Chen Sijing, Liu Jianhong, Peng Shiyi, Zheng Ying
Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, China.
Front Med (Lausanne). 2022 Aug 25;9:948709. doi: 10.3389/fmed.2022.948709. eCollection 2022.
To compare efficacy and safety of the levonorgestrel-releasing intrauterine system (LNG-IUS) with medical treatments for women with heavy menstrual bleeding.
We searched PubMed, Embase, the Cochrane Central Register of Controlled Trials, China National Knowledge Infrastructure (CNKI), and Wanfang databases for relevant randomized controlled trials (RCTs) in November 2021. All meta-analyses were performed using the random-effects model. PROSPERO registration number: CRD42021295379.
A total of trials (with 14 references) reporting on 1,677 women were included in this systematic review. The majority of the included RCTs were rated with low-to-unclear risk of bias in selection, detection, attrition, reporting, and other bias. All RCTs were rated as high risk in performance bias because blinding was difficult to ensure in the compared groups. Results of meta-analyses revealed that the number of clinical responders was greater in the LNG-IUS group than that in the medical treatments group at both 6-month (steroidal: five RCTs; = 490; risk ratio [RR]: 1.72 [1.13, 2.62]; = 92%; nonsteroidal: one RCT; = 42; RR: 2.34 [1.31, 4.19]) and 12-month (steroidal: three RCTs; = 261; RR: 1.31 [1.01, 1.71]; = 74%) endpoints, with no clear differences on number of dropouts, and the incidence of adverse events.
Evidence indicates that LNG-IUS is superior to the medical treatments in short-term and medium-term clinical responses, blood loss control, compliance, and satisfaction. Meanwhile, frequency of adverse events related to LNG-IUS is acceptable.
PROSPERO, identifier CRD42021259335, https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021295379.
比较左炔诺孕酮宫内节育系统(LNG-IUS)与药物治疗对月经过多女性的疗效和安全性。
我们于2021年11月检索了PubMed、Embase、Cochrane对照试验中心注册库、中国知网(CNKI)和万方数据库,以查找相关随机对照试验(RCT)。所有荟萃分析均采用随机效应模型。PROSPERO注册号:CRD42021295379。
本系统评价共纳入了报道1677名女性的试验(含14篇参考文献)。纳入的大多数RCT在选择、检测、失访、报告及其他偏倚方面的偏倚风险为低至不清楚。所有RCT在实施偏倚方面均被评为高风险,因为在比较组中难以确保盲法。荟萃分析结果显示,在6个月(甾体类药物:5项RCT;n = 490;风险比[RR]:1.72[1.13,2.62];I² = 92%;非甾体类药物:1项RCT;n = 42;RR:2.34[1.31,4.19])和12个月(甾体类药物:3项RCT;n = 261;RR:1.31[1.01,1.71];I² = 74%)的终点时,LNG-IUS组的临床反应者数量均多于药物治疗组,在失访数量和不良事件发生率方面无明显差异。
证据表明,LNG-IUS在短期和中期临床反应、失血控制、依从性和满意度方面优于药物治疗。同时,与LNG-IUS相关的不良事件发生率是可接受的。
PROSPERO,标识符CRD42021259335,https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021295379