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Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021
BACKGROUND: Tranexamic acid (TA) administration in aneurysmal subarachnoid hemorrhage (SAH) within the first 24 hours may reduce the incidence of early aneurysmal rebleeding. However, this is also the potential for an increased risk of delayed cerebral ischemia if TA is administered for more than 72...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088487/ https://www.ncbi.nlm.nih.gov/pubmed/33948326 http://dx.doi.org/10.25259/SNI_242_2021 |
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author | Lo, Benjamin W. Y. Fukuda, Hitoshi Tsang, Anderson C. O. Langer, David J. Miyawaki, Satoru Koyanagi, Masaomi Lui, Matthew Wai-Man |
author_facet | Lo, Benjamin W. Y. Fukuda, Hitoshi Tsang, Anderson C. O. Langer, David J. Miyawaki, Satoru Koyanagi, Masaomi Lui, Matthew Wai-Man |
author_sort | Lo, Benjamin W. Y. |
collection | PubMed |
description | BACKGROUND: Tranexamic acid (TA) administration in aneurysmal subarachnoid hemorrhage (SAH) within the first 24 hours may reduce the incidence of early aneurysmal rebleeding. However, this is also the potential for an increased risk of delayed cerebral ischemia if TA is administered for more than 72 hours following the initial aneurysmal rupture. METHODS: In the ultra-early tranexamic acid after subarachnoid hemorrhage randomized controlled trial by Post et al., patients were randomized to receive TA within the first 24 hours, or until start of aneurysm treatment. These results were compared to a matched control group. RESULTS: Ultra-early administration (≤24 h) of TA reduced the incidence of rebleeding, and did not alter the incidence of delayed cerebral ischemia and/or extracranial thrombosis. Further, no significant differences were noted between the TA group and control arm in the incidence of good (modified Rankin scores 0-3) clinical outcomes at 6 months. CONCLUSION: Ultra-early administration of TA (≤24 h) resulted in a lower rate of recurrent hemorrhage, without increasing the incidence of delayed cerebral ischemia in SAH patients. |
format | Online Article Text |
id | pubmed-8088487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-80884872021-05-03 Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021 Lo, Benjamin W. Y. Fukuda, Hitoshi Tsang, Anderson C. O. Langer, David J. Miyawaki, Satoru Koyanagi, Masaomi Lui, Matthew Wai-Man Surg Neurol Int Commentary BACKGROUND: Tranexamic acid (TA) administration in aneurysmal subarachnoid hemorrhage (SAH) within the first 24 hours may reduce the incidence of early aneurysmal rebleeding. However, this is also the potential for an increased risk of delayed cerebral ischemia if TA is administered for more than 72 hours following the initial aneurysmal rupture. METHODS: In the ultra-early tranexamic acid after subarachnoid hemorrhage randomized controlled trial by Post et al., patients were randomized to receive TA within the first 24 hours, or until start of aneurysm treatment. These results were compared to a matched control group. RESULTS: Ultra-early administration (≤24 h) of TA reduced the incidence of rebleeding, and did not alter the incidence of delayed cerebral ischemia and/or extracranial thrombosis. Further, no significant differences were noted between the TA group and control arm in the incidence of good (modified Rankin scores 0-3) clinical outcomes at 6 months. CONCLUSION: Ultra-early administration of TA (≤24 h) resulted in a lower rate of recurrent hemorrhage, without increasing the incidence of delayed cerebral ischemia in SAH patients. Scientific Scholar 2021-04-14 /pmc/articles/PMC8088487/ /pubmed/33948326 http://dx.doi.org/10.25259/SNI_242_2021 Text en Copyright: © 2021 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Commentary Lo, Benjamin W. Y. Fukuda, Hitoshi Tsang, Anderson C. O. Langer, David J. Miyawaki, Satoru Koyanagi, Masaomi Lui, Matthew Wai-Man Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021 |
title | Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021 |
title_full | Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021 |
title_fullStr | Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021 |
title_full_unstemmed | Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021 |
title_short | Commentary on Post, et al. Ultra-early tranexamic acid after subarachnoid hemorrhage: A randomized controlled trial. Lancet 2021 |
title_sort | commentary on post, et al. ultra-early tranexamic acid after subarachnoid hemorrhage: a randomized controlled trial. lancet 2021 |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088487/ https://www.ncbi.nlm.nih.gov/pubmed/33948326 http://dx.doi.org/10.25259/SNI_242_2021 |
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