2022
DOI: 10.1016/j.ucl.2022.02.001
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Medical Treatment of Female Sexual Dysfunction

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Cited by 21 publications
(10 citation statements)
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“…Currently, there are no recommended treatments for sexual dysfunction in national guidelines, and international guidelines lack specific recommendations for addressing sexual dysfunction in women with PD, despite its negative impact on their quality of life [ 36 ]. However, treatments such as menopause hormone therapy, local estrogen therapy, and vaginal dehydroepiandrosterone are available for women with sexual dysfunctions [ 37 ]. Studies on their effectiveness in women with PD are necessary to update the guidelines and provide recommendations for both sexes.…”
Section: Discussionmentioning
confidence: 99%
“…Currently, there are no recommended treatments for sexual dysfunction in national guidelines, and international guidelines lack specific recommendations for addressing sexual dysfunction in women with PD, despite its negative impact on their quality of life [ 36 ]. However, treatments such as menopause hormone therapy, local estrogen therapy, and vaginal dehydroepiandrosterone are available for women with sexual dysfunctions [ 37 ]. Studies on their effectiveness in women with PD are necessary to update the guidelines and provide recommendations for both sexes.…”
Section: Discussionmentioning
confidence: 99%
“… 28 In addition, vaginal estrogen therapy plays a critical role in the management of pelvic floor dysfunction and sexual health. 29 , 30 Although the data are limited, a small US-based study suggests that hysterectomy adversely affects pelvic floor function, irrespective of menopausal status. 31 While hysterectomy alone has not been shown to worsen sexual function, rr-BSO independently and when combined with hysterectomy adversely affects sexual health because of the induced hypoestrogenic state.…”
Section: Limitations Of the Current Literature Informing Rr-hysterect...mentioning
confidence: 99%
“…Because the literature on pharmacologic therapies continues to differentiate between HSDD and FSAD, they will continue to be referred to separately in this review. Development to date has been primarily aimed at the centrally acting excitatory (dopamine, noradrenaline, melanocortin) and inhibitory (serotonin, endocannabinoid, opioid) receptors to augment the sexual desire response [35]. Although our understanding of the neurochemical basis for HSDD is poor, the prevailing hypothesis is that an interplay between the serotoninergic system and other neurochemical pathways leads to increased inhibition or decreased excitation, and pharmaceutical development has been aimed at these pathways [36].…”
Section: Hypoactive Sexual Desire Disorder and Female Sexual Arousal ...mentioning
confidence: 99%