Women's experiences of endometriosis: a systematic review and synthesis of qualitative research

<jats:sec><jats:title>Background</jats:title><jats:p>Endometriosis is experienced by approximately 10% of women worldwide; it is associated with significant burden on the woman, her family, and society.</jats:p></jats:sec><jats:sec><jats:title>Aim</jats:title><jats:p>The aim of this systematic review was to synthesise the available qualitative literature to increase our understanding of the effects of endometriosis on women's lives.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Seven social science and medical databases (PubMed, Medline, CINAHL, Web of Science, ScienceDirect, PsycInfo and Embase) and Google Scholar were searched for peer-reviewed papers published in English of research using qualitative methods.</jats:p></jats:sec><jats:sec><jats:title>Results and conclusions</jats:title><jats:p>Eighteen papers reporting 11 studies met the inclusion criteria. Participant numbers ranged from 15 to 61 women, all recruited from support groups and specialised clinics. Studies were conducted in high-income, Anglophone countries. The review identified four prominent themes: Life, Symptoms, Medical Experience, and Self. Women's reported experiences demonstrated opportunities for enhancing current clinical practice, including improved education about endometriosis for health professionals, the need to take a comprehensive approach to pain treatment, and initiating appropriate discussion of the impact on sex life. Significant evidence gaps were identified: there was inadequate investigation of women's experiences of endometriosis-associated infertility and of the impact of reduced social participation on perceived support and emotional well-being, and limited or no inclusion of the experiences of adolescent and post-menopausal women, women from low socioeconomic backgrounds, women who do not identify as Caucasian, and non-heterosexual women.</jats:p></jats:sec>