Breau Rodney H, Lavallée Luke T, Cagiannos Ilias, Momoli Franco, Bryson Gregory L, Kanji Salmaan, Morash Christopher, Turgeon Alexis F, Zarychanski Ryan, Houston Brett L, McIsaac Daniel I, Mallick Ranjeeta, Knoll Greg A, Kulkarni Girish, Izawa Jonathan, Saad Fred, Kassouf Wassim, Fradet Vincent, Rendon Ricardo, Shayegan Bobby, Fairey Adrian, Drachenberg Darrel E, Fergusson Dean
Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.
JAMA Surg. 2024 Dec 1;159(12):1355-1363. doi: 10.1001/jamasurg.2024.4183.
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.
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.
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.
The primary outcome was receipt of RBC transfusion up to 30 days after surgery.
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.
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.
ClinicalTrials.gov Identifier: NCT01869413.
在癌症手术中,需要进行开放性根治性膀胱切除术的患者红细胞(RBC)输血风险最高。预防性使用氨甲环酸(TXA)可减少心脏和骨科手术中的失血,在根治性膀胱切除术中可能也会观察到TXA的类似效果。
确定在切口前及根治性膀胱切除术全程给予TXA是否能减少患者术后30天内接受的RBC输血量。
设计、设置和参与者:膀胱切除术中氨甲环酸试验(TACT)是一项双盲、安慰剂对照、随机临床试验,于2013年6月至2021年1月进行入组。该多中心试验在10个学术中心开展。连续入选的患者若计划接受开放性根治性膀胱切除术治疗膀胱癌则符合条件。
在切口前,干预组患者接受静脉注射TXA负荷剂量10mg/kg,随后在手术全程以每小时5mg/kg的速度持续输注。对照组患者接受难以区分的匹配安慰剂。
主要结局是术后30天内接受RBC输血情况。
共评估了386例患者的 eligibility,33例不符合条件。在353例随机分组患者(中位[四分位间距]年龄,69[62 - 75]岁;263例男性[74.5%])中,344例纳入意向性分析。TXA组173例患者中有64例(37.0%)在术后30天内接受了RBC输血,安慰剂组171例患者中有64例(37.4%)接受了输血(相对风险,0.99;95%置信区间,0.83 - 1.18)。TXA组与安慰剂组的次要结局无差异,包括平均(标准差)RBC输注单位数(0.9[1.5]单位对1.1[1.8]单位;P = 0.43)、估计失血量(927[733]mL对963[624]mL;P = 0.52)、术中输血(28.3%[173例中的49例]对24.0%[171例中的41例];P = 0.08)或静脉血栓栓塞事件(3.5%[173例中的6例]对2.9%[171例中的5例];P = 0.57)。两组非输血相关不良事件相似。
这项随机临床试验结果显示,TXA并未减少接受开放性根治性膀胱切除术治疗膀胱癌患者的输血情况。基于该试验,不建议在开放性根治性膀胱切除术中常规使用TXA。
ClinicalTrials.gov标识符:NCT01869413 。