Factors associated with outcomes of patients on extracorporeal membrane oxygenation support: a 5-year cohort study

1Extracorporeal membrane oxygenation (ECMO) is a rescue therapy to support severe cardiac and/or pulmonary failure. Both veno-venous (VV) and veno-arterial (VA) ECMO (or extracorporeal life support (ECSL)) are increasingly being used. VV ECMO support for severe influenza A (H1N1) pneumonitis was reported during the 2009 pandemic. Despite increasing experience with ECMO and recent technical improvements, the mortality of patients receiving ECMO remains high, but varies between centres, patient subgroups and by indication. While more randomised controlled trials are needed to define the place of ECMO in critically ill patient management, observational series may provide some useful data on factors associated with mortality and complications.

2Outcome of patients on ECMO is influenced not only by factors independent of ECMO (patient illness severity, type of illness, other organ support) but also by the potential complications related to ECMO. Clarification of the impact of key ECMO complications on outcome could inform safer care and improve outcomes. ECMO complications may be mechanical (relating to the ECMO circuit components) or medical. The latter are the most frequent and include bleeding, infection, embolism causing vascular and neurological complications, and limb ischaemia. Haemorrhage and infection are the most frequent adverse events. Nonetheless, neurologic complications are probably underestimated and can have devastating consequences on the prognosis. Vascular complications such as amputation may be delayed and also perhaps under-reported. Bloodstream infections during ECMO have been associated with a poor outcome in paediatric patients but the association remains uncertain in adults. Bleeding is another frequent adverse event in these patients who are critical ill, exposed to anticoagulation and susceptible to coagulopathy and platelet dysfunction. The impact of bleeding on prognosis depends in part on how bleeding events are defined and recorded in the studies. Mechanical complications and haemolysis have decreased with the introduction of centrifugal pumps, low-resistance polymethylpentene membranes and modern heparin-coated surfaces.

3This study describes the experience of a single ECMO referral centre during a stable period of practice. The aim of this study was also to identify factors that were independently associated with outcome for VV and VA ECMO.

4The Alfred Hospital is a university referral hospital in Melbourne (Australia), which provides heart and lung transplantation services for the states of Victoria, South Australia and Tasmania. It is one of two adult trauma centres in Victoria and is the state Burns Centre. The intensive care unit (ICU) is one of the largest Australian ICUs with capacity for 45 beds and more than 2,000 admissions a year. The Alfred ICU operates an ECMO referral service and retrieves patients on ECMO from the southern Australian states.

5Data were retrospectively extracted from a prospectively updated local registry of ECMO patients and ICU clinical database. Further clinical details were obtained from retrospective review of patient medical records. This study was approved by the Alfred Health Human Research Ethics Committee and no consent was needed.

6Patients over the age of 16 years who received ECMO support between January 2005 and June 2011 were included. Demographics, co-morbidities, hospital and ICU lengths of stay, acute physiology and chronic health evaluation (APACHE II) score and main diagnosis at admission were recorded. The following parameters were collected at ECMO initiation: presence of cardiac arrest, sequential organ failure assessment (SOFA) score, plasma lactate level and arterial partial pressure of oxygen to inspired oxygen fraction (PaO2/FiO2) ratio. Days in ICU and days on mechanical ventilation (MV) before ECMO, days on ECMO, and the requirement for catecholamines and renal replacement therapy (RRT) were recorded.

7The decision to use ECMO was made by the treating intensive care specialist or cardiac surgeon (for intra-operative cardiac support). Criteria for assessing the need to commence VV ECMO for severe respiratory failure and VA ECMO for severe cardiac failure are listed in Table 1. For respiratory failure, VV ECMO was delivered through percutaneously placed single-stage femoro-femoral cannulae (Medtronic, Minneapolis, MN, USA) under ultrasound guidance with an additional jugular access cannula inserted if required. Double lumen jugular cannulae (Avalon Elite™; Avalon Laboratories, Rancho Dominguez, CA, USA) were used in two patients. Mechanical ventilation settings were not standardised in patients undergoing MV. Our practice generally involved pressure-controlled ventilation with low respiratory rate and maintenance of tidal volume below 6 ml/kg (predicted body weight) and peak pressure below 30 cm H2O. Percutaneous VA ECMO for cardiac support was delivered through peripheral femoro-femoral ECMO cannulae and routinely included an ante-grade 8.5 French distal perfusion cannula (Mayo, Rochester, MN, USA) to prevent limb ischaemia. Central VA ECMO was initiated intra-operatively at the discretion of the managing cardiac surgeon. Management of failing heart was not standardised but low doses of inotropes were administered to maintain pulsatility and some native cardiac output, if these were severely depressed on support. Femoral artery cannulation sites were repaired surgically after decannulation. Continuous renal replacement (Prisma™ and then Prismaflex™; Gambro, Lund, Sweden) was performed via the ECMO circuit. ECMO care was delivered using Rotaflow pumps and Quadrox or PLS membranes with simplified Bioline-coated circuits (Maquet, Rastatt, Germany) without connectors, bridges or venous saturation monitoring. To avoid air emboli, we did not monitor pre-pump pressure and there were no pre-pump circuit access ports. Bedside care was delivered by trained ICU nursing staff with a patient-nurse ratio of 1:1 under the supervision of ECMO-trained intensive care specialists.

8Invasive procedures were minimised while on ECMO. Platelet transfusions were given to maintain platelet count > 80,000/mm3. Minimum haemoglobin of 80 g/l was generally targeted, consistent with reported literature. Patients with no active bleeding received heparin targeted to an activated partial thromboplastin time (APTT) of 50 to 70 seconds. Heparin was withheld at the discretion of the intensivist in patients who required surgical procedures or in those who had clinically significant bleeding. Administration of clotting factors, platelets, antifibrinolytics or recombinant factor VIIa for bleeding patients was determined by the intensivist in consultation with a specialist haematologist. Pre and post oxygenator pressures were monitored to detect progressive oxygenator thrombosis. Screening for haemolysis (plasma-free haemoglobin) and fibrinolysis (fibrinogen and D-dimer levels) was performed at least daily. Elective circuit changes were performed if significant trends in fibrinogen decline and D-dimer elevation were observed.

9Antibiotic prophylaxis for ECMO was not routine. Patients undergoing open heart surgery were given prophylaxis with cefazolin plus rifampicin or vancomycin plus rifampicin in the operating room in accordance with hospital guidelines. Suspected and/or confirmed sepsis was routinely treated with antibiotics following specimens being taken for culture.

10The following complications were recorded: i) haemorrhagic and coagulopathy: surgical interventions for bleeding (recorded prospectively), transfusion requirement: total red blood cell (RBC) units, total of platelets bags, fresh frozen plasma (FFP) and cryoprecipitate issued during ECMO at the Alfred hospital (recorded retrospectively); ii) bloodstream infections: defined using the Centre for Disease Control and Prevention/National Nosocomial Infections Surveillance System criteria and occurring between 48 hours after ECMO initiation and 72 hours after ECMO cessation (recorded retrospectively); iii) neurologic: defined as a cerebral haemorrhage or ischaemia reported on CT scan with no other potential aetiology; iv) vascular: vascular repair, fasciotomy, embolectomy or a limb amputation during or after ECMO (recorded prospectively).

11Primary outcomes considered were the proportion of patients successfully weaned from ECMO without bridging support and hospital mortality. When they occurred, deaths were classified as related to the primary illness, ECMO care, or occurring subsequently after weaning from ECMO. Hospital and ICU length of stay (LOS), ICU mortality and the percentage of survivors discharged home after hospital discharge were also recorded.

12All analyses were performed using Stata 10.0 (College Station, TX, USA). VV and VA ECMO were analysed separately. However, changes over the study period considered all the ECMO episodes in the same analysis. When ECMO was initiated in another centre, only the days at the Alfred hospital were taken into account for the number of RBC units given per day on ECMO. When the mode of ECMO was changed, only the first type was considered for analysis. Categorical variables were compared between groups with a Fisher exact test and continuous variables were compared with a Mann-Whitney U test for non-parametric data. Statistical regression models were constructed based on factors found to be associated with hospital mortality using backwards stepwise regression based on P < 0.02 or factors considered relevant. In the mortality models, data available at the time of starting ECMO were considered in a prognostic model and the effect of complications was considered in a complications model. To avoid interaction between days on support and number of RBC units per day, the number of RBC units transfused has been considered when applicable. When variables were expected to be collinear (for example SOFA score and APACHE II score), only one was included in the model. A two-sided P value of 0.05 was considered to be statistically significant.

13Between January 2005 and June 2011, there were 9,350 adult admissions to ICU; 151 (1.7%) patients were hospitalised and underwent ECMO support on 158 occasions. Ninety-nine patients underwent 105 VA ECMO for a median duration of 7 days (first and third quartiles: 5 to 10 days), while 52 patients underwent 53 episodes of VV ECMO for a median duration of 10 days (first and third quartiles: 6 to 16 days). The primary indications for ECMO support according to the type of ECMO are described in Figure 1. Forty patients were transferred to the hospital on ECMO, they were mostly on VV ECMO (41% versus 22%, P = 0.002), and in 34 (85%) patients, ECMO was initiated less than 24 hours prior to arrival. Two patients changed modes from VA to VV ECMO. Patients and ECMO characteristics are detailed per type of ECMO in Table 2. In the VA ECMO group, the SOFA score before ECMO initiation was higher in patients with peripheral ECMO than in those with central ECMO (12 (first and third quartiles: 11 to 14) versus 11 (first and third quartiles: 10 to 12.5), P = 0.0225).

14Haemorrhagic complications were an issue for most of the patients on VA and VV ECMO and only four of them did not receive a RBC transfusion (one patient on VA ECMO post heart transplant was a Jehovah's Witness, a second had VA ECMO for acute myocardial ischaemia, and two others (one VV and one VA) were on ECMO for less than 48 hours). More than one-third of patients on VA ECMO required surgery for bleeding, while 17% of the patients on VV ECMO underwent surgery for bleeding issues. Surgical details on procedures to achieve haemostasis were not collected. The median number of RBC units transfused per day on ECMO was higher in patients who underwent VA ECMO than VV ECMO (Table 2) and was higher in patients who died regardless the types of ECMO (Tables 3, 4; Figure 2). Central VA ECMO was associated with a higher requirement of blood products than peripheral VA ECMO (17 RBC units (first and third quartiles: 12 to 26) versus 10 RBC units (first and third quartiles: 5 to 24), P = 0.005; and a median of 2.8 RBC units per day (first and third quartiles: 2 to 3.6) versus 2 RBC units per day (first and third quartiles: 1 to 3.3), P = 0.0018). Platelets, FFP and cryoprecipitate transfusion was also consistent, especially in the VA ECMO group, with only four patients who did not received platelets in the group (Table 2).

15Bloodstream infections ranked second behind haemorrhagic complications, in both types of ECMO. Of the 146 ECMO episodes that were continued for more than 48 hours, 24 bloodstream infections occurred during 21 ECMO episodes (14.4%). The median delay between ECMO initiation and bloodstream infection occurrence was 8 days (range 2 to 59 days) and the most frequent pathogens were Gram-negative bacilli including Enterobacteriaeceae, Candida sp. and Enterococcus sp. Neurologic complications of ECMO occurred in one patient in each ECMO type group. One patient, who was on heparin and had an international normalised ratio (INR) equal to 2, had a bilateral cerebral hemisphere haemorrhage, the other patient, who also was on heparin, had an intracerebral haematoma with intraventricular extension. Vascular complications occurred in eight patients, all who received VA ECMO (1/43 (2.3%) central and 7/62 (11.2%) peripheral, P = 0.14). The vascular complications were: a false aneurysm (one case), dissection of the femoral artery (one case), ischaemia secondary to delayed insertion of the distal perfusion cannula (two cases), venous thrombosis following surgical repair (one case) and data were not available for three cases. Two patients required a lower limb amputation because of ECMO. One had femoral vein injury and thrombosis following surgical repair of the artery at ECMO decannulation and developed venous infarction, the other did not have backflow cannula and developed arterial ischaemia.

16Of the 39 patients who died in the VA ECMO group (Table 5), mortality was attributed to the ECMO procedure in six (15%), to other treatment-related complications in 14 (36%) patients and to the primary illness in 19 cases (49%). The factors associated with increased risk of death in the univariate analysis are shown in Table 3. In the multivariate logistic regression analysis, the only factor independently associated with death was the number of RBC units (OR = 1.058, 95% CI 1.016 to 1.102, P = 0.007) (Table 6).

17Of the 20 patients who died in the VV ECMO group (Table 5), mortality was attributed to the ECMO procedure in five (25%), to other treatment-related complications in three (15%) patient and to the primary illness in 12 cases (60%) (Table 5). In univariate analysis, the number of RBC units and platelets transfused were associated with mortality (Table 4). In multivariate analysis, only platelet transfusion remained significantly and independently associated with hospital mortality (OR = 1.458, 95% CI 1.087 to 1.955, P = 0.012) (Table 6).

18Among the 27 VA ECMO episodes unsuccessfully weaned (25.7%), 16 involved patients who were never weaned from ECMO and 11 involved patients who underwent bridging procedures to transplantation. In univariate analysis, vascular complications were negatively associated with successful weaning, while post-operative VA ECMO had a higher chance to be successfully weaned (Additional file 1). Sixteen patients who underwent VV ECMO were never weaned; the volume of platelets transfused was predictive of unsuccessful weaning (Additional file 1).

19Fifty-six percent and 45% of patients were discharged directly home in the VA and the VV ECMO group, respectively, while the others were transferred to another health service, including rehabilitation (Table 5).

20Trends over time were considered in two periods; from 2005 to 2007 when less than 20 ECMO procedures a year (a total of 59 ECMO) were performed, and from 2008 to 2011 when more than 20 ECMO episodes a year (a total of 99 ECMO) were performed. The proportion of VV ECMO trended to increase (25.4% of all the procedures during the first period versus 38.4% in the second period, P = 0.118). Peripheral ECMO became more frequent than central VA ECMO (22/44 during the first period versus 40/61 during the second period, P = 0.321). Between the first and the second periods, patient aged 44 (first and third quartiles: 30 to 58) years versus 48 (first and third quartiles: 36 to 57) years, P = 0.0869) and patient illness severity (APACHE II (19 (first and third quartiles: 14 to 23) versus 20 (first and third quartiles: 14 to 26), P = 0.292) and SOFA score (12 (first and third quartiles: 11 to 14) versus 11 (first and third quartiles: 10 to 14), P = 0.0661) were not significantly different. There was no difference in the number of RBC units transfused between the first study period (14 (first and third quartiles: 7 to 22) RBC units/episode or 1.8 (first and third quartiles: 0.9 to 3.3) RBC unit per day) and the second study period (12 (first and third quartiles: 5 to 25) RBC units/episode or 1.5 (first and third quartiles: 0.7 to 2.4) RBC unit per day). In addition, the occurrence of vascular (7/59 versus 5/99, P = 0.218), neurological (1/59 versus 1/99 versus, P = 1.0) complications and bloodstream infection (7/53, versus 17/93, P = 0.493) were similar between both study periods. There was also no statistical difference in mortality in the two time periods (40.68% versus 34.34%, P = 0.496).

21We report the experience of a large Australian ECMO referral centre over a period of 5 1/2 years. For both types of ECMO, bleeding complications were the most frequent. For VA ECMO, bleeding complications, when expressed by the number of RBC units transfused during ECMO, was an independent factor of mortality. In patients who underwent VV ECMO, volume of platelets transfused was independently associated with hospital mortality.

22Around a quarter of ECMO episodes required surgery for haemorrhage, which is similar to the 10 to 30% of haemorrhagic complication reported in the literature. Surgery for haemorrhage was not associated with an increased risk of death while mortality increased with the number of RBC units transfused, suggesting that a readily identifiable and correctable site of bleeding was not as important as ongoing bleeding and transfusion. These results are comparable to previous publications and may also highlight the negative consequences of RBC transfusion in ICU patients. Bleeding complications using alternative definitions have also been associated with poorer outcomes. For instance, in a study in paediatric cardiac surgical patients, bleeding complication defined as 'uncontrolled mediastinal bleeding requiring surgical intervention' was independently predictive of death. Bleeding events also estimated by gastrointestinal or pulmonary haemorrhage still affected the prognosis of 1,473 adults with ECMO. Furthermore, we found that VA ECMO required more RBC units and other blood products than VV ECMO, possibly because half of VA ECMO was instituted in the operating room and intraoperative transfusions were included or because bleeding was a common feature of open chest central VA ECMO. In addition, transfusion policies in specific patient groups differ; for example, the transfusion threshold is higher in cardiac patients with uncorrected ischaemic heart disease. The association between the number of RBC units transfused and mortality in patients who underwent VA ECMO may be related to potential confounders including blood administered in the theatre for post-surgery ECMO. Interestingly transfusion of platelets was associated with a higher risk of death only for VV ECMO. The significance of this association remains uncertain. Platelet transfusion in VA ECMO may be only related to peri-operative haemorrhagic complications, while thrombocytopenia in patients on VV ECMO could be related either to coagulopathy that occurred on ECMO, or illness severity.

23Infection ranked second among the complications, with bloodstream infections affecting 13% regardless of the type of ECMO. Our findings are in accordance with the literature reported where the percentage of patients who experienced bloodstream infections varied between 3.4% and 11.4%. The impact of such infection on the outcome is controversial. Some authors highlight that sepsis and nosocomial infections acquired on ECMO increase the risk of death whereas others do not report an independent relationship between infection and mortality. Our findings support that bloodstream infections were not independently associated with an increased risk of death; however, our study may be underpowered to detect such association. Neurologic complications were rare in our series and may have been underestimated because of the difficulty in performing brain imaging procedures and the absence of systematic post mortem determination of intracranial pathology. Neurologic complications are highly variable in terms of incidence (between 4 and 37%). The majority consists of haemorrhage. Vascular complications including leg amputation occurred exclusively in patients undergoing VA ECMO and in the same proportion as those reported by Wang et al. in a cohort of 62 VA ECMO for cardiogenic shock. We found that vascular complications were associated with unsuccessful weaning in univariate analysis. In a cohort of 174 VV and VA ECMO episodes, vascular complications were not associated with mortality. Larger studies are required to evaluate the impact of these complications on the chance of successful weaning.

24We found that the lactate level before VA ECMO deployment was associated with poor outcome in univariate analysis but not in multivariate analysis (possibly because of a lack of power). Other studies have described plasma lactate 24 hours or 48 hours after ECMO initiation (as a marker of the adequacy of tissue perfusion) was a good predictor of death. The absence of correlation between PaO2/FiO2 ratio prior to VV ECMO deployment and outcome was not surprising and in accordance with a recent report. In our study, spontaneous cardiac arrest prior to ECMO initiation was not predictive of death. This result is in contrast to other studies, some of which included both before and after ECMO initiation. Finally, for both types of ECMO, the duration of ECMO did not influence mortality in accordance with a previous report.

25Although no change was significant between both periods of the study, ECMO patients in the second period tended to be older, have a higher severity of illness, whilst mortality tended to decrease.

26Our study has several limitations. First, this is a single-centre retrospective study. Nonetheless, ECMO data and patients' characteristics were collected prospectively. Second, although this represents the totality of our experience over more than 5 years, the numbers of ECMO episodes was not high, precluding detailed subgroup analyses, which are likely to be underpowered for some outcomes. Although we did not collect data on haemoglobin levels prior to transfusion, previous work has suggested a high rate of concordance with the National Australian Transfusion Guidelines. Furthermore, the study did not allow us to classify the bleeding complications and to explore the presence of coagulopathy or the anticoagulation characteristics. Similarly, information about oxygenator changes was not available and any correlation between oxygenator exchange and bleeding could not be done. We focused our infections analysis on bloodstream infections, because bloodstream infections have the highest impact on prognosis. Describing all infection types was not the aim of this study and has been already performed. In addition, we were not able to establish correlation between infections and ECMO. Quality of life, really relevant outcome in this population, was not available and we were not able to evaluate long-term disability. Finally, our study did not include 'traditional' complications such as oxygenator failure, pump malfunction, air embolism, haemolysis or tubing rupture. Although current technology, staff training and simplified circuits have greatly reduced or completely removed the impact of these complications, the incidence of these complications was not recorded and therefore we were unable to assess their impact.

27In conclusion, ECMO implemented in a referral centre is a useful supportive therapy for temporary life-threatening cardiac and/or respiratory failure. Among the pre-ECMO parameters and the ECMO complications, the number of RBC units was independently associated with the mortality of patients on VA ECMO, while the volume of platelets transfused was associated with the risk of death in patients with VV ECMO. Our work supports the need to further explore prospectively the association between bleeding, blood products transfusion and mortality in patients with VV ECMO and VA ECMO.

28• Bleeding is the most frequent issue in patients undergoing ECMO.

29• Our study identified the volume of blood transfusion during ECMO, surrogate of bleeding, as an independent risk factor of mortality for VA ECMO.

30• Platelet volume requirement in patients undergoing VV ECMO is an independent risk factor of death suggesting that coagulopathy in these patient group impacts on the outcome.

31• Further studies identifying bleeding risk factors and coagulopathy management should occur to improve ECMO management and prognostic.

32APACHE: acute physiology and chronic health evaluation; APTT: activated partial thromboplastin time; ECLS: extracorporeal life support; ECMO: extracorporeal membrane oxygenation; FFP: fresh frozen plasma; ICU: intensive care unit; INR: international normalised ratio; LOS: length of stay; MV: mechanical ventilation; PaO2/FiO2: arterial partial pressure of oxygen to inspired oxygen fraction ratio; RBC unit: red blood cell unit; RRT: renal replacement therapy; SOFA: sequential organ failure assessment; VA ECMO: veno-arterial ECMO; VV ECMO: veno-venous ECMO.

33The authors declare they have no competing interests.

34VP maintained prospectively the ECMO registry and DP maintained the ICU clinical database. CA collected clinical and biological data not available in the original databases and built a unique database. CA and AC performed the statistical analysis. CA, AC, DP and VP analysed the results. CA, AC, DP and VP wrote the manuscript. TL, CS, JC, GM helped to draft the manuscript. All authors revised and approved the final version of the manuscript.