Alyousef Mahdi Yousef, Alaqaili Sadiq Issa, Alzayer Mohammed Ali, Alsultan Ali Sultan, Abusultan Ammar J, Alzahrani Mohammad M, Alqahtani Saad M
Department of Orthopedic Surgery, Dammam Medical Complex, Dammam, Saudi Arabia.
Department of Orthopedic Surgery, McGill University Health Centre, Montreal, Quebec, Canada.
Shoulder Elbow. 2024 Oct;16(6):595-604. doi: 10.1177/17585732231207972. Epub 2023 Oct 17.
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).
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.
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.
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 I; Systematic Review and Meta-analysis of Randomized Controlled Trials.
对研究氨甲环酸(TXA)在关节镜下肩袖修补术(ARCR)患者中的有效性的随机对照试验(RCT)进行系统评价和荟萃分析。
截至2022年12月18日,对五个数据库进行了筛选。对纳入的RCT进行偏倚风险评估,并在随机效应模型中汇总终点指标为平均差/标准化平均差(MD/SMD)或风险比(RR)以及95%置信区间(CI)。
分析了7项RCT,共510例患者(TXA组 = 261例,对照组/安慰剂组 = 249例)。四项和三项RCT的总体偏倚风险分别为“低”和“不清楚”。与对照组相比,TXA组的平均手术时间(n = 5项RCT,MD = -9.64分钟,95% CI [-15.74, -3.54],p = 0.002)和术后第1天的平均术后疼痛评分(n = 5项RCT,MD = -0.56,95% CI [-1.06, -0.05],p = 0.03)显著降低。然而,两组在视野清晰度、冲洗液量和估计术中失血量方面无显著差异。
在接受ARCR的患者中,术前使用TXA并未减少术中失血量或改善视野清晰度。然而,与对照组相比,使用TXA在手术时间和术后第1天疼痛评分方面有显著(统计学上)降低。一级;随机对照试验的系统评价和荟萃分析。