Cook Lynley A, Pun Asha, Gallo Maria F, Lopez Laureen M, Van Vliet Huib A A M
Public Health and General Practice, University of Otago, Box 4345, Christchurch, Canterbury, New Zealand, 8140.
Cochrane Database Syst Rev. 2014 Mar 30;2014(3):CD004112. doi: 10.1002/14651858.CD004112.pub4.
Currently, the two most common surgical techniques for approaching the vas during vasectomy are the incisional method and the no-scalpel technique. Whereas the conventional incisional technique involves the use of a scalpel to make one or two incisions, the no-scalpel technique uses a sharp-pointed, forceps-like instrument to puncture the skin. The no-scalpel technique aims to reduce adverse events, especially bleeding, bruising, hematoma, infection and pain and to shorten the operating time.
The objective of this review was to compare the effectiveness, safety, and acceptability of the incisional versus no-scalpel approach to the vas.
In February 2014, we searched the computerized databases of CENTRAL, MEDLINE, POPLINE and LILACS. We looked for recent clinical trials in ClinicalTrials.gov and the International Clinical Trials Registry Platform. Previous searches also included in EMBASE. For the initial review, we searched the reference lists of relevant articles and book chapters.
Randomized controlled trials and controlled clinical trials were included in this review. No language restrictions were placed on the reporting of the trials.
We assessed all titles and abstracts located in the literature searches and two authors independently extracted data from the articles identified for inclusion. Outcome measures included safety, acceptability, operating time, contraceptive efficacy, and discontinuation. We calculated Peto odds ratios (OR) with 95% confidence intervals (CI) for the dichotomous variables.
Two randomized controlled trials evaluated the no-scalpel technique and differed in their findings. The larger trial demonstrated less perioperative bleeding (OR 0.49; 95% CI 0.27 to 0.89) and pain during surgery (OR 0.75; 95% CI 0.61 to 0.93), scrotal pain (OR 0.63; 95% 0.50 to 0.80), and incisional infection (OR 0.21; 95% CI 0.06 to 0.78) during follow up than the standard incisional group. Both studies found less hematoma with the no-scalpel technique (OR 0.23; 95% CI 0.15 to 0.36). Operations using the no-scalpel approach were faster and had a quicker resumption of sexual activity. The smaller study did not find these differences; however, the study could have failed to detect differences due to a small sample size as well as a high loss to follow up. Neither trial found differences in vasectomy effectiveness between the two approaches to the vas.
AUTHORS' CONCLUSIONS: The no-scalpel approach to the vas resulted in less bleeding, hematoma, infection, and pain as well as a shorter operation time than the traditional incision technique. No difference in effectiveness was found between the two approaches.
目前,输精管结扎术中两种最常用的输精管手术方法是切开法和无手术刀技术。传统的切开技术是用手术刀做一到两个切口,而无手术刀技术则使用一种类似镊子的尖锐器械穿刺皮肤。无手术刀技术旨在减少不良事件,尤其是出血、瘀伤、血肿、感染和疼痛,并缩短手术时间。
本综述的目的是比较输精管切开法与无手术刀法的有效性、安全性和可接受性。
2014年2月,我们检索了Cochrane系统评价数据库(CENTRAL)、医学文献数据库(MEDLINE)、人口与健康数据库(POPLINE)和拉丁美洲及加勒比地区健康科学文献数据库(LILACS)的计算机化数据库。我们在ClinicalTrials.gov和国际临床试验注册平台上查找近期的临床试验。之前的检索还包括EMBASE。对于初次综述时,我们检索了相关文章和书籍章节的参考文献列表。
本综述纳入随机对照试验和对照临床试验。试验报告无语言限制。
我们评估了文献检索中找到的所有标题和摘要,两位作者独立从确定纳入的文章中提取数据。结局指标包括安全性、可接受性、手术时间、避孕效果和停用情况。我们计算了二分变量的Peto比值比(OR)及其95%置信区间(CI)。
两项随机对照试验评估了无手术刀技术,结果有所不同。规模较大的试验表明,与标准切开组相比,无手术刀技术组围手术期出血较少(OR 0.49;95%CI 0.27至0.89)、手术期间疼痛较轻(OR 0.75;95%CI 0.61至0.93)、随访期间阴囊疼痛较轻(OR 0.63;95%CI 0.50至0.80)以及切口感染较少(OR 0.21;95%CI 0.06至0.78)。两项研究均发现无手术刀技术导致的血肿较少(OR 0.23;95%CI 0.15至0.36)。采用无手术刀方法的手术速度更快,性功能恢复也更快。规模较小的研究未发现这些差异;然而,由于样本量小以及随访失访率高,该研究可能未能检测到差异。两项试验均未发现两种输精管手术方法在输精管结扎效果上存在差异。
与传统切开技术相比,无手术刀输精管手术方法导致的出血、血肿、感染和疼痛更少,手术时间更短。两种方法在有效性方面未发现差异。