Department of Obstetrics and Gynecology, CHA Gangnam Medical Center, CHA University, Seoul, Korea.
Am J Obstet Gynecol. 2013 Oct;209(4):317.e1-9. doi: 10.1016/j.ajog.2013.07.004. Epub 2013 Jul 13.
To assess the current evidence regarding the efficiency, safety, and potential advantages of laparoendoscopic single-site surgery (LESS) for treating gynecologic diseases.
We comprehensively searched PubMed, Embase, and the Cochrane Library from their inception to December 2012. Two authors screened out duplicates and independently reviewed eligibility of each study. We included randomized controlled trials comparing LESS with conventional laparoscopy (CL) for treating gynecologic diseases. The primary outcomes were perioperative complication rate, conversion rate, postoperative pain, and cosmetic satisfaction.
We included 6 randomized controlled trials with 439 participants in the final analysis. There were no significant differences between LESS and CL in terms of perioperative complication rate (15.5% and 14.3%; risk ratio, 1.11; 95% confidence interval [CI], 0.74-1.67; P = .61), conversion rate (3.8% and 1.1%; risk ratio, 2.75; 95% CI, 0.73-10.33; P = .13), postoperative pain (weighted mean difference [WMD], -0.22; 95% CI, -1.29 to 0.85; P = .68), analgesic requirement (WMD, 0.41; 95% CI, -1.69 to 2.51; P = .70), and cosmetic satisfaction (WMD, 0.19; 95% CI, -0.30 to 0.68; P = .46). There were also no differences in terms of operative time (P = .65), hemoglobin change (P = .23), time to first flatus (P = .17), and length of hospital stay (P = .99) between both techniques.
This metaanalysis provides evidence that LESS is comparable in the efficacy and safety, but does not offer potential advantage such as better cosmesis and lesser pain compared with CL for treating gynecologic diseases.
评估经脐单孔腹腔镜手术(LESS)治疗妇科疾病的有效性、安全性和潜在优势的现有证据。
我们全面检索了 PubMed、Embase 和 Cochrane 图书馆,检索时间截至 2012 年 12 月。两位作者筛选出重复文献,并独立审查了每一项研究的纳入标准。我们纳入了比较 LESS 与传统腹腔镜(CL)治疗妇科疾病的随机对照试验。主要结局为围手术期并发症发生率、中转开腹率、术后疼痛和美容满意度。
最终有 6 项随机对照试验(439 例患者)纳入分析。LESS 与 CL 在围手术期并发症发生率(15.5%和 14.3%;风险比,1.11;95%置信区间[CI],0.74-1.67;P=0.61)、中转开腹率(3.8%和 1.1%;风险比,2.75;95% CI,0.73-10.33;P=0.13)、术后疼痛(加权均数差[WMD],-0.22;95% CI,-1.29 至 0.85;P=0.68)、镇痛需求(WMD,0.41;95% CI,-1.69 至 2.51;P=0.70)和美容满意度(WMD,0.19;95% CI,-0.30 至 0.68;P=0.46)方面均无显著差异。在手术时间(P=0.65)、血红蛋白变化(P=0.23)、首次排气时间(P=0.17)和住院时间(P=0.99)方面,LESS 与 CL 也无差异。
本荟萃分析提供的证据表明,LESS 在疗效和安全性方面与 CL 相当,但在治疗妇科疾病方面,LESS 并未表现出潜在优势,如更好的美容效果和更少的疼痛。