Nkangu Miriam, Frisendahl Caroline, Polis Chelsea, Chen Tracy, Sterling Evan, Gomperts Rebecca, Plagianos Marlena, Haddad Lisa, Gemzell-Danielsson Kristina
University of Ottawa, Ottawa, Ontario, Canada
Population Council Center for Biomedical Research, New York City, New York, USA.
BMJ Open. 2024 Dec 4;14(12):e090402. doi: 10.1136/bmjopen-2024-090402.
Mifepristone is a selective progesterone receptor modulator with decades of data demonstrating its potential as a highly effective emergency as well as non-emergency contraceptive. Despite considerable evidence pointing to the potential effectiveness of mifepristone as a non-emergency contraceptive, no systematic review has been conducted to synthesise the available evidence. This systematic review aims to synthesise the current evidence on the use of mifepristone as a non-emergency contraceptive to prevent pregnancy among cisgender girls and women of reproductive age.
We developed an electronic search strategy in collaboration with the research librarian. We will search five databases (Ovid Medline, CINAHL, EMBASE, Cochrane-Central Trials and Global Health) from inception and identify additional studies using several grey literature search strategies. All databases will be searched from inception, and we planned to complete the search by 30 June 2024. An Ovid Medline search strategy conducted on 24 May 2024 is provided as an example. We will include all studies that involve cisgender girls and/or women of reproductive age (defined as 54 years or younger), which assessed mifepristone as a non-emergency contraceptive to prevent pregnancy. The primary outcome is contraceptive effectiveness. Two independent reviewers will screen studies for eligibility through title, abstract, and full-text review. We will extract data with Covidence software using a Cochrane Effective Practice and Organisation of Care (EPOC)-adapted data-extraction tool and will assess risk of bias using the EPOC risk of bias tool and the Newcastle-Ottawa Scale. If sufficient data are available, we will conduct a meta-analysis using fixed and/or random effect models. However, if we are unable to conduct a meta-analysis, we will present the results narratively using the synthesis without meta-analysis guidelines and the EPOC table recommended for presenting findings without meta-analysis. Grades of Recommendation, Assessment, Development and Evaluation will be used to assess the quality of the evidence. We will report this review according to Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols guidelines.
This review is focused on secondary data and does not require any ethical approval. We aim to publish the review in a peer-reviewed scientific journal to promote knowledge transfer and present results using other knowledge translation mediums.
CRD42024554720.
米非司酮是一种选择性孕激素受体调节剂,数十年的数据表明其作为高效紧急避孕药以及非紧急避孕药的潜力。尽管有大量证据表明米非司酮作为非紧急避孕药具有潜在有效性,但尚未进行系统评价来综合现有证据。本系统评价旨在综合当前关于米非司酮作为非紧急避孕药在预防顺性别育龄女孩和妇女怀孕方面应用的证据。
我们与研究馆员合作制定了电子检索策略。我们将从数据库建库起检索五个数据库(Ovid Medline、CINAHL、EMBASE、Cochrane - 中央试验库和全球健康库),并使用多种灰色文献检索策略识别其他研究。所有数据库将从建库起进行检索,我们计划在2024年6月30日前完成检索。以2024年5月24日进行的Ovid Medline检索策略为例。我们将纳入所有涉及顺性别育龄女孩和/或妇女(定义为54岁及以下)的研究,这些研究评估了米非司酮作为非紧急避孕药预防怀孕的效果。主要结局是避孕效果。两名独立评审员将通过标题、摘要和全文评审筛选研究的合格性。我们将使用Covidence软件,采用经过Cochrane有效实践与护理组织(EPOC)改编的数据提取工具提取数据,并使用EPOC偏倚风险工具和纽卡斯尔 - 渥太华量表评估偏倚风险。如果有足够的数据,我们将使用固定效应和/或随机效应模型进行荟萃分析。然而,如果我们无法进行荟萃分析,我们将根据无荟萃分析的综合指南和推荐用于呈现无荟萃分析结果的EPOC表格以叙述方式呈现结果。将使用推荐分级、评估、制定与评价方法来评估证据质量。我们将根据系统评价与荟萃分析方案的首选报告项目指南报告本评价。
本评价聚焦于二手数据,无需任何伦理批准。我们旨在将本评价发表在同行评审的科学期刊上,以促进知识传播,并使用其他知识转化媒介呈现结果。
PROSPERO注册号:CRD42024554720。