Patient–Physician Interactions Regarding Dyspareunia with Endometriosis: Online Survey Results
An online survey found that women with endometriosis-related dyspareunia experience severe pain impacting their lives and often receive inadequate treatment from healthcare providers.
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This study used an anonymous 24-question international online survey to characterize women aged 19–55 with self-identified endometriosis and painful sexual intercourse within the prior 2 years, focusing on dyspareunia experiences, life impacts, and patient–physician interactions. Among 638 completed responses (860 total; 74% completion), participants reported high dyspareunia severity (mean 7.4/10; 50% reporting 8–10), with 47% reporting pain lasting at least 24 hours post-intercourse; 34% reported avoiding and 29% stopping intercourse due to pain, and many reported substantial psychosocial and relationship impacts. Regarding healthcare interactions, 10% feared seeking help, and among those who approached practitioners, 36% reported not receiving effective treatment. This paper is centrally about endometriosis — it specifically examines patient experiences and perceived clinician interactions related to endometriosis-associated dyspareunia.
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