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绝经后女性泌尿生殖系统综合征阴道用雌激素产品治疗的疗效和安全性的系统评价。

A systematic review of the efficacy and safety of vaginal estrogen products for the treatment of genitourinary syndrome of menopause.

机构信息

TherapeuticsMD, Boca Raton, FL.

出版信息

Menopause. 2019 Apr;26(4):431-453. doi: 10.1097/GME.0000000000001221.

Abstract

OBJECTIVE

We updated a systematic review to evaluate the totality of evidence available for the efficacy and safety of vaginal estrogen products for the treatment of genitourinary syndrome of menopause (GSM) based on published randomized controlled trials.

METHODS

We searched the Cochrane Library, Ovid, PubMed, Medline, Embase, and Clinicaltrials.gov for English-language articles from database inception to June 2018. Our search consolidated 2,086 potential sources to 53 full-text articles that were reviewed and found relevant to our systematic review.

RESULTS

We identified 53 studies that met the inclusion criteria that evaluated the efficacy and safety of vaginal estrogen versus placebo or other hormone and nonhormone controls. Compared with placebo, all vaginal estrogens demonstrated superiority in objective endpoints and subjective endpoints of GSM, whereas some trials demonstrated superiority versus placebo in urogenital symptoms. No significant difference was observed between various dosages and dosage forms of vaginal estrogen products. Vaginal estrogen showed superiority over vaginal lubricants and moisturizers for the improvement of objective clinical endpoints of vulvovaginal atrophy but not for subjective endpoints. Unopposed vaginal estrogens seemed safe, although studies were not powered to detect a long-term estrogenic side effect.

CONCLUSION

Estrogen products were found to be clinically effective for the treatment of GSM with doses as low as 4 μg. Vaginal estrogen products seem to be safe with few adverse effects, although there is a lack of long-term controlled clinical trial safety data. This review supports the use of commercially available vaginal estrogen therapies as an effective and safe first-line therapy for the treatment of moderate-to-severe GSM.

摘要

目的

我们更新了一项系统评价,以评估基于已发表的随机对照试验的阴道雌激素产品治疗女性生殖泌尿系统绝经综合征(GSM)的疗效和安全性的全部证据。

方法

我们在 Cochrane 图书馆、Ovid、PubMed、Medline、Embase 和 Clinicaltrials.gov 上搜索了从数据库建立到 2018 年 6 月的英文文章。我们的搜索整合了 2086 个潜在来源,筛选出 53 篇全文文章进行审查,发现与我们的系统评价相关。

结果

我们确定了 53 项符合纳入标准的研究,这些研究评估了阴道雌激素与安慰剂或其他激素和非激素对照药物治疗 GSM 的疗效和安全性。与安慰剂相比,所有阴道雌激素在 GSM 的客观终点和主观终点方面都表现出优越性,而一些试验在泌尿生殖症状方面表现出优于安慰剂的效果。不同剂量和剂型的阴道雌激素产品之间没有观察到显著差异。阴道雌激素在改善外阴阴道萎缩的客观临床终点方面优于阴道润滑剂和保湿剂,但在主观终点方面没有优势。未拮抗的阴道雌激素似乎是安全的,尽管这些研究没有足够的力量来检测长期的雌激素副作用。

结论

雌激素产品被发现对治疗 GSM 具有临床疗效,剂量低至 4μg。阴道雌激素产品似乎是安全的,副作用很少,尽管缺乏长期的对照临床试验安全性数据。这篇综述支持使用市售的阴道雌激素疗法作为治疗中重度 GSM 的有效和安全的一线治疗方法。

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