In-hospital and 6-month outcomes in patients with COVID-19 supported with extracorporeal membrane oxygenation (EuroECMO-COVID): a multicentre, prospective observational study
Language English Country Great Britain, England Media print-electronic
Document type Observational Study, Multicenter Study, Journal Article
PubMed
36402148
PubMed Central
PMC9671669
DOI
10.1016/s2213-2600(22)00403-9
PII: S2213-2600(22)00403-9
Knihovny.cz E-resources
- MeSH
- COVID-19 * therapy MeSH
- Middle Aged MeSH
- Humans MeSH
- Extracorporeal Membrane Oxygenation * MeSH
- Aftercare MeSH
- Hospitals MeSH
- Infant, Newborn MeSH
- Patient Discharge MeSH
- Prospective Studies MeSH
- Retrospective Studies MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
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.
Cardiothoracic Critical Care Unit Whythenshawe Hospital Manchester UK
Cardiothoracic Intensive Care Unit University Hospital Copenhagen Denmark
Critical Care Department Val d'Hebron Research Institute Barcelona Spain
Department of Anesthesia and Intensive Care IRCCS San Raffaele Scientific Institute Milan Italy
Department of Cardiac Surgery Heinrich Heine University Dusseldorf Germany
Department of Cardiac Surgery Louis Pradel Hospital Lyon France
Department of Cardiac Surgery Medical University Hospital of Vienna Vienna Austria
Department of Intensive Care Erasme Hospital Université Libre de Bruxelles Brussels Belgium
Department of Internal Medicine 2 University Hospital of Regensburg Regensburg Germany
Department of Medicine Paracelsus Medical University Nuremberg Germany
Intensive Care Unit Royal Brompton and Harefield hospitals London UK
Medizinische Klinik Uniklinik Rheinisch Westfälische Technische Hochschule Aachen Germany
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ClinicalTrials.gov
NCT04366921