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Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis
BACKGROUND: Although some studies have shown that tranexamic acid is beneficial to patients with intracranial haemorrhage, the efficacy and safety of tranexamic acid for intracranial haemorrhage remain controversial. METHOD: The PubMed, EMBASE, and Cochrane Library databases were systematically sear...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065302/ https://www.ncbi.nlm.nih.gov/pubmed/37000863 http://dx.doi.org/10.1371/journal.pone.0282726 |
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author | Xiong, Yu Guo, Xiumei Huang, Xinyue Kang, Xiaodong Zhou, Jianfeng Chen, Chunhui Pan, Zhigang Wang, Linxing Goldbrunner, Roland Stavrinou, Lampis Stavrinou, Pantelis Lin, Shu Chen, Yuping Hu, Weipeng Zheng, Feng |
author_facet | Xiong, Yu Guo, Xiumei Huang, Xinyue Kang, Xiaodong Zhou, Jianfeng Chen, Chunhui Pan, Zhigang Wang, Linxing Goldbrunner, Roland Stavrinou, Lampis Stavrinou, Pantelis Lin, Shu Chen, Yuping Hu, Weipeng Zheng, Feng |
author_sort | Xiong, Yu |
collection | PubMed |
description | BACKGROUND: Although some studies have shown that tranexamic acid is beneficial to patients with intracranial haemorrhage, the efficacy and safety of tranexamic acid for intracranial haemorrhage remain controversial. METHOD: The PubMed, EMBASE, and Cochrane Library databases were systematically searched. The review followed PRISMA guidelines. Data were analyzed using the random-effects model. RESULTS: Twenty-five randomized controlled trials were included. Tranexamic acid significantly inhibited hematoma growth in intracranial hemorrhage (ICH) and traumatic brain injury (TBI) patients. (ICH: mean difference -1.76, 95%CI -2.78 to -0.79, I(2) = 0%, P < .001; TBI: MD -4.82, 95%CI -8.06 to -1.58, I(2) = 0%, P = .004). For subarachnoid hemorrhage (SAH) patients, it significantly decreased the risk of hydrocephalus (OR 1.23, 95%CI 1.01 to 1.50, I(2) = 0%, P = .04) and rebleeding (OR, 0.52, 95%CI 0.35 to 0.79, I(2) = 56% P = .002). There was no significance in modified Rankin Scale, Glasgow Outcome Scale 3–5, mortality, deep vein thrombosis, pulmonary embolism, or ischemic stroke/transient ischemic. CONCLUSION: Tranexamic acid can significantly reduce the risk of intracranial haemorrhage growth in patients with ICH and TBI. Tranexamic acid can reduce the incidence of complications (hydrocephalus, rebleeding) in patients with SAH, which can indirectly improve the quality of life of patients with intracranial haemorrhage. |
format | Online Article Text |
id | pubmed-10065302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100653022023-04-01 Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis Xiong, Yu Guo, Xiumei Huang, Xinyue Kang, Xiaodong Zhou, Jianfeng Chen, Chunhui Pan, Zhigang Wang, Linxing Goldbrunner, Roland Stavrinou, Lampis Stavrinou, Pantelis Lin, Shu Chen, Yuping Hu, Weipeng Zheng, Feng PLoS One Research Article BACKGROUND: Although some studies have shown that tranexamic acid is beneficial to patients with intracranial haemorrhage, the efficacy and safety of tranexamic acid for intracranial haemorrhage remain controversial. METHOD: The PubMed, EMBASE, and Cochrane Library databases were systematically searched. The review followed PRISMA guidelines. Data were analyzed using the random-effects model. RESULTS: Twenty-five randomized controlled trials were included. Tranexamic acid significantly inhibited hematoma growth in intracranial hemorrhage (ICH) and traumatic brain injury (TBI) patients. (ICH: mean difference -1.76, 95%CI -2.78 to -0.79, I(2) = 0%, P < .001; TBI: MD -4.82, 95%CI -8.06 to -1.58, I(2) = 0%, P = .004). For subarachnoid hemorrhage (SAH) patients, it significantly decreased the risk of hydrocephalus (OR 1.23, 95%CI 1.01 to 1.50, I(2) = 0%, P = .04) and rebleeding (OR, 0.52, 95%CI 0.35 to 0.79, I(2) = 56% P = .002). There was no significance in modified Rankin Scale, Glasgow Outcome Scale 3–5, mortality, deep vein thrombosis, pulmonary embolism, or ischemic stroke/transient ischemic. CONCLUSION: Tranexamic acid can significantly reduce the risk of intracranial haemorrhage growth in patients with ICH and TBI. Tranexamic acid can reduce the incidence of complications (hydrocephalus, rebleeding) in patients with SAH, which can indirectly improve the quality of life of patients with intracranial haemorrhage. Public Library of Science 2023-03-31 /pmc/articles/PMC10065302/ /pubmed/37000863 http://dx.doi.org/10.1371/journal.pone.0282726 Text en © 2023 Xiong et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Xiong, Yu Guo, Xiumei Huang, Xinyue Kang, Xiaodong Zhou, Jianfeng Chen, Chunhui Pan, Zhigang Wang, Linxing Goldbrunner, Roland Stavrinou, Lampis Stavrinou, Pantelis Lin, Shu Chen, Yuping Hu, Weipeng Zheng, Feng Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis |
title | Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis |
title_full | Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis |
title_fullStr | Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis |
title_full_unstemmed | Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis |
title_short | Efficacy and safety of tranexamic acid in intracranial haemorrhage: A meta-analysis |
title_sort | efficacy and safety of tranexamic acid in intracranial haemorrhage: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065302/ https://www.ncbi.nlm.nih.gov/pubmed/37000863 http://dx.doi.org/10.1371/journal.pone.0282726 |
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