In-hospital and 6-month outcomes in patients with COVID-19 supported with extracorporeal membrane oxygenation (EuroECMO-COVID): a multicentre, prospective observational study.

BACKGROUND

Extracorporeal membrane oxygenation (ECMO) has been widely used in patients with COVID-19, but uncertainty remains about the determinants of in-hospital mortality and data on post-discharge outcomes are scarce. The aims of this study were to investigate the variables associated with in-hospital outcomes in patients who received ECMO during the first wave of COVID-19 and to describe the status of patients 6 months after ECMO initiation.

METHODS

EuroECMO-COVID is a prospective, multicentre, observational study developed by the European Extracorporeal Life Support Organization. This study was based on data from patients aged 16 years or older who received ECMO support for refractory COVID-19 during the first wave of the pandemic-from March 1 to Sept 13, 2020-at 133 centres in 21 countries. In-hospital mortality and mortality 6 months after ECMO initiation were the primary outcomes. Mixed-Cox proportional hazards models were used to investigate associations between patient and management-related variables (eg, patient demographics, comorbidities, pre-ECMO status, and ECMO characteristics and complications) and in-hospital deaths. Survival status at 6 months was established through patient contact or institutional charts review. This study is registered with ClinicalTrials.gov, NCT04366921, and is ongoing.

FINDINGS

Between March 1 and Sept 13, 2020, 1215 patients (942 [78%] men and 267 [22%] women; median age 53 years [IQR 46-60]) were included in the study. Median ECMO duration was 15 days (IQR 8-27). 602 (50%) of 1215 patients died in hospital, and 852 (74%) patients had at least one complication. Multiorgan failure was the leading cause of death (192 [36%] of 528 patients who died with available data). In mixed-Cox analyses, age of 60 years or older, use of inotropes and vasopressors before ECMO initiation, chronic renal failure, and time from intubation to ECMO initiation of 4 days or more were associated with higher in-hospital mortality. 613 patients did not die in hospital, and 547 (95%) of 577 patients for whom data were available were alive at 6 months. 102 (24%) of 431 patients had returned to full-time work at 6 months, and 57 (13%) of 428 patients had returned to part-time work. At 6 months, respiratory rehabilitation was required in 88 (17%) of 522 patients with available data, and the most common residual symptoms included dyspnoea (185 [35%] of 523 patients) and cardiac (52 [10%] of 514 patients) or neurocognitive (66 [13%] of 512 patients) symptoms.

INTERPRETATION

Patient's age, timing of cannulation (<4 days vs ≥4 days from intubation), and use of inotropes and vasopressors are essential factors to consider when analysing the outcomes of patients receiving ECMO for COVID-19. Despite post-discharge survival being favourable, persisting long-term symptoms suggest that dedicated post-ECMO follow-up programmes are required.

FUNDING

None.

Informations de copyright

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Déclaration de conflit d'intérêts

Declaration of interests RL and JBe are past chairmen of the European Extracorporeal Life Support Organization (ELSO) Steering Committee. NB is the current chairman of the European ELSO Steering Committee. MVA, NB, JBe, MB, MDM, TM, JR, and JS are European ELSO Steering Committee members. RL reports personal fees from Abiomed and Xenios and honoraria payed institution from Medtronic, LivaNova, Getinge and Eurosets, unrelated to the submitted works. FST is advisory member for Eurosets unrelated to the submitted work. DW is proctor for Abbott and scientific advisor for Fresenius. NB is advisory board for ALung. JR reports lecture and advisory fees from Medtronic and Werfen outside the submitted work. PS reports advisory fees from Getinge but not related to the submitted work. AV received consultant fees from Inspira Technologies. MB is an advisory member for Eurosets, congress speaker for Hamilton Medical, and course speaker for Estor, all unrelated to the submitted work. LMB is advisory board for Eurosets and Xenios and is board member of EuroELSO Enterprise, unrelated to the present work. JBe reports consultancy and lecture fees from Abiomed and Getinge and is advisory board member of AstraZeneca and Boehringer Ingelheim. SL is advisory member of Inspira Technologies, unrelated to the present work. All other authors declare no competing interests.