Vincent Obstetrics and Gynecology, Massachusetts General Hospital, Boston.
Department of Obstetrics, Gynecology and Reproductive Biology, Harvard Medical School, Boston, Massachusetts.
JAMA Intern Med. 2018 May 1;178(5):681-690. doi: 10.1001/jamainternmed.2018.0116.
Nearly half of postmenopausal women report bothersome vulvovaginal symptoms, but few data support the efficacy of 2 commonly recommended treatments.
To compare the efficacy of a low-dose vaginal estradiol tablet and a vaginal moisturizer, each vs placebo, for treatment of moderate-to-severe postmenopausal vulvovaginal symptoms.
DESIGN, SETTING, AND PARTICIPANTS: This 12-week multicenter randomized clinical trial enrolled postmenopausal women with moderate to severe symptoms of vulvovaginal itching, pain, dryness, irritation, or pain with penetration.
Vaginal 10-μg estradiol tablet (daily for 2 weeks, then twice weekly) plus placebo gel (3 times a week) (n = 102) vs placebo tablet plus vaginal moisturizer (n = 100) vs dual placebo (n = 100).
The main outcome was decrease in severity (0-3) of most bothersome symptom (MBS) between enrollment and 12 weeks. Additional measures included a composite vaginal symptom score, Female Sexual Function Index (FSFI) score (2-36), modified Female Sexual Distress Score-Revised item 1, treatment satisfaction and meaningful benefit, Vaginal Maturation Index, and vaginal pH.
The 302 women had a mean (SD) age of 61 (4) years and were primarily white (267 [88%]), college educated (200 [66%]), and sexually active (245 [81%]). Most women (294 [97%]) provided data for the primary analysis. The most commonly reported MBS was pain with vaginal penetration (182 [60%]), followed by vulvovaginal dryness (63 [21%]). Mean baseline MBS severity was similar between treatment groups: estradiol, 2.4 (95% CI, 2.3 to 2.6); moisturizer, 2.5 (95% CI, 2.3 to 2.6); placebo, 2.5 (95% CI, 2.4 to 2.6). All treatment groups had similar mean reductions in MBS severity over 12 weeks: estradiol, -1.4 (95% CI, -1.6 to -1.2); moisturizer, -1.2 (95% CI, -1.4 to -1.0); and placebo, -1.3 (95% CI, -1.5 to -1.1). No significant differences were seen between estradiol (P = .25) or moisturizer (P = .31) compared with placebo. Mean total FSFI improvement was similar between estradiol (5.4; 95% CI, 4.0 to 6.9) and placebo (4.5; 95% CI, 2.8 to 6.1) (P = .64), and between moisturizer (3.1; 95% CI, 1.7 to 4.5) and placebo (P = .17).
Our results suggest that neither prescribed vaginal estradiol tablet nor over-the-counter vaginal moisturizer provides additional benefit over placebo vaginal tablet and gel in reducing postmenopausal vulvovaginal symptoms.
clinicaltrials.gov Identifier: NCT02516202.
近一半的绝经后妇女报告有令人烦恼的外阴阴道症状,但很少有数据支持两种常用治疗方法的疗效。
比较低剂量阴道雌二醇片和阴道保湿剂与安慰剂治疗绝经后中度至重度外阴阴道症状的疗效。
设计、地点和参与者:这是一项为期 12 周的多中心随机临床试验,招募了有中度至重度外阴阴道瘙痒、疼痛、干燥、刺激或性交疼痛症状的绝经后妇女。
阴道 10-μg 雌二醇片(每日 2 周,然后每周 2 次)加安慰剂凝胶(每周 3 次)(n = 102)与安慰剂片加阴道保湿剂(n = 100)与双安慰剂(n = 100)。
主要结果是在招募和 12 周之间最令人烦恼的症状(MBS)的严重程度(0-3)下降。其他措施包括阴道症状综合评分、女性性功能指数(FSFI)评分(2-36)、改良女性性困扰评分修订项目 1、治疗满意度和显著获益、阴道成熟指数和阴道 pH 值。
302 名女性的平均(SD)年龄为 61(4)岁,主要为白人(267 [88%])、大学学历(200 [66%])和有性生活(245 [81%])。大多数女性(294 [97%])提供了主要分析的数据。最常见的报告 MBS 是阴道插入疼痛(182 [60%]),其次是外阴阴道干燥(63 [21%])。治疗组之间基线 MBS 严重程度相似:雌二醇组为 2.4(95%CI,2.3 至 2.6);保湿剂组为 2.5(95%CI,2.3 至 2.6);安慰剂组为 2.5(95%CI,2.4 至 2.6)。所有治疗组在 12 周内 MBS 严重程度都有相似的平均降低:雌二醇组为-1.4(95%CI,-1.6 至-1.2);保湿剂组为-1.2(95%CI,-1.4 至-1.0);安慰剂组为-1.3(95%CI,-1.5 至-1.1)。雌二醇(P =.25)或保湿剂(P =.31)与安慰剂相比,无显著差异。雌二醇(5.4;95%CI,4.0 至 6.9)和安慰剂(4.5;95%CI,2.8 至 6.1)(P =.64)以及保湿剂(3.1;95%CI,1.7 至 4.5)和安慰剂(P =.17)之间的平均总 FSFI 改善相似。
我们的结果表明,与安慰剂阴道片剂和凝胶相比,处方阴道雌二醇片剂和非处方阴道保湿剂在减轻绝经后外阴阴道症状方面没有额外的益处。
clinicaltrials.gov 标识符:NCT02516202。