Assessing the Clinical Efficacy of Sildenafil for the Treatment of Female Sexual Dysfunction
Objective: To review the clinical data regarding the efficacy and safety of sildenafil for the treatment of female sexual dysfunction (FSD). Data Sources: A MEDLINE search from 1950 to February 2009 was conducted using the key words sildenafil and female sexual dysfunction. Human studies and publica...
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Veröffentlicht in: | The Annals of pharmacotherapy 2009-07, Vol.43 (7), p.1275-1285 |
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creator | Brown, Dana A Kyle, Jeffrey A Ferrill, Mary J |
description | Objective:
To review the clinical data regarding the efficacy and safety of sildenafil for the treatment of female sexual dysfunction (FSD).
Data Sources:
A MEDLINE search from 1950 to February 2009 was conducted using the key words sildenafil and female sexual dysfunction. Human studies and publication in English were used as primary limits. A combination of several publication-type limits was used to locate the clinical trials (eg, clinical trial, controlled clinical trial, randomized clinical trial). A bibliographic search was also performed of all located articles.
Study Selection and Data Extraction:
Clinical trials involving sildenafil treatment of premenopausal and postmenopausal women with FSD and women with FSD due to concomitant medications and/or disease states were reviewed.
Data Synthesis:
An increasing number of clinical trials have been published regarding the treatment of FSD with sildenafil. Eight studies demonstrated a possible benefit from treatment for FSD in patients receiving sildenafil, regardless of dose, while 4 trials did not show any significant differences with treatment. It appears that sildenafil might be beneficial for women with FSD caused by diseases such as multiple sclerosis, type 1 diabetes, spinal cord injury, and use of antidepressant medications.
Conclusions:
Although data suggest a possible role of sildenafil for the treatment of FSD, the information should be interpreted cautiously, as many of the studies included small sample sizes, used inappropriate statistical tests, and used nonvalidated assessment tools. A better FSD classification system and consistent use of validated assessment tools might help alleviate differences among clinical trials and provide a more cohesive foundation for assessing the safety and efficacy of sildenafil for the treatment of FSD. |
doi_str_mv | 10.1345/aph.1L691 |
format | Article |
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To review the clinical data regarding the efficacy and safety of sildenafil for the treatment of female sexual dysfunction (FSD).
Data Sources:
A MEDLINE search from 1950 to February 2009 was conducted using the key words sildenafil and female sexual dysfunction. Human studies and publication in English were used as primary limits. A combination of several publication-type limits was used to locate the clinical trials (eg, clinical trial, controlled clinical trial, randomized clinical trial). A bibliographic search was also performed of all located articles.
Study Selection and Data Extraction:
Clinical trials involving sildenafil treatment of premenopausal and postmenopausal women with FSD and women with FSD due to concomitant medications and/or disease states were reviewed.
Data Synthesis:
An increasing number of clinical trials have been published regarding the treatment of FSD with sildenafil. Eight studies demonstrated a possible benefit from treatment for FSD in patients receiving sildenafil, regardless of dose, while 4 trials did not show any significant differences with treatment. It appears that sildenafil might be beneficial for women with FSD caused by diseases such as multiple sclerosis, type 1 diabetes, spinal cord injury, and use of antidepressant medications.
Conclusions:
Although data suggest a possible role of sildenafil for the treatment of FSD, the information should be interpreted cautiously, as many of the studies included small sample sizes, used inappropriate statistical tests, and used nonvalidated assessment tools. A better FSD classification system and consistent use of validated assessment tools might help alleviate differences among clinical trials and provide a more cohesive foundation for assessing the safety and efficacy of sildenafil for the treatment of FSD.</description><identifier>ISSN: 1060-0280</identifier><identifier>EISSN: 1542-6270</identifier><identifier>DOI: 10.1345/aph.1L691</identifier><identifier>PMID: 19509350</identifier><identifier>CODEN: APHRER</identifier><language>eng</language><publisher>Los Angeles, CA: Harvey Whitney Books</publisher><subject>Biological and medical sciences ; Clinical Trials as Topic ; Dose-Response Relationship, Drug ; Female ; Humans ; Medical sciences ; Pharmacology. Drug treatments ; Phosphodiesterase Inhibitors - administration & dosage ; Phosphodiesterase Inhibitors - adverse effects ; Phosphodiesterase Inhibitors - therapeutic use ; Piperazines - administration & dosage ; Piperazines - adverse effects ; Piperazines - therapeutic use ; Purines - administration & dosage ; Purines - adverse effects ; Purines - therapeutic use ; Sexual Dysfunctions, Psychological - drug therapy ; Sexual Dysfunctions, Psychological - etiology ; Sildenafil Citrate ; Sulfones - administration & dosage ; Sulfones - adverse effects ; Sulfones - therapeutic use</subject><ispartof>The Annals of pharmacotherapy, 2009-07, Vol.43 (7), p.1275-1285</ispartof><rights>2009 SAGE Publications</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-fb9663b75a5b553730fdc08bedf6d3d2083af0a2d6fcb8eb66ce64971e88ea983</citedby><cites>FETCH-LOGICAL-c375t-fb9663b75a5b553730fdc08bedf6d3d2083af0a2d6fcb8eb66ce64971e88ea983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1345/aph.1L691$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1345/aph.1L691$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,777,781,21800,27905,27906,43602,43603</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21883930$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19509350$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brown, Dana A</creatorcontrib><creatorcontrib>Kyle, Jeffrey A</creatorcontrib><creatorcontrib>Ferrill, Mary J</creatorcontrib><title>Assessing the Clinical Efficacy of Sildenafil for the Treatment of Female Sexual Dysfunction</title><title>The Annals of pharmacotherapy</title><addtitle>Ann Pharmacother</addtitle><description>Objective:
To review the clinical data regarding the efficacy and safety of sildenafil for the treatment of female sexual dysfunction (FSD).
Data Sources:
A MEDLINE search from 1950 to February 2009 was conducted using the key words sildenafil and female sexual dysfunction. Human studies and publication in English were used as primary limits. A combination of several publication-type limits was used to locate the clinical trials (eg, clinical trial, controlled clinical trial, randomized clinical trial). A bibliographic search was also performed of all located articles.
Study Selection and Data Extraction:
Clinical trials involving sildenafil treatment of premenopausal and postmenopausal women with FSD and women with FSD due to concomitant medications and/or disease states were reviewed.
Data Synthesis:
An increasing number of clinical trials have been published regarding the treatment of FSD with sildenafil. Eight studies demonstrated a possible benefit from treatment for FSD in patients receiving sildenafil, regardless of dose, while 4 trials did not show any significant differences with treatment. It appears that sildenafil might be beneficial for women with FSD caused by diseases such as multiple sclerosis, type 1 diabetes, spinal cord injury, and use of antidepressant medications.
Conclusions:
Although data suggest a possible role of sildenafil for the treatment of FSD, the information should be interpreted cautiously, as many of the studies included small sample sizes, used inappropriate statistical tests, and used nonvalidated assessment tools. A better FSD classification system and consistent use of validated assessment tools might help alleviate differences among clinical trials and provide a more cohesive foundation for assessing the safety and efficacy of sildenafil for the treatment of FSD.</description><subject>Biological and medical sciences</subject><subject>Clinical Trials as Topic</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Phosphodiesterase Inhibitors - administration & dosage</subject><subject>Phosphodiesterase Inhibitors - adverse effects</subject><subject>Phosphodiesterase Inhibitors - therapeutic use</subject><subject>Piperazines - administration & dosage</subject><subject>Piperazines - adverse effects</subject><subject>Piperazines - therapeutic use</subject><subject>Purines - administration & dosage</subject><subject>Purines - adverse effects</subject><subject>Purines - therapeutic use</subject><subject>Sexual Dysfunctions, Psychological - drug therapy</subject><subject>Sexual Dysfunctions, Psychological - etiology</subject><subject>Sildenafil Citrate</subject><subject>Sulfones - administration & dosage</subject><subject>Sulfones - adverse effects</subject><subject>Sulfones - therapeutic use</subject><issn>1060-0280</issn><issn>1542-6270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0E1PwyAYwHFiNE6nB7-A6UUTD51QBoXjMjc1WeJh82ZCKH3YWLp2gS5z3172Er14ekj4AeGP0B3BPUL77FmvFz0y4ZKcoSvC-lnKsxyfxzXmOMWZwB10HcISYyxJJi9Rh0iGJWX4Cn0NQoAQXD1P2gUkw8rVzugqGVkbp9kljU2mriqh1tZViW38wc086HYFdbvfH8NKV5BM4XsTT77sgt3UpnVNfYMurK4C3J5mF32OR7PhWzr5eH0fDiapoTlrU1tIzmmRM80KxmhOsS0NFgWUlpe0zLCg2mKdldyaQkDBuQHelzkBIUBLQbvo6Xiv8U0IHqxae7fSfqcIVvtCKhZSh0LR3h_telOsoPyTpyQRPJyADrGE9bo2Lvy6jAhBJd27x6MLeg5q2Wx8Hf_474snuHDzxdZ5UCH2quL7RG232z5VuSJZzugPTI2I6g</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Brown, Dana A</creator><creator>Kyle, Jeffrey A</creator><creator>Ferrill, Mary J</creator><general>Harvey Whitney Books</general><general>SAGE Publications</general><general>Whitney</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20090701</creationdate><title>Assessing the Clinical Efficacy of Sildenafil for the Treatment of Female Sexual Dysfunction</title><author>Brown, Dana A ; Kyle, Jeffrey A ; Ferrill, Mary J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-fb9663b75a5b553730fdc08bedf6d3d2083af0a2d6fcb8eb66ce64971e88ea983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Biological and medical sciences</topic><topic>Clinical Trials as Topic</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphodiesterase Inhibitors - administration & dosage</topic><topic>Phosphodiesterase Inhibitors - adverse effects</topic><topic>Phosphodiesterase Inhibitors - therapeutic use</topic><topic>Piperazines - administration & dosage</topic><topic>Piperazines - adverse effects</topic><topic>Piperazines - therapeutic use</topic><topic>Purines - administration & dosage</topic><topic>Purines - adverse effects</topic><topic>Purines - therapeutic use</topic><topic>Sexual Dysfunctions, Psychological - drug therapy</topic><topic>Sexual Dysfunctions, Psychological - etiology</topic><topic>Sildenafil Citrate</topic><topic>Sulfones - administration & dosage</topic><topic>Sulfones - adverse effects</topic><topic>Sulfones - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brown, Dana A</creatorcontrib><creatorcontrib>Kyle, Jeffrey A</creatorcontrib><creatorcontrib>Ferrill, Mary J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The Annals of pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brown, Dana A</au><au>Kyle, Jeffrey A</au><au>Ferrill, Mary J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessing the Clinical Efficacy of Sildenafil for the Treatment of Female Sexual Dysfunction</atitle><jtitle>The Annals of pharmacotherapy</jtitle><addtitle>Ann Pharmacother</addtitle><date>2009-07-01</date><risdate>2009</risdate><volume>43</volume><issue>7</issue><spage>1275</spage><epage>1285</epage><pages>1275-1285</pages><issn>1060-0280</issn><eissn>1542-6270</eissn><coden>APHRER</coden><abstract>Objective:
To review the clinical data regarding the efficacy and safety of sildenafil for the treatment of female sexual dysfunction (FSD).
Data Sources:
A MEDLINE search from 1950 to February 2009 was conducted using the key words sildenafil and female sexual dysfunction. Human studies and publication in English were used as primary limits. A combination of several publication-type limits was used to locate the clinical trials (eg, clinical trial, controlled clinical trial, randomized clinical trial). A bibliographic search was also performed of all located articles.
Study Selection and Data Extraction:
Clinical trials involving sildenafil treatment of premenopausal and postmenopausal women with FSD and women with FSD due to concomitant medications and/or disease states were reviewed.
Data Synthesis:
An increasing number of clinical trials have been published regarding the treatment of FSD with sildenafil. Eight studies demonstrated a possible benefit from treatment for FSD in patients receiving sildenafil, regardless of dose, while 4 trials did not show any significant differences with treatment. It appears that sildenafil might be beneficial for women with FSD caused by diseases such as multiple sclerosis, type 1 diabetes, spinal cord injury, and use of antidepressant medications.
Conclusions:
Although data suggest a possible role of sildenafil for the treatment of FSD, the information should be interpreted cautiously, as many of the studies included small sample sizes, used inappropriate statistical tests, and used nonvalidated assessment tools. A better FSD classification system and consistent use of validated assessment tools might help alleviate differences among clinical trials and provide a more cohesive foundation for assessing the safety and efficacy of sildenafil for the treatment of FSD.</abstract><cop>Los Angeles, CA</cop><pub>Harvey Whitney Books</pub><pmid>19509350</pmid><doi>10.1345/aph.1L691</doi><tpages>11</tpages></addata></record> |
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subjects | Biological and medical sciences Clinical Trials as Topic Dose-Response Relationship, Drug Female Humans Medical sciences Pharmacology. Drug treatments Phosphodiesterase Inhibitors - administration & dosage Phosphodiesterase Inhibitors - adverse effects Phosphodiesterase Inhibitors - therapeutic use Piperazines - administration & dosage Piperazines - adverse effects Piperazines - therapeutic use Purines - administration & dosage Purines - adverse effects Purines - therapeutic use Sexual Dysfunctions, Psychological - drug therapy Sexual Dysfunctions, Psychological - etiology Sildenafil Citrate Sulfones - administration & dosage Sulfones - adverse effects Sulfones - therapeutic use |
title | Assessing the Clinical Efficacy of Sildenafil for the Treatment of Female Sexual Dysfunction |
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