Continuous vs. cyclic combined hormonal contraceptives for treatment of dysmenorrhea: a systematic review

Q2 Medicine Contraception: X Pub Date : 2019-01-01 DOI:10.1016/j.conx.2019.100002
Tiffany Damm , Georgine Lamvu , Jorge Carrillo , Chensi Ouyang , Jessica Feranec
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引用次数: 9

Abstract

Objective

This systematic review aims to evaluate the benefits of oral continuous combined hormonal contraceptives (CHCs) in managing dysmenorrhea by comparing randomized controlled trials (RCTs) evaluating the efficacy of continuous vs. cyclic CHC use for the following outcomes: (a) reducing dysmenorrhea duration and frequency, (b) severity, (c) recurrence and (d) interference with daily activity.

Study design

Cochrane, PUBMED and Popline databases were searched from 1934 to 2018 for all relevant studies evaluating CHC for treatment of dysmenorrhea. A study was selected if it (a) compared continuous regimen vs. cyclic regimen of oral CHC, (b) measured dysmenorrhea as a primary or secondary outcome, (c) was an RCT and (d) was published in English. Due to differences in CHC used and outcome measurement, a systematic analysis of individual study results and a limited meta-analysis were conducted.

Results

Of 780 studies that were screened by title and abstract, 8 were included in the final analysis; 6 evaluated cyclic vs. continuous CHC, and 2 evaluated cyclic vs. extended/flexible CHC use. Quality of evidence was low for all outcome measures. Overall, compared to cyclic use, flexible/extended CHC resulted in 4 fewer days of dysmenorrhea. Studies revealed conflicting results for interference with daily activity, pain severity and pain recurrence. Side effects were few in both comparison groups.

Conclusions

Continuous or extended/flexible CHC use may reduce dysmenorrhea duration compared to cyclic regimen; however, more rigorous research is needed.

Implications

This systematic review shows that continuous CHC use may reduce dysmenorrhea duration compared to cyclic regimen, although the quality of evidence is low. Future double-blinded RCTs with more rigorous study design, consistent outcome measures and comprehensive outcome reporting are needed.

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连续与循环联合激素避孕药治疗痛经:系统回顾
目的:本系统综述旨在通过比较随机对照试验(RCTs)来评价口服连续联合激素避孕药(CHCs)在治疗痛经方面的益处,这些随机对照试验评估了连续与循环使用CHCs在以下方面的疗效:(a)减少痛经持续时间和频率,(b)严重程度,(c)复发和(d)对日常活动的干扰。研究设计检索cochrane、PUBMED和Popline数据库,从1934年到2018年检索所有评价CHC治疗痛经的相关研究。如果:(A)比较口服CHC的连续方案与循环方案,(b)测量痛经作为主要或次要结局,(c)是一项随机对照试验,(d)以英文发表,则选择一项研究。由于使用的CHC和结果测量的差异,我们对个别研究结果进行了系统分析和有限的荟萃分析。结果通过题目和摘要筛选的780篇研究中,有8篇纳入最终分析;6个评估循环与连续CHC, 2个评估循环与延长/灵活CHC使用。所有结果测量的证据质量都很低。总的来说,与循环使用相比,灵活/延长的CHC导致痛经时间减少4天。研究显示,干扰日常活动、疼痛严重程度和疼痛复发的结果相互矛盾。两组的副作用都很少。结论与循环用药相比,持续或延长/灵活使用CHC可缩短痛经持续时间;然而,还需要更严格的研究。本系统综述显示,尽管证据质量较低,但与循环用药相比,持续使用CHC可缩短痛经持续时间。未来的双盲随机对照试验需要更严格的研究设计、一致的结果测量和全面的结果报告。
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来源期刊
Contraception: X
Contraception: X Medicine-Obstetrics and Gynecology
CiteScore
5.10
自引率
0.00%
发文量
17
审稿时长
22 weeks
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