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Non-pharmacological interventions for treating sexual dysfunction in postpartum women: a systematic review protocol

机译:非药物治疗产后女性性功能障碍的干预措施:系统评价方案

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Introduction Sexual dysfunction in the postpartum period is a very common and relevant clinical problem, which has a significant adverse impact on the health of women. We aim to analyse the efficacy and safety of non-pharmacological interventions for treating sexual dysfunction in postpartum women. Our review aims to provide accurate data for effective policy-making and improve our understanding of the treatment of postpartum sexual dysfunction with non-pharmacological therapies.Methods and analysis The Cochrane Central Register of Controlled Trials in The Cochrane Library, clinicaltrials.gov, Medline/PubMed, CINAHL (Cumulative Index to Nursing and Allied Health Literature), LILACS (Literatura Latino-americana e do Caribe em Ciências da Saúde) and Embase will be used to search for articles dated from database inception to July 2019. Randomised controlled clinical trials and large prospective cohorts with control groups using non-pharmacological treatments for sexual dysfunction in postpartum women will be included. Sexual problems are directly linked to sexual dysfunction; thus, the primary outcome will be the absolute number or percentage of sexual issues in each treatment group. The secondary outcomes will be assessed by decreased sexual problems, such as lack of lubrication, decreased libido and difficulty reaching orgasm. Three reviewers will independently select trials and extract data from the original publications. The citations will be screened independently by reviewers in duplicate. The risk of bias of the included studies will be assessed according to the Cochrane risk of bias tool. Data synthesis will be performed using Review Manager (RevMan) software V.5.2.3. In the event that a meta-analysis is possible, we will assess the heterogeneity across the studies by computing the I2 statistic.Ethics and dissemination As the design of this study includes a review of published data, the need to obtain ethical approval was waived by our institutional review committee. We intend to publish the findings of this systematic review in a peer-reviewed journal.PROSPERO registration number CRD42018103077.
机译:简介产后性功能障碍是一个非常普遍且相关的临床问题,对妇女的健康有严重的不利影响。我们旨在分析非药物干预措施治疗产后妇女性功能障碍的有效性和安全性。我们的综述旨在为有效的决策提供准确的数据,并增进我们对采用非药物疗法治疗产后性功能障碍的理解。方法与分析Cochrane图书馆的Cochrane对照试验中央登记册,clinicaltrials.gov,Medline PubMed,CINAHL(护理和相关健康文献的累积索引),LILACS(拉丁美洲文学的萨乌德文学)和Embase将用于搜索从数据库开始到2019年7月的文章。随机对照临床试验和包括与对照组一起使用非药物疗法治疗产后妇女性功能障碍的大量前瞻性队列研究。性问题与性功能障碍直接相关;因此,主要结果将是每个治疗组中性问题的绝对数量或百分比。次要结果将通过减少性问题来评估,例如缺乏润滑,性欲降低和难以达到性高潮。三名审稿人将独立选择试验并从原始出版物中提取数据。审阅者将一式两份地独立筛选引文。将根据Cochrane偏倚风险工具评估纳入研究的偏倚风险。数据综合将使用Review Manager(RevMan)软件V.5.2.3执行。如果可能进行荟萃分析,我们将通过计算I2统计量来评估研究之间的异质性。伦理与传播由于本研究的设计包括对已发表数据的审查,因此免除了获得伦理批准的需要。我们的机构审查委员会。我们打算将此系统评价的结果发布在同行评审期刊上.PROSPERO注册号CRD42018103077。

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