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The Experiences of Endometriosis Patients During Primary Healthcare Encounters

Project 566

566

Research Team

  • Sarah Harris
  • Laila J. Tata
  • Nadeem Qureshi
  • Et al

Abstract Endometriosis affects 10% of those assigned-female-at-birth worldwide. Diagnosis typically takes between 5–12 years. This qualitative systematic review explored endometriosis patients’ experiences with primary healthcare professionals from presentation before diagnosis to post-diagnosis follow-up. Six electronic databases were searched: CINAHL, MEDLINE, Embase, PubMed, Scopus, and PsycINFO. A total of 37 articles were included and synthesized thematically. Findings showed common issues that patients were experiencing during their interactions with primary healthcare professionals, including dismissal regarding their symptoms, delayed referral to secondary care, and lack of knowledge regarding endometriosis. This review highlights a need for improved education and awareness surrounding endometriosis amongst primary healthcare professionals.

Information

Type

Journal article

Publisher

Informa UK Ltd

Addresses

This study is part of a PhD being undertaken by Sarah Harris, which is funded by the National Institute for Health and Care Research (NIHR) School for Primary Care Research (reference: C105).

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