<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kartika T</submitter><funding>NHLBI NIH HHS</funding><pagination>566-576</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11034845</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>112(4)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>We aimed to evaluate thrombotic and hemorrhagic complications with heparin versus bivalirudin use in veno-venous extracorporeal membrane oxygenation (V-V ECMO).&lt;h4>Methods&lt;/h4>We performed a retrospective cohort study of adult patients placed on V-V ECMO with intravenous anticoagulation with either heparin or bivalirudin. Time to thrombotic event and major bleed were analyzed in addition to related outcomes.&lt;h4>Results&lt;/h4>We identified 95 patients placed on V-V ECMO: 61 receiving heparin, 34 bivalirudin. The bivalirudin group had a higher rate of severe COVID-19, higher BMI, and longer ECMO duration. Despite this, bivalirudin was associated with reduced risk of thrombotic event (HR 0.14, 95% CI 0.06-0.32, p &lt; .001) and increased average lifespan of the circuit membrane lung (16 vs. 10 days, p = 0.004). While there was no difference in major bleeding, the bivalirudin group required fewer transfusions of packed red blood cells and platelets per 100 ECMO days (means of 13 vs. 39, p = 0.004; 5 vs. 19, p = .014, respectively). Lastly, the bivalirudin group had improved survival to ECMO decannulation in univariate analysis (median OS 53 vs. 26 days, p = .015).&lt;h4>Conclusions&lt;/h4>In this real-world analysis of bivalirudin versus heparin, bivalirudin is a viable option for V-V ECMO and associated with lower risk of thrombotic complications and fewer transfusion requirements.</pubmed_abstract><journal>European journal of haematology</journal><pubmed_title>Comparison of bleeding and thrombotic outcomes in veno-venous extracorporeal membrane oxygenation: Heparin versus bivalirudin.</pubmed_title><pmcid>PMC11034845</pmcid><funding_grant_id>T32 HL083808</funding_grant_id><funding_grant_id>R01 HL144113</funding_grant_id><funding_grant_id>R01 HL151367</funding_grant_id><funding_grant_id>R01 HL101972</funding_grant_id><pubmed_authors>McCarty OJT</pubmed_authors><pubmed_authors>Pfeffer M</pubmed_authors><pubmed_authors>Hinds MT</pubmed_authors><pubmed_authors>Zakhary B</pubmed_authors><pubmed_authors>Beardshear R</pubmed_authors><pubmed_authors>Kartika T</pubmed_authors><pubmed_authors>Zonies D</pubmed_authors><pubmed_authors>Oetken HJ</pubmed_authors><pubmed_authors>Migneco G</pubmed_authors><pubmed_authors>Moore K</pubmed_authors><pubmed_authors>Mathews R</pubmed_authors><pubmed_authors>Shatzel JJ</pubmed_authors><pubmed_authors>Kaempf AJ</pubmed_authors><pubmed_authors>DeLoughery TG</pubmed_authors><pubmed_authors>Bundy T</pubmed_authors><pubmed_authors>Case J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparison of bleeding and thrombotic outcomes in veno-venous extracorporeal membrane oxygenation: Heparin versus bivalirudin.</name><description>&lt;h4>Objectives&lt;/h4>We aimed to evaluate thrombotic and hemorrhagic complications with heparin versus bivalirudin use in veno-venous extracorporeal membrane oxygenation (V-V ECMO).&lt;h4>Methods&lt;/h4>We performed a retrospective cohort study of adult patients placed on V-V ECMO with intravenous anticoagulation with either heparin or bivalirudin. Time to thrombotic event and major bleed were analyzed in addition to related outcomes.&lt;h4>Results&lt;/h4>We identified 95 patients placed on V-V ECMO: 61 receiving heparin, 34 bivalirudin. The bivalirudin group had a higher rate of severe COVID-19, higher BMI, and longer ECMO duration. Despite this, bivalirudin was associated with reduced risk of thrombotic event (HR 0.14, 95% CI 0.06-0.32, p &lt; .001) and increased average lifespan of the circuit membrane lung (16 vs. 10 days, p = 0.004). While there was no difference in major bleeding, the bivalirudin group required fewer transfusions of packed red blood cells and platelets per 100 ECMO days (means of 13 vs. 39, p = 0.004; 5 vs. 19, p = .014, respectively). Lastly, the bivalirudin group had improved survival to ECMO decannulation in univariate analysis (median OS 53 vs. 26 days, p = .015).&lt;h4>Conclusions&lt;/h4>In this real-world analysis of bivalirudin versus heparin, bivalirudin is a viable option for V-V ECMO and associated with lower risk of thrombotic complications and fewer transfusion requirements.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-07-04T03:06:06.184Z</modification><creation>2025-07-04T03:06:06.184Z</creation></dates><accession>S-EPMC11034845</accession><cross_references><pubmed>38088062</pubmed><doi>10.1111/ejh.14146</doi></cross_references></HashMap>