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DOI 10.1177/00031348241268109

Медицинская библиотека · The American surgeon · 2024

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

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

СтатьяМногоцентровое исследованиеНаблюдательное исследованиеПеревод в очереди

Аннотация

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.

Для цитирования: 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. Tranexamic Acid and Pulmonary Complications: A Secondary Analysis of an EAST Multicenter Trial.. The American surgeon. 2024. DOI: 10.1177/00031348241268109.

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