A COMPARATIVE STUDY OF FEMALE SEXUAL DYSFUNCTION AMONG WOMEN ON PAROXETINE, SERTRALINE AND ESCITALOPRAM VISITING A RURAL TERTIARY HOSPITAL

Main Article Content

Dr Sanjana ilavarasu
Dr Abhishek Nagakumar
Dr Kasthuri pandiyan

Keywords

Female Sexual Dysfunction; Escitalopram; Paroxetine; Sertraline; SSRI emergent sexual dysfunction.

Abstract

Background


Female Sexual Dysfunction (FSD) is a common clinical issue globally, linked to various medical, gynaecological, psychiatric conditions, and medications. With increased psychotropic use, particularly SSRIs, drug-induced FSD is becoming more prevalent. SSRIs are well-known to impair sexual function, which may reduce adherence, worsen underlying conditions, and negatively impact quality of life and relationships. This study aims to assess the prevalence, incidence, and extent of FSD among SSRI users, along with the specific domains of sexual function affected.


Aim


To study and compare the female sexual dysfunction among patients on Sertraline, Paroxetine and Escitalopram.


Methods


This cross-sectional study included 100 female subjects in remission from primary depressive or anxiety disorders, treated with Paroxetine, Sertraline, or Escitalopram. A semi-structured proforma was used to gather sociodemographic data and premorbid sexual functioning. Female Sexual Dysfunction was assessed using the Female Sexual Function Index (FSFI).


Results


The prevalence of Female Sexual Dysfunction (FSD) was 46.66%, highest with Paroxetine, followed by Sertraline and Escitalopram. All six FSFI domains were affected, with the most common being loss of desire (45%), delay/lack of orgasm (29%), and difficulty with arousal (14%). Paroxetine caused significantly more orgasmic dysfunction compared to Escitalopram. No significant differences were found across other domains or among sociodemographic variables.


Interpretation And Conclusion


The prevalence of drug induced Sexual Dysfunction is of clinical significance which can adversely affect drug compliance and it is an often-underreported side effect. Clinicians must be trained adequately to identify and manage the resultant adverse effects.


 


 

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