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Association between tranexamic acid administration and mortality based on the trauma phenotype: a retrospective analysis of a nationwide trauma registry in Japan.

Authors :
Tachino, Jotaro
Seno, Shigeto
Matsumoto, Hisatake
Kitamura, Tetsuhisa
Hirayama, Atsushi
Nakao, Shunichiro
Katayama, Yusuke
Ogura, Hiroshi
Oda, Jun
Source :
Critical Care; 3/19/2024, Vol. 28 Issue 1, p1-14, 14p
Publication Year :
2024

Abstract

Background: In trauma systems, criteria for individualised and optimised administration of tranexamic acid (TXA), an antifibrinolytic, are yet to be established. This study used nationwide cohort data from Japan to evaluate the association between TXA and in-hospital mortality among all patients with blunt trauma based on clinical phenotypes (trauma phenotypes). Methods: A retrospective analysis was conducted using data from the Japan Trauma Data Bank (JTDB) spanning 2019 to 2021. Results: Of 80,463 patients with trauma registered in the JTDB, 53,703 met the inclusion criteria, and 8046 (15.0%) received TXA treatment. The patients were categorised into eight trauma phenotypes. After adjusting with inverse probability treatment weighting, in-hospital mortality of the following trauma phenotypes significantly reduced with TXA administration: trauma phenotype 1 (odds ratio [OR] 0.68 [95% confidence interval [CI] 0.57–0.81]), trauma phenotype 2 (OR 0.73 [0.66–0.81]), trauma phenotype 6 (OR 0.52 [0.39–0.70]), and trauma phenotype 8 (OR 0.67 [0.60–0.75]). Conversely, trauma phenotypes 3 (OR 2.62 [1.98–3.47]) and 4 (OR 1.39 [1.11–1.74]) exhibited a significant increase in in-hospital mortality. Conclusions: This is the first study to evaluate the association between TXA administration and survival outcomes based on clinical phenotypes. We found an association between trauma phenotypes and in-hospital mortality, indicating that treatment with TXA could potentially influence this relationship. Further studies are needed to assess the usefulness of these phenotypes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13648535
Volume :
28
Issue :
1
Database :
Complementary Index
Journal :
Critical Care
Publication Type :
Academic Journal
Accession number :
176145283
Full Text :
https://doi.org/10.1186/s13054-024-04871-w