Impact of chronic pelvic pain on quality of life in diverse young adults
This study investigated the impact of chronic pelvic pain on the quality of life among a diverse group of young adults.
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This cross-sectional survey study examined the relationship between quality of life (QoL) and chronic pelvic pain (CPP) in young adults aged 18–25 who menstruate, recruited from Midwestern U.S. college campuses (n=585), using the WHOQOL-BREF and the Impact of Female Chronic Pelvic Pain Questionnaire. Participants reporting CPP (153; 26%) or being unsure they had CPP (95; 16%) had lower QoL scores across all four WHOQOL domains, with statistically significant lower scores in physical health, social relationships, and environment compared with those answering “no.” Respondents identifying as Black, Indigenous, or People of Color had significantly lower QoL in physical health and environment domains than white respondents. The authors’ key caveat is that the design is cross-sectional and thus cannot establish causality. Relevance to endometriosis: endometriosis is discussed in the paper’s reference list within prior work on racial disparities in uterine fibroids and endometriosis, though the study itself focuses broadly on chronic pelvic pain and QoL rather than specifically on endometriosis or adenomyosis.
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