**Background:** The COVID-19 pandemic created an urgent need for guidance on using venovenous extracorporeal membrane oxygenation (VV-ECMO) for severe ARDS, but high-quality evidence was lacking. This international expert consensus aimed to address controversial topics in ECMO for COVID-19 patients and provide guidance for future pandemics.
**Methods:** The coordinating center was the ECMO center at King Saud Medical City (Riyadh, Saudi Arabia) through the Saudi Arabia Ministry of Health National ECMO program. The scientific committee comprised five chairpersons with >5 years of ECMO experience. Thirty-two experts were invited; the faculty included 22 panelists representing both sexes, various countries and ethnicities, with half not active members of ELSO. The process used a mix of modified Delphi technique rounds and nominal group technique (NGT) through three face-to-face meetings and anonymous voting. The project was conducted in compliance with CREDES and SQUIRE standards. Five phases were completed over approximately 8 months (December 2021–August 2022): identifying knowledge gaps, validation, statement formulation, voting, and drafting. Voting used a 10-point scale (1–3 low, 4–7 intermediate, 8–10 high agreement). Strong consensus required >80% high scores or mean >8; weak consensus required 70–80% or mean 7–8; no consensus was <70% or mean <6.
**Key Results:** In Phase I, 52 questions were identified. After Phase II validation, 32 questions across nine domains remained (validation rate >75%). In Phase III, 25 questions were used to formulate 14 statements; six questions achieved no consensus. After two voting rounds (R1: June 25, 2022; R2: July 12, 2022), 14 statements reached consensus across four domains. In R1, 10 statements reached strong consensus; four reached weak consensus and were modified. In R2, two of those four reached strong consensus. The final 14 statements: Domain 1 (Patient Selection) — Statement 1: Duration of IMV before ECMO should not be the primary determinant for candidacy (strong consensus, mean 8.2, 90.4%). Statement 2: No validated scoring system exists for COVID-19 ECMO prognosis; non-COVID-19 scores should not be used (strong consensus, mean 7.9, R2 81%). Statement 3: Days on NIMV/HFNC should not be used alone for selection (strong consensus, mean 8.3, 80.9%). Statement 4: Cutoff age may vary by resource availability; national/regional policy advised (strong consensus, mean 9.1, 90.4%). Statement 5: EOLIA criteria should be followed without deviation (strong consensus, mean 8.7, 85.7%). Domain 2 (ECMO Management) — Statement 6: Prone positioning may be considered during ECMO in experienced centers with sufficient resources (weak consensus, mean 7.9, R2 71.9%). Statement 7: Lung transplantation for late COVID-19 respiratory failure is feasible but should be considered only after prolonged ECMO without recovery (weak consensus, mean 7.4, R2 76.2%). Statement 8: Post-ECMO follow-up should be initiated (strong consensus, mean 9.1, 95.2%). Statement 9: Weaning strategy including spontaneous breathing during ECMO is feasible (strong consensus, mean 8.5, 76.1%). Domain 3 (Operational/Logistics) — Statement 10: Starting a new centralized ECMO service pre-pandemic is feasible (strong consensus, mean 8.7, 85.7%). Statement 11: Establishing new ECMO programs in areas lacking services is feasible with precautions (strong consensus, mean 8.5, 80.9%). Statement 12: Transport of COVID-19 patients on ECMO does not pose appreciable risk to trained teams with appropriate PPE (strong consensus, mean 9, 95.2%). Domain 4 (Ethics) — Statement 13: ECMO futility should not be determined solely by run duration; withdrawal not advised until recovery, transplantation, or irreversible multiorgan failure (strong consensus, mean 9, 85.7%). Statement 14: No evidence-based scoring system guides ECMO prioritization during resource limitations; factors predicting poor outcomes may be used (strong consensus, mean 7.9, R2 85.7%).
**Clinical Implications:** This consensus provides practical guidance for ECMO practitioners on patient selection, clinical management, operational logistics, and ethics during pandemics. The panel emphasized that pre-ECMO ventilation duration should not be the primary determinant for candidacy, that existing prognostic scores developed for non-COVID-19 patients should not be applied to COVID-19 patients, and that ECMO should not be withheld or withdrawn based solely on run duration. Regional centralization of ECMO services is recommended. Important topics where no consensus was reached include anticoagulation, pregnancy, immunocompromised cases, cost of services, supply chain solutions, ECMO team models during resource scarcity, and pediatric/neonatal ECMO for COVID-19. The authors acknowledge that consensus does not replace guidelines, randomized trials, or clinical judgment.