Center for Care Delivery & Outcomes Research, VA Health Care System, and Department of Medicine, University of Minnesota, Minneapolis, Minnesota (E.R.D., S.D.).
Center for Care Delivery & Outcomes Research, VA Health Care System, Minneapolis, Minnesota (C.S., K.E.U., N.Z., M.A., C.K., A.L., N.G.).
Ann Intern Med. 2024 Oct;177(10):1400-1414. doi: 10.7326/ANNALS-24-00610. Epub 2024 Sep 10.
Postmenopausal women commonly experience vulvovaginal, urinary, and sexual symptoms associated with genitourinary syndrome of menopause (GSM).
To evaluate effectiveness and harms of vaginal estrogen, nonestrogen hormone therapies, and vaginal moisturizers for treatment of GSM symptoms.
Medline, Embase, and CINAHL through 11 December 2023.
Randomized controlled trials (RCTs) of at least 8 weeks' duration enrolling postmenopausal women with at least 1 GSM symptom and reporting effectiveness or harms of hormonal interventions or vaginal moisturizers.
Risk of bias and data extraction were performed by one reviewer and verified by a second reviewer. Certainty of evidence (COE) was assessed by one reviewer and verified by consensus.
From 11 993 citations, 46 RCTs evaluating vaginal estrogen ( = 22), nonestrogen hormones ( = 16), vaginal moisturizers ( = 4), or multiple interventions ( = 4) were identified. Variation in populations, interventions, comparators, and outcomes precluded meta-analysis. Compared with placebo or no treatment, vaginal estrogen may improve vulvovaginal dryness, dyspareunia, most bothersome symptom, and treatment satisfaction. Compared with placebo, vaginal dehydroepiandrosterone (DHEA) may improve dryness, dyspareunia, and distress, bother, or interference from genitourinary symptoms; oral ospemifene may improve dryness, dyspareunia, and treatment satisfaction; and vaginal moisturizers may improve dryness (all low COE). Vaginal testosterone, systemic DHEA, vaginal oxytocin, and oral raloxifene or bazedoxifene may provide no benefit (low COE) or had uncertain effects (very low COE). Although studies did not report frequent serious harms, reporting was limited by short-duration studies that were insufficiently powered to evaluate infrequent serious harms.
Most studies were 12 weeks or less in duration and used heterogeneous GSM diagnostic criteria and outcome measures. Few studies enrolled women with a history of cancer.
Vaginal estrogen, vaginal DHEA, oral ospemifene, and vaginal moisturizers may improve some GSM symptoms in the short term. Few long-term data exist on efficacy, comparative effectiveness, tolerability, and safety of GSM treatments.
Agency for Healthcare Research and Quality and Patient-Centered Outcomes Research Institute. (PROSPERO: CRD42023400684).
绝经后妇女常出现与女性生殖泌尿系统综合征(GSM)相关的外阴阴道、泌尿系统和性功能障碍症状。
评估阴道雌激素、非雌激素激素疗法和阴道保湿剂治疗 GSM 症状的有效性和危害。
通过 Medline、Embase 和 CINAHL 数据库,检索截至 2023 年 12 月 11 日的相关研究。
纳入至少有 1 种 GSM 症状且报告激素干预或阴道保湿剂有效性或危害的绝经后妇女,至少进行 8 周随访的随机对照试验(RCT)。
由一名评审员进行偏倚风险和数据提取,并由另一名评审员进行验证。由一名评审员评估证据确定性(COE),并通过共识进行验证。
从 11993 条引文筛选出 46 项 RCT,评估阴道雌激素(=22)、非雌激素激素(=16)、阴道保湿剂(=4)或多种干预措施(=4)。由于人群、干预措施、对照和结局存在差异,因此无法进行荟萃分析。与安慰剂或不治疗相比,阴道雌激素可能改善外阴阴道干燥、性交痛、最困扰症状和治疗满意度。与安慰剂相比,阴道脱氢表雄酮(DHEA)可能改善干燥、性交痛和泌尿系统症状引起的不适、烦恼或干扰;口服奥昔孕诺可能改善干燥、性交痛和治疗满意度;阴道保湿剂可能改善干燥(所有证据的 COE 均为低)。阴道睾酮、全身 DHEA、阴道催产素和口服雷洛昔芬或巴多昔芬可能没有益处(COE 低)或效果不确定(COE 极低)。尽管研究未报告常见的严重危害,但由于短期研究报告中缺乏评价罕见严重危害的充分数据,报告受限。
大多数研究持续时间为 12 周或更短,使用了不同的 GSM 诊断标准和结局指标。很少有研究纳入有癌症病史的女性。
阴道雌激素、阴道 DHEA、口服奥昔孕诺和阴道保湿剂可能在短期内改善一些 GSM 症状。关于 GSM 治疗的疗效、相对有效性、耐受性和安全性的长期数据很少。
美国卫生保健研究与质量局和患者导向的医疗结果研究所。(PROSPERO:CRD42023400684)。