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Liberal or Restrictive Postoperative Transfusion in Patients at High Cardiac Risk The TOP Randomized Clinical Trial

  • Panos Kougias
  • , Sherene E. Sharath
  • , Min Zhan
  • , Jeffrey L. Carson
  • , L. Erin Norman
  • , Zhibao Mi
  • , Rupsi Pal
  • , Hasan Dosluoglu
  • , J. Gregory Modrall
  • , George A. Sarosi
  • , Peter Nelson
  • , Shipra Arya
  • , Alexandra Scrymgeour
  • , Jade Ollison
  • , Lawrence A. Calais
  • , Vijay Nambi
  • , L. Parker Gregg
  • , Shuaib M. Abdullah
  • , Shirling Tsai
  • , Natasha Becker
  • Justin C. Choi, Louisa Chiu, Salvatore Scali, Neal R. Barshes, Samir Awad, Mohammed Moursi, Matthew C. Koopmann, Mitchell Sally, Daniel Ihnat, Archana Ramaswamy, Warren Gasper, Edith Tzeng, Mark A. Wilson, Gale Tang, Grant Huang, Kousick Biswas
  • SUNY Downstate Health Sciences University
  • VA Cooperative Studies Program Coordinating Center
  • Rutgers - The State University of New Jersey, New Brunswick
  • University of Texas Southwestern Medical Center
  • University of Florida
  • University of Oklahoma
  • Stanford University
  • Cooperative Studies Program Clinical Research Pharmacy Coordinating Center
  • and Resource Team
  • Baylor College of Medicine
  • University of Arkansas for Medical Sciences
  • Portland VA Medical Center
  • Oregon Health and Science University
  • University of Minnesota Twin Cities
  • University of California at San Francisco
  • University of Pittsburgh
  • University of Washington

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Importance Postoperative red blood cell transfusion guidelines recommend transfusion for hemoglobin levels less than 7 g/dL. However, the safety of this strategy in patients at high risk of cardiac events undergoing major operations remains unclear. Objective To evaluate the risk of death or major ischemic events within 90 days after a liberal transfusion strategy compared with a restrictive transfusion strategy in patients at high risk of cardiac events who had undergone major vascular or general surgery operations and developed postoperative anemia. Design, Setting, and Participants This parallel, single-blind, randomized clinical superiority trial included 1428 veterans (≥18 y) at high cardiac risk undergoing major vascular or general surgery operations. Participants were enrolled from February 2018 to March 2023 across 16 Veterans Affairs Medical Centers in the US. Interventions Seven hundred fourteen participants with postoperative hemoglobin less than 10 g/dL were randomized to a liberal strategy (transfusion trigger at hemoglobin level <10 g/dL) and 714 to a restrictive strategy (transfusion trigger at hemoglobin <7 g/dL). Main Outcomes and Measures The primary end point was a composite of all-cause death, myocardial infarction, coronary revascularization, acute kidney failure, or ischemic stroke within 90 days after randomization. Secondary end points included a composite of cardiac complications other than myocardial infarction (arrhythmias, heart failure, and nonfatal cardiac arrest). Results Of the 1424 analyzed veterans (mean age, 69.9 [SD, 7.9] years; 1393 male [97.8%]; 268 Black [18.8%]; 48 Hispanic [4.1%]; 1071 White [75.2%]), 1297 (91.1%) underwent vascular surgical procedures. The mean hemoglobin difference between transfusion strategies was 2.0 g/dL on day 5 after randomization. The primary outcome rate in the liberal group was 9.1% (61 of 670) compared with 10.1% (71 of 700) in the restrictive group (relative risk, 0.90; 95% CI, 0.65-1.24). The secondary end point of cardiac complications without myocardial infarction, which was 1 of 5 secondary end points, occurred in 5.9% (38 of 647) of patients in the liberal group and 9.9% (67 of 678) of patients in the restrictive group (relative risk, 0.59; 99% CI, 0.36-0.98). Conclusions and relevance After major vascular or general surgery operations among patients at high risk of a cardiac event, a liberal transfusion strategy did not reduce 90-day death or major ischemic outcome rates compared with a restrictive strategy.

Original languageEnglish
Pages (from-to)2197-2207
Number of pages11
JournalJAMA
Volume334
Issue number24
DOIs
StatePublished - Dec 23 2025

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