Wang Feng, Huang Li-Yan, Li Yue-Juan, Wang Deng-Chao
College of Nursing and Optometry, Jiangxi Teachers College, Yingtan, 335000, Jiangxi, China.
Department of Pathology, West China Second Hospital of Sichuan University, Chengdu, 610000, Sichuan, China.
Updates Surg. 2024 Dec;76(8):2733-2743. doi: 10.1007/s13304-024-02025-9. Epub 2024 Oct 24.
There is a debate over whether to transect or completely reduce the hernia sac during laparoscopic tension-free repair of inguinal hernia. This study endeavors to systematically assess the efficacy and safety of two approaches, namely transected sac (TS) and completely reduced sac (RS), in laparoscopic tension-free repair of inguinal hernia. Utilizing a meta-analysis methodology, we aim to provide a comprehensive analysis of these techniques. A comprehensive search was conducted across PubMed, Embase, Cochrane Library, Web of Science, and ClinicalTrials.gov databases to identify comparative studies focusing on laparoscopic tension-free repair of inguinal hernia, specifically comparing TS and RS techniques. The selected studies were subjected to meta-analysis using RevMan 5.3 software. A total of 8 studies, involving 2995 patients with inguinal hernia, were included in the analysis. The meta-analysis results revealed that the TS group had a higher incidence of seroma compared to the RS group [OR = 1.74, 95% CI (1.35, 2.25), P < 0.0001], and a prolonged time to return to normal activity postoperatively [MD = 0.99, 95% CI (0.85, 1.14), P < 0.00001]. However, no statistically significant differences were observed between the two groups in terms of operation time [MD = -1.75, 95% CI (- 8.72, 5.22), P = 0.62], incidence of postoperative pain [OR = 1.00, 95% CI (0.41, 2.44), P = 1.00], overall postoperative complication rate [OR = 0.98, 95% CI (0.43, 2.20), P = 0.95], and recurrence rate fOR = 2.53, 95% CI (0.61, 10.39), P = 0.20]. Transected sac in laparoscopic inguinal hernia repair is associated with an increased incidence of seroma and a longer recovery time for patients to return to normal activity. Clinical trial registration Registration number is INPLASY20223110070.
在腹股沟疝腹腔镜无张力修补术中,对于是否横断或完全回纳疝囊存在争议。本研究旨在系统评估腹股沟疝腹腔镜无张力修补术中两种方法,即横断疝囊(TS)和完全回纳疝囊(RS)的疗效和安全性。我们采用荟萃分析方法,旨在对这些技术进行全面分析。通过全面检索PubMed、Embase、Cochrane图书馆、Web of Science和ClinicalTrials.gov数据库,以识别聚焦于腹股沟疝腹腔镜无张力修补术的比较研究,特别是比较TS和RS技术的研究。使用RevMan 5.3软件对所选研究进行荟萃分析。共有8项研究,涉及2995例腹股沟疝患者,纳入了分析。荟萃分析结果显示,与RS组相比,TS组血清肿发生率更高[比值比(OR)=1.74,95%置信区间(CI)(1.35,2.25),P<0.0001],术后恢复正常活动的时间延长[平均差(MD)=0.99,95%CI(0.85,1.14),P<0.00001]。然而,两组在手术时间[MD=-1.75,95%CI(-8.72,5.22),P=0.62]、术后疼痛发生率[OR=1.00,95%CI(0.41,2.44),P=1.00]、总体术后并发症发生率[OR=0.98,95%CI(0.43,2.20),P=0.95]和复发率[OR=2.53,95%CI(0.61,10.39),P=0.20]方面未观察到统计学上的显著差异。腹腔镜腹股沟疝修补术中横断疝囊与血清肿发生率增加以及患者恢复正常活动的时间延长有关。临床试验注册 注册号为INPLASY20223110070。