Restrictive vs liberal red blood cell transfusion strategies in patients with acute myocardial infarction and anemia: Rationale and design of the REALITY trial

dc.contributor.authorDucrocq, Gregory
dc.contributor.authorCalvo, Gonzalo
dc.contributor.authorGonzález Juanatey, José Ramón
dc.contributor.authorDurand Zaleski, Isabelle
dc.contributor.authorAvendano Sola, Cristina
dc.contributor.authorPuymirat, Etienne
dc.contributor.authorLemesle, Gilles
dc.contributor.authorArnáiz, Joan Albert
dc.contributor.authorMartínez Sellés Oliveria Soares, Manuel
dc.contributor.authorREALITY investigators
dc.contributor.authorEt al.
dc.date.accessioned2021-02-11T19:25:26Z
dc.date.available2021-02-11T19:25:26Z
dc.date.issued2021
dc.description.abstractBackground: Anemia is common in patients with acute myocardial infarction (AMI), and is an independent predictor of mortality. The optimal transfusion strategy in these patients is unclear. Hypothesis: We hypothesized that a "restrictive" transfusion strategy (triggered by hemoglobin ≤8 g/dL) is clinically noninferior to a "liberal" transfusion strategy (triggered by hemoglobin ≤10 g/dL), but is less costly. Methods: REALITY is an international, randomized, multicenter, open-label trial comparing a restrictive vs a liberal transfusion strategy in patients with AMI and anemia. The primary outcome is the incremental cost-effectiveness ratio (ICER) at 30 days, using the primary composite clinical outcome of major adverse cardiovascular events (MACE; comprising all-cause death, nonfatal stroke, nonfatal recurrent myocardial infarction, or emergency revascularization prompted by ischemia) as the effectiveness criterion. Secondary outcomes include the ICER at 1 year, and MACE (and its components) at 30 days and at 1 year. Results: The trial aimed to enroll 630 patients. Based on estimated event rates of 11% in the restrictive group and 15% in the liberal group, this number will provide 80% power to demonstrate clinical noninferiority of the restrictive group, with a noninferiority margin corresponding to a relative risk equal to 1.25. The sample size will also provide 80% power to show the cost-effectiveness of the restrictive strategy at a threshold of €50 000 per quality-adjusted life year. Conclusions: REALITY will provide important guidance on the management of patients with AMI and anemia.spa
dc.description.filiationUEMspa
dc.description.impact3.287 JCR (2021) Q3, 74/143 Cardiac & Cardiovascular Systemsspa
dc.description.impact0.983 SJR (2021) Q1, 82/356 Cardiology and Cardiovascular Medicinespa
dc.description.impactNo data IDR 2021spa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationDucrocq, G., Calvo, G., González-Juanatey, J. R., Durand-Zaleski, I., Avendano-Sola, C., Puymirat, E., Lemesle, G., Arnáiz, J. A., Martínez-Sellés, M., Rousseau, A., Cachanado, M., Vicaut, E., Silvain, J., Karam, C., Danchin, N., Simón, T., Steg, P. G., & REALITY investigators (2021). Restrictive vs liberal red blood cell transfusion strategies in patients with acute myocardial infarction and anemia: Rationale and design of the REALITY trial. Clinical Cardiology, 44(2), 143–150. https://doi.org/10.1002/clc.23453spa
dc.identifier.doi10.1002/clc.23453
dc.identifier.issn1932-8737
dc.identifier.issn0160-9289
dc.identifier.urihttp://hdl.handle.net/11268/9842
dc.language.isoengspa
dc.peerreviewedSispa
dc.relation.publisherversionhttp://ezproxy.universidadeuropea.es/login?url=http://dx.doi.org/10.1002/clc.23453spa
dc.rights.accessRightsrestricted accessspa
dc.subject.otherInsuficiencia cardíacaspa
dc.subject.otherTransfusión sanguíneaspa
dc.subject.otherReacción a la transfusiónspa
dc.subject.unescoSistema cardiovascularspa
dc.subject.unescoEnfermedad cardiovascularspa
dc.subject.unescoTratamiento médicospa
dc.titleRestrictive vs liberal red blood cell transfusion strategies in patients with acute myocardial infarction and anemia: Rationale and design of the REALITY trialspa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublicationa14a4cbe-6878-47e7-8b7b-ffdd4a82573a
relation.isAuthorOfPublication.latestForDiscoverya14a4cbe-6878-47e7-8b7b-ffdd4a82573a

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