Restrictive or Liberal Transfusion Strategy in Myocardial Infarction and Anemia.

Authors

Jeffrey L. Carson, Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ
Maria Mori Brooks, Departments of Epidemiology and Biostatistics, School of Public Health, University of Pittsburgh
Paul C. Hébert, Bruyere Research Institute, University of Ottawa, Pittsburgh
Shaun G. Goodman, Ottawa, St. Michael's Hospital, University of Toronto, Toronto
Marnie Bertolet, Departments of Epidemiology and Biostatistics, School of Public Health, University of Pittsburgh
Simone A. Glynn, National Heart, Lung, and Blood Institute, Bethesda, MD
Bernard R. Chaitman, St. Louis University School of Medicine, St. Louis
Tabassome Simon, FACT (French Alliance for Cardiovascular Trials); Hôpital Saint Antoine, Sorbonne Université
Renato D. Lopes, Duke Clinical Research Institute, Duke University, Durham, France
Andrew M. Goldsweig, Department of Medicine, Baystate Medical Center, Springfield
Andrew P. DeFilippis, Department of Medicine, Vanderbilt University Medical Center, Nashville
J Dawn Abbott, Lifespan Cardiovascular Institute and the Department of Medicine, Division of Cardiology, Alpert Medical School of Brown University, Providence, RI
Brian J. Potter, Edmonton, CHUM Research Centre
Francois Martin Carrier, Department of Anesthesiology and Pain Medicine, Université de Montréal
Sunil V. Rao, Department of Medicine, NYU Langone Health System
Howard A. Cooper, New York, and the Department of Cardiology, Westchester Medical Center, Valhalla
Shahab Ghafghazi, Department of Medicine, University of Louisville, Louisville, KY
Dean A. Fergusson, Clinical Epidemiology Program, Ottawa Hospital Research Institute
William J. Kostis, Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ
Helaine Noveck, Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ
Sarang Kim, Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ
Meechai Tessalee, UChicago AdventHealth Heart and Vascular
Gregory Ducrocq, FACT (French Alliance for Cardiovascular Trials); Université Paris-Cité, INSERM Unité 1148 and AP-HP, Hôpital Bichat
Pedro Gabriel Melo de Barros E Silva, Brazilian Clinical Research Institute, Sao Paulo
Darrell J. Triulzi, Department of Pathology, Division of Transfusion Medicine, University of Pittsburgh School of Medicine
Caroline Alsweiler, Green Lane Coordinating Center, Auckland, New Zealand
Mark A. Menegus, Department of Medicine, Montefiore Medical Center
John D. Neary, Montreal, the Department of Medicine, McMaster University, Hamilton, ON
Lynn Uhl, Department of Pathology
Jordan B. Strom, Richard A. and Susan F. Smith Center for Outcomes Research in Cardiology
Christopher B. Fordyce, Division of Cardiology and Centre for Cardiovascular Innovation, Vancouver General Hospital and University of British Columbia, Vancouver
Emile Ferrari, Paris, Hôpital Pasteur, Service de Cardiologie, CHU Nice, Nice
Johanne Silvain, Sorbonne Université, ACTION Study Group, INSERM UMRS1166, Hôpital Pitié-Salpêtrière AP-HP
Frances O. Wood, Department of Medicine, WakeMed Health and Hospitals, Winston-Salem
Benoit Daneault, Centre Hospitalier Universitaire (CHU) de Sherbrooke, Université de Sherbrooke, Sherbrooke, QC
Tamar S. Polonsky, Department of Medicine, University of Chicago Medicine
Manohara Senaratne, Department of Medicine, Grey Nuns Hospital
Etienne Puymirat, AP-HP, Hôpital Européen Georges Pompidou, Department of Cardiology, Université de Paris
Claire Bouleti, University Hospital of Poitiers, Clinical Investigation Center (INSERM 1204), Cardiology Department, Poitiers
Benoit Lattuca, Nimes University Hospital, Montpelier University, ACTION Group, Nimes
Harvey D. White, Green Lane Coordinating Center, Auckland, New Zealand
Sheryl F. Kelsey, Departments of Epidemiology and Biostatistics, School of Public Health, University of Pittsburgh
P Gabriel Steg, FACT (French Alliance for Cardiovascular Trials); Université Paris-Cité, INSERM Unité 1148 and AP-HP, Hôpital Bichat
John H. Alexander, Duke Clinical Research Institute, Duke University, Durham
MINT Investigators
Jay Raval, MINT Investigator; University of New Mexico, Department of Pathology

Document Type

Article

Publication Date

12-28-2023

Abstract

BACKGROUND: A strategy of administering a transfusion only when the hemoglobin level falls below 7 or 8 g per deciliter has been widely adopted. However, patients with acute myocardial infarction may benefit from a higher hemoglobin level.

METHODS: In this phase 3, interventional trial, we randomly assigned patients with myocardial infarction and a hemoglobin level of less than 10 g per deciliter to a restrictive transfusion strategy (hemoglobin cutoff for transfusion, 7 or 8 g per deciliter) or a liberal transfusion strategy (hemoglobin cutoff,deciliter). The primary outcome was a composite of myocardial infarction or death at 30 days.

RESULTS: A total of 3504 patients were included in the primary analysis. The mean (±SD) number of red-cell units that were transfused was 0.7±1.6 in the restrictive-strategy group and 2.5±2.3 in the liberal-strategy group. The mean hemoglobin level was 1.3 to 1.6 g per deciliter lower in the restrictive-strategy group than in the liberal-strategy group on days 1 to 3 after randomization. A primary-outcome event occurred in 295 of 1749 patients (16.9%) in the restrictive-strategy group and in 255 of 1755 patients (14.5%) in the liberal-strategy group (risk ratio modeled with multiple imputation for incomplete follow-up, 1.15; 95% confidence interval [CI], 0.99 to 1.34; P = 0.07). Death occurred in 9.9% of the patients with the restrictive strategy and in 8.3% of the patients with the liberal strategy (risk ratio, 1.19; 95% CI, 0.96 to 1.47); myocardial infarction occurred in 8.5% and 7.2% of the patients, respectively (risk ratio, 1.19; 95% CI, 0.94 to 1.49).

CONCLUSIONS: In patients with acute myocardial infarction and anemia, a liberal transfusion strategy did not significantly reduce the risk of recurrent myocardial infarction or death at 30 days. However, potential harms of a restrictive transfusion strategy cannot be excluded. (Funded by the National Heart, Lung, and Blood Institute and others; MINT ClinicalTrials.gov number, NCT02981407.).

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