Defining Endometriosis for Doctors and Patients
This chapter explores how accurate and consistent communication about endometriosis can improve health literacy and patient management, especially for adolescents and their families.
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This chapter discusses the need for consistent and accurate communication about endometriosis, focusing on how information is conveyed to healthcare professionals, adolescents, and their families in order to improve health literacy and support more adequate management of the condition. It is framed in a context where patients, including adolescents, are taking a more empowered role in their own healthcare, and it argues that defining what is said about endometriosis—how, to whom, and by whom—is crucial given that the disease remains relatively unknown even among healthcare professionals. A stated limitation is that the work is presented as a communication/definition chapter rather than as original clinical or experimental research with patient outcomes. This paper is centrally about endometriosis — specifically how endometriosis should be defined and communicated to doctors and adolescent patients.
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References (15)
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- Endometriosis in an Adolescent Population: The Emory Experience via openalex
- Impact of endometriosis on quality of life and work productivity: a multicenter study across ten countries via openalex
- Laparoscopic evaluation and management of chronic pelvic pain during adolescence. via openalex
- Laparoscopy in the diagnosis of chronic pelvic pain in adolescent women. via openalex
- Prevalence of Endometriosis in Adolescent Girls With Chronic Pelvic Pain Not Responding to Conventional Therapy via openalex
- Research Priorities for Endometriosis: Recommendations From a Global Consortium of Investigators in Endometriosis via openalex
- The burden of endometriosis: costs and quality of life of women with endometriosis and treated in referral centres via openalex
- W6600095811 via openalex
- W2141909819 via openalex
- W2416713714 via openalex
- W2338444 via openalex
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