Restrictive Versus Liberal Transfusion in Patients With Type 1 or Type 2 Myocardial Infarction: A Prespecified Analysis of the MINT Trial
- PMID: 39206549
- PMCID: PMC11611643
- DOI: 10.1161/CIRCULATIONAHA.124.071208
Restrictive Versus Liberal Transfusion in Patients With Type 1 or Type 2 Myocardial Infarction: A Prespecified Analysis of the MINT Trial
Abstract
Background: The MINT trial (Myocardial Ischemia and Transfusion) raised concern for harm from a restrictive versus liberal transfusion strategy in patients with acute myocardial infarction (MI) and anemia. Type 1 and type 2 MI are distinct pathophysiologic entities that may respond differently to blood transfusion. This analysis sought to determine whether the effects of transfusion varied among patients with a type 1 or a type 2 MI and anemia. The authors hypothesized that the liberal transfusion strategy would be of greater benefit in type 2 than in type 1 MI.
Methods: The authors compared rates of death or MI at 30 days in patients with type 1 (n=1460) and type 2 (n=1955) MI and anemia who were randomly allocated to a restrictive (threshold, 7-8 g/dL) or a liberal (threshold, 10 g/dL) transfusion strategy.
Results: The primary outcome of death or MI was observed in 16% of type 1 MI and 15.4% of type 2 MI patients. The rate of death or MI was higher in patients with type 1 MI randomized to a restrictive (18.2%) versus liberal (13.8%) transfusion strategy (relative risk [RR], 1.32 [95% CI, 1.04-1.67]) with no difference observed between the restrictive (15.8%) and liberal (15.1%) transfusion strategies in patients with type 2 MI (RR, 1.05 [95% CI, 0.85-1.29]). The test for a differential effect of transfusion strategy by MI type was not statistically significant (Pinteraction = 0.16).
Conclusions: The concern for harm with a restrictive transfusion strategy in patients with acute MI and anemia raised in the MINT primary outcome manuscript may be more apparent in patients with type 1 than type 2 MI.
Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02981407.
Keywords: acute coronary syndrome; blood transfusion; clinical trials as topic; myocardial infarction.
Conflict of interest statement
Dr DeFilippis reports research grants from Ionis Pharmaceutical; and consulting for Velkor, Inc and Novo Nordisk. Dr Abbott reports consulting for Abbott, Medtronic, Penumbra. Research Boston Scientific, Recor, Med Alliance, Shockwave, and Microport. Dr White reports grant support paid to the institution for: ODYSSEY OUTCOMES trial (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab; from Sanofi and Regeneron Pharmaceuticals); STRENGTH trial (Long-Term Outcomes Study to Assess Statin Residual Risk With Epanova in High Cardiovascular Risk Patients With Hypertriglyceridemia; Omthera Pharmaceuticals); HEART-FID Study (Ferric Carboxymaltose in Heart Failure With Iron Deficiency; American Regent); Dal GenE study (Study Effect of Dalcetrapib Versus Placebo on CV Risk in a Genetically Defined Population With a Recent ACS; DalCor Pharma UK Inc); AEGIS II study (CSL Behring); Clear Outcomes Study (Cholesterol Lowering via Bempedoic Acid, an ACL-Inhibiting Regimen; Esperion Therapeutics); SOLIST-WHF (Effect of Sotagliflozin on Cardiovascular Events in Patients With Type 2 Diabetes Post Worsening Heart Failure) and SCORED (Effect of Sotagliflozin on Cardiovascular and Renal Events in Patients With Type 2 Diabetes and Moderate Renal Impairment Who Are at Cardiovascular Risk) studies (Sanofi Aventis Australia Pty Ltd); Librexia AF (A Study of Milvexian Versus Apixaban in Participants With Atrial Fibrillation) and ACS (A Study of Milvexian in Participants After a Recent Acute Coronary Syndrome) studies (Janssen); and ISCHEMIA (International Study of Comparative Health Effectiveness With Medical and Invasive Approaches) and MINT ([Myocardial Ischemia and Transfusion] National Institutes of Health); and personal fees as a steering committee member from DalCor Pharma UK, CSL Behring, Sanofi Australia Pty Ltd, Janssen, and Esperion Therapeutics; as well as membership on advisory boards for CSL Behring and Genentech. Dr Lopes reports grant support or contracts from Amgen, Bristol Myers Squibb, GlaxoSmithKline, Medtronic, Pfizer, and Sanofi-Aventis; funding for educational activities or lectures from Pfizer, Daiichi Sankyo, and Novo Nordisk; and funding for consulting or other services from Bayer, Boehringer Ingelheim, Bristol Myers Squibb, and Novo Nordisk. Dr Alexander reports grant support (to Duke University) from Artivion/CryoLife, Bayer, Bristol Myers Squibb, CSL Behring, Ferring, United States Food and Drug Administration, Humacyte, and National Institutes of Health; and advisory board or consulting payments from AbbVie, Artivion/CryoLife, AtriCure, Bayer, Bristol-Myers Squibb, Eli Lilly, Ferring, GlaxoSmithKline, Janssen, Novostia, Pfizer, Portola, Theravance, and Veralox. Drs Carson and Hébert report participation on the data safety monitoring board for Cerus. Dr Goodman reports research grant support (eg, steering committee or data and safety monitoring committee) and/or speaker/consulting honoraria (eg, advisory boards) from Amgen, Anthos Therapeutics, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol Myers Squibb, CSL Behring, CYTE Ltd, Daiichi-Sankyo/American Regent, Eli Lilly, Esperion, Ferring Pharmaceuticals, HLS Therapeutics, Idorsia, JAMP Pharma, Merck, Novartis, Novo Nordisk A/C, Pendopharm/Pharmascience, Pfizer, Regeneron, Sanofi, Servier, Tolmar Pharmaceuticals, and Valeo Pharma; and salary support/honoraria from the Canadian Heart Failure Society, Canadian Heart Research Centre and MD Primer, Canadian VIGOUR Centre, Cleveland Clinic Coordinating Centre for Clinical Research, Duke Clinical Research Institute, New York University Clinical Coordinating Centre, PERFUSE Research Institute, Peter Munk Cardiac Centre Clinical Trials and Translation Unit, and Thrombolysis in Myocardial Infarction Study Group (Brigham Health). The other authors report no conflicts.
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