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Tranexamic Acid and Pulmonary Complications: A Secondary Analysis of an EAST Multicenter Trial

Authors :
Raza, Shariq S.
Tatum, Danielle
Nordham, Kristen D.
Broome, Jacob M.
Keating, Jane
Maher, Zoe
Goldberg, Amy J.
Chang, Grace
Mendiola Pla, Michelle
Haut, Elliott R.
Tatebe, Leah
Toraih, Eman
Anderson, Christofer
Ninokawa, Scott
Maluso, Patrick
Burruss, Sigrid
Reeves, Matthew
Coleman, Lauren E.
Shatz, David V.
Goldenberg-Sandau, Anna
Bhupathi, Apoorva
Spalding, Chance
LaRiccia, Aimee
Bird, Emily
Noorbakhsh, Matthew R.
Babowice, James
Nelson, Marsha C.
Jacobson, Lewis E.
Williams, Jamie
Vella, Michael
Dellonte, Kate
Hayward, Thomas Z.
Holler, Emma
Lieser, Mark J.
Berne, John D.
Mederos, Dalier R.
Askari, Reza
Okafor, Barbara
Etchill, Eric
Fang, Raymond
Roche, Samantha L.
Whittenburg, Laura
Bernard, Andrew C.
Haan, James M.
Lightwine, Kelly L.
Norwood, Scott H.
Murry, Jason
Gamber, Mark A.
Carrick, Matthew M.
Bugaev, Nikolay
Tatar, Antony
Duchesne, Juan
Taghavi, Sharven
Source :
The American Surgeon; January 2025, Vol. 91 Issue: 1 p107-114, 8p
Publication Year :
2025

Abstract

Background Anti-inflammatory effects of tranexamic acid (TXA) in reducing trauma endotheliopathy may protect from acute lung injury. Clinical data showing this benefit in trauma patients is lacking. We hypothesized that TXA administration mitigates pulmonary complications in penetrating trauma patients.Materials and Methods This is a post-hoc analysis of a multicenter, prospective, observational study of adults (18+ years) with penetrating torso and/or proximal extremity injury presenting at 25 urban trauma centers. Tranexamic acid administration in the prehospital setting or within three hours of admission was examined. Participants were propensity matched to compare similarly injured patients. The primary outcome was development of pulmonary complication (ARDS and/or pneumonia).Results A total of 2382 patients were included, and 206 (8.6%) received TXA. Of the 206, 93 (45%) received TXA prehospital and 113 (55%) received it within three hours of hospital admission. Age, sex, and incidence of massive transfusion did not differ. The TXA group was more severely injured, more frequently presented in shock (SBP < 90 mmHg), developed more pulmonary complications, and had lower survival (P< 0.01 for all). After propensity matching, 410 patients remained (205 in each cohort) with no difference in age, sex, or rate of shock. On logistic regression, increased emergency department heart rate was associated with pulmonary complications. Tranexamic acid was not associated with different rate of pulmonary complications or survival on logistic regression. Survival was not different between the groups on logistic regression or propensity score–matched analysis.Conclusions Tranexamic acid administration is not protective against pulmonary complications in penetrating trauma patients.

Details

Language :
English
ISSN :
00031348 and 15559823
Volume :
91
Issue :
1
Database :
Supplemental Index
Journal :
The American Surgeon
Publication Type :
Periodical
Accession number :
ejs67102749
Full Text :
https://doi.org/10.1177/00031348241268109