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Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants
BACKGROUND: Sexual dysfunction is a common side effect of Serotonergic antidepressants (SA) treatment, and persists in some patients despite drug discontinuation, a condition termed post-SSRI sexual dysfunction (PSSD). The risk for PSSD is unknown but is thought to be rare and difficult to assess. T...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122283/ https://www.ncbi.nlm.nih.gov/pubmed/37085865 http://dx.doi.org/10.1186/s12991-023-00447-0 |
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author | Ben-Sheetrit, Joseph Hermon, Yehonathan Birkenfeld, Shlomo Gutman, Yehiel Csoka, Antonei B. Toren, Paz |
author_facet | Ben-Sheetrit, Joseph Hermon, Yehonathan Birkenfeld, Shlomo Gutman, Yehiel Csoka, Antonei B. Toren, Paz |
author_sort | Ben-Sheetrit, Joseph |
collection | PubMed |
description | BACKGROUND: Sexual dysfunction is a common side effect of Serotonergic antidepressants (SA) treatment, and persists in some patients despite drug discontinuation, a condition termed post-SSRI sexual dysfunction (PSSD). The risk for PSSD is unknown but is thought to be rare and difficult to assess. This study aims to estimate the risk of erectile dysfunction (ED) and PSSD in males treated with SAs. METHODS: A 19-year retrospective cohort analysis was conducted using a computerized database of the largest HMO in Israel. ED was defined by phosphodiesterase-5 inhibitors prescriptions. 12,302 males aged 21–49 met the following criteria: non-smokers, no medical or psychiatric comorbidities or medications associated with ED, no alcohol or substance use. Logistic regression was used for estimation of ED risk in SA-treated subjects compared to non-SA-treated controls, assessed with and without the effects of age, body mass index (BMI), socioeconomic status (SES), depression and anxiety, yielding crude and adjusted odds ratios (cOR and aOR, respectively). RESULTS: SAs were associated with an increased risk for ED (cOR = 3.6, p < 0.000001, 95% CI 2.8–4.8), which remained significant after adjusting for age, SES, BMI, depression and anxiety (aOR = 3.2, p < 0.000001, 95% CI 2.3–4.4). The risk for PSSD was 1 in 216 patients (0.46%) treated with SAs. The prevalence of PSSD was 4.3 per 100,000. CONCLUSIONS: This work offers a first assessment of the small but significant risk of irreversible ED associated with the most commonly prescribed class of antidepressants which should enhance the process of receiving adequate informed consent for therapy. |
format | Online Article Text |
id | pubmed-10122283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101222832023-04-23 Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants Ben-Sheetrit, Joseph Hermon, Yehonathan Birkenfeld, Shlomo Gutman, Yehiel Csoka, Antonei B. Toren, Paz Ann Gen Psychiatry Research BACKGROUND: Sexual dysfunction is a common side effect of Serotonergic antidepressants (SA) treatment, and persists in some patients despite drug discontinuation, a condition termed post-SSRI sexual dysfunction (PSSD). The risk for PSSD is unknown but is thought to be rare and difficult to assess. This study aims to estimate the risk of erectile dysfunction (ED) and PSSD in males treated with SAs. METHODS: A 19-year retrospective cohort analysis was conducted using a computerized database of the largest HMO in Israel. ED was defined by phosphodiesterase-5 inhibitors prescriptions. 12,302 males aged 21–49 met the following criteria: non-smokers, no medical or psychiatric comorbidities or medications associated with ED, no alcohol or substance use. Logistic regression was used for estimation of ED risk in SA-treated subjects compared to non-SA-treated controls, assessed with and without the effects of age, body mass index (BMI), socioeconomic status (SES), depression and anxiety, yielding crude and adjusted odds ratios (cOR and aOR, respectively). RESULTS: SAs were associated with an increased risk for ED (cOR = 3.6, p < 0.000001, 95% CI 2.8–4.8), which remained significant after adjusting for age, SES, BMI, depression and anxiety (aOR = 3.2, p < 0.000001, 95% CI 2.3–4.4). The risk for PSSD was 1 in 216 patients (0.46%) treated with SAs. The prevalence of PSSD was 4.3 per 100,000. CONCLUSIONS: This work offers a first assessment of the small but significant risk of irreversible ED associated with the most commonly prescribed class of antidepressants which should enhance the process of receiving adequate informed consent for therapy. BioMed Central 2023-04-21 /pmc/articles/PMC10122283/ /pubmed/37085865 http://dx.doi.org/10.1186/s12991-023-00447-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ben-Sheetrit, Joseph Hermon, Yehonathan Birkenfeld, Shlomo Gutman, Yehiel Csoka, Antonei B. Toren, Paz Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants |
title | Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants |
title_full | Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants |
title_fullStr | Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants |
title_full_unstemmed | Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants |
title_short | Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants |
title_sort | estimating the risk of irreversible post-ssri sexual dysfunction (pssd) due to serotonergic antidepressants |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122283/ https://www.ncbi.nlm.nih.gov/pubmed/37085865 http://dx.doi.org/10.1186/s12991-023-00447-0 |
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