首页> 美国卫生研究院文献>Patient preference and adherence >Efficacy and safety of ultra-low-dose Vagifem (10 mcg)
【2h】

Efficacy and safety of ultra-low-dose Vagifem (10 mcg)

机译:超低剂量Vagifem(10 mcg)的功效和安全性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Vulvovaginal atrophy [VVA] is defined as inflammation of the vaginal epithelium due to atrophy secondary to decreased levels of circulating estrogen. There is currently only one approved method for the treatment of VVA, and that is the administration of exogenous estrogens. Overall, the ideal VVA treatment must have benefits, minimize risks, and enhance compliance in the patient while optimizing cost-effectiveness. Unfortunately, of the approximate 25% of symptomatic women that are thought to seek medical help, the proportion that receives hormone therapy may be small and its duration of use is short. Women have been very reluctant to take hormone therapy due to widely publicized results of the risks associated with hormone therapy. Thus, while menopausal hormone therapy was once accepted as the ideal approach for optimizing changes associated with menopause, prospective randomized clinical trials have challenged that view and have led to a marked decrease in the use of such therapy and increased search for low-dose therapies. This article will highlight the efficacy and safety of recently FDA-approved Vagifem (10 mcg) in treatment of VVA.
机译:阴道阴道萎缩[VVA]定义为由于循环雌激素水平降低引起的萎缩引起的阴道上皮炎症。当前只有一种批准的用于治疗VVA的方法,即外源性雌激素的给药。总体而言,理想的VVA治疗必须具有收益,最大程度地降低风险并增强患者的依从性,同时优化成本效益。不幸的是,在大约25%的被认为有症状的有症状的女性中,接受激素治疗的比例可能很小,使用时间也很短。由于激素治疗相关风险的广泛宣传结果,女性一直不愿接受激素治疗。因此,尽管绝经激素疗法曾经被认为是优化与绝经有关的变化的理想方法,但前瞻性随机临床试验已经对该观点提出了挑战,并导致这种疗法的使用明显减少,并且对低剂量疗法的寻求增加。本文将重点介绍最近FDA批准的Vagifem(10 mcg)治疗VVA的功效和安全性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号