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[JAMA Surg发表论文]:根治性膀胱切除术中使用氨甲环酸
2024年11月26日 时讯速递, 进展交流 [JAMA Surg发表论文]:根治性膀胱切除术中使用氨甲环酸已关闭评论

Original Investigation 

October 2, 2024

Tranexamic Acid During Radical Cystectomy: A Randomized Clinical Trial

Rodney H. Breau, Luke T. Lavallée, Ilias Cagiannos, et al

JAMA Surg. Published online October 2, 2024. doi:10.1001/jamasurg.2024.4183

Key Points

Question  Does intraoperative prophylactic tranexamic acid reduce blood transfusion in patients undergoing open radical cystectomy?

Findings  In this randomized clinical trial that included 353 adults undergoing open radical cystectomy for bladder cancer, 37.0% of patients treated with tranexamic acid received a red blood cell transfusion compared with 37.4% of patients treated with placebo.

Meaning  Tranexamic acid did not reduce red blood cell transfusion in patients undergoing open radical cystectomy for bladder cancer.

Abstract

Importance  Among cancer surgeries, patients requiring open radical cystectomy have the highest risk of red blood cell (RBC) transfusion. Prophylactic tranexamic acid (TXA) reduces blood loss during cardiac and orthopedic surgery, and it is possible that similar effects of TXA would be observed during radical cystectomy.

Objective  To determine whether TXA, administered before incision and for the duration of radical cystectomy, reduced the number of RBC transfusions received by patients up to 30 days after surgery.

Design, Setting, and Participants  The Tranexamic Acid During Cystectomy Trial (TACT) was a double-blind, placebo-controlled, randomized clinical trial with enrollment between June 2013 and January 2021. This multicenter trial was conducted in 10 academic centers. A consecutive sample of patients was eligible if the patients had a planned open radical cystectomy for the treatment of bladder cancer.

Intervention  Before incision, patients in the intervention arm received a loading dose of intravenous TXA, 10 mg/kg, followed by a maintenance infusion of 5 mg/kg per hour for the duration of the surgery. In the control arm, patients received indistinguishable matching placebo.

Main Outcomes and Measures  The primary outcome was receipt of RBC transfusion up to 30 days after surgery.

Results  A total of 386 patients were assessed for eligibility, and 33 did not meet eligibility. Of 353 randomized patients (median [IQR] age, 69 [62-75] years; 263 male [74.5%]), 344 were included in the intention-to-treat analysis. RBC transfusion up to 30 days occurred in 64 of 173 patients (37.0%) in the TXA group and 64 of 171 patients (37.4%) in the placebo group (relative risk, 0.99; 95% CI, 0.83-1.18). There were no differences in secondary outcomes among the TXA group vs placebo group including mean (SD) number of RBC units transfused (0.9 [1.5] U vs 1.1 [1.8] U; P = .43), estimated blood loss (927 [733] mL vs 963 [624] mL; P = .52), intraoperative transfusion (28.3% [49 of 173] vs 24.0% [41 of 171]; P = .08), or venous thromboembolic events (3.5% [6 of 173] vs 2.9% [5 of 171]; P = .57). Non–transfusion-related adverse events were similar between groups.

Conclusions and Relevance  Results of this randomized clinical trial reveal that TXA did not reduce blood transfusion in patients undergoing open radical cystectomy for bladder cancer. Based on this trial, routine use of TXA during open radical cystectomy is not recommended.

Trial Registration  ClinicalTrials.gov Identifier: NCT01869413

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