<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Peetermans M</submitter><funding>Research Fund of the University Hospitals Leuven</funding><funding>FWO Vlaanderen</funding><pagination>404</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12465718</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>ECMO outcomes in COVID-19-related respiratory failure among solid organ transplant (SOT) and hematopoietic stem-cell transplant recipients (HSCT) are poorly described. We investigated: (1) whether transplant patients (SOT/HSCT) with COVID-19 have worse outcomes than non-immunocompromised (IC) COVID-19 patients, and (2) whether among transplant recipients (SOT/HSCT), those with COVID-19 have worse outcomes than those with non-COVID-19-related respiratory failure. Additionally, we aimed to identify factors independently associated with mortality among COVID-19 transplants.&lt;h4>Methods&lt;/h4>Retrospective analyses of the Extracorporeal Life Support Organization Registry from 1/1/2017 to 31/07/2023. Two comparisons were made: (1) transplant COVID-19 versus non-IC COVID-19, and (2) transplant COVID-19 versus transplant non-COVID-19 patients. Outcomes were analyzed using propensity score (PS)-adjusted, multivariable, and PS-matched analyses, adjusting for a priori identified confounders. Primary outcome was in-hospital mortality.&lt;h4>Results&lt;/h4>Among 38,270 runs, 146 transplant COVID-19, 12,552 non-IC-COVID-19 and 886 transplant non-COVID-19 runs were identified. In-hospital mortality in transplant COVID-19 patients was 75.3% and the risk was invariably increased compared to non-IC-COVID-19 (PS-adjusted OR: 2.36 [95%CI:1.61-3.46], p &lt; 0.001, multivariable OR:2.35 [95%CI:1.59-3.49], p &lt; 0.001, and PS-matched analysis OR: 1.89 [95%CI:1.21-2.95], p &lt; 0.005) and transplant non-COVID-19 patients (PS-adjusted OR: 4.20 [95%CI:2.74-6.44], p &lt; 0.001, multivariable OR: 3.79 [95%CI:2.51-5.74], p &lt; 0.001, and PS-matched analyses OR: 3.17 [95%CI:1.90-5.28], p &lt; 0.001). Mortality difference remained stable over time. Older age independently associated with higher mortality. This was accompanied by higher need for renal replacement therapy compared to non-IC-COVID-19 patients. Compared to transplant non-COVID-19 patients, ECMO runs and time-to-live discharge were invariably prolonged. Hemorrhagic, metabolic, pulmonary and infectious complications consistently occurred more frequently.&lt;h4>Conclusions&lt;/h4>Mortality was high in COVID-19 transplant ECMO patients, warranting cautious use of ECMO in this population.</pubmed_abstract><journal>Critical care (London, England)</journal><pubmed_title>Outcomes of transplant recipients on ECMO for COVID-19 respiratory failure: an ELSO registry study.</pubmed_title><pmcid>PMC12465718</pmcid><funding_grant_id>S67501</funding_grant_id><funding_grant_id>1805121N</funding_grant_id><pubmed_authors>Hermans G</pubmed_authors><pubmed_authors>Vlaar APJ</pubmed_authors><pubmed_authors>Wauters J</pubmed_authors><pubmed_authors>Belmans A</pubmed_authors><pubmed_authors>Peetermans M</pubmed_authors><pubmed_authors>Lubnow M</pubmed_authors><pubmed_authors>Bohyn A</pubmed_authors><pubmed_authors>Combes A</pubmed_authors><pubmed_authors>Muller T</pubmed_authors><pubmed_authors>Meersseman P</pubmed_authors><pubmed_authors>Wilmer A</pubmed_authors><pubmed_authors>Meyns B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcomes of transplant recipients on ECMO for COVID-19 respiratory failure: an ELSO registry study.</name><description>&lt;h4>Background&lt;/h4>ECMO outcomes in COVID-19-related respiratory failure among solid organ transplant (SOT) and hematopoietic stem-cell transplant recipients (HSCT) are poorly described. We investigated: (1) whether transplant patients (SOT/HSCT) with COVID-19 have worse outcomes than non-immunocompromised (IC) COVID-19 patients, and (2) whether among transplant recipients (SOT/HSCT), those with COVID-19 have worse outcomes than those with non-COVID-19-related respiratory failure. Additionally, we aimed to identify factors independently associated with mortality among COVID-19 transplants.&lt;h4>Methods&lt;/h4>Retrospective analyses of the Extracorporeal Life Support Organization Registry from 1/1/2017 to 31/07/2023. Two comparisons were made: (1) transplant COVID-19 versus non-IC COVID-19, and (2) transplant COVID-19 versus transplant non-COVID-19 patients. Outcomes were analyzed using propensity score (PS)-adjusted, multivariable, and PS-matched analyses, adjusting for a priori identified confounders. Primary outcome was in-hospital mortality.&lt;h4>Results&lt;/h4>Among 38,270 runs, 146 transplant COVID-19, 12,552 non-IC-COVID-19 and 886 transplant non-COVID-19 runs were identified. In-hospital mortality in transplant COVID-19 patients was 75.3% and the risk was invariably increased compared to non-IC-COVID-19 (PS-adjusted OR: 2.36 [95%CI:1.61-3.46], p &lt; 0.001, multivariable OR:2.35 [95%CI:1.59-3.49], p &lt; 0.001, and PS-matched analysis OR: 1.89 [95%CI:1.21-2.95], p &lt; 0.005) and transplant non-COVID-19 patients (PS-adjusted OR: 4.20 [95%CI:2.74-6.44], p &lt; 0.001, multivariable OR: 3.79 [95%CI:2.51-5.74], p &lt; 0.001, and PS-matched analyses OR: 3.17 [95%CI:1.90-5.28], p &lt; 0.001). Mortality difference remained stable over time. Older age independently associated with higher mortality. This was accompanied by higher need for renal replacement therapy compared to non-IC-COVID-19 patients. Compared to transplant non-COVID-19 patients, ECMO runs and time-to-live discharge were invariably prolonged. Hemorrhagic, metabolic, pulmonary and infectious complications consistently occurred more frequently.&lt;h4>Conclusions&lt;/h4>Mortality was high in COVID-19 transplant ECMO patients, warranting cautious use of ECMO in this population.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T21:22:22.683Z</modification><creation>2026-05-01T03:11:01.188Z</creation></dates><accession>S-EPMC12465718</accession><cross_references><pubmed>40999467</pubmed><doi>10.1186/s13054-025-05636-9</doi></cross_references></HashMap>