中年和老年妇女的雄激素治疗:拉丁美洲妇科内分泌学会(ALEG)的立场声明。

IF 3.2 4区 医学 Q1 OBSTETRICS & GYNECOLOGY
Susana Pilnik, Alejandra Belardo, Lucas Bandeira Marchesan, Adriana Camero-Lascano, Margot Acuña-San Martín, Alejandra Elizalde-Cremonte, Eliana Ojeda, Alejandro Manzur, Peter Chedraui
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引用次数: 0

摘要

目的:雄激素已被用于缓解中年妇女的症状,但关于益处和风险的证据仍然有限,没有明确确定的睾酮治疗适应症。在许多拉丁美洲国家,睾酮的处方没有具体的指导方针,这使得很难确定可能受益的患者。本立场声明旨在总结证据,并提供拉丁美洲对中年和老年妇女雄激素治疗的看法。方法:数据收集自Cochrane综述、安慰剂对照研究、荟萃分析、国际指南、共识声明和2000年至今发表的政府法规。分析的重点是中年和老年妇女雄激素治疗的有效性、安全性和临床建议。结果:绝经后妇女的睾酮治疗应限于通过正式的生物心理社会评估(a级:高)确诊的性欲减退(HSDD)患者。常规血清睾酮或其他雄激素测量不建议用于诊断(A级:高),但在治疗前应检查基线水平,以排除浓度升高(C级:低)。治疗监测应在3-6周内进行,将睾酮维持在绝经前生理范围内(C级:低)。透皮制剂优先。由于超生理剂量的风险和证据不足,不推荐皮下微丸和复合“生物同源”睾酮(C级:低)。不建议全身口服脱氢表雄酮(DHEA) (A级:高)。阴道脱氢表雄酮仅被批准用于更年期的泌尿生殖系统综合征。结论:女性应该接受符合当前临床指南的咨询。在开始睾酮治疗之前,必须告知患者其使用是标签外的。迄今为止的证据并不支持全身性脱氢表雄酮作为性症状的有效治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Androgen therapy in midlife and older women: a position statement of the Latin American Association of Gynecological Endocrinology (ALEG).

Objective: Androgens have been prescribed to alleviate symptoms in midlife women, but evidence regarding benefits and risks remains limited, with no clearly established indications for Testosterone therapy. In many Latin American countries, Testosterone is prescribed without specific guidelines, making it difficult to identify patients who might benefit. This position statement aims to summarize evidence and provide a Latin American perspective on androgen therapy in midlife and older women.

Method: Data were collected from Cochrane reviews, placebo-controlled studies, meta-analyses, international guidelines, consensus statements, and government regulations published between 2000 and the present. Analyses focused on efficacy, safety, and clinical recommendations for androgen therapy in midlife and older women.

Results: Testosterone therapy for postmenopausal women should be limited to those with hypoactive sexual desire disorder (HSDD) confirmed through a formal biopsychosocial evaluation (Grade A: High). Routine serum measurements of Testosterone or other androgens are not recommended for diagnosis (Grade A: High), but baseline levels should be checked before therapy to exclude elevated concentrations (Grade C: Low). Treatment monitoring should occur within 3-6 weeks, maintaining Testosterone within the premenopausal physiological range (Grade C: Low). Transdermal formulations are preferred. Subcutaneous pellets and compounded "bioidentical" Testosterone are not recommended due to risks of supraphysiological dosing and insufficient evidence (Grade C: Low). Oral dehydroepiandrosterone (DHEA) is not advised systemically (Grade A: High). Vaginal DHEA is approved only for genitourinary syndrome of menopause.

Conclusion: Women should receive counseling aligned with current clinical guidelines. Prior to initiating Testosterone therapy, patients must be informed that its use is off-label. Evidence to date does not support systemic DHEA as an effective treatment for sexual symptoms.

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来源期刊
Climacteric
Climacteric 医学-妇产科学
CiteScore
1.70
自引率
7.10%
发文量
53
审稿时长
1 months
期刊介绍: Climacteric is the official journal of the International Menopause Society (IMS). As an international peer-reviewed journal it publishes original research and reviews of all aspects of aging in women. Climacteric was founded by the IMS in 1998 and today has become a leading journal in the publication of peer-reviewed papers on the menopause, climacteric and mid-life health. Topics covered include endocrine changes, symptoms attributed to the menopause and their treatment, hormone replacement and alternative therapies, lifestyles, and the counselling and education of peri- and postmenopausal women. Climacteric, published bimonthly, also features regular invited reviews, editorials and commentaries on recent developments. The editorial review board of Climacteric includes leading scientific and clinical experts in the field of midlife medicine and research and is headed by its Editor-in-Chief, Professor Rod Baber of Australia. He and his team of Associate Editors act independently to set a clear editorial policy, co-ordinate peer review, and ensure a rapid response to submitted papers.
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