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Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding

Data on the use of activated prothrombin complex concentrate (aPCC) for the management of warfarin associated major bleeding is sparse. The objective of the study was to assess the achievement of effective clinical hemostasis using aPCC in patients presenting with major bleeding while on warfarin. W...

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Autores principales: Sheikh-Taha, Marwan, Crawley, R. Monroe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810750/
https://www.ncbi.nlm.nih.gov/pubmed/35110612
http://dx.doi.org/10.1038/s41598-022-05803-w
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author Sheikh-Taha, Marwan
Crawley, R. Monroe
author_facet Sheikh-Taha, Marwan
Crawley, R. Monroe
author_sort Sheikh-Taha, Marwan
collection PubMed
description Data on the use of activated prothrombin complex concentrate (aPCC) for the management of warfarin associated major bleeding is sparse. The objective of the study was to assess the achievement of effective clinical hemostasis using aPCC in patients presenting with major bleeding while on warfarin. We also assessed the safety of the drug. This retrospective study was conducted at a tertiary care teaching center in the USA where patients with major bleeding while receiving warfarin, and received aPCC were included. Efficacy of aPCC in achieving effective hemostasis was assessed according to the International Society of Thrombosis and Hemostasis Scientific and Standardization Subcommittee criteria. Efficacy was also assessed by achieving INR < 1.5 after treatment. The primary safety endpoint was the occurrence of any thromboembolic complications. A total of 67 patients were included in the study. The most common site for bleeding was intracerebral hemorrhage (n = 37, 55.2%), followed by gastrointestinal bleed (n = 26, 38.8%). Clinical hemostasis was achieved in 46 (68.7%) patients and of the 21 (31.3%) patients who did not achieve clinical hemostasis, 16 died. Thirty nine (58.2%) patients achieved INR < 1.5. Five (7.5%) patients developed thromboembolic complications. This study suggests that the use of aPCCs is effective in achieving effective hemostasis in patients on warfarin presenting with major bleeding.
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spelling pubmed-88107502022-02-03 Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding Sheikh-Taha, Marwan Crawley, R. Monroe Sci Rep Article Data on the use of activated prothrombin complex concentrate (aPCC) for the management of warfarin associated major bleeding is sparse. The objective of the study was to assess the achievement of effective clinical hemostasis using aPCC in patients presenting with major bleeding while on warfarin. We also assessed the safety of the drug. This retrospective study was conducted at a tertiary care teaching center in the USA where patients with major bleeding while receiving warfarin, and received aPCC were included. Efficacy of aPCC in achieving effective hemostasis was assessed according to the International Society of Thrombosis and Hemostasis Scientific and Standardization Subcommittee criteria. Efficacy was also assessed by achieving INR < 1.5 after treatment. The primary safety endpoint was the occurrence of any thromboembolic complications. A total of 67 patients were included in the study. The most common site for bleeding was intracerebral hemorrhage (n = 37, 55.2%), followed by gastrointestinal bleed (n = 26, 38.8%). Clinical hemostasis was achieved in 46 (68.7%) patients and of the 21 (31.3%) patients who did not achieve clinical hemostasis, 16 died. Thirty nine (58.2%) patients achieved INR < 1.5. Five (7.5%) patients developed thromboembolic complications. This study suggests that the use of aPCCs is effective in achieving effective hemostasis in patients on warfarin presenting with major bleeding. Nature Publishing Group UK 2022-02-02 /pmc/articles/PMC8810750/ /pubmed/35110612 http://dx.doi.org/10.1038/s41598-022-05803-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sheikh-Taha, Marwan
Crawley, R. Monroe
Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding
title Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding
title_full Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding
title_fullStr Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding
title_full_unstemmed Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding
title_short Efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin K antagonist major bleeding
title_sort efficacy and safety of activated prothrombin complex concentrate for the reversal of vitamin k antagonist major bleeding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810750/
https://www.ncbi.nlm.nih.gov/pubmed/35110612
http://dx.doi.org/10.1038/s41598-022-05803-w
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