Volume-dependent effect of stored red blood cells: A secondary analysis of the Age of Blood Evaluation trial.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
09 2020
Historique:
received: 21 11 2019
revised: 09 04 2020
accepted: 17 04 2020
pubmed: 29 8 2020
medline: 30 6 2021
entrez: 29 8 2020
Statut: ppublish

Résumé

An increased risk of complications, including death, has been associated with stored red blood cell (RBC) units in observational studies but not in randomized trials. We aimed to evaluate for volume-dependent effects attributable to length of RBC storage in a secondary analysis of the Age of Blood Evaluation (ABLE) trial. In the 2510 critically ill adults from the ABLE trial randomized to receive RBC units stored not more than 7 days or the oldest compatible RBC units, we estimated the hazard ratio (HR) for death by intensive care unit (ICU) and hospital discharge and by days 28, 90, and 180, within subgroups defined by the number of RBC units received. Extended Cox proportional hazards regression was used to model the HR. A volume-dependent effect of storage age on survival was present for death by 90 and 180 days, but not earlier endpoints. The HR for death by 90 days was 0.55 (95% confidence interval [CI], 0.11-0.98, fresh vs standard) after transfusion of 6 RBC units but 1.45 (95% CI, 1.06-1.98) after transfusion of 1 RBC unit. In this exploratory analysis, volume-dependent effects related to RBC storage were documented in the ABLE trial. The harms associated with small volumes of fresh RBC units and large volumes of older RBC units should be further explored.

Sections du résumé

BACKGROUND
An increased risk of complications, including death, has been associated with stored red blood cell (RBC) units in observational studies but not in randomized trials. We aimed to evaluate for volume-dependent effects attributable to length of RBC storage in a secondary analysis of the Age of Blood Evaluation (ABLE) trial.
STUDY DESIGN AND METHODS
In the 2510 critically ill adults from the ABLE trial randomized to receive RBC units stored not more than 7 days or the oldest compatible RBC units, we estimated the hazard ratio (HR) for death by intensive care unit (ICU) and hospital discharge and by days 28, 90, and 180, within subgroups defined by the number of RBC units received. Extended Cox proportional hazards regression was used to model the HR.
RESULTS
A volume-dependent effect of storage age on survival was present for death by 90 and 180 days, but not earlier endpoints. The HR for death by 90 days was 0.55 (95% confidence interval [CI], 0.11-0.98, fresh vs standard) after transfusion of 6 RBC units but 1.45 (95% CI, 1.06-1.98) after transfusion of 1 RBC unit.
CONCLUSION
In this exploratory analysis, volume-dependent effects related to RBC storage were documented in the ABLE trial. The harms associated with small volumes of fresh RBC units and large volumes of older RBC units should be further explored.

Identifiants

pubmed: 32856734
doi: 10.1111/trf.15933
doi:

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1929-1939

Subventions

Organisme : Fonds de Recherche du Québec - Santé
ID : Programme FRQS/MSSS de formation pour les médecin
Organisme : MSS: Ministère de la Santé et des Services Sociaux du Québec

Informations de copyright

© 2020 AABB.

Références

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Auteurs

Johnathan Mack (J)

Department of Medicine, Ottawa General Hospital, University of Ottawa, Ottawa, Ontario, Canada.

Susan R Kahn (SR)

Department of Medicine and Lady Davis Institute, Jewish General Hospital, McGill University, Montréal, Québec, Canada.

Alan Tinmouth (A)

Department of Medicine, Ottawa General Hospital, University of Ottawa, Ottawa, Ontario, Canada.

Dean Fergusson (D)

Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Ontario, Canada.

Paul C Hébert (PC)

Division of Critical Care, Centre Hospitalier Universitaire de Montréal, Université de Montréal, Montréal, Québec, Canada.

Jacques Lacroix (J)

Division of Pediatric Critical Care Medicine, Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Québec, Canada.

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