Department of Urology, Sun Yat-Sen University Cancer Center.
Department of Bone and Joint Surgery and Sports Medicine Center, The First Affiliated Hospital, Jinan University, Guangzhou, People's Republic of China.
Int J Surg. 2023 Mar 1;109(3):438-448. doi: 10.1097/JS9.0000000000000267.
The meta-analysis aimed to integrate the evidence of randomized control trials to estimate the efficacy of prophylactic tamsulosin on postoperative urinary retention (POUR).
The PubMed, Embase, Web of Science, and Cochrane Library databases were searched through 1 March 2022 using predetermined keywords. Randomized control trials reporting the preventive efficacy of prophylactic tamsulosin against POUR were identified according to the PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) guideline. Pooled risk ratios (RRs) were calculated using a random-effects model or a fixed-effects model based on the results of heterogeneity assessment. A meta-regression analysis was performed to explore the potential sources of heterogeneity.
There were 14 studies with 1102 patients in the Tamsulosin group and 1119 patients in the Control group. The risk of POUR was significantly lower in the Tamsulosin group (156/1102 [14.2%] vs. 238/1119 [21.3%]; RR=0.65; 95% CI: 0.50-0.86; P =0.002; Heterogeneity: I2 =51%; P =0.01). Tamsulosin administration was associated with a higher risk of adverse events (65/614 [10.6%] vs. 39/626 [6.2%]; RR=1.72; 95% CI: 1.19-2.48; P =0.004; Heterogeneity: I2 =0%; P =0.70). The meta-regression identified the mean age of patients as the only potential source of heterogeneity. Subgroup analysis showed that the younger patients (age <50 years) might benefit more from tamsulosin intake (RR=0.36; 95% CI: 0.19-0.70; P =0.003; Heterogeneity: I2 =49%; P =0.14).
The current meta-analysis suggested that prophylactic tamsulosin contributed to the prevention of POUR, and younger patients (<50 years) might benefit more from this preventive regimen. Tamsulosin was also associated with a higher risk of adverse events.
本荟萃分析旨在整合随机对照试验的证据,以评估坦索罗辛预防术后尿潴留(POUR)的疗效。
通过预定的关键词,于 2022 年 3 月 1 日之前检索了 PubMed、Embase、Web of Science 和 Cochrane Library 数据库。根据 PRISMA(系统评价和荟萃分析的首选报告项目)指南,确定了报告坦索罗辛预防 POUR 疗效的随机对照试验。使用随机效应模型或固定效应模型,根据异质性评估结果计算汇总风险比(RR)。进行了荟萃回归分析以探索潜在的异质源。
共有 14 项研究,坦索罗辛组 1102 例患者,对照组 1119 例患者。坦索罗辛组 POUR 的风险明显较低(156/1102 [14.2%] vs. 238/1119 [21.3%];RR=0.65;95%CI:0.50-0.86;P=0.002;异质性:I2=51%;P=0.01)。坦索罗辛给药与不良事件风险增加相关(65/614 [10.6%] vs. 39/626 [6.2%];RR=1.72;95%CI:1.19-2.48;P=0.004;异质性:I2=0%;P=0.70)。荟萃回归分析确定患者的平均年龄是唯一潜在的异质源。亚组分析显示,年轻患者(<50 岁)可能从坦索罗辛摄入中获益更多(RR=0.36;95%CI:0.19-0.70;P=0.003;异质性:I2=49%;P=0.14)。
本荟萃分析表明,坦索罗辛有助于预防 POUR,年轻患者(<50 岁)可能从这种预防方案中获益更多。坦索罗辛也与更高的不良事件风险相关。