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Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review

OBJECTIVE: To review available data on tranexamic acid (TXA) plasma concentration needed to inhibit fibrinolysis and the time to achieve this concentration when giving TXA by different routes in humans. To identify ongoing trials assessing alternatives to intravenous TXA administration. METHODS: We...

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Autores principales: Shakur‐Still, Haleema, Grassin‐Delyle, Stanislas, Muhunthan, Kopalasuntharam, Ahmadzia, Homa K., Faraoni, David, Arribas, Monica, Roberts, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327714/
https://www.ncbi.nlm.nih.gov/pubmed/35762806
http://dx.doi.org/10.1002/ijgo.14201
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author Shakur‐Still, Haleema
Grassin‐Delyle, Stanislas
Muhunthan, Kopalasuntharam
Ahmadzia, Homa K.
Faraoni, David
Arribas, Monica
Roberts, Ian
author_facet Shakur‐Still, Haleema
Grassin‐Delyle, Stanislas
Muhunthan, Kopalasuntharam
Ahmadzia, Homa K.
Faraoni, David
Arribas, Monica
Roberts, Ian
author_sort Shakur‐Still, Haleema
collection PubMed
description OBJECTIVE: To review available data on tranexamic acid (TXA) plasma concentration needed to inhibit fibrinolysis and the time to achieve this concentration when giving TXA by different routes in humans. To identify ongoing trials assessing alternatives to intravenous TXA administration. METHODS: We updated two previous systematic reviews by searching MEDLINE, EMBASE, OviSP, and ISI Web of Science from database inception to July 2021. We also searched the WHO International Clinical Trials Registry Platform for ongoing trials to July 2021. Titles and abstracts were screened for relevant trials. Two reviewers independently reviewed and agreed the trials to be included. RESULTS: Plasma TXA concentrations over 10 mg/L provide near maximal inhibition of fibrinolysis, with concentrations over 5 mg/L providing partial inhibition. Oral TXA tablets take about 1 h to reach a plasma concentration of 5 mg/L in postpartum women. Studies in healthy volunteers and shocked trauma patients show that intramuscular TXA achieves a plasma level of over 10 mg/L within 15 min. One trial is ongoing to determine the pharmacokinetics of intramuscular and oral solution TXA in pregnant women. CONCLUSION: Intramuscular TXA in healthy volunteers and shocked trauma patients reaches therapeutic concentration rapidly. Oral TXA tablets take too long to reach the minimum therapeutic concentration in postpartum women.
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spelling pubmed-93277142022-07-30 Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review Shakur‐Still, Haleema Grassin‐Delyle, Stanislas Muhunthan, Kopalasuntharam Ahmadzia, Homa K. Faraoni, David Arribas, Monica Roberts, Ian Int J Gynaecol Obstet Supplement Articles OBJECTIVE: To review available data on tranexamic acid (TXA) plasma concentration needed to inhibit fibrinolysis and the time to achieve this concentration when giving TXA by different routes in humans. To identify ongoing trials assessing alternatives to intravenous TXA administration. METHODS: We updated two previous systematic reviews by searching MEDLINE, EMBASE, OviSP, and ISI Web of Science from database inception to July 2021. We also searched the WHO International Clinical Trials Registry Platform for ongoing trials to July 2021. Titles and abstracts were screened for relevant trials. Two reviewers independently reviewed and agreed the trials to be included. RESULTS: Plasma TXA concentrations over 10 mg/L provide near maximal inhibition of fibrinolysis, with concentrations over 5 mg/L providing partial inhibition. Oral TXA tablets take about 1 h to reach a plasma concentration of 5 mg/L in postpartum women. Studies in healthy volunteers and shocked trauma patients show that intramuscular TXA achieves a plasma level of over 10 mg/L within 15 min. One trial is ongoing to determine the pharmacokinetics of intramuscular and oral solution TXA in pregnant women. CONCLUSION: Intramuscular TXA in healthy volunteers and shocked trauma patients reaches therapeutic concentration rapidly. Oral TXA tablets take too long to reach the minimum therapeutic concentration in postpartum women. John Wiley and Sons Inc. 2022-06-28 2022-06 /pmc/articles/PMC9327714/ /pubmed/35762806 http://dx.doi.org/10.1002/ijgo.14201 Text en © 2022 The Authors. International Journal of Gynecology & Obstetrics published by John Wiley & Sons Ltd on behalf of International Federation of Gynecology and Obstetrics. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement Articles
Shakur‐Still, Haleema
Grassin‐Delyle, Stanislas
Muhunthan, Kopalasuntharam
Ahmadzia, Homa K.
Faraoni, David
Arribas, Monica
Roberts, Ian
Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review
title Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review
title_full Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review
title_fullStr Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review
title_full_unstemmed Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review
title_short Alternative routes to intravenous tranexamic acid for postpartum hemorrhage: A systematic search and narrative review
title_sort alternative routes to intravenous tranexamic acid for postpartum hemorrhage: a systematic search and narrative review
topic Supplement Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327714/
https://www.ncbi.nlm.nih.gov/pubmed/35762806
http://dx.doi.org/10.1002/ijgo.14201
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