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Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data

Randomized controlled trials (RCTs) have found no evidence that the storage time of transfused red blood cell (RBC) units affects recipient survival. However, inherent difficulties in conducting RBC transfusion RCTs have prompted critique of their design, analyses, and interpretation. Here, we addre...

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Autores principales: Bruun-Rasmussen, Peter, Kragh Andersen, Per, Banasik, Karina, Brunak, Søren, Johansson, Pär Ingemar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9227103/
https://www.ncbi.nlm.nih.gov/pubmed/35482965
http://dx.doi.org/10.1182/blood.2022015892
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author Bruun-Rasmussen, Peter
Kragh Andersen, Per
Banasik, Karina
Brunak, Søren
Johansson, Pär Ingemar
author_facet Bruun-Rasmussen, Peter
Kragh Andersen, Per
Banasik, Karina
Brunak, Søren
Johansson, Pär Ingemar
author_sort Bruun-Rasmussen, Peter
collection PubMed
description Randomized controlled trials (RCTs) have found no evidence that the storage time of transfused red blood cell (RBC) units affects recipient survival. However, inherent difficulties in conducting RBC transfusion RCTs have prompted critique of their design, analyses, and interpretation. Here, we address these issues by emulating hypothetical randomized trials using large real-world data to further clarify the adverse effects of storage time. We estimated the comparative effect of transfusing exclusively older vs fresher RBC units on the primary outcome of death, and the secondary composite end point of thromboembolic events, or death, using inverse probability weighting. Thresholds were defined as 1, 2, 3, and 4 weeks of storage. A large Danish blood transfusion database from the period 2008 to 2018 comprising >900 000 transfusion events defined the observational data. A total of 89 799 patients receiving >340 000 RBC transfusions during 28 days of follow-up met the eligibility criteria. Treatment with RBC units exclusively fresher than 1, 2, 3, and 4 weeks of storage was found to decrease the 28-day recipient mortality with 2.44 percentage points (pp) (0.86 pp, 4.02 pp), 1.93 pp (0.85 pp, 3.02 pp), 1.06 pp (–0.20 pp, 2.33 pp), and −0.26 pp (–1.78 pp, 1.25 pp) compared with transfusing exclusively older RBC units, respectively. The 28-day risk differences for the composite end point were similar. This study suggests that transfusing exclusively older RBC units stored for >1 or 2 weeks increases the 28-day recipient mortality and risk of thromboembolism or death compared with transfusing fresher RBC units.
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spelling pubmed-92271032022-07-06 Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data Bruun-Rasmussen, Peter Kragh Andersen, Per Banasik, Karina Brunak, Søren Johansson, Pär Ingemar Blood Transfusion Medicine Randomized controlled trials (RCTs) have found no evidence that the storage time of transfused red blood cell (RBC) units affects recipient survival. However, inherent difficulties in conducting RBC transfusion RCTs have prompted critique of their design, analyses, and interpretation. Here, we address these issues by emulating hypothetical randomized trials using large real-world data to further clarify the adverse effects of storage time. We estimated the comparative effect of transfusing exclusively older vs fresher RBC units on the primary outcome of death, and the secondary composite end point of thromboembolic events, or death, using inverse probability weighting. Thresholds were defined as 1, 2, 3, and 4 weeks of storage. A large Danish blood transfusion database from the period 2008 to 2018 comprising >900 000 transfusion events defined the observational data. A total of 89 799 patients receiving >340 000 RBC transfusions during 28 days of follow-up met the eligibility criteria. Treatment with RBC units exclusively fresher than 1, 2, 3, and 4 weeks of storage was found to decrease the 28-day recipient mortality with 2.44 percentage points (pp) (0.86 pp, 4.02 pp), 1.93 pp (0.85 pp, 3.02 pp), 1.06 pp (–0.20 pp, 2.33 pp), and −0.26 pp (–1.78 pp, 1.25 pp) compared with transfusing exclusively older RBC units, respectively. The 28-day risk differences for the composite end point were similar. This study suggests that transfusing exclusively older RBC units stored for >1 or 2 weeks increases the 28-day recipient mortality and risk of thromboembolism or death compared with transfusing fresher RBC units. American Society of Hematology 2022-06-23 /pmc/articles/PMC9227103/ /pubmed/35482965 http://dx.doi.org/10.1182/blood.2022015892 Text en © 2022 by The American Society of Hematology. https://creativecommons.org/licenses/by-nc-nd/4.0/Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
spellingShingle Transfusion Medicine
Bruun-Rasmussen, Peter
Kragh Andersen, Per
Banasik, Karina
Brunak, Søren
Johansson, Pär Ingemar
Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data
title Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data
title_full Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data
title_fullStr Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data
title_full_unstemmed Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data
title_short Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data
title_sort intervening on the storage time of rbc units and its effects on adverse recipient outcomes using real-world data
topic Transfusion Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9227103/
https://www.ncbi.nlm.nih.gov/pubmed/35482965
http://dx.doi.org/10.1182/blood.2022015892
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