Acessibilidade / Reportar erro

The use of phosphodiesterase inhibitors in the treatment of female sexual dysfunction: scoping review

Abstract

Objective

The purpose of this study was to analyze the available evidence regarding the efficacy of iPDE5 in the treatment of female sexual dysfunction (FSD).

Methods

A comprehensive literature search was conducted in March 2023 through the main scientific databases.

Results

A total of 53 articles were identified, out of which, 6 met the predefined inclusion criteria. All of these were randomized controlled trials. Among the included studies, 4 demonstrated the effectiveness of sildenafil in improving sexual response and addressing FSD, while 2 studies failed to establish its efficacy in this context.

Conclusion

Overall, the efficacy of sildenafil in the treatment of FSD remains controversial and inconclusive based on the available evidence. Further research is necessary to clarify the therapeutic potential of iPDE5 in addressing FSD and to better understand the factors that influence treatment outcomes.

Libido; Female; Sexual dysfunction; Phosphodiesterase inhibitor; Sildenafil

Introduction

According to the World Health Organization (WHO), health encompasses a comprehensive state of physical, psychological, and social well-being, extending beyond the mere absence of disease. This inclusive concept of health also incorporate sexual health.(11. World Health Organization. Brief sexuality-related communication: recomendations for a public health approach. Geneva: WHO; 2015 [cited 2023 Jul 15]. Available from: https://apps.who.int/iris/bitstream/handle/ 10665/170251/9789241549004_eng.pdf
https://apps.who.int/iris/bitstream/hand...
) The definition of Female Sexual Dysfunction (FSD) has evolved over time and currently aligns with the International Classification of Diseases 11th Revision (ICD-11). FSD are syndromes that comprise the various ways in which an adult may have difficulty experiencing personally satisfying, non-coercive sexual activities. Sexual response is a complex interaction of psychological, interpersonal, social, cultural and physiological processes and one or more of these factors may affect any stage of the sexual response. In order to be considered a sexual dysfunction, the dysfunction must occur frequently, although it may be absent on some occasions; have been present for at least several months; and be associated with clinically significant distress. The FSD can be divided into Hypoactive Sexual Desire Dysfunction (HSDD), Sexual Arousal Dysfunction and Orgasmic Dysfunction.(22. World Health Organization. International Classification of Diseases (ICD). 2022 [cited 2023 Dec 4]. Available from: https:// www.who.int/standards/classifications/classification-of-diseases
https:// www.who.int/standards/classific...
)

The estimated prevalence of FSD ranges from 40% to 70%, with HSDD being the most prevalent diagnosis.(33. Cereja AC. Disfunção sexual feminina: prevalência e factores relacionados. Rev Port Med Geral Fam. 2006;22(6):701-20. doi: 10.32385/rpmgf.v22i6.10303
https://doi.org/10.32385/rpmgf.v22i6.103...

4. Nobre PJ, Pinto-Gouveia J, Gomes FA. Prevalence and comorbidity of sexual dysfunctions in a Portuguese clinical sample. J Sex Marital Ther. 2006;32(2):173-82. doi: 10.1080/00926230500442334
https://doi.org/10.1080/0092623050044233...

5. Pablo C, Soares C. As disfunções sexuais femininas. Rev Port Med Geral Fam. 2004;20(3):357-70. doi: 10.32385/rpmgf.v20i3.10044
https://doi.org/10.32385/rpmgf.v20i3.100...

6. Zhang H, Yip PS. Female sexual dysfunction among young and middle-aged women in Hong Kong: prevalence and risk factors. J Sex Med. 2012;9(11):2911-8. doi: 10.1111/j.1743-6109.2012.02773.x
https://doi.org/10.1111/j.1743-6109.2012...
-77. Lou WJ, Chen B, Zhu L, Han SM, Xu T, Lang JH, et al. Prevalence and factors associated with female sexual dysfunction in Beijing, China. Chin Med J. 2017;130(12):1389-94. doi: 10.4103/0366-6999.207466
https://doi.org/10.4103/0366-6999.207466...
)Given its high prevalence, it is imperative to familiarize oneself with its diagnosis and stay abreast of therapeutic possibilities.

In recent years, there has been a growing interest in identifying pharmaceutical agents suitable for treating FSD. Among these, phosphodiesterase 5 inhibitors (iPDE5) serve as notable examples. While these drugs have already received approval and are in use for male erectile dysfunction, their approval for treating FSD in all countries remains pending. Nevertheless, due to their underlying mechanism of action, there is a belief that a parallel may exist between the two conditions, thus driving the interest in understanding their efficacy in women. Studies have shown that treatment with iPDE5 in women also induces relaxation of the smooth muscles in the clitoris and increases blood flow in this region. Consequently, iPDE5 were hypothesized to be a promising therapeutic option for FSD, namely sexual arousal dysfunction, however the function of the female sexuality is complex.(88. Goldstein I, Berman JR. Vasculogenic female sexual dysfunction: vaginal engorgement and clitoral erectile insufficiency syndromes. Int J Impot Res. 1998; 10 Suppl 2:S84-90.)

The objective of this scoping review is to conduct a comprehensive analysis of the existing scientific evidence regarding the efficacy of phosphodiesterase 5 inhibitors in the treatment of female sexual dysfunction.

Methods

A literature search was conducted in March 2023 using the keywords (“libido” OR “sexual dysfunction”) AND (“sildenafil” OR “phosphodiesterase inhibitors”) to identify relevant systematic reviews, meta-analyses, original studies, and published clinical guidelines published from the year 2000 up to March 2023 in both Portuguese and English. The following databases were utilized: National Guideline Clearinghouse, Canadian Medical Association Practice Guidelines Infobase, PubMed, The Cochrane Library, DARE, Bandolier, Evidence-Based Medicine Online, TRIP Database, and National Institute for Health and Care Excellence (NICE). The references of the included articles on the subject of the present study were also carefully reviewed to complete the search. The search results from these databases were merged and duplicates were deleted.

The inclusion criteria was women aged 18 years or older, diagnosed with female sexual dysfunction (FSD), who were administered oral phosphodiesterase 5 inhibitors (specifically sildenafil) at any dose and posology, compared to placebo. The primary focus of evaluation of improvement in FSD was through the use of validated questionnaires. Studies were excluded if the participants were concurrently receiving therapy or had an underlying pathology that could contribute to or cause sexual dysfunction. Additionally, studies involving women on medications other than phosphodiesterase 5 inhibitors for FSD treatment were excluded.

The articles included in this review were selected after careful analysis and unanimous agreement among all three authors. The selection of related articles was performed in two separate stages. In the screening phase, article titles were initially reviewed to determine inclusion. In cases of ambiguity, abstracts were examined to align with inclusion and exclusion criteria. Articles with were ambiguous and did not clearly fit the criteria proceeded to the second stage for a more careful analysis. In the second phase, the full text of articles was reviewed, and those meeting the inclusion and exclusion criteria were included in the scoping review.

To assign levels of evidence and strengths of recommendation, the Strength of Recommendation Taxonomy (SORT) scale developed by the American Academy of Family Physicians was employed.

Results

A comprehensive search yielded a total of 1835 articles, which underwent an initial selection based on an abstract screening and subsequent full-text evaluation. Ultimately, only 6 articles met the eligibility criteria and were included in this review. The selection process of the included articles is presented in figure 1. Out of the 11 articles selected for full- text review, two systematic reviews and three randomized clinical trials were excluded. The reasons for exclusion were as follows: the two systematic reviews included articles that did not meet the predefined inclusion and exclusion criteria, influence FSD. Moreover, one of the systematic reviews only included a single relevant article of interest. The three randomized clinical trials were excluded based on concerns regarding their methodological quality.

Figure 1
Flow chart of study selection including studies involving women with underlying pathologies that could potentially

All articles included in this review were randomized controlled trials (RCTs) of the placebo-controlled design (Chart 1), with a combined total sample size of 1188 women. The most frequently employed phosphodiesterase inhibitor was on-demand sildenafil, administered 1 hour prior to sexual intercourse. The dosages used varied among the studies, with one study utilizing a dosage of 100 mg, six studies using 50 mg, one study using 25 mg, and another study using 10 mg. Only one study employed a daily dosage of 50 mg of sildenafil. Sexual function assessment was conducted in all studies using validated questionnaires specifically designed for this purpose. However, it should be noted that the questionnaires employed were not uniform across the studies. Among the subset of five studies in which the intervention involved on- demand administration of sildenafil one hour prior to sexual activity, three studies demonstrated efficacy or observed certain benefits in the treatment of female sexual dysfunction.

Chart 1
Summary of the Randomized Clinical Trials included in this review

Caruso et al.(99. Caruso S, Intelisano G, Lupo L, Agnello C. Premenopausal women affected by sexual arousal disorder treated with sildenafil: a double-blind, cross-over, placebo- controlled study. BJOG. 2001;108(6):623-8. doi: 10.1111/j.1471-0528.2001.00143.x
https://doi.org/10.1111/j.1471-0528.2001...
)conducted an RCT with 59 premenopausal women diagnosed with FSAD. The participants were randomized to receive placebo, 25 mg of sildenafil, or 50 mg of sildenafil for 4 weeks, with a 1-week washout period between treatment phases. The women were instructed to take the medication 1 hour before sexual intercourse. The Personal Experience Questionnaire was administered before the intervention and at the end of each 4-week treatment phase, assessing levels of excitement, orgasm, frequency of fantasies and sexual intercourse, satisfaction with frequency, and overall satisfaction with sexual activity. In all assessed parameters, both 25 mg and 50 mg of sildenafil showed improvement compared to placebo, but there was no statistically significant difference between the two dosages. The authors concluded that sildenafil may improve FSAD. Two studies by Basson et al.(1010. Basson R, McInnes R, Smith MD, Hodgson G, Koppiker N. Efficacy and safety of sildenafil citrate in women with sexual dysfunction associated with female sexual arousal disorder. J Womens Health Gend Based Med. 2002;11(4):367-77. doi: 10.1089/152460902317586001
https://doi.org/10.1089/1524609023175860...
)and Basson and Brotto(1111. Basson R, Brotto LA. Sexual psychophysiology and effects of sildenafil citrate in oestrogenised women with acquired genital arousal disorder and impaired orgasm: a randomised controlled trial. BJOG. 2003;110(11):1014-24. doi: 10.1111/j.1471-0528.2003.02438.x
https://doi.org/10.1111/j.1471-0528.2003...
) were included in this review. In both studies, sildenafil was found to be ineffective.

In the study conducted in 2002,(1010. Basson R, McInnes R, Smith MD, Hodgson G, Koppiker N. Efficacy and safety of sildenafil citrate in women with sexual dysfunction associated with female sexual arousal disorder. J Womens Health Gend Based Med. 2002;11(4):367-77. doi: 10.1089/152460902317586001
https://doi.org/10.1089/1524609023175860...
)a total of 781 women with FSD were divided into two groups: Group 1 included premenopausal or menopausal women on hormone replacement therapy (HRT), and Group 2 included postmenopausal women without HRT. After an initial 4-week period without treatment, the women were randomized to receive either 10 mg, 50 mg, or 100 mg of sildenafil or placebo in Group 1, while Group 2 received only 50 mg of sildenafil or placebo. At the end of the 12-week follow-up, there was no statistically significant difference between sildenafil and placebo in terms of sexual function parameters, global efficacy, life satisfaction, or sexual function questionnaire scores. Thus, sildenafil did not demonstrate efficacy in this sample of women with a broad spectrum of FSD complaints. The authors suggested conducting a study in women with FSD without HSDD, a more particular subgroup.

The study by Basson and Brotto, in 2003(1111. Basson R, Brotto LA. Sexual psychophysiology and effects of sildenafil citrate in oestrogenised women with acquired genital arousal disorder and impaired orgasm: a randomised controlled trial. BJOG. 2003;110(11):1014-24. doi: 10.1111/j.1471-0528.2003.02438.x
https://doi.org/10.1111/j.1471-0528.2003...
)included a subgroup of 34 postmenopausal women who had been on HRT for at least 6 months and had a diagnosis of FSAD with significant loss or delayed and/or decreased intensity of orgasm. These women were randomized to receive 50 mg of sildenafil or placebo in a crossover design. The intervention consisted of watching a 30-minute erotic film while using a standard intensity portable vibrator with direct clitoral stimulation. The primary outcomes assessed were orgasm latency and intensity. Subjective intensity of orgasm, awareness of genital sensations, and subjective ratings of overall sexual excitement were evaluated using self- report questionnaires. There was no statistically significant difference between sildenafil and placebo in these assessed parameters, indicating that the efficacy of sildenafil was not demonstrated in this group of women.

Berman et al.(1212. Berman JR, Berman LA, Toler SM, Gill J, Haughie S; Sildenafil Study Group. Safety and efficacy of sildenafil citrate for the treatment of female sexual arousal disorder: a double- blind, placebo controlled study. J Urol. 2003;170(6 Pt 1):2333-8. doi: 10.1097/01.ju.0000090966.74607.34
https://doi.org/10.1097/01.ju.0000090966...
)conducted an RCT with 208 postmenopausal women on HRT or hysterectomized women with free testosterone levels >0.9 pg/ml and estradiol levels >40 pg/ml. The participants were randomized into two groups: one group received

50 mg of sildenafil 1 hour before sexual intercourse, and the other received placebo. Women with symptoms of FSAD, with or without HSDD, were recruited. The study consisted in a 4-week period without intervention, followed by a 12-week intervention phase. The primary endpoint of the study was improvement in the Female Intervention Efficacy Index (FIEI) scores for increased genital sensation during sexual intercourse and greater satisfaction with sexual intercourse and/or foreplay. All women in the sildenafil group achieved the primary endpoint compared to the placebo group (p=0.017 and p=0.015, respectively). However, statistical analysis revealed an interaction between sildenafil administration and the concomitant diagnosis of HSDD. When analyzing the results in women with FSAD and HSDD versus women with FSAD only, it was found that the former did not reach the primary endpoint, while the latter did. Therefore, the administration of 50 mg of sildenafil 1 hour before sexual activity may be effective in women with FSAD without HSDD. The authors also mentioned that the population in this study received HRT or had adequate levels of free testosterone and estradiol, as the authors believe that these factors may enhance the efficacy of sildenafil.

Cavalcanti et al.(1313. Cavalcanti AL, Bagnoli VR, Fonseca AM, Pastore RA, Cardoso EB, Paixão JS, et al. Effect of sildenafil on clitoral blood flow and sexual response in postmenopausal women with orgasmic dysfunction. Int J Gynaecol Obstet. 2008;102(2):115-9. doi: 10.1016/j.ijgo.2008.03.020
https://doi.org/10.1016/j.ijgo.2008.03.0...
)recruited a group of 22 postmenopausal women with FSD. The participants were randomized to receive a daily dose of 50 mg of sildenafil for 15 days or placebo. This study evaluated responses to the GRISS questionnaire and clitoral artery blood flow using Doppler ultrasound. However, for the purpose of this review, only the data related to the questionnaire were analyzed. The results are presented in chart 1. The authors concluded that sildenafil may improve sexual response in postmenopausal women with orgasmic disorders.

Zeinalzadeh et al.(1414. Zeinalzadeh S, Akbarzadeh M, Faridi P, Ali Mohagheghzadeh A, Sayadi M. Effect of sildenafil citrate on women affected by sexual dysfunction referred to health clinics. Fam Med Prim Care Rev. 2017;19(2):167-72. doi: 10.5114/fmpcr.2017.67873
https://doi.org/10.5114/fmpcr.2017.67873...
)conducted a study with 84 premenopausal women diagnosed with FSD. The participants were randomized to receive either 50 mg of sildenafil 1 hour before sexual intercourse for 4 weeks or placebo every 12 hours for 35 days. The various parameters of the Female Sexual Function Index (FSFI) were evaluated before and after the intervention. The findings of the study showed that sildenafil was effective in increasing sexual desire, arousal, orgasm, and sexual satisfaction. However, considering the sample size of the study, further research is needed on this topic.

Discussion

Phosphodiesterase inhibitors have demonstrated relative success in the treatment of erectile dysfunction (ED) in men. These inhibitors act by inhibiting phosphodiesterases, which are enzymes responsible for the breakdown of cyclic guanosine monophosphate (cGMP) and cyclic adenosine monophosphate (cAMP), intracellular messengers that mediate hormone and neurotransmitter responses. Among the various phosphodiesterases, phosphodiesterase 5 (PDE5) is the target for ED treatment due to its location in the corpus cavernosum, leading to vasodilation and increased blood flow.(88. Goldstein I, Berman JR. Vasculogenic female sexual dysfunction: vaginal engorgement and clitoral erectile insufficiency syndromes. Int J Impot Res. 1998; 10 Suppl 2:S84-90.,1515. Ückert S, Kuczyk MA, Oelke M. Phosphodiesterase inhibitors in clinical urology. Expert Rev Clin Pharmacol. 2013;6(3):323-32. doi: 10.1586/ecp.13.16
https://doi.org/10.1586/ecp.13.16...
) A similar mechanism occurs in women: relaxation of the smooth muscle of the vagina and clitoris and increased blood flow to these organs is one of the essential phase of the female sexual response and results in increased vaginal lubrication, engorgement of the walls and luminal diameter, as well as an increase in the length and diameter of the clitoris. Although this biological effect exists, it remains unproven whether it translates into increased and improved female sexual response, given the complex and multifactorial nature of FSD.(88. Goldstein I, Berman JR. Vasculogenic female sexual dysfunction: vaginal engorgement and clitoral erectile insufficiency syndromes. Int J Impot Res. 1998; 10 Suppl 2:S84-90.)

The present review aimed to analyze the available scientific evidence on the efficacy of using iPDE5 in the treatment of FSD. In this review, four studies demonstrated improvement in certain parameters with the use of iPDE5 in FSD, while two studies failed to establish its efficacy. Although all of these studies were randomized and placebo- controlled, with well-established methodologies, they suffered from small sample sizes and short follow-up periods. Three of the studies(1010. Basson R, McInnes R, Smith MD, Hodgson G, Koppiker N. Efficacy and safety of sildenafil citrate in women with sexual dysfunction associated with female sexual arousal disorder. J Womens Health Gend Based Med. 2002;11(4):367-77. doi: 10.1089/152460902317586001
https://doi.org/10.1089/1524609023175860...

11. Basson R, Brotto LA. Sexual psychophysiology and effects of sildenafil citrate in oestrogenised women with acquired genital arousal disorder and impaired orgasm: a randomised controlled trial. BJOG. 2003;110(11):1014-24. doi: 10.1111/j.1471-0528.2003.02438.x
https://doi.org/10.1111/j.1471-0528.2003...
-1212. Berman JR, Berman LA, Toler SM, Gill J, Haughie S; Sildenafil Study Group. Safety and efficacy of sildenafil citrate for the treatment of female sexual arousal disorder: a double- blind, placebo controlled study. J Urol. 2003;170(6 Pt 1):2333-8. doi: 10.1097/01.ju.0000090966.74607.34
https://doi.org/10.1097/01.ju.0000090966...
)received support from Pfizer. However, they were included in the review due to their rigorous methodology, and only one of them demonstrated a positive effect of the drug.

The total sample size across the studies was 1188 women, reflecting a substantial number of participants. Among the subset of five studies in which the intervention involved on-demand administration of sildenafil one hour prior to sexual activity, three studies demonstrated efficacy or observed certain benefits in the treatment of FSD. This finding suggests a potential positive effect of sildenafil in improving sexual function and addressing FSD in women.

These findings suggest that sildenafil may have a positive impact on sexual function in women with FSD. Notably, the positive outcomes were observed in various domains of sexual function, including increased genital sensation during sexual intercourse, greater satisfaction with sexual intercourse and/or foreplay, improved sexual desire, arousal, orgasm, and sexual satisfaction. The improvement in these parameters is in the line with the mechanism of iPDE5 and the female sexual response.

The participants in these studies were generally healthy women, but the samples varied, including premenopausal and postmenopausal women with or without hormone replacement therapy (HRT), leading to heterogeneity within the study population. It is important to recognize that a woman’s sexual function changes throughout her life and is influenced by various factors. Therefore, these factors may introduce limitations when interpreting the results, particularly considering that individual, relational, and cultural factors shape the experience of sexuality, especially considering that the populations across the different studies were from different countries with diverse cultural backgrounds.

Another limitation pertains to the broad definition and diagnosis of FSD, which, despite being well-established, still engenders controversy regarding the differentiation of various concepts within this overarching diagnosis. This limitation is evident in certain articles where differences in drug efficacy were observed among women presenting different complaints and symptoms along the spectrum of FSD.

Most studies administered the drug on-demand, while only one study used a daily dosage regimen. There was a lack of consensus regarding the most effective dosage, further complicating the interpretation of the results. Additionally, we chose not to include articles that investigated the concurrent use of iPDE5 and testosterone, as the scope of this review was solely to evaluate the efficacy of iPDE5.

Lastly, it is worth noting that the assessment of sexual function and the various instruments used to measure outcomes were also characterized by heterogeneity across the studies, posing an additional challenge in the interpretation of results.

Conclusion

This scoping review evaluated the available literature on the use of iPDE5 in the treatment of FSD. The search process yielded a substantial number of articles, with a rigorous selection procedure resulting in the inclusion of six RCT in this review. Among the selected studies, the majority employed on-demand administration of sildenafil, one hour prior to sexual activity. The dosages of iPDE5 varied across the studies, with sildenafil being the most commonly used drug. Notably, three out of the five studies focusing on on-demand sildenafil demonstrated efficacy or observed some beneficial effects in the treatment of FSD. However, the heterogeneity of the study populations, encompassing both premenopausal and postmenopausal women with or without hormone replacement therapy, may have influenced the interpretation of results. The complex and multifactorial nature of FSD, influenced by individual, relational, and cultural factors, adds further complexity to the assessment of treatment outcomes. In conclusion, this review contributes with valuable insights into the efficacy of iPDE5 in the context of FSD (SORT B). Further research with larger sample sizes, longer follow-up periods, standardized assessment tools, and awareness of diverse cultural backgrounds is essential to enhance the understanding of the role of iPDE5 in the treatment of FSD.

References

  • 1
    World Health Organization. Brief sexuality-related communication: recomendations for a public health approach. Geneva: WHO; 2015 [cited 2023 Jul 15]. Available from: https://apps.who.int/iris/bitstream/handle/ 10665/170251/9789241549004_eng.pdf
    » https://apps.who.int/iris/bitstream/handle/ 10665/170251/9789241549004_eng.pdf
  • 2
    World Health Organization. International Classification of Diseases (ICD). 2022 [cited 2023 Dec 4]. Available from: https:// www.who.int/standards/classifications/classification-of-diseases
    » https:// www.who.int/standards/classifications/classification-of-diseases
  • 3
    Cereja AC. Disfunção sexual feminina: prevalência e factores relacionados. Rev Port Med Geral Fam. 2006;22(6):701-20. doi: 10.32385/rpmgf.v22i6.10303
    » https://doi.org/10.32385/rpmgf.v22i6.10303
  • 4
    Nobre PJ, Pinto-Gouveia J, Gomes FA. Prevalence and comorbidity of sexual dysfunctions in a Portuguese clinical sample. J Sex Marital Ther. 2006;32(2):173-82. doi: 10.1080/00926230500442334
    » https://doi.org/10.1080/00926230500442334
  • 5
    Pablo C, Soares C. As disfunções sexuais femininas. Rev Port Med Geral Fam. 2004;20(3):357-70. doi: 10.32385/rpmgf.v20i3.10044
    » https://doi.org/10.32385/rpmgf.v20i3.10044
  • 6
    Zhang H, Yip PS. Female sexual dysfunction among young and middle-aged women in Hong Kong: prevalence and risk factors. J Sex Med. 2012;9(11):2911-8. doi: 10.1111/j.1743-6109.2012.02773.x
    » https://doi.org/10.1111/j.1743-6109.2012.02773.x
  • 7
    Lou WJ, Chen B, Zhu L, Han SM, Xu T, Lang JH, et al. Prevalence and factors associated with female sexual dysfunction in Beijing, China. Chin Med J. 2017;130(12):1389-94. doi: 10.4103/0366-6999.207466
    » https://doi.org/10.4103/0366-6999.207466
  • 8
    Goldstein I, Berman JR. Vasculogenic female sexual dysfunction: vaginal engorgement and clitoral erectile insufficiency syndromes. Int J Impot Res. 1998; 10 Suppl 2:S84-90.
  • 9
    Caruso S, Intelisano G, Lupo L, Agnello C. Premenopausal women affected by sexual arousal disorder treated with sildenafil: a double-blind, cross-over, placebo- controlled study. BJOG. 2001;108(6):623-8. doi: 10.1111/j.1471-0528.2001.00143.x
    » https://doi.org/10.1111/j.1471-0528.2001.00143.x
  • 10
    Basson R, McInnes R, Smith MD, Hodgson G, Koppiker N. Efficacy and safety of sildenafil citrate in women with sexual dysfunction associated with female sexual arousal disorder. J Womens Health Gend Based Med. 2002;11(4):367-77. doi: 10.1089/152460902317586001
    » https://doi.org/10.1089/152460902317586001
  • 11
    Basson R, Brotto LA. Sexual psychophysiology and effects of sildenafil citrate in oestrogenised women with acquired genital arousal disorder and impaired orgasm: a randomised controlled trial. BJOG. 2003;110(11):1014-24. doi: 10.1111/j.1471-0528.2003.02438.x
    » https://doi.org/10.1111/j.1471-0528.2003.02438.x
  • 12
    Berman JR, Berman LA, Toler SM, Gill J, Haughie S; Sildenafil Study Group. Safety and efficacy of sildenafil citrate for the treatment of female sexual arousal disorder: a double- blind, placebo controlled study. J Urol. 2003;170(6 Pt 1):2333-8. doi: 10.1097/01.ju.0000090966.74607.34
    » https://doi.org/10.1097/01.ju.0000090966.74607.34
  • 13
    Cavalcanti AL, Bagnoli VR, Fonseca AM, Pastore RA, Cardoso EB, Paixão JS, et al. Effect of sildenafil on clitoral blood flow and sexual response in postmenopausal women with orgasmic dysfunction. Int J Gynaecol Obstet. 2008;102(2):115-9. doi: 10.1016/j.ijgo.2008.03.020
    » https://doi.org/10.1016/j.ijgo.2008.03.020
  • 14
    Zeinalzadeh S, Akbarzadeh M, Faridi P, Ali Mohagheghzadeh A, Sayadi M. Effect of sildenafil citrate on women affected by sexual dysfunction referred to health clinics. Fam Med Prim Care Rev. 2017;19(2):167-72. doi: 10.5114/fmpcr.2017.67873
    » https://doi.org/10.5114/fmpcr.2017.67873
  • 15
    Ückert S, Kuczyk MA, Oelke M. Phosphodiesterase inhibitors in clinical urology. Expert Rev Clin Pharmacol. 2013;6(3):323-32. doi: 10.1586/ecp.13.16
    » https://doi.org/10.1586/ecp.13.16

Edited by

Associate Editor: Lucia Alves da Silva Lara (https://orcid.org/0000-0003-1073-238X) Universidade de São Paulo, Ribeirão Preto, SP, Brazil

Publication Dates

  • Publication in this collection
    12 Aug 2024
  • Date of issue
    2024

History

  • Received
    3 Aug 2023
  • Accepted
    7 Feb 2024
Federação Brasileira das Sociedades de Ginecologia e Obstetrícia Av. Brigadeiro Luís Antônio, 3421, sala 903 - Jardim Paulista, 01401-001 São Paulo SP - Brasil, Tel. (55 11) 5573-4919 - Rio de Janeiro - RJ - Brazil
E-mail: editorial.office@febrasgo.org.br