An update on the pharmacological management of female sexual dysfunction

被引:18
|
作者
Fooladi, Ensieh [1 ]
Davis, Susan R. [2 ]
机构
[1] Monash Univ, Sch Publ Hlth & Prevent Med, Womens Hlth Program, Alfred Ctr, Melbourne, Vic 3004, Australia
[2] Monash Univ, Sch Publ Hlth & Prevent Med, Womens Hlth Res Program, Melbourne, Vic 3004, Australia
关键词
DHEA; estrogens; female sexual dysfunction; hormonal therapy; testosterone; tibolone; SURGICALLY MENOPAUSAL WOMEN; PLACEBO-CONTROLLED TRIAL; INTRAVAGINAL DEHYDROEPIANDROSTERONE PRASTERONE; MELANOCORTIN RECEPTOR AGONIST; RANDOMIZED CONTROLLED-TRIAL; QUALITY-OF-LIFE; POSTMENOPAUSAL WOMEN; AROUSAL DISORDER; DESIRE DISORDER; PREMENOPAUSAL WOMEN;
D O I
10.1517/14656566.2012.725046
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Female sexual dysfunction (FSD) is a global health issue, with as many as 12% of women over 18 years old reporting sexual difficulties associated with distress. It is a multifaceted problem with psychological and biological causes. Affected women tend to have an impaired quality of life, a decreased level of well-being and relationship issues. Hence there is a need for management options for affected women. Areas covered: This paper focuses on current pharmacological options for the treatment of FSD, particularly estrogens and androgens, which have been extensively studied. Some investigational drugs are also described, including the centrally acting agents such as flibanserin and bupropion, and intravaginal DHEA and testosterone, which may be useful as an alternative for women with specific conditions, such as breast cancer survivors. Expert opinion: Although approval for the use of testosterone for treatment of FSD is limited to some European countries and restricted to surgically menopausal women, there is extensive off-label use for this purpose. No other product has yet achieved regulatory approval for treatment of FSD. Completion of studies of nonhormonal FSD therapies and safety studies of testosterone may result in regulatory approval of such products for the treatment of FSD in the near future.
引用
收藏
页码:2131 / 2142
页数:12
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