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      Post-SSRI sexual dysfunction: barriers to quantifying incidence and prevalence

      editorial
      1 , , 2 , 3
      Epidemiology and Psychiatric Sciences
      Cambridge University Press
      adverse effects, antidepressants, sexual dysfunction, suicide

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          Abstract

          While sexual dysfunction is a well-known side effect of taking selective serotonin reuptake inhibitors (SSRIs), in an undetermined number of patients, sexual function does not return to pre-drug baseline after stopping SSRIs. The condition is known as post-SSRI sexual dysfunction (PSSD) and is characterised most commonly by genital numbness, pleasureless or weak orgasm, loss of libido and erectile dysfunction. This article provides a commentary on the incidence and prevalence of PSSD based on a combination of academic literature as well as clinical and research experience. A number of obstacles to quantifying the occurrence of PSSD are outlined including difficulty in designing a suitable study method. Other contextual obstacles include patient embarrassment at raising sexual concerns, the response of healthcare professionals, inability to stop an antidepressant due to withdrawal issues in a proportion of patients and patient unawareness that their sexual difficulties are linked to prior medication compounded by variability of online information and a lack of information aimed at public education. A definition of PSSD with diagnostic criteria has been published. A MedDRA code for PSSD has also been introduced, but this is yet to be adopted by regulators.

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          Most cited references52

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          TEMPORARY REMOVAL: A systematic review into the incidence, severity and duration of antidepressant withdrawal effects: Are guidelines evidence-based?

          The U.K.'s current National Institute for Health and Care Excellence and the American Psychiatric Association's depression guidelines state that withdrawal reactions from antidepressants are 'self-limiting' (i.e. typically resolving between 1 and 2weeks). This systematic review assesses that claim.
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            Adverse effect of paroxetine on sperm.

            To assess the effects of a selective serotonin reuptake inhibitor on semen parameters. Prospective study. Academic medical center. Thirty-five healthy male volunteers, 18-65 years old. Paroxetine administration for 5 weeks. Serum hormone levels, semen analyses, percent sperm DNA fragmentation, and questionnaire assessment of sexual function assessed before, during, and 1 month after drug administration. Mean sperm DNA fragmentation was significantly higher for men while on paroxetine (30.3%) versus baseline (13.8%). Before paroxetine, 9.7% of patients had a terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) score>or=30% compared with 50% at week 4 of treatment. The odds ratio (OR) of having abnormal DNA fragmentation while taking paroxetine was 9.33 (95% confidence interval, 2.3-37.9]. Multivariate logistic regression correcting for age and body mass index confirmed this correlation (OR, 11.12). Up to 35% of men noted significant changes in erectile function and up to 47% of men reported ejaculatory difficulties on medication. Recovery to near-normal sexual function was noted after stopping treatment. Standard semen parameters were not significantly altered during paroxetine treatment. In men with normal semen parameters, paroxetine induced abnormal sperm DNA fragmentation in a significant proportion of subjects, without a measurable effect on semen parameters. The fertility potential of a substantial number of men on paroxetine may be adversely affected by these changes in sperm DNA integrity. Copyright (c) 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.
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              Post-SSRI Sexual Dysfunction: A Literature Review.

              Selective serotonin reuptake inhibitors (SSRIs) are a widely used class of drug. Post-SSRI sexual dysfunction (PSSD) is a condition in which patients continue to have sexual side effects after discontinuation of SSRI use. The prevalence of persistent sexual side effects after discontinuing SSRIs is unknown. The recognition and study of PSSD will increase our knowledge base of this underreported and distressing condition.
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                Author and article information

                Journal
                Epidemiol Psychiatr Sci
                Epidemiol Psychiatr Sci
                EPS
                Epidemiology and Psychiatric Sciences
                Cambridge University Press (Cambridge, UK )
                2045-7960
                2045-7979
                2024
                18 September 2024
                : 33
                : e40
                Affiliations
                [1 ]Data Based Medicine , Wales, UK
                [2 ]Department of Family Medicine, McMaster University , Hamilton, ON, Canada
                [3 ]Department of General Practice, University of Otago , Christchurch, New Zealand
                Author notes
                Corresponding author: David Healy; Email: david.healy54@ 123456googlemail.com
                Author information
                https://orcid.org/0000-0002-6340-9247
                https://orcid.org/0000-0003-2149-9376
                Article
                S2045796024000441
                10.1017/S2045796024000441
                11450419
                39289881
                c2ca71df-3f22-46ea-ba81-7b1663a9d939
                © The Author(s) 2024

                This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.

                History
                : 25 June 2024
                : 01 July 2024
                Page count
                References: 61, Pages: 5
                Categories
                Editorial

                adverse effects,antidepressants,sexual dysfunction,suicide

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