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Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism

The increased risk of venous thromboembolism (VTE) associated with pregnancy is well-known and prophylaxis guidelines consider a number of risk factors. Although non-O blood group and red blood cell (RBC) transfusion are known to be associated with VTE risk, their contribution to pregnancy-associate...

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Autores principales: Wang, Chen, Le Ray, Isabelle, Lee, Brian, Wikman, Agneta, Reilly, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753067/
https://www.ncbi.nlm.nih.gov/pubmed/31537816
http://dx.doi.org/10.1038/s41598-019-49566-3
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author Wang, Chen
Le Ray, Isabelle
Lee, Brian
Wikman, Agneta
Reilly, Marie
author_facet Wang, Chen
Le Ray, Isabelle
Lee, Brian
Wikman, Agneta
Reilly, Marie
author_sort Wang, Chen
collection PubMed
description The increased risk of venous thromboembolism (VTE) associated with pregnancy is well-known and prophylaxis guidelines consider a number of risk factors. Although non-O blood group and red blood cell (RBC) transfusion are known to be associated with VTE risk, their contribution to pregnancy-associated VTE has received little attention. This study was conducted in a population-based cohort of 1,000,997 deliveries to women with no prior history of VTE or thrombophilia. The independent contributions of ABO blood type and RBC transfusion to the risks of antepartum, peripartum and postpartum VTE are reported as odds ratios adjusted for risk factors that are considered in current prophylaxis guidelines and other potential confounders. Compared with type O, A and B blood types have higher risk of antepartum and postpartum VTE, with odds ratios between 1.4 and 1.8. Transfusion around delivery has the largest increased risks and a dose-response effect, with adjusted odds ratios from 2.60 (1.71–3.97) for 1–2 units to 3.55 (1.32–9.55) for more than 5 units. ABO blood type and RBC transfusion were found to be independent risk factors for pregnancy-associated VTE. Further research is required to understand the underlying mechanisms and to conduct a risk-benefit assessment of the small volumes of RBCs transfused around delivery.
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spelling pubmed-67530672019-10-01 Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism Wang, Chen Le Ray, Isabelle Lee, Brian Wikman, Agneta Reilly, Marie Sci Rep Article The increased risk of venous thromboembolism (VTE) associated with pregnancy is well-known and prophylaxis guidelines consider a number of risk factors. Although non-O blood group and red blood cell (RBC) transfusion are known to be associated with VTE risk, their contribution to pregnancy-associated VTE has received little attention. This study was conducted in a population-based cohort of 1,000,997 deliveries to women with no prior history of VTE or thrombophilia. The independent contributions of ABO blood type and RBC transfusion to the risks of antepartum, peripartum and postpartum VTE are reported as odds ratios adjusted for risk factors that are considered in current prophylaxis guidelines and other potential confounders. Compared with type O, A and B blood types have higher risk of antepartum and postpartum VTE, with odds ratios between 1.4 and 1.8. Transfusion around delivery has the largest increased risks and a dose-response effect, with adjusted odds ratios from 2.60 (1.71–3.97) for 1–2 units to 3.55 (1.32–9.55) for more than 5 units. ABO blood type and RBC transfusion were found to be independent risk factors for pregnancy-associated VTE. Further research is required to understand the underlying mechanisms and to conduct a risk-benefit assessment of the small volumes of RBCs transfused around delivery. Nature Publishing Group UK 2019-09-19 /pmc/articles/PMC6753067/ /pubmed/31537816 http://dx.doi.org/10.1038/s41598-019-49566-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Chen
Le Ray, Isabelle
Lee, Brian
Wikman, Agneta
Reilly, Marie
Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism
title Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism
title_full Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism
title_fullStr Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism
title_full_unstemmed Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism
title_short Association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism
title_sort association of blood group and red blood cell transfusion with the incidence of antepartum, peripartum and postpartum venous thromboembolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753067/
https://www.ncbi.nlm.nih.gov/pubmed/31537816
http://dx.doi.org/10.1038/s41598-019-49566-3
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