Rahn David D, Carberry Cassandra, Sanses Tatiana V, Mamik Mamta M, Ward Renée M, Meriwether Kate V, Olivera Cedric K, Abed Husam, Balk Ethan M, Murphy Miles
University of Texas Southwestern Medical Center, Dallas, Texas; Women & Infants Hospital, Alpert Medical School of Brown University and the Center for Evidence Based Medicine, Brown University, Providence, Rhode Island; the University of Maryland School of Medicine, Baltimore, Maryland; the Icahn School of Medicine at Mount Sinai, New York, New York; Vanderbilt University Medical Center, Nashville, Tennessee; the University of New Mexico Health Sciences Center, Albuquerque, New Mexico; Henry Ford Health System, Detroit, Michigan; and the Institute for Female Pelvic Medicine and Reconstructive Surgery, North Wales, Pennsylvania.
Obstet Gynecol. 2014 Dec;124(6):1147-1156. doi: 10.1097/AOG.0000000000000526.
To comprehensively review and critically assess the literature on vaginal estrogen and its alternatives for women with genitourinary syndrome of menopause and to provide clinical practice guidelines.
MEDLINE and Cochrane databases were searched from inception to April 2013. We included randomized controlled trials and prospective comparative studies. Interventions and comparators included all commercially available vaginal estrogen products. Placebo, no treatment, systemic estrogen (all routes), and nonhormonal moisturizers and lubricants were included as comparators.
We double-screened 1,805 abstracts, identifying 44 eligible studies. Discrepancies were adjudicated by a third reviewer. Studies were individually and collectively assessed for methodologic quality and strength of evidence.
TABULATION, INTEGRATION, AND RESULTS: Studies were extracted for participant, intervention, comparator, and outcomes data, including patient-reported atrophy symptoms (eg, vaginal dryness, dyspareunia, dysuria, urgency, frequency, recurrent urinary tract infection (UTI), and urinary incontinence), objective signs of atrophy, urodynamic measures, endometrial effects, serum estradiol changes, and adverse events. Compared with placebo, vaginal estrogens improved dryness, dyspareunia, urinary urgency, frequency, and stress urinary incontinence (SUI) and urgency urinary incontinence (UUI). Urinary tract infection rates decreased. The various estrogen preparations had similar efficacy and safety; serum estradiol levels remained within postmenopausal norms for all except high-dose conjugated equine estrogen cream. Endometrial hyperplasia and adenocarcinoma were extremely rare among those receiving vaginal estrogen. Comparing vaginal estrogen with nonhormonal moisturizers, patients with two or more symptoms of vulvovaginal atrophy were substantially more improved using vaginal estrogens, but those with one or minor complaints had similar symptom resolution with either estrogen or nonhormonal moisturizer.
All commercially available vaginal estrogens effectively relieve common vulvovaginal atrophy-related complaints and have additional utility in patients with urinary urgency, frequency or nocturia, SUI and UUI, and recurrent UTIs. Nonhormonal moisturizers are a beneficial alternative for those with few or minor atrophy-related symptoms and in patients at risk for estrogen-related neoplasia.
PROSPERO International prospective register of systematic reviews, http://www.crd.york.ac.uk/PROSPERO/, CRD42013006656.
全面回顾并严格评估关于绝经后泌尿生殖综合征女性使用阴道雌激素及其替代疗法的文献,并提供临床实践指南。
检索MEDLINE和Cochrane数据库,检索时间从建库至2013年4月。我们纳入了随机对照试验和前瞻性比较研究。干预措施和对照措施包括所有市售的阴道雌激素产品。安慰剂、不治疗、全身用雌激素(所有给药途径)以及非激素保湿剂和润滑剂均作为对照措施。
我们对1805篇摘要进行了双盲筛选,确定了44项符合条件的研究。分歧由第三位评审员裁决。对研究进行了单独和综合评估,以确定其方法学质量和证据强度。
制表、整合与结果:提取了研究中的参与者、干预措施、对照措施和结局数据,包括患者报告的萎缩症状(如阴道干燥、性交困难、排尿困难、尿急、尿频、复发性尿路感染(UTI)和尿失禁)、萎缩的客观体征、尿动力学测量、子宫内膜影响、血清雌二醇变化以及不良事件。与安慰剂相比,阴道雌激素改善了阴道干燥、性交困难、尿急、尿频、压力性尿失禁(SUI)和急迫性尿失禁(UUI),尿路感染率降低。各种雌激素制剂具有相似的疗效和安全性;除高剂量结合马雌激素乳膏外,所有制剂的血清雌二醇水平均保持在绝经后正常范围内。接受阴道雌激素治疗的患者中,子宫内膜增生和腺癌极为罕见。将阴道雌激素与非激素保湿剂进行比较,有两种或更多外阴阴道萎缩症状的患者使用阴道雌激素后改善更为明显,但有一两种轻微症状的患者使用雌激素或非激素保湿剂后的症状缓解情况相似。
所有市售的阴道雌激素均可有效缓解常见的外阴阴道萎缩相关症状,对尿急、尿频或夜尿症、SUI和UUI以及复发性UTI患者还有额外的治疗作用。非激素保湿剂是萎缩相关症状较少或轻微以及有雌激素相关肿瘤风险患者的有益替代选择。
PROSPERO国际前瞻性系统评价注册库,http://www.crd.york.ac.uk/PROSPERO/,CRD42013006656。