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黑升麻对更年期症状的疗效与安全性。西班牙更年期协会声明。

Black cohosh efficacy and safety for menopausal symptoms. The Spanish Menopause Society statement.

作者信息

Castelo-Branco Camil, Navarro Concepción, Beltrán Estanislao, Losa Fernando, Camacho Marta

机构信息

Institut Clinic de Ginecologia, Obstetrícia i Neonatologia, Hospital Clinic Barcelona, Barcelona, Spain.

Facultat de Medicina, Universitat de Barcelona, Barcelona, Spain.

出版信息

Gynecol Endocrinol. 2022 May;38(5):379-384. doi: 10.1080/09513590.2022.2056591. Epub 2022 Apr 11.

Abstract

OBJECTIVE

The increasing interest in Western countries regarding phytotherapy use to treat menopause-related symptoms has led the Spanish Menopause Society (AEEM) to update its position statement performed in 2009 on the role of black cohosh () for the treatment of menopausal symptoms.

MATERIAL AND METHODS

A panel of experts from both clinical and research backgrounds were assembled to investigate the best available evidence. Selected studies were obtained by an electronic search, including the Internet search engines MEDLINE-Pubmed (1997-December 2021) and the Cochrane Controlled Trials Register.

RESULTS

Most of the well-designed studies published in recent years have been conducted with the isopropanolic extract of black cohosh/. The most common dose is 40 mg/day capable of achieving a significant reduction in hot flushes (particularly in women with intense hot flushes) and an improvement in mood. Used at the recommended doses, produces no significant adverse reactions.

CONCLUSION

Black cohosh is an effective and safe treatment option for the relieving of vasomotor symptoms. Finally, further clinical trials with sufficient patient enrollment and longer study follow-up are needed.

摘要

目的

西方国家对使用植物疗法治疗更年期相关症状的兴趣日益浓厚,这促使西班牙更年期协会(AEEM)更新其在2009年发表的关于黑升麻治疗更年期症状作用的立场声明。

材料与方法

组建了一个由临床和研究背景专家组成的小组,以调查现有的最佳证据。通过电子检索获取选定的研究,包括互联网搜索引擎MEDLINE-Pubmed(1997年至2021年12月)和Cochrane对照试验注册库。

结果

近年来发表的大多数设计良好的研究都是使用黑升麻异丙醇提取物进行的。最常见的剂量是40毫克/天,能够显著减少潮热(尤其是潮热严重的女性)并改善情绪。按推荐剂量使用,不会产生明显的不良反应。

结论

黑升麻是缓解血管舒缩症状的一种有效且安全的治疗选择。最后,需要进行更多有足够患者入组和更长研究随访期的临床试验。

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