The efficacy of preoperative tranexamic acid administration among patients undergoing arthroscopic rotator cuff repair: A systematic review and meta-analysis of randomized controlled trials

IF 1.5 Q3 ORTHOPEDICS
Mahdi Yousef Alyousef, Sadiq Issa Alaqaili, Mohammed Ali Alzayer, Ali Sultan Alsultan, Ammar J Abusultan, Mohammad M Alzahrani, Saad M Alqahtani
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Abstract

Aim To conduct a systematic review and meta-analysis of randomized controlled trials (RCTs) that investigated the effectiveness of tranexamic acid (TXA) among patients undergoing arthroscopic rotator cuff repair (ARCR). Methods Five databases were screened until December 18, 2022. The included RCTs were assessed for risk of bias, and the endpoints were summarized as mean difference/standardized mean difference (MD/SMD) or risk ratio (RR) with the 95% confidence interval (CI) in a random-effects model. Results Seven RCTs with 510 patients (TXA = 261 and control/placebo = 249) were analyzed. The overall risk of bias was “low” and “unclear” in four and three RCTs, respectively. The mean operative time (n = 5 RCTs, MD = −9.64 min, 95% CI [−15.74, −3.54], p = 0.002) and mean postoperative pain score on postoperative day 1 (n = 5 RCTs, MD = −0.56, 95% CI [−1.06, −0.05], p = 0.03) were significantly reduced in the TXA group compared with the control group. However, there were no significant differences between both groups regarding visual clarity, amount of irrigation solution, and estimated intraoperative blood loss. Conclusion Among patients undergoing ARCR, preoperative TXA did not reduce intraoperative blood loss or improve visual clarity. However, TXA administration correlated with significant reductions (statistically) in operative time and postoperative day 1 pain score compared with the control group. Level of evidence: Level I; Systematic Review and Meta-analysis of Randomized Controlled Trials
关节镜下肩袖修复术患者术前给予氨甲环酸的疗效:随机对照试验的系统回顾和荟萃分析
目的对随机对照试验(RCTs)进行系统回顾和荟萃分析,研究氨甲环酸(TXA)在接受关节镜下肩袖修复(ARCR)患者中的有效性。方法筛选5个数据库至2022年12月18日。对纳入的rct进行偏倚风险评估,终点总结为随机效应模型中95%可信区间的均差/标准化均差(MD/SMD)或风险比(RR)。结果7项随机对照试验共510例患者(TXA = 261例,对照组/安慰剂= 249例)。在4项和3项随机对照试验中,总体偏倚风险分别为“低”和“不明确”。与对照组相比,TXA组的平均手术时间(n = 5 RCTs, MD = - 9.64 min, 95% CI [- 15.74, - 3.54], p = 0.002)和术后第1天的平均疼痛评分(n = 5 RCTs, MD = - 0.56, 95% CI [- 1.06, - 0.05], p = 0.03)均显著降低。然而,两组在视觉清晰度、冲洗液量和估计术中出血量方面没有显著差异。结论在接受ARCR的患者中,术前TXA并没有减少术中出血量或改善视力。然而,与对照组相比,TXA给药与手术时间和术后第1天疼痛评分显著减少(统计学上)相关。证据等级:一级;随机对照试验的系统评价和荟萃分析
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来源期刊
Shoulder and Elbow
Shoulder and Elbow Medicine-Rehabilitation
CiteScore
2.80
自引率
0.00%
发文量
91
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