Ezebialu Ifeanyichukwu, Okafo Obiamaka, Oringanje Chukwudi, Ogbonna Udoezuo, Udoh Ekong, Odey Friday, Meremikwu Martin M
Department of Obstetrics and Gynecology, Faculty of Clinical Medicine, College of Medicine, Anambra State University, Awka, Nigeria.
University of Calabar, Calabar, Nigeria.
Int J Gynaecol Obstet. 2017 Feb;136 Suppl 1:34-37. doi: 10.1002/ijgo.12048.
Vulvar and clitoral pain are known complications of female genital mutilation (FGM). Several interventions have been used to treat these conditions. This review focuses on surgical and nonsurgical interventions to improve vulvar and clitoral pain in women living with FGM.
To evaluate the impact of nonsurgical and surgical interventions for alleviating vulvar and clitoral pain in women living with any type of FGM and to assess the associated adverse events.
The search included the following major databases: Cochrane Central Register for Controlled Trials (CENTRAL), MEDLINE, Scopus, Web of Science, and ClinicalTrials.gov. These were searched from inception until August 10, 2015 without any language restrictions.
Study designs included randomized controlled trials, cluster randomized trials, nonrandomized trials, cohort studies, case-control studies, controlled before-and-after studies, historical control studies, and interrupted time series with reported data comparing outcomes among women with FGM who were treated for clitoral or vulvar pain with either surgical or nonsurgical interventions.
Two team members independently screened studies for eligibility.
No studies were included.
Limited information exists on management of vulvar and clitoral pain in women living with FGM. This constitutes an important area for further research.
CRD42015024521.
外阴和阴蒂疼痛是女性生殖器切割(FGM)已知的并发症。已经采用了几种干预措施来治疗这些病症。本综述重点关注手术和非手术干预措施,以改善接受女性生殖器切割女性的外阴和阴蒂疼痛。
评估非手术和手术干预措施对缓解任何类型女性生殖器切割女性的外阴和阴蒂疼痛的影响,并评估相关不良事件。
检索包括以下主要数据库:Cochrane对照试验中央注册库(CENTRAL)、MEDLINE、Scopus、科学网和ClinicalTrials.gov。从数据库建立至2015年8月10日进行检索,无任何语言限制。
研究设计包括随机对照试验、整群随机试验、非随机试验、队列研究、病例对照研究、前后对照研究、历史对照研究以及中断时间序列研究,要求报告接受手术或非手术干预治疗阴蒂或外阴疼痛的女性生殖器切割女性之间的结果比较数据。
两名团队成员独立筛选研究以确定其是否符合纳入标准。
未纳入任何研究。
关于接受女性生殖器切割女性的外阴和阴蒂疼痛管理的信息有限。这是一个需要进一步研究的重要领域。
PROSPERO注册编号:CRD42015024521。