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Tranexamic acid for post-partum haemorrhage: What, who and when

Tranexamic acid reduces bleeding by inhibiting the breakdown of blood clots. It is cost-effective and heat-stable with a long shelf life. In the WOMAN trial, tranexamic acid reduced deaths due to bleeding with no increase in thromboembolic events. The effect was greatest when women received tranexam...

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Autores principales: Brenner, Amy, Ker, Katharine, Shakur-Still, Haleema, Roberts, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891248/
https://www.ncbi.nlm.nih.gov/pubmed/31128974
http://dx.doi.org/10.1016/j.bpobgyn.2019.04.005
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author Brenner, Amy
Ker, Katharine
Shakur-Still, Haleema
Roberts, Ian
author_facet Brenner, Amy
Ker, Katharine
Shakur-Still, Haleema
Roberts, Ian
author_sort Brenner, Amy
collection PubMed
description Tranexamic acid reduces bleeding by inhibiting the breakdown of blood clots. It is cost-effective and heat-stable with a long shelf life. In the WOMAN trial, tranexamic acid reduced deaths due to bleeding with no increase in thromboembolic events. The effect was greatest when women received tranexamic acid within 3 h of childbirth (RR = 0.69, 95% CI 0.52–0.91). The WHO recommends that women with post-partum haemorrhage receive 1 g tranexamic acid intravenously as soon as possible after giving birth, followed by a second dose if bleeding continues after 30 min or restarts within 24 h since the first dose. Urgent treatment is critical because women with post-partum haemorrhage bleed to death quickly, and tranexamic acid is most effective when given early. Evidence suggests there is no benefit when the drug is given more than 3 h after bleeding onset. Alternative routes of administration and use of tranexamic acid in the prevention of post-partum haemorrhage are research priorities.
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spelling pubmed-68912482019-12-16 Tranexamic acid for post-partum haemorrhage: What, who and when Brenner, Amy Ker, Katharine Shakur-Still, Haleema Roberts, Ian Best Pract Res Clin Obstet Gynaecol Article Tranexamic acid reduces bleeding by inhibiting the breakdown of blood clots. It is cost-effective and heat-stable with a long shelf life. In the WOMAN trial, tranexamic acid reduced deaths due to bleeding with no increase in thromboembolic events. The effect was greatest when women received tranexamic acid within 3 h of childbirth (RR = 0.69, 95% CI 0.52–0.91). The WHO recommends that women with post-partum haemorrhage receive 1 g tranexamic acid intravenously as soon as possible after giving birth, followed by a second dose if bleeding continues after 30 min or restarts within 24 h since the first dose. Urgent treatment is critical because women with post-partum haemorrhage bleed to death quickly, and tranexamic acid is most effective when given early. Evidence suggests there is no benefit when the drug is given more than 3 h after bleeding onset. Alternative routes of administration and use of tranexamic acid in the prevention of post-partum haemorrhage are research priorities. Elsevier 2019-11 /pmc/articles/PMC6891248/ /pubmed/31128974 http://dx.doi.org/10.1016/j.bpobgyn.2019.04.005 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Brenner, Amy
Ker, Katharine
Shakur-Still, Haleema
Roberts, Ian
Tranexamic acid for post-partum haemorrhage: What, who and when
title Tranexamic acid for post-partum haemorrhage: What, who and when
title_full Tranexamic acid for post-partum haemorrhage: What, who and when
title_fullStr Tranexamic acid for post-partum haemorrhage: What, who and when
title_full_unstemmed Tranexamic acid for post-partum haemorrhage: What, who and when
title_short Tranexamic acid for post-partum haemorrhage: What, who and when
title_sort tranexamic acid for post-partum haemorrhage: what, who and when
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891248/
https://www.ncbi.nlm.nih.gov/pubmed/31128974
http://dx.doi.org/10.1016/j.bpobgyn.2019.04.005
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