avoid further damage to the patient's organ functions.

Background: Extracorporeal membrane oxygenation (ECMO) is a rapidly expanding, life-supporting therapy for critically ill patients with severe respiratory and/or cardiovascular failure. Cerebrovascular impairment can result in hemorrhagic and ischemic complications commonly seen in the patients supported on ECMO. The healthy brain is protected by cerebral autoregulation, which maintains an adequate cerebral blood flow in face of blood pressure changes.¹ Pre-ECMO factors, such as hypoxia, hypercarbia, and hypertension, can disrupt blood flow regulation, leaving the brain vulnerable to changes in blood pressure.² Cannulation of large blood vessels³ and alterations of pulsatile flow patterns during ECMO also play a role in altered cerebral autoregulation.⁴

A reliable methodology that can assess the status of cerebral autoregulation during ECMO and provide early indication of neurological injury is critical for optimization of bedside management to improve clinical outcomes. Wavelet transform coherence (WTC) is a time–frequency domain analysis that characterizes the cross-correlation and relative phase between spontaneous fluctuations in blood pressure and cerebral oxygenation measurement by oximetry.

We implemented WTC⁵ to assess the degree of cerebral autoregulation impairment in neonatal and pediatric ECMO and evaluated its usefulness as an early predictor of acute neurological complications. Further, we examined cerebrovascular parameters, blood gas changes, and anticoagulation parameters as potential causes of autoregulation impairment during ECMO. Methods: Spontaneous fluctuations of mean arterial pressure (MAP) and cerebral tissue oxygen saturation (SctO2) were continuously measured during the ECMO run. The dynamic relationship between the MAP and SctO2 fluctuations were assessed based on wavelet transform coherence (WTC) to derive an index of cerebral autoregulation impairment. The Institutional Review Board at the University of Texas Southwestern Medical Center at Dallas approved the study. Results: A total of 25 neonatal (11) and pediatric (14) patients were studied. In-phase coherence between the MAP and SctO2 fluctuations was predominant in a time scale range of 8–32 min. Significant correlations between individual autoregulation indices and neuroimaging scores were found in both neonates and children. There was a significant association between individual blood pressure variations with autoregulation indices in the children, but not in the neonates (Figure 1). Discussion and conclusion: We found that intra-ECMO autoregulation impairments derived from WTC were apparent even before clinically observable changes occur at the bedside. Furthermore, these impairments correlated with the patients' neuroimaging abnormalities. This finding remained constant for both VA ECMO and VV ECMO in contrast to evidence of increased incidence of neurological complication with carotid artery cannulation in the literature. Blood pressure variability in ECMO patients appeared to be associated with impaired autoregulation in the non-neonatal population.

Continuous assessment of cerebral autoregulation based on WTC has the potential to be a useful bedside tool to predict acute neurological events in patients on ECMO. Our study shows that high blood pressure viability, for which these patients are at risk, appears to be a cause of cerebral autoregulation impairment. This finding suggests a new approach to bedside management that may lead to a decrease in cerebral autoregulation impairment, thereby improving neurological outcomes in these patients.

Survival of patients with malignancy over the last 30 years has continually improved due to advancements in aggressive chemotherapeutic regimens as well as supportive measures toward treatment and prevention of infection.^1,2 Even though cancer remains a significant cause of mortality in children, 5-year survival for childhood cancers, including hematologic malignancies and solid tumors, is greater than 80%. In these children, critical illness occurs either as a result of their malignancies and/or complications from treatment. Given improvements in survival, a more aggressive approach to the management of these complications in pediatric patients with malignancies has been encouraged, which has enlightened the medical community to the use of extracorporeal life support (ECLS) in this complex population. Evidence of this new approach was reported in 2009 by Gow et al.³ when a survey of ECLS centers regarding utilization of ECLS for patients with malignancy found that 95% of respondent ECLS centers felt that malignancy was not a contraindication to ECLS. This is further supported by the Extracorporeal Life Support Organization (ELSO) registry, which documents that, since 1997, the use of ECLS, including extracorporeal membrane oxygenation (ECMO) for pediatric cancer patients has been steadily rising.

Up until 2007, pediatric patients with malignancy comprised 0.5% of all ECLS patients. Limitation in the use of ECLS for patients with cancer was most likely influenced by cancer-related mortality as well as the ideology of ECLS being a support modality offered only to acutely ill “healthy” patients. Since 2009, a number of reports describing ECLS use for patients with malignancy have been published, implying that its use is increasing in this population most likely due to noted improved oncologic survival compounded by more widespread ECLS use in complex patient populations. Utilization of this support modality in pediatric malignancy, although still low compared with other populations, is increasing. In 2008–2012, the ELSO registry documented 178 patients with malignancy who received ECLS, which equates to 1% and a doubling of utilization compared with that reported previously. Although there is still a small portion of ECLS patients, education regarding the use of this modality of support for patients with malignancy will likely lead to further increases in utilization.^4,5

Background: Harlequin syndrome is a rare autonomic disorder, characterized by unilateral diminished sweating and flushing of the face in response to heat or exercise.¹

Harlequin syndrome is described in patients receiving peripheral veno-arterial extracorporeal membrane oxygenation (VA-ECMO), where differential oxygen saturation is observed between the upper and lower parts of the body.

It is a phenomenon related to cannulation, where upper body hypoxia occurs due to compromised arterial return despite an initial correct bifemoral cannula insertion. Case report: A 9-month-old child presented to the Royal Hospital, Oman, with a 1-day history of tachypnea and potential case of chocking, which rapidly progressed into ARDS and refractory respiratory failure despite providing maximum supportive measures: different modes of conventional mechanical ventilation and high-frequency oscillatory ventilator (HFOV), steroids, inhaled surfactant, inhaled iloprost, and prone positioning. Inhaled nitric oxide was not available. Rigid bronchoscopy excluded foreign body aspiration and echocardiography showed normal heart structure and function. As all measures failed and oxygen index remained low, ECMO was initiated. She was initially cannulated for VA-ECMO; two femoral venous cannulas of sizes 16F and 10F were inserted into both sides for adequate drainage and a size 8F femoral artery cannula was inserted into the right side; VV-ECMO cannulas were not available. The ECMO machine delivered a flow rate of about 80 ml/kg/min, BP 90/46, HR 130, CVP 14, Hb 12.6 g/dl, and milrinone 0.5 μg/kg/min. There was differential oxygen saturation between the upper and lower parts of the body; saturation was 50–60% in the upper part and 100% in the lower part, and FiO2 was 100%.

To solve the problem, VA-ECMO was changed from peripheral to central through insertion of a venous cannula into the right atrium and an arterial cannula in the aorta with a flow rate of about 110 ml/kg/min.

The child was successfully decannulated after 10 days of ECMO support and discharged home 2 months after admission. Respiratory viral panel was positive for adenovirus. Discussion: Harlequin syndrome is a rare complication of peripheral VA-ECMO. However, it can be as high as 8.8%.²

It occurs when the heart function is preserved or recovering, but the lungs are still poorly functioning, so the native cardiac output flows against the pumped blood, usually in the aortic arch region.² The reinfusion jet flows retrograde up the aorta and may meet resistance from antegrade flow generated by the left ventricle.

Depending on the amount of native cardiac function, the location of the interface between antegrade and retrograde flow will vary, and in circumstances where there is impaired native gas exchange with a significant amount of poorly oxygenated blood ejected from the left ventricle, the oxygenated reinfused blood may not reach the aortic arch.³ Subsequently, the coronary arteries, and to a variable degree the supra-aortic vessel as well, are provided with hypoxic blood, and the heart and brain can be affected.²

Therapeutic options consist of relocation of the arterial cannula into the right subclavian artery or aorta,² or converting to central VA-ECMO. It can also be solved by converting the system into a VA-V setting, where an additional return cannula may be added to the configuration with a “Y” connection off the femoral arterial reinfusion cannula, with insertion into an internal jugular vein.³Conclusion: Harlequin syndrome is a known complication of peripheral VA-ECMO, where the upper part of the body is poorly oxygenated. It occurs when the native heart function is preserved but the lungs are poorly functioning. Therapeutic options include converting to central VA-ECMO or VA-V-ECMO.

Extracorporeal membrane oxygenation (ECMO) is a form of mechanical circulatory support that can be lifesaving in people with potentially reversible heart or lung injuries. ECMO is nearly always used urgently, when all other treatment options for cardiopulmonary injury have failed and high mortality is otherwise expected. Standard ECMO treatment involves venous drainage from the femoral vein or left atrium with artificial extra-circulatory oxygen exchange. Return to the body is through the same veins (veno-venous) or arterial system via the femoral artery or ascending aorta (veno-arterial). Compared with cardiopulmonary bypass circuit, ECMO is transportable, smaller, closed to the atmosphere, and can treat a patient for several days to weeks.

Neurological consequences of severe respiratory failure and its different management strategies in adults are likely common but uncharacterized and poorly described in the reviewed literature.

Development of severe respiratory failure (SRF) occurs in 20–25% of patients with isolated severe traumatic brain injury (TBI) and is associated with a threefold increase in mortality, or patients remaining in a vegetative state.¹ It has been attributed mostly to aspiration, infection, neurogenic pulmonary edema, and release of pro-inflammatory mediators into the systemic circulation causing ultrastructural damage in type II pneumocyte.² This decreases the pulmonary tolerance of subsequent mechanical stress due to mechanical ventilation. Actually, some data suggest that the main feature of ALI/ARDS in brain-injured patients is the presence of a poor oxygenation (reduced PaO2/FiO2 ratio) accompanied by a moderate increase in the elastance of the respiratory system even though these patients had a normal chest X-ray.

Ventilatory support for such patients could be difficult with a lot of challenges to keep optimal oxygenation and acceptable level of blood carbon dioxide. It involves the application of positive end-expiratory pressure (PEEP) to recruit collapsed alveoli, improve arterial oxygenation, and reduce elastance of the respiratory system. Although improving oxygenation is a key factor for optimizing O2 delivery to the brain, clinical studies provide contradictory information on the use of PEEP in patients with acute lung injury (ALI) complicating severe brain injury.

Furthermore, we tend to use higher tidal volumes in patients with acute brain injury because mild hypocapnia is a key factor in the clinical management of raised intracranial pressure, which is a frequent abnormality in such patients;^3,4 this would be an injurious ventilator strategy and may present a further relevant inflammatory stimulus. Moreover, it has been shown that the use of high tidal volumes for the first 48 h after ICU admission is associated with the development of ventilator-induced lung injury.⁴

In addition, one of the recognized methods in improving oxygenation in SRF patients is the use of prone position, because it improves the lung mechanics and augments oxygenation. Studies have demonstrated that patients with unstable intracranial pressure (ICP) have higher ICP in the horizontal position sideways. Therefore, the recommended position for this patient cohort is a 30-degree head-up tilt combined with a straight head position.⁴

Furthermore, TBI patients who require ECMO support for their SRF will need full anticoagulation, as the circuit poses considerable derangement in the hemostatic system with increased platelet consumption and a higher risk of intracranial bleeding. There have been several reports of ECMO without anticoagulation therapy, but so far with no evidence or good literature to support this notion.⁵

Although some controversy and difficulties exist, it seems that multiorgan clinical approach instead of single-organ approach represents the optimal way in clinical management of patients with ALI/SRF and TBI.

Background: Obesity, defined according to body mass index (BMI > 30 kg/m²), is an increasing problem in the world's population. The proportion of extremely obese patients (BMI > 40 kg/m²) in intensive care units varies between 2.8 and 6.8%.¹ A BMI higher than 40 kg/m² seems to be associated with an increased risk of developing acute respiratory distress syndrome (ARDS) along with greater morbidity, length of stay, and duration of mechanical ventilation in the intensive care unit (ICU).²

The use of veno-venous extracorporeal membrane oxygenation (ECMO) has reemerged as an option for acute respiratory distress syndrome (ARDS) refractory to conventional support.³ In addition to cannulation difficulty, morbid obesity can pose a significant challenge to obtaining sufficient circuit flow, indexed to either weight or body surface area (BSA), required to sustain lung rest and recovery.⁴ Owing to this hypothetical obstacle, there remains significant hesitancy in many centers to offer ECMO support to this patient population. However, Zachary N and his colleague in 2015 proved the efficacy of veno-venous ECMO in this patient population.⁵Methods: In King Fahd Jeddah ECMO center, Patients requiring ECMO for ARDS between April 2014 and May 2016 were reviewed retrospectively with institutional review board approval. Demographics, ECMO variables, and outcomes were assessed. Obesity, morbid obesity, and super obesity were defined as a body mass index (BMI) greater than 30 kg/m², greater than 40 kg/m², and greater than 50 kg/m², respectively. Results: Forty-nine patients (36M/13F) with ARDS were placed on ECMO during the study period. Fifteen were obese with a BMI of 32.7 kg/m² (interquartile range [IQR]: 31.6–34.9 kg/m²). Four were morbidly obese with a BMI of 46 kg/m² (IQR: 43.5–48.5 kg/m²). Nine were super morbidly obese with a BMI of 59 kg/m² (IQR: 54.5–69.5 kg/m²). Pre-ECMO mechanical ventilator support and indices of disease severity were similar between the three groups, as were the cannulation strategy and the duration of ECMO support.

The 90-day survival rate was 71% (20/28) in patients with a BMI more than 30 kg/m² compared with 42% (9/21) in the non-obese group. Subgroup analysis showed improved survival in morbidly obese patients as 75% (3/4), and super morbidly obese patients as 88.8% (8/9). There were four bleeding complications, two in each morbidly and super morbidly obese group. Conclusions: ECMO in obese patients is feasible and life-saving. Therefore, a percutaneous cannulation remains feasible. The goals of the ECMO therapy include early spontaneous breathing, tracheotomy, rapid reduction of sedation, and adequate analgesia.

Interstitial lung disease comprises a heterogeneous group of histologically distinct pathological entities characterized by a diffuse inflammatory process affecting the lung parenchyma. Classification of interstitial lung disease is complex and usually determined by a combination of clinical features, radiological, particularly computed tomography, appearance, and findings at lung biopsy. Interstitial lung disease presentations can range from slowly progressive interstitial pneumonitis to more rapidly progressive vasculitic, eosinophilic, and acute fibrotic diseases. In the acute form, interstitial lung disease can, over a period of days, manifest as bilateral diffuse pulmonary infiltrates, causing a significant disturbance of respiratory function. Patients characteristically have very poor dynamic compliance and poor gas exchange. The outcome of patients with interstitial lung disease admitted to the Intensive Care Unit (ICU) has historically been very poor. This is thought to be a combination of both the lack of reversibility of the underlying respiratory problem and further damage to the lungs associated with necessarily invasive mechanical ventilation.^1–3 The pro-inflammatory effects of invasive ventilation have been well described and are proportional to both tidal ventilation and pressure within the lung. There are a number of potential treatment options now available, which may help to modify the course of the disease,⁴ particularly in cases where there is a very high level of inflammation within the lung. Treatment options currently available include high-dose steroids, rituximab, and cyclophosphamide. Recently patients with acute interstitial lung disease have been offered extracorporeal membrane oxygenation (ECMO) as both a life-sustaining supportive therapy and a means of avoiding ventilator-induced lung injury, and results are improving, particularly in patients with acute interstitial lung disease.⁵ One of the benefits of ECMO is that it can allow patients to be awake and undertake physical and pulmonary rehabilitation.⁶ This may be of particular benefit in the interstitial lung disease population, where a bridge to transplant is being considered. The latest evidence for the use of ECMO in interstitial lung disease will be reviewed, including clinical phenotypes which appear to particularly benefit from ECMO as a bridge to recovery. Some patients who present with what is assumed to be an infective pneumonia will ultimately progress to developing a progressive acute interstitial lung disease and it is essential to differentiate such patients from those with acute respiratory distress syndrome. In patients with acute interstitial lung disease, there are treatments which may modify the course of the disease, whereas the predominant management of acute respiratory distress syndrome is largely avoiding lung inflammation to prevent the progression. A strategy for investigation and the key clinical and physiological indicators of potential acute interstitial lung disease will be discussed.

Extracorporeal membrane oxygenation (ECMO) is increasingly being used in adult patients with either cardiac or respiratory failure or both in many settings.^1,2 This includes pregnant patients and those who are postpartum experiencing cardiac or respiratory failure, a particularly vulnerable population where both the mother and the fetus are at risk.

There is scant literature addressing the use of ECMO for either cardiac or respiratory failure in patients who are pregnant or postpartum. However, there are many potential indications, such as the acute respiratory distress syndrome (due to pneumonia, especially influenza pneumonia; aspiration; transfusion-related lung injury; or non-pulmonary sepsis), pulmonary embolism, amniotic fluid embolism, management of pre-existing or newly diagnosed pulmonary hypertension, cardiomyopathy (including postpartum cardiomyopathy), extracorporeal cardiopulmonary resuscitation (most frequently in the setting of pulmonary embolism or amniotic fluid embolism), and other conditions that are less commonly seen in the pregnant and peripartum patient population, which nevertheless may be encountered by clinicians.

Case reports and case series are beginning to illuminate the management of such patients and suggest that ECMO in this setting may be beneficial to save the lives of both the mother and child. A case series of four patients reported survival in all four mothers and in three of the four fetuses.³ The largest case series in the literature reported on 18 peripartum patients, four of whom were pregnant at the time of cannulation.⁴ Mortality in that series was 11.1% with only two patients not surviving to hospital discharge. Fetal survival was 100% in those patients cannulated after fetal viability – overall fetal survival was 77.8%. One-third of the patients in this cohort had bleeding as a complication of their ECMO with no fetal complications attributable to ECMO. Other complications in the mothers included: DIC, as well as occlusive and non-occlusive deep vein thromboses. The risk of complications must be weighed against any potential benefits of using ECMO in these patients. A subset of patients were able to participate in active physical therapy while receiving ECMO (38.9%), with four patients being able to ambulate around the intensive care unit while receiving ECMO. The duration of ECMO was relatively brief overall (median 6.6 days), which was similar in both of these series.^3,4

While ECMO appears from case reports and case series to be both feasible and reasonably safe in patients who are pregnant or postpartum with cardiac or respiratory failure, more data are clearly needed to better appreciate the potential indications, contraindications, and specific techniques involved. However, given the potential for recovery in a population that skews younger and healthier than the general population, deploying ECMO, even in severely critically ill patients in this setting, may be appropriate in centers experienced with the use of ECMO for cardiac and respiratory failure. For centers that do not have this experience, early referral is encouraged in those cases where deterioration may be anticipated.

Pulmonary vasculitis is a rare disease that typically shows inflammation in pulmonary vessel walls and necrosis.¹ The disease is usually immune mediated, common in young patients, triggered by many factors, and with wide clinical and radiologic presentations. Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAVs) is the main focus in most literature and includes granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), Churg–Strauss syndrome (CSS), idiopathic pauci immune pulmonary capillaritis (IPIPC), secondary to systemic lupus erythematosus, and other types like anti-glomerular basement membrane disease, drug-induced vasculitis after cannabis and glue inhalation.² Diagnosis is usually established after careful history taking clinical, radiologic, and laboratory evidence; bilateral lung infiltrates with or without pulmonary hemorrhages and peripheral distribution, positive ANCA-P component, proteinase-3 ELISA test, anti-glomerular basement membrane antibody, and other antibodies associated with immunologic disease like systemic lupus erythematosus. Sometimes, lung biopsy may be needed but because of the low yield of bronchoscopic biopsies and the need for open lung biopsy, this tool is rarely used specially in critically ill patients. Treatment is by the use of steroids and cytotoxic medications like cyclophosphamide and mycophenolate mofetil. In refractory cases, plasmapheresis or the monoclonal antibody rituximab may be used. Pulmonary hemorrhage is a common manifestation in vasculitic lung syndromes; however, many other disease and toxins can trigger pulmonary hemorrhage, which can be life threatening.³ The diagnosis of pulmonary hemorrhage is generally considered based on clinical and radiological findings and is characterized by acute bilateral patchy lung infiltrates more centrally located but may be diffuse. Sequential aliquots of bronchoalveolar lavage yield progressively bloodier return and help in diagnosis.⁴ Treatment depends largely on the cause. Extracorporeal membrane oxygenation (ECMO) is a life support modality that can be used in severe cases of pulmonary vasculitis and hemorrhage with great caution and careful assessment of risk of bleeding with anticoagulation and benefit of use as life-saving support. With newer ECMO circuits used (either heparin- or bioline-coated circuits), several days of heparin-free ECMO runs may be successful. In some reported cases, citrate was used as an anticoagulant.⁵ The ECMO modality shall be carefully chosen especially in the presence of pulmonary hypertension, which may affect the veno-venous (VV) ECMO flow, and hence, echocardiographic assessment before initiation is mandatory to avoid low-efficiency runs. In cases with severe pulmonary hypertension, veno-arterial (VA) ECMO would be more suitable. Institution of treatment using steroids and cytotoxic drugs in addition to plasmapheresis is warranted upon suspected diagnosis. The rapid initiation of treatment may be the key point of survival in such cases. There are some case reports where plasmapheresis and immunosuppressive therapies were used based on clinical and radiographic data alone⁵ with successful outcome. There is paucity of data regarding drug doses of immunosuppressive drugs used during the ECMO run, and the duration of treatment was variable. Most of the cases reported started with 1 g of methylprednisolone for 3 days followed by either plasmapheresis and cyclophosphamide or cyclophosphamide and rituximab.⁶ The plasmapheresis circuit installation needs to be addressed whether to be incorporated into the ECMO circuit⁷ or not.

Pulmonary infection and respiratory failure are the most common causes of admission to the intensive care unit (ICU) in human immunodeficiency virus (HIV)-positive patients.^1,2

In our experience, in a developing nation (despite the advent of HAART), the commonest cause of admission to ICU and mechanical ventilation still remains Pneumocystis jiroveci pneumonia (PJP). Most of these patients presenting with PJP have not been on antiretroviral therapy (ART) or been treated with PJP prophylaxis, and it is highly likely that this is their first time presentation to hospital.³ The advent of highly active antiretroviral therapy (HAART) has allowed for more effective treatment of HIV-positive patients; however, despite this, PJP remains the most common acquired immunodeficiency syndrome (AIDS)-defining condition and is associated with much morbidity and mortality, in both developing and developed nations.⁴ In developed countries, mortality may reach up to 85%, while, in developing countries, the mortality figure nears 100%.^3,5 In consideration of the above mortality figures, it may be said that conventional mechanical ventilation (CMV) has failed to improve outcomes (and reduce morbidity) in HIV-positive patients who present with severe acute respiratory failure (ARF), especially in cases caused by PJP.

This has opened the door to using extracorporeal membrane oxygenation (ECMO) as a treatment modality. We found that ECMO was used with good success in treating these patients, with a much improved survival rate (see Table 1). Most of our patients were newly diagnosed HIV positive, and were not on HAART at the time of admission. HAART was immediately initiated in the ICU once the HIV diagnosis was made. We found a 68% overall survival of our HIV-positive patients who received ECMO treatment and a 61% survival of the PJP subset of patients. Of note is the median duration of ventilation required: 9 days. This is significantly shorter than our pre-ECMO experience in severe ARDS PJP patients (p = 0.020), where most patients were ventilated for significantly longer than 9 days. Also noteworthy is that the median duration of ECMO was 9.5 days.

While on ECMO, we identified two factors that were clearly associated with poor outcomes in our series of patients with PJP:

[1]  Duration of ECMO. Patients who survived had an ECMO run of 7 days on average and those who died were on ECMO for >13 days; [2]  The need for inotropic support while on ECMO was a strong predictor of mortality.

We found that CD4 count was not a predictor of mortality.

This suggests that ECMO is a viable and effective treatment for HIV-positive patients who present with severe ARDS.

Congenital diaphragmatic hernia (CDH) remains a common defect in infants and occurs worldwide at a rate of 0.8–4.5 per 10,000 live births. It is associated with high mortality and morbidity. Veno-arterial (VA) support remains common in neonates with CDH, although venovenous support has also been used.¹ Criteria for extracorporeal membrane oxygenation (ECMO) in CDH patients remain an inexact science. Studies have evaluated the role of achievable gas exchange (both carbon dioxide and oxygen), fetal lung-to-head ratio, lung volume estimates, and other factors in predicting outcomes, but none have proven to be highly accurate.² Currently, observed/expected lung-to-head ratio of < 1 and liver position up in chest are associated with poor outcomes in some reports. Fetal therapies to encourage lung growth with tracheal occlusion are also occurring in cases of predicted severe CDH. Following birth, use of “gentle” ventilation is recommended to limit mechanical ventilator-induced lung injury. Use of inhaled nitric oxide to alleviate pulmonary hypertension may be helpful in some patients as well. High-frequency oscillatory ventilation is often provided. If the patient remains unstable or has severe hypercarbia or hypoxia, ECMO is considered. Despite many years of experience with CDH and ECMO, it should be noted that survival remains only about 50% and has not markedly improved over time.³ There is little consensus on when to repair the CDH, with some clinicians performing surgery while on ECMO and others preferring that the patient be weaned off ECMO successfully prior to surgical hernia repair.⁴ Survivors often have residual problems such as frequent respiratory illnesses that bring them into the hospital even after they get successfully discharged. Coexistent cardiac or genetic abnormalities have also been associated with poor outcome in patients with CDH, with or without ECMO support.⁵ CDH care is also expensive, especially in patients who require ECMO or prolonged hospital stays. It is hoped that future research will result in improvements in prevention and treatment for these fragile infants. Until that time, ECMO will continue to hold a place in support of these patients.

Extracorporeal membrane oxygenation (ECMO) is an increasingly used life support modality in both respiratory and cardiac cases. The ECMO run may last from a few hours to several months and is usually associated with many major and minor events that can be overseen and may not always be documented. These ECMO complications are related to the circuit, the patient, or other factors such as procedures, drugs, environment, and personnel. The circuit may show some events that are usually predictable, manageable but require training to be dealt with effectively without compromising patient safety. Fortunately, the circuit-related complications are the most documented,¹ which include: oxygenator failure, clotting, inflammatory response, disseminated intravascular coagulopathy, thrombopenia, hemolysis, air embolism, cannula-related blood stream infections, cannula dislodgement, bleeding, injury during insertion, malpositioning, recirculation, hypothermia, chattering, and oxygenator malfunction. The commonest complications include the oxygenator failure (occurs in 10% of ECMO runs), infections (reported in 17% of ECMO runs), and cannula-related problems (present in 19–20% of ECMO runs in one form or another).¹ Patient-related complications include: neurologic complications including hemorrhages or strokes, infections, bed sores due to prolonged recumbency, deep vein thrombosis and subsequent pulmonary embolism, limb ischemia, sepsis and septic shock, acute kidney injury, pneumothorax and pneumomediastinum, psychological complications, musculoskeletal weakness, and hemolysis.¹ Procedures-related complications include pneumothorax, surgical emphysema, catheter-related complications, and others. Drug-related issues include hemorrhage from anticoagulation, acute kidney injury from antibiotics, heparin-induced thrombocytopenia,^2–4 some other iatrogenic incidents related to the staff, equipment, and facility (environment), which may include transport-related complications, electricity-related events, and medical gases-related events, and these are usually unexpected and require special skills in communication and management.^5,6 These complications may represent a major distress to the patient, caring medical team, and family members. Proper training, adequate preparation in anticipation of potential issues, and team work are the key and only way to handle these complications.⁷ Among other nightmares are ethical and legal considerations about the end of life that are still a major area of debate especially in countries without transplantation programs and clear legalization to support withdrawal.⁸ In summary, nightmares during ECMO runs may occur, and hence, they should be expected. Complications and incidents may occur at any point in time during ECMO runs, and hence, careful and continuous monitoring and regular staff training to manage these complications are the key principles for safe daily ECMO practice.

With the introduction of veno-venous extracorporeal membrane oxygenation (VV-ECMO) to Qatar, the medical intensive care unit (MICU) team started to face new and challenging ethical dilemmas. These ethical questions have subjected the team of physicians, nurses, and other healthcare professionals to mental stress in addition to the physical stress already encountered running the ECMO service.

In this article, we reviewed the literature for similar ethical dilemmas to the ones we have faced comparing our experience with that of other centers around the world.¹

The main principles that we applied were justice, beneficence, non-maleficence, and avoiding cruelty.² The principle of justice was practiced by making ECMO service available to all residents of Qatar, regardless of their social, cultural, or economic background.

Applying this principle has not incurred any injustice to the other fields of medicine as the health system in Qatar provides full medical coverage to all residents of Qatar. The principle of beneficence was applied by lowering the threshold of accepting acute respiratory distress syndrome (ARDS) cases regardless of the inciting cause. As such, ECMO support was started for patients with ARDS due to medical, surgical, and trauma-related conditions.

The two principles of non-maleficence and avoiding cruelty were most challenging.³ The team faced these two principles when dealing with a patient who ended with permanently damaged lungs due to open TB and ARDS with no favorable outcome; lung transplantation was not available in Qatar. What made the situation difficult was the fact that the patient was alert, communicating, and able to make decisions. The patient clearly indicated wanting to stay on ECMO support to stay alive, hoping to return home. Although some argued against continuing ECMO to avoid complications which will harm the patient, others argued against stopping ECMO as it would lead to death. As there was a clear conflict among the team members, the Ethics Committee was consulted and more than one meeting were conducted. At the end, the decision was to continue with full ECMO support, including changing the circuit and/or membrane if needed. The patient eventually succumbed to acute severe right heart failure after more than 9 months on ECMO support.

In conclusion, the ethical challenges that we faced and will most likely continue to face in the ECMO program in Qatar are similar to those faced in other parts of the world. The main difference remains that withdrawing care from futile cases is not accepted in general. This is governed by the local cultural, religious backgrounds, and the level of awareness among the medical staff and the public at large. We believe that any ECMO program should include in its training discussions about potential ethical dilemmas that will most likely be faced in the course of managing the critically ill patients.

Background: Veno-venous extracorporeal membrane oxygenation (VV-ECMO) provides the respiratory support in acute severe respiratory failure until the underlying acute lung pathology improves.^1,2 VV-ECMO support for >100 days is rare and in most situations requires a destination therapy of lung transplant.^3,4 This may not be an option in some centers. We had our longest ECMO case of >300 days with severe residual fibrotic lung disease and inability to wean off ECMO. This presentation briefly discusses the multifaceted challenges and lessons learned from this experience. Discussion/lessons learned: Prolonged ECMO can lead to various challenges, some of which are briefly described below.

1. General ECMO-related issues: These are more common due to prolonged ECMO run and include membrane failure, thrombosis, DIC, etc. Right ventricular failure may prove to be a terminal event in these patients.

2. Rare ECMO-related issues: Prolonged heparin therapy may lead to osteoporosis and heparin-induced thrombocytopenia (HIT). Our patient had positive HIT and was managed with prolonged argatroban therapy.

3. Unusual complications: Extensive fibrocavitary lung disease can lead to large lung cavities impairing gas exchange. Percutaneous pleuropulmonary procedures are at high risk during ECMO. We performed percutaneous drainage of a large bullous lesion without any untoward event. Unexpected hypoglycemia and type II lactic acidosis were also unusual events in our patient. Potential etiologies and management of these rare events will be discussed during the presentation.

4. Team morale and psychosocial support: Prolonged ECMO patient care with no destination therapy can be extremely stressful for care givers. Frequent debriefing sessions may help to mitigate these issues. Formal personal psychological support should be readily available to all team members to mitigate stress-related complications.

5. Skin integrity and musculoskeletal function: Besides the adequate nutrition, mobility and muscle exercises are extremely important to maintain musculoskeletal functional status. We were actively mobilizing our patient while on ECMO to prevent these complications.

6. Psychosocial issues for the patient: Prolonged ECMO, ICU stay, limited mobility, and limited family connections are a rich recipe for depression and other psychosocial issues. Team members from patient's country, birthday and other celebrations, involvement of embassy staff, and use of social media to communicate with the family back home may help to mitigate some of these issues.

7. Ethical and other considerations: ECMO to “nowhere” creates tension among the team members due to different views about the ongoing care of these patients.⁵ Consideration of withdrawal of care is a major ethical issue and needs to be resolved by involvement of all team members, local ethics committee, religious scholars' input, consideration of local policies, and input from the patient and any available family members.

8. ECMO to “nowhere” to “somewhere”: Exploration for non-regional transplant centers and resolution of financial constraints by support from the local embassy, social services support, hospital administration, charitable organization, and conducting fund-raising activities. Conclusion: Prolonged ECMO therapy poses its unique challenges. Good team dynamics, frequent debriefing sessions, and ethic consultations are extremely important during care of these patients. Innovative solutions and collaboration with regional and distant transplant centers may provide an opportunity for destination therapy in these patients.

Aim: Extracorporeal membrane oxygenation (ECMO) may be lifesaving for patients with severe cardiac/respiratory failure. Typically, ECMO is provided by specialized or regional centers, and patients may have to be transported by road or air ambulance. Herein, we will review the essential requirements for road transport of adult ECMO patients, also known as “mobile ECMO”. Background: Interfacility transport on ECMO is defined as “primary” where the ECMO team cannulates the patient at the referring facility and subsequently transports the patient to the ECMO center. In “secondary” transport, the patient is already on ECMO support at the referring facility but a need to transfer to another center has arisen.¹ Patient safety is the overriding priority in any mode of transport; however, in primary transports there is also a need to expedite the arrival of the ECMO team.¹

Interhospital transfer of critically ill patients on multi-modal organ support can be hazardous and adherence to protocols is recommended.^2,3 ECMO patients represent the extreme condition of pathophysiology and therefore meticulous planning, competent personnel, checklists, and attention to details are necessary for ensuring patient safety. Mobile ECMO team: The team composition and specific roles vary considerably between centers. There is no consensus on the exact composition or number of the members. An ECMO nurse or physician can be trained to prime the circuit. Some centers do not include a respiratory therapist (RT) in the mobile ECMO team. ELSO team composition includes a cannulating physician and a surgical assistant (to perform cannulation), an ECMO physician, and specialist in addition to a RT.

Our model in Qatar is composed of two ECMO consultants, an ECMO nurse, a perfusionist, a RT, and a Critical Care Paramedic.

Whatever the configuration is, the mobile ECMO team should have the necessary skills and competency to safely initiate, maintain, and trouble-shoot any ECMO or clinical emergency. The team has to be able to manage the critically ill patient on ECMO, medications, ventilator, and invasive monitoring. Due to lack of back up, the mobile team must have all necessary skills for the mission.¹ECMO transport vehicle: It should provide adequate space to accommodate the patient, stretcher, and all attached equipment including ECMO console. Appropriate electric, oxygen, and gas supply, suction, climate control, and lighting are required.^4,5 Ground transport is recommended for distances up to 400 km,¹ generally using a custom-made mobile ECMO unit (Fig. 1).Figure 1.  HMC Mobile ECMO team (with permission). Note the 360° access, space, adequate lighting, and ancillary equipment within the ambulance.

Equipment: The use of checklists is recommended.¹ Mobile ECMO team should be self-sufficient and ensure adequate supply of all ECMO-specific equipment. Limited space during transportation mandates careful selection of transport equipment without exposing the patient or team to risk. The ECMO team must be familiar with equipment and items in sealed pre-packs help expedite the team dispatch.⁴Medications: The same medications used for in-house ECMO are typically used during transport. The team must ensure adequate supply of medication for the duration of the mission and anticipate possible delays. Equipment and medication redundancy, immediate availability of emergency medications, and use of a medication list further enhance patient safety.^1,4Conclusion: Adequately trained personnel, appropriate vehicle, equipment, and medication in addition to meticulous planning are key elements for safe ECMO transport.

Transport of extracorporeal membrane oxygenation (ECMO) patients in India, where there are very few ECMO centres, is a real challenge due to the huge area and large population of the country, and the diversities of resources between urban and rural areas. Road and air transportation are well established but another common mode of transport not fully developed is the train. Road transportation is used in almost 98% of our ECMO transfers. It is cheaper but its limitations are traffic congestions, road conditions, and travel times. The maximum distance covered is up to 250 miles,¹ which represents almost 5–6 h of travel time. Air transportation is a good option for long distances but is costly.² The average cost of air transportation (fixed wing) in India is around US $1600–2500 per hour, and the average run time is 4–6 h. Helicopter is not a preferred aeromedical transportation modality in India. Train transport services could be ideal in India as many superfast trains are covering the length and breadth of the country but the coaches are currently not suitable.

As an alternative option we developed the concept of a mobile ECMO unit, keeping in mind safety and cost effectiveness. It involves taking the ECMO team to the referring hospitals rather than transferring the patient. It is a viable practice as cardiac surgical skills are available in tertiary hospitals. Patients can be cannulated locally and managed by an expert visiting ECMO team in association with the referring team. Advantages:

•  Safer – no patient transfer •  Cheaper – no aeromedical patient retrieval •  Creates more awareness and utilization of ECMO services in different parts of India •  Opportunity to train and develop regional centres.

Drawbacks:

•  Staff need to get adjusted to different environments, cultures, and languages •  Coordinating teamwork with an entire new team

Retrospective case series of patients managed by our mobile ECMO team from August 2010 to August 2016 shows that we have had 45 patients transported during or before ECMO, without loss of life or major clinical or technical issues during the transport phase. Of the 45 patients, 39 had intrahospital transport for investigation like CT scan and for therapeutic procedures in the operating theatre. Of the 39 patients, 35 (90%) were transported on ECMO, while 4 were transported with conventional ventilation before initiating ECMO. Six patients had interhospital road transport while on VV ECMO with an average distance of 130 km (Ranging of 9–250 km). Of the 6 interhospital transport patients, 4 survived (67%) and were discharged alive from the hospital, and the other two patients died after 5 and 7 days on ECMO. The team has provided mobile ECMO services to 121 patients in different tertiary care hospitals and covered so far eight states of India, roughly 20 cities, and more than 50 tertiary care hospitals. The average survival remained around 45%. The average ECMO expense per patient was US $7340 (Range: US $4500–$23,000).

A dedicated mobile team allows safe road transportation of patients with severe ARDS;³ however, in India, where healthcare is self-sponsored, mobilizing the ECMO team and equipment to put a patient on ECMO in the referring hospital is more cost effective and safer. Our ultimate objective is to develop affordable transport services to reduce healthcare costs. Inclusion of ECMO as part of the curriculum for critical care consultants and cardiac surgeons is essential for improving awareness and getting hands on experience in initiating and streamlining the process of ECMO teaching and training. A definitive roadmap for developing Indian critical care services is crucial.

This study reports India's first international extracorporeal membrane oxygenation (ECMO) transfer as a joint operation between Hamad Medical Corporation (HMC) (Doha, Qatar), International Critical Care Air Transfer Team (ICATT), and Apollo Hospital (Chennai, India).

Severe respiratory failure (SRF) patients can be transferred safely, and there may be a survival advantage in transferring such patients to regional centers of expertise.¹ Patients can also be transported between facilities while on ECMO.² In the case reported below, ECMO was initiated as a bridge for lung transplant,³ which is currently not a procedure available in Qatar. ECMO support as a bridge for these patients could provide acceptable 1-year survival.⁴ It is also important to note that newer ECMO pumps are small and compact, and can safely be used to transfer patients by air.⁵

The first contact between the HMC and ICATT teams was made a month prior to the transfer of an ECMO patient due for the lung transplant. The patient was a middle-aged male with a very complicated and stormy ICU course, known to have interstitial lung disease (ILD) and ECMO-dependent referred for lung transplant.

The patient issues were:

[1]  Advanced ILD [2]  ECMO-dependent [3]  Resolving septic shock [4]  Frequent sepsis with multiple organisms, bacterial and fungal [5]  Hemothorax [6]  Pneumomediastinum [7]  Deep vein thrombosis [8]  Low body mass index (BMI) of 19 kg/m² [9]  Pulmonary embolism [10]  Bilateral brain microhemorrhages

The challenges were:

[11]  Air logistic [12]  Cost [13]  Long-distance ECMO transfer (Qatar to India) [14]  Complicated patient factor [15]  Poor understanding of ECMO among airport authorities [16]  Pump exchange on arrival

There were initial discussions for the ECMO team from India to aeromedically retrieve the patient from Doha, but considering the cost factor, it was more economically viable for the ECMO team from Doha to perform the transfer and return by the same carrier. An appropriate aircraft was chosen to fit all the equipment and the mobile ECMO team. Preparation of an appropriately staffed and equipped intensive care unit (ICU) ambulance (“Mobile ECMO unit”) along with patient stabilization was performed before the transfer to the airport. A bed in the receiving ICU in India was arranged. A mobile communication application was used from the onset of the transfer to communicate among all the relevant team members, referring hospital, receiving hospital, and the aviation team. It included the intensivists, transplant surgeons, ECMO specialists, perfusionists, logistical lead, and the transplant co-coordinator. The patient was mobilized from the medical ICU in Doha to the mobile ECMO unit, while in India the airport and receiving hospital team re-visited the entire operation from the landing to the airport exit of the ambulance to the hospital. Passport details of the patient and team from Doha were obtained and the immigration officer at Chennai airport, India, was appraised about the criticality and the complexity of the operation. A fully loaded ECMO capable ambulance was mobilized with the full team and stationed at the airport, pre-empting and preparing for a possible pump exchange in the event of any possible complication. Nine hours after leaving the hospital, the team from Doha safely landed with the stable patient. Following multiple negotiations, permission for the tarmac transfer of the patient from the air ambulance to the land ambulance was obtained. The patient arrived safely in at Apollo Hospital, Chennai, India, nearly 6 h after leaving the HMC's MICU.

Background: Transport of patients on ECMO has been demonstrated to be safe, if undertaken by well-trained teams.^1–3 Incorporating an Ambulance Service Critical Care Paramedic (CCP) into the team provides a seamless team dynamic during retrieval improving safety.⁴ The CCP helps to co-ordinate logistics, monitors patient and team safety and provides an additional resource for advanced life support during ECMO patient transport. In addition, they provide a link to decision-making and execution of patient movement systems and help access any additional resources within the Ambulance Service. Seamless team dynamics: The success of each retrieval depends as much on team dynamics as on the technical skills of the individual specialties represented in the team.⁵ In recognition of the central role of the Ambulance Service in ECMO transport, CCPs were included in the working group, training and development process for ECMO at Hamad Medical Corporation in Doha, Qatar. Based on their experience, they led the design of the retrieval service Mobile Intensive Care Vehicle and High-Acuity Patient Transport Trolley, helping to develop a platform and system that provides redundancy and limits the requirement for the ECMO team to carry additional backup equipment. In addition, they are part of activities like developing and participating in ECMO transport multidisciplinary simulations. Patient and team safety: Multitasking is a potential source of medical error.⁴ To allow each member of the team to focus on their specific tasks, the CCP takes a patient and team safety role, oversees the various aspects of the process, and ensures the timing of each process and completion of all tasks before movement. Each step in the patient preparation and movement is confirmed as per the safety checklist to ensure nothing is overlooked, and the risk of accidental snagging of lines, trip hazards and subsequent dislodgment of invasive lines or ET tubes is assessed at each step and thus minimised. Logistics: Successful cannulation by the ECMO team requires them to be self-sufficient and independent of the referral hospital for supplies. Prior to the ECMO team activation, the CCP is responsible to ensure that all equipment boxes, required for cannulation and patient care, are loaded into the transport vehicles, and the subsequent delivery of these boxes to the appropriate venue at the referral hospital. The CCP, being familiar with ambulance service equipment (oxygen, power sources, and electronic equipment placement within the ambulance), is there to ensure appropriate connection, trip hazard and snag risk reduction, and troubleshooting on route. ALS and clinical support: Critical Care or Intensive Care Paramedics have received additional training in Critical Care Transport and Aeromedical Medicine. CCPs within the Ambulance Service are able to provide advanced airway interventions (rapid sequence induction intubation), use multimodal mechanical ventilation and provide advanced cardiovascular life support – including infusion devices, inotropes, external pacing and mechanical chest compression devices. The CCP also plays a support role for the ECMO nurse specialist in preparing the patient for transfer to theatre (infusions, monitoring and ventilation), and becomes lead for the safe movement of the patient from the unit to the theatre, and later to the ambulance.

Extracorporeal membrane oxygenation (ECMO) is a highly complex, resource-intensive intervention. The use of veno-venous ECMO for the management of patients with acute, reversible lung failure has increased significantly over the past 10 years.¹ Advances in ECMO technology have resulted in the development of simpler, safer circuits, which are associated with fewer complications. Concomitantly with the clinical and technological changes in ECMO, the role of the ECMO specialist has evolved to manage patient–circuit interaction and the clinical needs of the patient, and to ensure safety of the ECMO circuit through continuous surveillance, assessment and troubleshooting, as well as preventing and managing circuit emergencies.

The Extracorporeal Life Support Organization (ELSO) defines the specialist as “the technical specialist trained to manage the ECMO system and clinical needs of the patient on ECMO under direction and supervision of an ECMO trained physician”.² Internationally, specialists come from a range of professional backgrounds including perfusion, nursing, physiotherapy and medicine. Each ECMO center, depending on the local needs and the availability of resources, in terms of both manpower and finances, has developed its own local specialist role, training program and staffing arrangements. A recent international survey confirmed that despite variation in funding and practice, the staffing arrangement implemented by most centers responding to the survey was the ECMO specialist nurse providing 24/7 ECMO care supported by perfusionist backup for the technical aspects of circuit management.³ Most centers responding to the survey reported a “two carers” approach to nurse staffing with the ECMO specialist nurse working collaboratively with the bedside nurse to ensure the safe co-ordination and management of a critically ill patient with a wide range of complex needs, including multi-organ system support and complex haematological, fluid and sedation management. In addition to meeting the complex needs of the patient, the ECMO specialist nurse is responsible for ensuring the safe management of the ECMO circuit, which includes the titration of blood flow and sweep gas flow to achieve oxygen and carbon dioxide targets, titrations of blood flows and sweep gas flows to facilitate exercise and the management of emergency situations should they arise. Understanding the management of both patient and circuit and the potential patient–circuit interaction is an essential component of the ECMO specialist nurse role. While other professionals have the educational background and technical skills to function in the role of the ECMO specialist, the advantage of the ECMO specialist with a nursing background is their ability to provide 24-hour care managing all aspects of patients' needs, including administration of medication, and to have the technical skills and knowledge to safely manage the ECMO circuit with perfusion backup for the more complicated aspects of circuit management.

As part of the National Health Strategy in the State of Qatar to improve the healthcare sector, the Critical Care Service in Hamad General Hospital (HGH) sets up an extracorporeal membrane oxygenation (ECMO) service within the Medical Intensive Care Unit (MICU) to enhance the care provided to critically ill patients. The new service demands a new technology and specific staff training in order to maintain high standards and safe care. Therefore, our initial investment was in training the team following ELSO guidelines and the purchase of ECMO equipment, especially for the adult population in our case.

In the State of Qatar, the first use of ECMO treatment as respiratory support was in May 2014. Our experience supports other research that this technique requires expert knowledge and skills to deliver best and safe practice.¹ We believe that this can be developed through regular practice and interaction at the bedside with patients and the ECMO technical equipment. Moreover, planning a robust ECMO education programme for the team is central to improving the quality of care and safety that we provide to these vulnerable patients. As part of our preparation process, in November 2013, six ICU nurses attended the ECMO specialist training course in London (UK). Since then, continuing educational programme has been established to train all the whole MICU nursing team focused on ECMO patient care. Several in-house training workshops and external re-training programmes were provided to nurses to develop their theoretical knowledge and technical skills with other members of the clinical team. In addition, we have performed simulation training that focused on multidisciplinary team, emphasising that teamwork is important and necessary for the care of such patients.

The ECMO specialised nurse who takes care of these patients is educated to provide specialised assessment, appropriate monitoring, and clinical reasoning interventions. In addition to manipulating the ECMO machine, understanding ventilation requirements and the patient's medical treatment is crucial to help the ECMO nurses detect the signs of deterioration early and intervene immediately. Therefore, naturally, the role of the ECMO nurse has expanded and tends to be developed with theoretical and technological developments.² The primary roles being close monitoring of alterations in blood flow and observation and maintenance of the circuit, and also an ability to assess the risks and assist with patient care.

We also compared the role of the ECMO specialist nurse versus the role of the perfusionist. We believe in the importance of both roles; however, we argue that when the ECMO nurse works alongside the ICU bedside nurse, the bedside care becomes more effective. Both nurses and perfusionists are able to understand the patient's overall condition and needs during the ECMO run, and have better interpretation regarding observed changes.³ The partnership promotes the continuity of patient care and allows better communication and support of the family as an aspect of care. This also increases the opportunity of bedside training and education and allows developing other nurses under supervision.

Overall, with proper planning, education, and structuring of ECMO care, we were able to obtain outcomes that are similar to those reported internationally. We aim to further improve patient outcome, especially regarding post-ICU discharge as part of holistic nursing care.

Extracorporeal membrane oxygenation (ECMO) or extracorporeal life support (ECLS) is a highly specialized procedure relying on advanced technology, and specific attention is required to ensure safe operation. Who should or can accomplish this procedure is roughly defined by the ELSO guidelines.¹ Before starting an ECMO program, proper assessment of resource adequacy is crucial, and developing the structure for the program is mandatory. Recommendations can be found on the Extracorporeal Life Support Organization (ELSO) website.² Formal training of the whole team is desired, not to say highly recommended, to be able to provide the best patient care possible.

In the UAE, the need for an ECMO program was identified and formalized in 2009. Two batches of nurses were consequently sent to a high-volume ECMO center in Europe to acquire both theoretical knowledge and practical training in the waterlab to master the required technical skills. Observation of clinical shifts and daily routine for ECMO as well as sharing protocols and policies provided for a safe startup in the UAE. When volume increased and the need for more trained nursing specialists was identified, we developed a three-day specific training course: first day for general introduction, second day for veno-arterial (VA) ECMO, and third day dedicated to veno-venous (VV) ECMO. The course is backed by competency assessment during supervised bedside shifts.

Maintenance of task skills for our ECMO team is achieved during monthly waterlab sessions (de-airing, pump failure, etc.) when not only manual practice is done, but also case presentations and reviews are discussed, team debriefing is done, and lectures are delivered to ensure up-to-date knowledge and understanding. The importance of simulation for ECMO has been described,³ and we made it a focus of our specialist ECMO training. Our concept of training has since then spread over the Middle East area and South Africa.

In 2010, following the H1N1 swine flu pandemic,¹ five severe respiratory centers were commissioned in England. These were established to provide veno-venous ECMO (extracorporeal membrane oxygenation) for patients with refractory respiratory failure. Moreover, it was a condition set out by the commissioning body that each center would carry out a minimum of 20 cases per year to remain certified. The reality of the situation has proved somewhat different. At Guy's and St Thomas’ NHS foundation Trust (GSTT), the annual number of cases has steadily increased. In 2015, the Trust carried out almost 100 veno-venous ECMO cases.² These recent developments in available therapies for patients with refractory respiratory failure or cardiac failure meant that intensive care staff have been exposed to equipment with which they have been hitherto unfamiliar. Clinical perfusion scientists, previously “shackled” to the heart lung machine, have found themselves thrust into clinical, supportive, and educational roles, teaching both nurses and medical staff the ins and outs of the ECMO equipment and being an integral part of the multidisciplinary team retrieving patients from tertiary centers.

This increase in workload has necessitated an increase in staffing requirements across all specialties and an ever evolving training program. All ECMO specialist nurses are required to undergo a comprehensive training program.³ This serves to familiarize them with the equipment used, give them a good understanding of the nuances of the ECMO circuit, and train them to an accepted level of competency in ECMO emergencies. All water laboratory training is carried out by perfusion ECMO trainers. The competencies practiced have evolved to include emergency procedures that staff have encountered over the years since the service began. Since 2009, at Guy's and St Thomas’ NHS Foundation Trust, we have developed a robust and comprehensive training program to ensure that we have a large cohort of well-trained, confident, and competent intensive care staff who are able to handle any ECMO emergencies in a safe and timely manner.

ECMO specialist training involves water drills approximately 3 days a week prior to “signing off” and then mandatory updates every 3 months.³ ECMO consultants and medical fellows also undergo the same training and have yearly updates.

This presentation explains how the role of the clinical perfusionist at GSTT has evolved outside the operating theater environment in training, supportive, and clinical roles.

It also explains the role of the perfusionist in the retrieval process as well as outlining the training program and the three-day bi-annual high-fidelity simulation course developed by the multidisciplinary team in the Trust.

Intensive care unit-acquired weakness is a common sequela of critical illness and is associated with deficits in physical strength, functional performance, and associated health-related quality of life.^1–3 Early rehabilitation in the intensive care unit (ICU) is recognised as safe and feasible.^4,5 Maintaining and restoring musculoskeletal strength and function is recognised as an essential element of therapy in critical care.³

Active rehabilitation of patients with femoral access veno-venous extracorporeal membrane oxygenation (VV ECMO) has been deemed a high-risk procedure and to the authors' knowledge is not a routine practice. There is limited published literature describing the rehabilitation of those requiring VV ECMO in critical care.^6–8 The aim of this study was to explore the active rehabilitation of those requiring VV ECMO.

A retrospective review of the medical records of patients admitted to the Intensive Care Unit at Saint Thomas’ Hospital requiring VV ECMO was undertaken. Owing to the nature of this observational retrospective study, it was exempt from ethical approval. Data were collected for the period from 1 September 2012 to 31 January 2015. Details of rehabilitation sessions were recorded daily on the electronic patient record by physiotherapists. Data on the frequency and type of active rehabilitation, time on VV ECMO, and patient characteristics, including diagnosis, were collected. Active rehabilitation was defined as any of the following interventions: active range of movement, bed mobility, sitting on the edge of the bed, step transfers, mobilisation, and leg cycle ergometer use.

During the study period, 56 patients (30 male) who required VV ECMO were identified. Of them, 55 were cannulated bi-femorally and 1 required femoral and jugular cannulation. The mean (SD) patient age was 44.2 (14.3) years and the diagnoses requiring VV ECMO were: bacterial pneumonia (n = 19), viral pneumonia (n = 20), interstitial lung disease (n = 5), aspiration (n = 2), asthma (n = 4), tuberculosis (n = 2), cancer (n = 1), and non-pulmonary ARDS (n = 3). The mean (SD) duration of VV ECMO was 32 (37.6) days.

Twenty-six patients (46%) participated in active rehabilitation. A total of 808 active rehabilitation sessions were carried out. The active rehabilitation interventions provided were: sitting on the edge of the bed (n = 683); step transfer to chair (n = 112); and cycle ergometer use (n = 13). Rehabilitation sessions generally involved two physiotherapists, one bedside nurse, and one ECMO clinical nurse specialist. Thirty patients (54%) did not participate in active rehabilitation. The reasons recorded for this were either a deterioration in the patient's condition or the indication that the patient did not meet the criteria for active rehabilitation, e.g. Richmond Agitation and Sedation Score <  − 2 or >+2; neurologically inappropriate; or unable to follow commands. No rehabilitation sessions had to be terminated due to adverse events.

This small retrospective cohort study showed that active rehabilitation is feasible in patients receiving VV ECMO, the majority (98%) of whom were cannulated bi-femorally. However, not all patients are suitable for active rehabilitation. Previous local evaluation data have shown that care for those requiring VV ECMO is resource intensive, requiring increased numbers of staff and time compared with those requiring conventional mechanical ventilation. Sufficient resource is essential to ensure a safe, structured, and co-ordinated approach, which enables active rehabilitation for those requiring VV ECMO. Further research is required, investigating the physiological response to exercise in this patient cohort, to inform future practice.

The last couple of decades has brought a lot of changes in thoughts and technology in the domain of simulation-based healthcare education, ranging from emergency preparedness using screen-based technology to the practice of precise surgical procedures with computerised simulators with haptic and performance feedback.¹ There is a perpetually evolving educational and technological simulation continuum available to educators and clinicians promoting the practical and cognitive aspects of healthcare delivery. It is becoming an increasingly competitive market area from an industry perspective as more and more governments invest on technology to support educational initiatives and programmes in order to increase patient safety and standards of care.² Although industry strives to develop more advanced and realistic simulators, it is increasingly argued that it is not necessarily linked to better learning outcomes.³ For an effective use of simulation as an educational approach, a key aspect is to focus on selecting the approach that best addresses the intended learning objectives.⁴

Extracorporeal membrane oxygenation (ECMO) is a bridge therapy that can be separated into several phases from a training perspective such as patient selection, cannulation type (veno-venous (VV)/venous-arterial (VA)/VVA) and process (ultrasound guided cannulation, fluoroscopy cannula placement, securing the cannula, etc.), ECMO patient management and issues, and ECMO circuit issues.⁵ Overall, it is a complex system that all ECMO team members need to grasp at least theoretically in order to be able to support one another at any stage when a problem occurs. The safest way to become familiar with ECMO is to use simulation; however, at present, there is no single simulation platform that allows us to seemingly practise the succession of phases without transiting from one type of simulator to another type, and this is what we are trying to address. At best, and generally only for demonstration purposes (appropriate in that case), we are “simulating the simulation” as a form of deception.⁴ We currently pretend the ultrasound or fluoroscopy procedure by playing a video making observers believe that it is a live view or we ask them to imagine a colour change in the oxygenated blood, which might be a more significant gap.

Several teams have developed their own simulation solution⁶ to bridge a gap in the market or save on the purchase of prohibitive technologically advanced simulators that still have limitations. The simulations for ECMO training often either start post cannulation, whereby a team of learners has to fix a machine or patient issue during the ECMO run, or they concentrate on very technical skills such as cannulation insertion and water drills to practise circuit change. Both aspects are critical but still leave room for missed educational opportunities involving the whole team. Collaboration, generally without commercial ambition, between clinicians, educators, and engineers is now pushing the boundaries of ECMO simulation, making it a more affordable and common practice, but ultimately industrial support is generally required to “mass-produce” and distribute the solutions as we need them: functional, effective, and affordable, so the use of simulation for ECMO training can become a common practice and clinical teams are better prepared to initiate ECMO and deal with emergency situations. We hope to introduce ELSO very soon with a collaboratively developed simulator that meets all key training requirements.

Transfer and retrieval of extracorporeal membrane oxygenation (ECMO) patients is an aspect of a severe respiratory failure (SRF) service, which has generally low volume and high risk thus necessitating attention to particular safety measures. One of the key aspects in preventing patient safety issues and minimising risks of harm during the transportation of an ECMO patient is to develop a well-prepared multiprofessional team. This is the key area where simulation can play a very important role in various stages of a patient care pathway. There is much more to ECMO patient transfer and retrieval than one may suspect as it involves a referral, a lot of planning regarding activation, tasking, transporting, and disposing of the patient at the receiving facility,¹ all of which should be done collaboratively and maintaining open and high communication standards to prevent mishaps.

Simulation is used not only to develop important ECMO-related clinical or teamwork skills, but also to identify potential safety threats.² There are several modalities of simulation that can be used to prepare the clinical team and test processes put in place.³ The modality needs to be selected according to the specific learning objectives expected to be addressed. The full-scale high-fidelity approach is usually the most complex to orchestrate as it would most likely involve the team members, a scenario, a patient simulator or simulated patient (Actor), real clinical equipment, and the patient care setting (ambulance and potentially the referring and/or receiving facility). For this type of simulation to be beneficial to more people than the immediate participants, it requires the scenario to be audio/video recorded with live broadcast into an observation room, where other learners could follow the event and then be engaged in the debriefing with the participants. This does not constitute the ideal starting point of developing an ECMO transport simulation programme but is certainly an objective to achieve to really prepare a team on all aspects of “Mobile ECMO”.

Our recommendation is to start more simply and gradually increase the level of realism and complexity, so that teething issues can be identified and fixed in a more manageable manner. Process testing, new staff orientation, emergency procedures, and understanding of roles and responsibilities are elements that should initially be addressed in a low-fidelity simulation context such as Visually Enhanced Mental Simulation.⁴ It is also important to realise that a scenario, of low or high fidelity, can simply be a snapshot of the Mobile ECMO process, as it helps focus on key pre-identified learning objectives. The starting point might be to simulate how a referral is evaluated via remote patient assessment and how the team is activated. A different phase might involve starting at the point of transferring the newly cannulated patient from the operating table onto the ambulance stretcher and moving through the hospital and loading onto the vehicle (Fig. 1). A whole scenario could take place inside the ambulance during the journey with the ECMO patient. As in real life, the possibilities offered by simulation are endless but need to serve a real educational purpose.

Simulation training is increasingly being used to provide clinical care providers with experience and competence in high-risk procedures that occur infrequently. Implementation of standardized extracorporeal life support (ECLS) simulation training improves multidisciplinary team processes and increases efficiency of establishing ECLS. The initiation of ECLS is a highly complex process that requires technical proficiency of the surgeon and frequently depends on advanced crisis-management skills. Human performance simulation systems can be designed to simulate complex surgical procedures and used to teach and assess technical skills and refine team management protocols. Furthermore, high-fidelity simulators may enhance technical competency and improve patient safety.

The use of ECLS cannulation simulation has been shown to improve proficiency of surgical cannulation.¹ However, advanced surgical skills simulators are generally expensive and require extensive setup time.² The use of commercially available simulation systems that cost >$500 USD per use represents a significant financial burden for many centers that are establishing an ECLS program.

Affordable ( < $10 USD per use), silicone-based ECLS cannulation simulators can be created using commercial available materials. Custom ECLS cannulation simulators may be designed to fulfill specific educational and quality improvement requirements in unique hospital settings. High-fidelity simulation models may be used to accurately recreate anatomic structures. When integrated into a comprehensive ECLS simulation program, cannulation simulators create a more realistic learning environment that more accurately represents clinical scenarios encountered in the clinical management of ECLS patients, including cannula malpositioning events, bleeding, air entrainment, and hypovolemia. In addition, ECLS cannulation simulators can be used to teach and reinforce proper techniques in a standardized manner.

Commercially available, silicone-based materials may be combined to reproduce layers of skin, subcutaneous tissue, blood vessels, and boney. Percutaneous models utilize similar materials but require additional processing to render ECLS cannulation models ultrasound compatible. Cannulation simulators may be integrated with low-cost compliance chambers and tubing to reproduce circulatory physiology after initiating ECLS. Although each cannulation simulator may be used only once, the raw materials for custom-made simulators cost less than $10 USD each. This low cost for production allows centers to use them frequently and incorporate them into existing skills-based ECLS training programs.

Percutaneous cannulation simulators that are designed to reproduce the cervical cannulation with dual-lumen veno-venous ECLS cannulae are being developed by our team. These novel simulators will enable users to perform ultrasound-guided percutaneous reproduce cannulation using standard dual-lumen cannulae and echocardiography. This system will facilitate communication between proceduralists and echocardiographers.

Background: Extracorporeal membrane oxygenation (ECMO) is a high-complexity life-saving procedure riddled with mechanical complications that can place the patient in a critical state where fast and coordinated actions are required to avoid mortality. Thus, patients on ECMO are supervised round the clock by highly trained nurses and perfusionists. Currently, ECMO training programs include patient emergency simulations performed with different levels of success. Some training facilities use mannequins that have computer-controlled physiological parameters such as heart rate and oxygen saturation. The circuit parameters such as pressure are manually adjusted per scenario; air and artificial blood are manually injected to indicate problems such as air embolism, and hypovolemia.¹ Despite being realistic, using an actual ECMO circuit for simulation training purposes has disadvantages such as the use of expensive disposable equipment (oxygenation membrane), lack of oxygenation color differentials, and manual circuit adjustments and injections. Methods: This paper describes the design of a modular ECMO simulator centered on the use of thermochromic ink and instructor/clinician interface. The goal is to re-create the ECMO circuit and its functionalities using affordable, reusable, and extensible mechanisms that do not require the presence of a real ECMO machine. Results: Oxygenation is visually simulated by heating and cooling thermochromic ink, allowing it to switch between dark and light red. A replica of an ECMO machine's console interface allows manual adjustment of parameters wirelessly through a tablet instructor application. Furthermore, the visual and audio cues of mechanical complications such as access line shattering can be easily implemented using mechanical vibrators. See proposed simulator design in Figure 1. Conclusions: Advantages of the proposed system include the removal of the cost barrier and inconvenience of current ECMO simulators, while adding modularity and customizability to simulate a multitude of emergency scenarios, thus increasing the accessibility, fidelity, and versatility of ECMO patient management training.

Background: In medical simulation and training, blood is used to exhibit its different behaviors in context. In some cases, blood color differential is an imperative visual effect to ensure high-fidelity training and practical understanding. High simulation realism is usually achieved by using animal or artificial blood (which mimics some biological features of blood), which has high cost, requires disposable equipment such as oxygenators, and entails contamination or infection risks. Methods: A novel method for blood simulation is introduced. Using the thermal properties of thermochromic ink, its color can be altered by adjustment of temperature.¹ The unique red color of blood can be mimicked to a high fidelity using a custom hue of thermochromic ink. Then, by adjusting its temperature, realistic dark and bright red can be employed to simulate the low and high oxygen concentrations of blood, respectively. Although thermochromic ink currently does not imitate other blood properties such as viscosity and clotting, it has superior merits when color change simulation is a paramount priority. The major advantages of the proposed solution are reusability and cost. Thermochromic ink can be used for multiple simulations without any noticeable change in quality. It also costs significantly less than using actual or artificial blood. Results: Testing results of the proposed solution in extracorporeal membrane oxygenation (ECMO) simulation has proven its efficacy as a practical solution for medical simulations (see Figure 1). To prevent membrane occlusion because of the thermochromic ink, the latter needs to be pierced. In addition to ECMO simulation, other medical applications are being considered. Conclusions: The use of thermochromic ink in medical training provides reproducible color change simulation features of blood while maintaining significantly lower equipment costs and contamination risks as all circuit components can be reused.

Background: Transport of critically ill patients especially on extracorporeal membrane oxygenation (ECMO) is a real challenge. In India, more than 98% of cases requiring transfer are transported by road and less than 2% of cases are transported by air due to costs involved. As an institutional policy, and considering the safety and cost effectiveness, we have decided to develop mobile teams who can go to the patients, cannulate them, and stay during the course of the ECMO run. The mobile team program was established in 2010 when there were less than 10 ECMO centers in the country.¹Methods: First, the ECMO intensivist talks to the referring physician to confirm the need for ECMO, and then the coordinator settles financial issues and organizes the team, equipment, and travel arrangements. The team composed of the nursing staff, perfusionist, and intensivist² leaves within 2 hours of receiving the confirmation. Results: Retrospective analysis of patients managed on ECMO by our mobile ECMO team from August 2010 to August 2016 shows that we received 170 referrals. Of these, 132 calls were confirmed, but we initiated ECMO in 121 patients only (Table 1). We visited the eight Indian states, roughly 20 cities, and more than 50 tertiary care hospitals.³ Only four patients were in secondary care centers and were transferred to nearby tertiary care units after initiation of ECMO and stabilization. The average time from call confirmation to initiation of ECMO was 8 hours, with a minimum of 4 hours and a maximum of 14 hours, mainly depending on the availability of a transport modality.

There was not much of mortality difference when ECMO is done in an ECMO center or when it is done by an expert mobile ECMO team out of the hospital.

Problems encountered included:

1. □ Forgetting part of the equipment or disposables in four cases, resulting in a 4-hour delay to ECMO initiation;
2. □ Getting adjusted to a different environment, different culture, and language;
3. □ Coordinating team work with an entire new team at the referring facility.

Background: The mission of the King Faisal Specialist Hospital and Research Center (KFSH&RC), Riyadh, Saudi Arabia, is to provide safe and effective care to patients. KFSH&RC is a 985-bed hospital that started its ECMO program in 2004. Based on the ELSO guidelines, KFSH&RC invested in establishing a successful ECMO program by upgrading the logistic, team composition, quality, and educational structure in the organization.¹Methods: The following key components were utilized including institutional commitment, to build a strong program block by block relying on the support of the following team structure: physician champion, multidisciplinary leadership, nursing-led ECMO program, ECMO coordinator, ECMO specialist, and organized training² that includes low- to high-fidelity simulations.³Results: The KFSH&RC ECMO nursing-led program caters for a diverse patient population and provides support in the following areas: bridge-to-transplant program such as heart and lung; adult and pediatric patients, including acute lung injury/acute respiratory distress syndrome (ARDS); and cardiac surgeries and congenital anomalies. In addition, KFSH&RC is establishing a referral and transport system to acknowledge our center as supporter to the surrounding organizations to refer patients.

In 2014, KFSH&RC provided 30 ECMO supports, of which 26 were for cardiac support. A total of 39 ECMO supports were provided in 2015, of which six were post-lung transplant and three related to acute lung injury.

A total of 66 patients were treated with veno-arterial ECMO with a survival to decannulation of 56.6 and 46.15% in 2014 and 2015, respectively.

With recent advancement, KSH&RC has initiated the extracorporeal cardiopulmonary resuscitation (ECPR) life support program and activation of code ECMO services under the facility with unified code pager and team. Conclusion: The results highlight that a developed nursing-led ECMO program can improve patient outcomes and provide safe transport services.¹ Further study is required to determine whether ECMO patient outcomes will continue to improve with less complications and good survival rate.

Background: Although there have been many developments related to specific strategies for treating patients after poisoning exposure, the mainstay of therapy remains symptomatic and supportive care. Objectives: To highlight different techniques of ECMO, indications, contraindications, and some case reports of its use in patients with poisoning. Methods: PubMed and the Cochrane database were searched using the terms “extracorporeal membrane oxygenation”, “ECMO”, and “poison”. Results: Two types of ECMO are used: veno-venous ECMO (VV-ECMO) and veno-arterial ECMO (VA-ECMO). Indications: As the clinical impact of intoxication is often temporary, ECMO can be used as a “bridge to recovery”. Contraindications: Absolute contraindications are uncontrolled coagulopathy and severe intracranial bleeding, which precludes the use of anticoagulation therapy. Relative contraindications to ECMO include advanced age, severe irreversible brain injury, untreatable metastatic cancer, and severe organ dysfunction.

In different case reports, ECMO has been successfully used in treating cases of aluminum phosphide poisoning,^1,2 hydrocarbon aspiration,³ and calcium channel blocker toxicity.^4,5

Patients with aluminum phosphide poisoning treated with ECMO recovered very well and were safely discharged from hospital.²

There is evidence that pulmonary parenchymal tissue can recover from hydrocarbon pneumonitis, but the degree of injury and recovery is variable. In the Extracorporeal Life Support Organization Registry, 19 children with hydrocarbon pneumonitis were treated with extracorporeal membrane oxygenation during 1985 to 1994 and 68% survived compared with the 52% overall survival of 883 pediatric cases who had a diagnosis of a respiratory condition.³

For calcium channel blocker toxicity, ECMO was an efficient and relatively safe last resort therapy in critically ill poisoned patients (i.e. cardiac arrest and refractory shock) who did not respond to conventional therapies.⁴Conclusions: Recently, ECMO equipment has improved considerably, rendering it more biocompatible, and it has been used more frequently as an assist device for patients needing oxygenation as well as circulatory support. ECMO is considered a bridge for patients who are severely poisoned with acute respiratory distress syndrome (ARDS) or refractory circulatory shock.

Background: Streptococcal toxic shock syndrome (STSS) is a life-threatening illness associated with invasive or non-invasive group A streptococcal (GAS) infection with rapid progression and a high mortality rate.¹ There are limited data on the use of extracorporeal membrane oxygenation (ECMO) in toxic shock syndrome (TSS) with few case reports in adults with TSS-induced cardiac dysfunction^2,3 and a pediatric series of severe group A streptococcal infections from Australia.¹ The mode of ECMO was veno-arterial (VA) in all these case reports due to significant myocardial failure. According to our knowledge, we present the first reported case of STSS in a child managed with veno-venous (VV) ECMO. Methods: Clinical presentation, investigations, management, and outcome of the child was followed from the health records. The study was exempt from ethical approval. Detailed search of the published medical articles did not reveal similar publication. Results: A 13-month-old, previously healthy child presented in a state of shock 3 days after sustaining a burn wound to the dorsum of the left hand. Blood and wound cultures were positive for Streptococcus pyogenes, and there were signs of multiorgan failure, satisfying the Center for Disease Control (CDC) criteria for STSS. Acute respiratory distress syndrome (ARDS) developed on day 2 of presentation, accompanied by hemodynamic instability requiring support with multiple inotropes with a modified inotropic score of 117.5. Echocardiography revealed a structurally normal heart with ejection fraction of 40%. Hemodynamics were found to be associated with blood oxygen saturation. Blood pressure increased on increasing SpO2 with no change in the inotropic support. VV ECMO was initiated when the oxygenation index reached 68 in spite of being on inotropes. Inotropic support was weaned and stopped after 12 h. The child remained on ECMO for 7 days before being successfully decannulated. Conclusions: As the underlying cause of STSS is frequently treatable, ECMO may be considered early in the management of these cases when conservative measures fail. Presence of inotropic support should not be considered as a contraindication for VV ECMO in pediatric STSS.^4,5

Background: Survival following extracorporeal membrane oxygenation (ECMO) has steadily improved over the past decade owing to better knowledge and training.^1,2 The objective of our study is to identify the predictors and trend of in-hospital morbidity and mortality during our initial experience. Methods: After obtaining an DSREC (Dubai Scientific Research Ethics Committee) review and exemption, we collected the clinical data of patients from May 2013 to November 2016 and analyzed for baseline characteristics, indication, type, undergoing cardiopulmonary resuscitation (CPR) or not, duration of ECMO treatment, morbidity, and mortality. Results: A total of 24 adults received ECMO (18 M/6 F), of which 22 were supported with veno-arterial (VA) ECMO and the remaining were converted from VA to veno-venous (VV) ECMO during the course of their treatment. There were 8 (6 M/2 F) survivors (30%) with two bridged for left ventricular assist device (LVAD) and one for heart transplant. The mortality pattern as shown in Figure 1 shows a consistent improvement of more than 50% from mid-2015. Weaning was overall successful in 30% of surgical and 38% of medical patients. CPR was necessary in 12 patients, none from the survivor group. The minimum to maximum duration of ECMO was 53–483 hours in the survivors versus 2–528 hours in the non-survivors, of which 8 (50%) survived less than 24 hours on ECMO. The most frequent complications were bleeding from catheterization or surgical site (58.3%), renal failure (29.1%), GI bleeding (20.8%), and leg ischemia (12.5%). Two patients had raised bilirubin and one altered response to medication, resulting in hypertension and bleeding.³ The percentage among survivors to non-survivors with reference to bleeding was 38% vs. 69%, leg ischemia 0% vs.18%, renal failure 12.5% vs. 37.5%, and GI bleeding 12.5% vs. 31.2%.Figure 1.  Mortality rate of ECMO patients at Dubai Hospital from 2013 to 2016.

Conclusions: In spite of a steep learning curve, a remarkable improvement in the reduction of mortality was achieved during the latter half of the term possibly due to better understanding, education, and training. The survival during this interval compared well with the previous results and Extracorporeal Life Support Organization (ELSO) reports.^4,5 The percentage of complications and the number of patients requiring CPR were less in the survivors' group, indicating that early referral and prevention of ECMO complications are equally important. These two elements could be the key to our success in the management of these patients.

Introduction: Bleeding is the most frequent complication in patients receiving veno-arterial or veno-venous extracorporeal membrane oxygenation (ECMO).^1,2 Recombinant activated factor VII (rFVIIa) has been used in these patients with conflicting results. We describe our experience in pediatric patients on ECMO who received rFVIIa for refractory bleeding in whom conventional management was not successful. This conventional management to stop the bleeding included adjustment of anticoagulation medications, substitution of clotting factors and platelets, and exclusion of surgical cause of bleeding.^3–6Methods: We reviewed the medical records of all the patients who underwent ECMO in our PICU from January 1999 to July 2014 and received rFVIIa for refractory bleeding. Clinical characteristics, demographics, type of congenital heart disease, surgical correction, bleeding, thrombotic complications, mortality, and rFVIIa dose were documented. Being based on retrospective hospital data, this study is exempt from IRB approval. Results: A total of 123 patients underwent ECMO in our unit since 1999, and five of them received rFVIIa for persistent refractory bleeding during veno-arterial ECMO. All of them had corrective cardiac surgery for congenital defects before installation of ECMO. Bleeding dramatically decreased in four patients (Figure 1), without a major thrombotic event. In one patient, bleeding remained significant and he developed left pulmonary artery thrombosis confirmed by cardiac catheterization, and this patient died. Four patients survived at 48-h after withdrawal from ECMO.Figure 1.  Rate of bleeding in the 3 h prior to the dose of rFVIIa and the 3 h after the dose of rFVIIa.

Conclusions: rFVIIa use for refractory bleeding in patients on ECMO was efficacious in four out of five patients in stopping bleeding without major thrombotic events. While the use of rFVIIa seems effective, indications for its use, modalities of administration, and precautions to be taken need to be better defined.

Background: ECMO has been successfully used to support patients with trauma-induced respiratory failure. Here, we present the successful application of ECMO in a patient with life-threatening polytrauma following a road traffic accident complicated by severe acute respiratory failure.¹Methods: This is a retrospective case report, and approval for presentation has been obtained from the department and can be submitted upon request.

The patient was 20 years old and found at the roadside after being hit by a vehicle. The patient was rushed into the ED by an ambulance, where the trachea was intubated due to the low Glasgow Coma Score. A trauma CT scan revealed severe head injury with possible diffuse axonal injury. The scan also confirmed fractures of the mandible, left transfers process of L3,4,5 and first sacral vertebrae, pelvis and comminuted fracture of the right tibia and fibula. The patient was admitted to the Trauma Intensive Care Unit (TICU). A subsequent head CT scan showed multiple hemorrhagic contusions and cerebral edema. The patient underwent ventriculostomy and intracranial pressure (ICP) monitoring insertion, and was treated by neuroprotective interventions including sedation, paralysis, hypothermia, and hyperosmolar therapy. Unfortunately, the patient developed ventilator-associated pneumonia (VAP), which resulted in severe ARDS. Despite appropriate antibiotics, lung-protective ventilation, rescue inhaled nitric oxide, and high-frequency oscillatory ventilation (HFOV), the patient continued to have severe respiratory failure. The patient was evaluated for rescue ECMO despite severe neurological injury.² Veno-venous ECMO was initiated using percutaneous femoral–jugular configuration with a 25 French access cannula in the inferior vena cava and a 21 French return cannula in the right internal jugular vein.³ Throughout the ECMO run, no systemic anticoagulation was used, except the initial 5,000 units heparin administered during cannulation.⁴ Percutaneous tracheostomy was placed and the patient was weaned off ECMO over the next week. ECMO decannulation was performed on day 7 and decannulation of tracheostomy on day 18 of ICU admission with good neurological outcome, and transferred for rehabilitation. Conclusion: ECMO may be an acceptable therapy for patients with profound respiratory failure secondary to trauma and intracranial pathology, contraindicating the use of systemic anticoagulation.^1,5 Neurological prognosis is difficult to predict in patients with intracranial pathology and multiple organ dysfunction.^2,6 Axonal injury based on imaging studies may not predict neurological recovery in individual patients, and salvage therapies, including ECMO, should not be denied in these patients.^6,7

Background: Intensive care patients are at high risk of increased mortality and morbidity and longer hospital stay secondary to prolonged immobility.¹Methods: Early mobilization and therapeutic exercises reduce delirium and days on mechanical ventilation, shorten ICU and hospital stay, improve physical function, and reduce healthcare costs.^2,3

Mobilization and exercise can be safely implemented for patients receiving mechanical ventilation and continuous hemofiltration.^4–6

The incidence of physical deconditioning and other ICU-acquired morbidities are very high among patients with severe respiratory failure. Protocol-directed progressive early mobilizations of these groups of patients are safe and feasible even if they are on ECMO.^7,8

Our ECMO patients are evaluated daily to assess hemodynamic and respiratory stability, and suitability for mobilization and exercise program. Assessment includes cardiovascular parameters, ECMO circuit, APTT and arterial blood gas results and targets, sedation level, muscle relaxation use, medical and nursing plan for the day, recent chest X-ray, and ECMO settings and recent changes. Figure 1 illustrates the continuum of early mobility protocol in the Hamad General Hospital Medical Intensive Care Unit (ICU). The mobilization level and exercises determined are based on these assessments. Adequate patient preparation is essential before initiating any exercises or mobilization.

Patient safety is a primary goal and to achieve this, the multidisciplinary ECMO team pays due attention to intravenous lines, ECMO cannulas, and monitoring devices in place. Maintenance of adequate oxygenation and hemodynamic stability has to be assured throughout mobilization and rehabilitation therapy.

The team must ensure that adequate ECMO tubing slack is available to allow safe movement of the patient without undue strain on the circuit, and a dedicated team member, typically a perfusionist or ECMO nurse, will be in charge of monitoring the circuit. ECMO sweep gas and blood flow rates as well as supplemental oxygen may all be increased. Hemodynamic or respiratory instability should be assessed immediately and the session can be stopped without delay. Conclusions: Goal-directed slow progressive early mobilization of ECMO patients is feasible and safe when undertaken by a multidisciplinary team. As evidence supports the implementation of rehabilitation in the ICU, particular attention should be made to incorporate mobility and exercises in the daily routine of ECMO patients.⁷

Background: Awake extracorporeal membrane oxygenation (ECMO) in conscious, extubated patients has been used successfully in adults and children, primarily as a bridge to lung or heart–lung transplantation and recovery from refractory cardiogenic shock.^1,2 However, this strategy has been reported only as an exceptional measure in neonatal patients. We present a case of neonatal respiratory failure where an infant was extubated while on ECMO and managed without invasive ventilation. Methods: The clinical details, laboratory investigations, management, and outcome of the patient were reviewed from the electronic health record. This single-patient case report was exempt from the IRB at our institution. The photograph was used with parental consent. Results: The patient was a 2950 g product of an uncomplicated term pregnancy, whose postnatal course was complicated by neonatal acute respiratory failure, pulmonary hypertension, and bilateral pneumothoraces. The infant was managed on veno-arterial (VA) ECMO. Despite the presence of thoracostomy tubes and rest ventilator settings while on VA ECMO, pneumothoraces persisted. On ECMO day 2, the patient was electively extubated to a humidified high-flow nasal cannula. At 96 h after extubation, there was complete resolution of bilateral pneumothoraces. The infant achieved adequate lung recruitment with only spontaneous respiration and underwent decannulation on ECMO day 6. He was electively intubated for decannulation and extubated 12 h later. At 5 days post-decannulation, the infant was weaned off respiratory support and discharged home 4 weeks after decannulation after weaning from sedation and establishing successful oral feedings. Conclusions: Awake neonatal ECMO appears to be safe and effective and may offer significant advantages over traditional management in certain clinical scenarios, particularly in cases of persistent air leak. To our knowledge, there have been no published studies comparing awake ECMO with traditional (ventilated) ECMO in neonatal patients, although we have successfully managed five patients in our neonatal intensive care unit using this strategy for various clinical indications. Extubation offers the advantages of mitigating ventilator-associated pneumonia (VAP) risk and tracheal trauma, facilitating resolution of air leak, de-escalating sedation, and promoting family bonding. Prospective comparison trials are warranted.

Background: Extracorporeal membrane oxygenation (ECMO) has evolved as a treatment option for patients having rev ersible severe respiratory failure who are deter iorating on conventional ventilation.^1,2 We describe our experience with a patient who received ECMO for refractory hypoxemic respiratory failure due to community-acquired pneumonia associated with systemic lupus erythematosus (SLE). Methods: This is a retrospective case report for which approval for presentation has been obtained from the administration of the department and can be submitted upon request. Our patient was an 18-year-old female with a long history of SLE with nephritis who was recently started on immunosuppression, admitted with azotemia, fluid overload, and respiratory failure, and initially improved with fluid removal.³ Her respiratory status later worsened with saturations in the low 80s despite 100% FiO2 and a positive end-expiratory pressure (PEEP) of 14 cm H2O. She had a trial of prone positioning together with PEEP optimization, but her condition continued to deteriorate.⁴ The patient was evaluated for rescue ECMO therapy as a life-saving measure.⁵ Both femoral veins were cannulated, and when ECMO started, there was immediate improvement in oxygenation. The ventilator was soon switched to the pressure control setting (PEEP 10 cm H2O/inspiratory pressure 10 cm H2O/rate 10 cycles/min) with 40% FiO2. The patient's hospital stay was complicated by lupus-induced thrombocytopenia, resulting in our decision to run heparin-free ECMO. She was decannulated after 25 days of ECMO without receiving any systemic anticoagulation. Results: The patient improved and was decannulated, extubated, and discharged from hospital, with no residual lung comorbidity. Conclusions: ECMO without any systemic anticoagulation is an acceptable therapy when there is profound respiratory failure secondary to infection in an immunosuppressed patient.⁵ Most of the literature reviews have already shown the good application of ECMO in SLE-induced diffuse alveolar hemorrhage.⁶ Our case report presents a promising application of rescue ECMO therapy in a lupus-induced immunosuppressed patient with pneumonia, acute respiratory distress syndrome,⁷ and thrombocytopenia.

Background: One of the Millennium Development Goals is to reduce childhood mortality by two-thirds by 2015 (www.un.org/millenniumgoals). This study was conducted to identify the clinical profile and pattern of disease, and to find out the commonest cause of mortality and morbidity of neonatal ICU patients in a Nepali teaching hospital. Methods: A retrospective study was conducted at a grade IIIA NICU in the Neonatal Intensive Care Unit of a tertiary care teaching hospital in the eastern part of Nepal to identify the clinical profile, pattern of disease, and outcome of patients. The data of all neonates were analyzed retrospectively from January 2012 to December 2012. IRB approval was exempted. Results: A total of 361 neonates were admitted in NICU during the study period, 65.6% were male and 34.4% were female. Of these neonates, 86 (23.8%) were admitted with a diagnosis of prematurity and 73 (20.2%) were admitted with a diagnosis of birth asphyxia. One of the commonest causes for birth asphyxia is the meconium aspiration syndrome. Among the neonates with birth asphyxia, 40 (54.8%) were in hypoxic ischemic encephalopathy (HIE) III, 20 (27.4%) in HIE II, and 13 (17.8%) in HIE I. The common causes for admission in NICU were sepsis (n = 118, 32.6%), prematurity (n = 86, 23.8%), and birth asphyxia (n = 73, 20.2%). The overall mortality was 20.2%. Among the ventilated cases, the mortality was 36.1%. In the non-ventilated cases, it was 13.25%. If two-thirds of the cases requiring ventilation would have survived thanks to a different treatment approach, we could have reduced our overall mortality to 15.7%. Conclusions: The neonatal phase is a very vulnerable period with a high risk of mortality and morbidity, most of which are preventable with good obstetric and subsequent neonatal care^1–2. Most of the NICU patients under mechanical ventilation may need advanced ventilation to reduce mortality further. There is a need for timely referral to a tertiary care hospital from peripheral and non-tertiary set-ups to prevent and control neonatal mortality and morbidity. The mortality rate can be reduced by giving advanced care such as extracorporeal membrane oxygenation (ECMO) to patients who fail to improve from conventional mechanical ventilation.³

The utilization of extracorporeal membrane oxygenation (ECMO) to support patients with respiratory and/or cardiac failure continues to increase annually, with growth primarily in the adult population.¹ The life-saving therapy requires a multidisciplinary team to deliver the highly technical treatment with clinical competency in three areas: cognitive knowledge, technical skills, and behavioral skills. The use of traditional methods of education in which knowledge is transmitted through lectures and reading materials results in limited retention and ability to apply learned information in the clinical setting.² Adult education theory promotes alternative methods of learning, which organizes abstract information through association with previous experiences and leads to mastery of knowledge through functional application.³ The educational tool which supports this approach to learning is simulation.

Multiple forms of simulation have been used to enhance ECMO education. These include task trainers, virtual patients, standardized patients, human patient simulator, and a combination of these models. High-fidelity ECMO simulation (fidelity on the ECMO circuit versus patient manikin) has been successfully implemented in many clinical centers and reported to have a greater impact on education in the three areas of required competency in ECMO care.^4,5 Using simulation in ECMO training, the technical aspects of routine and emergent care can be rehearsed and mastered. Scenarios can be designed with various objectives and can promote the critical thinking aspects of bedside management of these medically complex patients. Incorporating the lessons learned from the airline industry for effective teamwork in a crisis situation, Crew/Crisis Resource Management (CRM) proficiencies embedded in a scenario, also assists in the development of behavioral skills required for effective communication across multiple disciplines.⁶

The use of ECMO simulation incorporates all elements of adult learning theory and improves the learning experience of the clinical staff. The goal of this improved educational experience is to improve quality and safety in care, and ultimately, improve clinical outcomes.

This is a case presentation of a 16-year-old male patient who arrived in South Africa after a trip to Hong Kong. He had been on a sports tour. Previously, he had been healthy with no past medical history of note. Days prior to leaving Hong Kong, he had contracted a flu-like illness. On arrival at O.R. Tambo International Airport (in South Africa), he was showing signs and symptoms of deterioration in condition, including fever, coughing and confusion. He was tended to by paramedic staff at the airport, who transported him urgently to our emergency department (ED) by ambulance. He was extremely short of breath. At the time of arrival in the ED, he was not intubated. He had a quick sequential organ function assessment (qSOFA) score of 3, with a lactate level >2 mmol/l.

The patient's condition was found to be critical, with marked deterioration in his respiratory and haemodynamic status. Soon after arrival, he required resuscitation in the ED. With no return of spontaneous circulation (ROSC), despite aggressive resuscitation, it was decided to place him on veno-arterial extracorporeal membrane oxygenation (VA ECMO). He was cannulated femoral–femoral with a 23-French venous catheter and a 15-French arterial catheter. Extracorporeal cardiopulmonary resuscitation (ECPR)¹ was performed promptly with successful return of spontaneous circulation. Due to poor saturation and oxygenation on blood gas, veno-venous (VV) ECMO was concomitantly performed. An 18 French Avalon catheter was separately placed in the internal jugular vein. This required a second ECMO machine to be used, as his clinical condition was deemed to be too unstable to create a hybrid circuit (VA-V). The patient had good oxygen saturation levels with a satisfactory blood pressure, and hence, he was transferred to the Intensive Care Unit (ICU).

Appropriate clinical samples were sent (with a request for urgent influenza PCR test to be performed on a tracheal aspiration specimen), and a positive result was found for influenza B. As it was unusual for influenza B to result in such a severe septic shock clinical picture, a bacterial co-infection was suspected. He was started on empiric therapy with broad spectrum antibiotics, including Linezolid, to cover for Staphylococcus aureus infection. Urgent blood Gram stain confirmed Gram-positive cocci, and soon thereafter, a blood culture positive for Staphylococcus aureus was confirmed.

Despite comprehensive treatment, pharmaceutically and mechanically, the patient continued to deteriorate. All parameters did not improve. Discussions were held regarding the central cannulation² and it was decided to commence with the same immediately. The patient was transferred to the theatre for the placement of central ECMO. Despite successfully placing the cannula in the right atrium and aorta, the patient's condition did not improve, and flow³ and haemodynamics were deemed insufficient to maintain brain function. The patient had a cardiac arrest and was not further resuscitated in the theatre.

Profound septic shock was in keeping with Staphylococcus aureus septicaemia and toxic shock syndrome.⁴ This case was an example of combining full medical therapy with mechanical intervention, i.e. ECMO.

Note: Permission to report this case was obtained from the Hospital Administration on the basis that patient confidentiality was maintained. In addition, verbal consent was obtained from the patient's parents to present this case as a learning tool, also on the condition that anonymity is maintained.

Dr Robert Bartlett is the pioneer surgeon credited for moving extracorporeal life support (ECLS) from the operating room to the intensive care unit (ICU), where the therapy has given hope for survival to thousands of neonates, children, and adults with respiratory and/or cardiac failure. Dr Bartlett describes the ECMO timeline as ECMO 1 (1990–2008) and ECMO 2 (2008–present).¹ The first phase of ECMO utilized individual components, designed for other uses, assembled together to provide ECLS at the bedside. Circuit monitoring used equipment engineered for other functions, and hence, the need for clinical personnel to oversee the delivery of this technologically complex therapy was extensive. ECMO 2, the second phase in which we are currently practicing has been revolutionized by low-resistance oxygenators, centrifugal technology, and bicaval catheters that can be placed using the Seldinger technique.² ECMO systems are now integrated, simplified, self-monitoring, and self-regulating, and have allowed for changes in the bedside model of care. A remaining challenge in providing ECLS is the systemic inflammatory response (SIR) induced by blood exposure to the artificial circuitry. The renal, pulmonary, and neurologic dysfunction seen after cardiopulmonary bypass (CPB) has been attributed to the SIR.³ The development of miniaturized extracorporeal circuits (MECC) with reduced tubing length, smaller oxygenators, biocompatible coatings, and fewer components are hypothesized to reduce the blood–foreign surface contact area, and hence, reduce the SIR. A possible breakthrough in the reduction of a SIR may allow transition into the next era of ECMO care.

Published reports have shown laboratory evidence that MECC application in CPB blunts the systemic inflammatory response with decreases in C-reactive protein (CRP), leukocytes, and cytokines (IL-6, IL-8, TNF), SC5b-9 (an inflammation complement complex), and activated neutrophil factors.⁴ In studies evaluating the clinical outcome of patients who have undergone ECLS with MECC, the benefit remains debatable with respect to 30-day mortality, neurocognitive disturbance, cerebrovascular events, renal failure, and myocardial infarction. In the outcome criteria of ventilation period, hospital stay, and ICU stay, MECC showed benefit.⁵ In the meta-analysis report by Harling et al., the authors found other clinical benefits with MECC, which included the reduction in blood production transfusions.⁶

The use of MECC for prolonged ECLS has not been extensively reported in the literature, and may be related to the functional longevity of the oxygenator. A small number of case reports have been published and a conclusion cannot be made from the current level of MECC experience for its use as an alternative equipment option in ECMO. Further research in this area will be necessary before MECC can be clinically adapted for ECMO.

Introduction: At the start of every new extracorporeal membrane oxygenation (ECMO) center, safe and effective use of ECMO therapy requires unique institutional resources and strategies to optimize patient care and outcome. This is a report of the initial experience at the first ECMO center in Lebanon; the course of five patients is described, focusing on the monitoring considerations.^1–4 Lessons learnt help improve patient ECMO care, safety, and outcome. Methods: Two adult cases treated with veno-arterial (VA) ECMO for refractory cardiac failure, and three neonates (two veno-arterial and one veno-venous (VV) ECMO) treated for refractory respiratory failure were retrospectively reviewed with special focus on both medical and mechanical complications. Results: All complications were recognized early and managed successfully. The main complications encountered were: limb ischemia (1 patient), bleeding and clotting requiring circuit change (2 patients), overflow and aortic regurgitation (1 patient), hemolysis (1 patient), acute kidney injury and fluid overload (3 patients), patient–ventilator asynchrony, and technical problems (mainly related to cannula's positioning) (2 patients). In some instances, diagnosis was limited or delayed due to unavailability of monitoring tools, mainly multimodal coagulation studies. All five patients were successfully decannulated. Two patients died following decannulation and three patients were discharged home; one among them needed to go to a rehabilitation center for a few weeks before going back home. Conclusion: Optimal monitoring tools such as cerebral and somatic near infrared spectroscopy, echocardiography, head ultrasound, and multimodal coagulation studies (activated clotting time, aPTT, antiXa, thromboelastogram, and others) would allow for early recognition of complications. This would prevent or at least help anticipate catastrophic events, thus minimizing the impact of life-threatening complications and improving the quality of care and outcome. Furthermore, organizational structure with investment in training and technology is needed to optimize patient care.⁵

Background: “ECMO for Greater Poland” is a program being developed to serve the 3.5 million inhabitants of the Greater Poland region (Wielkopolska) based on an approach already implemented in the USA¹ or Qatar.^2,3Method: The program is complex and takes full advantage of the ECMO perfusion therapy opportunities to save the life of patients in the Greater Poland region.

The main implementation areas are:

– treatment of patients with hypothermia;⁴

– treatment of reversible severe respiratory failure;⁵

– treatment of acute intoxication resulting in cardiorespiratory failure⁶ or other critical conditions resulting in heart failure;

– in the absence of response to treatment and eventual death, and with donor authorization, there is possible organ transplantation from a non-heart beating donor (NHBD) to another patient.⁷ This led to the development of a program for donation after circulatory death (DCD). Study: The program will help to put in place a Medical Rescue System including ECMO (Figure 1). It requires training in specialized resuscitation, perfusion, and transplantation teams in the implementation of this “ECMO rescue chain”. The main strength of the program is the widespread use of extracorporeal perfusion. All program arms in the use of ECMO should be implemented in parallel to maximize its positive impact.Figure 1.  Organizational model of “ECMO for Greater Poland” – “ECMO rescue chain” scheme divided into three stages: prehospital, hospital/perfusion, and transplantation.

As this organizational model is complex and expensive, we used high-fidelity medical simulation to prepare for the real-life implementation of our ECMO program. During 4 months, we performed scenarios including:

  – “ECMO for DCD” which includes: prehospital identification, CPR ALS (cardiopulmonary resuscitation advanced life support), perfusion therapy (CPR-ECMO or DCD-ECMO), inclusion and exclusion criteria matching, mechanical chest compression, transport, DCD confirmation, and donor authorization, the veno-arterial (VA) cannulation of a mannequin's artificial vessels, and starting on-scene organ perfusion.⁷ – “ECMO for INTOXICATION” which includes: hospital identification (Department of Toxicology), poisoning treatment, CPR ALS, mechanical chest compression, VA cannulation, for the implementation of ECMO therapy and transport to another hospital (Department of Cardiac Surgery).⁶ – “ECMO for RRF” (reversible respiratory failure) which includes: hospital identification (Regional Department of Intensive Care) – inclusion and exclusion criteria matching, ECMO team transport (80 km), therapy confirmation, veno-venous cannulation for the implementation of perfusion therapy, and return transport (80 km) with ECMO to another hospital in a provincial city (Clinical Department of Intensive Care), where the veno-venous (VV) ECMO therapy was continued for the next 48 hours.⁵

The training programs, in a short time, resulted in a team being appropriately trained to successfully undertake the complex procedures. Soon after these simulations, Maastricht category II DCD procedures were performed involving real patients and resulting in two double successful kidney transplantations, for the first time in Poland. One month later, we treated two hypothermia patients and, for the first time in the region, also treated on ECMO an adult patient with reversible respiratory failure. Conclusions: The “ECMO for Greater Poland” program will allow the use of perfusion therapy for the inhabitants of Wielkopolska in a comprehensive manner, covering all critical disease states, by what appears to be a unique regional program in Poland. The full-scale, high-fidelity simulation enabled standardized training and testing of new, commonly, and rarely used procedures, and facilitated clinicians’ skills development.

Background: Poland is setting up its first regional ECMO program and relies heavily on the use of simulation in testing processes and training clinicians.¹ As ECMO is a complex and expensive procedure, we developed an advanced ECMO simulator for high-fidelity medical simulation training.^2–6 It can be used to modify any type of full-body patient simulator and allows for the creation of an unlimited number of scenarios. Methods: The system is equipped with an electronic core control unit (CCU) (Figure 1), a set of synthetic valves, pressure sensors, and hydraulic pumps. The major functions of the CCU are to stabilize the hydraulic system (flow of simulated blood, differential pressures in the arterial and venous lines), providing instant information about the system to the user via a display. Electric valves and sensors provide ‘on-the-fly’ information to the CCU about the actual system's status and it can be made to respond to specific instructions imitating the physiological circulatory system and simulating several scenarios (i.e. bleeding, low pressure, occlusion, reaction to proper and incorrect pharmacological treatment). It can be connected to an ECMO machine to act like the human body during ECMO run. Silicone tubes (modified polyethylene) that can be realistically cannulated using ultrasound imaging represent the artificial vessels. The CCU is made of electronic components that can be integrated to customize any mannequin as shown in Figure 1. The hardware includes both digital and analogue components that are controlled by a software run on a computer connected to the CCU via a serial port (RS232) (Figure 2). The software allows for the visualization of measurements obtained from the sensors and the control of the pumps and valves via electronic controllers. The controllers affect the ECMO circuit simulated blood flow, and hence the readings from the ECMO machine sensors, to recreate various clinical scenarios.Figure 1.  The modified patient simulator with circulatory loop prepared for VA ECMO cannulation and CCU (core control unit) for high-fidelity simulations.

Figure 2.  The ECMO simulator architecture.

Results: Every component used can be easily replaced. The total cost of the simulator modification, excluding the cost of the computer or future mobile device, is approximately 200 USD, and the consumable parts cost about 20 USD. It has been used to help simulate successfully a range of scenarios.¹ Although the system is currently tethered, the next prototype will include a wireless controller so that the system can be controlled from a mobile application. Conclusions: This advanced simulator allows for unlimited possibilities with regard to creating clinical scenarios. Our ambition is to become a reference ECMO training center in Poland so that our high-fidelity ECMO simulator can be used to its full potential and for the benefit of more clinicians and their patients around Poland.