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Communicating Endometriosis Pain in France and Australia: An Interview Study

Endometriosis is characterized by persistent, fluctuating pain associated with menstruation, a biological function which is socially invisible. The degree and quality of pain cannot easily be measured, observed, or documented. Difficulties in communicating pain pose particular challenges when seekin...

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Autores principales: Ilschner, Susanne, Neeman, Teresa, Parker, Melissa, Phillips, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984272/
https://www.ncbi.nlm.nih.gov/pubmed/35400132
http://dx.doi.org/10.3389/fgwh.2022.765762
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author Ilschner, Susanne
Neeman, Teresa
Parker, Melissa
Phillips, Christine
author_facet Ilschner, Susanne
Neeman, Teresa
Parker, Melissa
Phillips, Christine
author_sort Ilschner, Susanne
collection PubMed
description Endometriosis is characterized by persistent, fluctuating pain associated with menstruation, a biological function which is socially invisible. The degree and quality of pain cannot easily be measured, observed, or documented. Difficulties in communicating pain pose particular challenges when seeking diagnosis and support from health professionals. In this paper we explore the experiences and characterization of pain by thirteen Australian and thirteen French women with endometriosis. Data were collected through semi-structured interviews using a life-history approach to illness symptoms, diagnosis and treatment. We explore the experiences of women with endometriosis in two phases: from onset of symptoms to seeking advice from a clinician, and from first consulting a clinician to receiving a diagnosis. On average, initial pain symptoms were identified 2.1 years before consulting a health practitioner, after which women reported pain symptoms 8.5 years prior to diagnosis; that is, the time between consulting a clinician and receiving a diagnosis was almost four times the period between experiencing symptoms and consulting a doctor. Pain was often “made real” to doctors by findings consistent with endometriosis on ultrasound and MRI, mostly used in France, or laparoscopy, the predominant diagnostic tool in Australia. No woman described her practitioner using standardized pain assessment tools. Thus, the validation of pain relies largely on disease visibility and the clinician-classified degree of severity rather than self-reported grades of pain or impact on activities of daily living. The invisible and enigmatic pain of this chronic women's disease remains difficult to communicate to doctors, and the recognition of severe pain is often key to timely diagnostic procedures. Clinicians need to be more proactive about severe pain related to menstruation, taking into consideration women's individual circumstances, and maintain a high index of suspicion of underlying endometriosis as a condition characterized primarily by pain.
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spelling pubmed-89842722022-04-07 Communicating Endometriosis Pain in France and Australia: An Interview Study Ilschner, Susanne Neeman, Teresa Parker, Melissa Phillips, Christine Front Glob Womens Health Global Women's Health Endometriosis is characterized by persistent, fluctuating pain associated with menstruation, a biological function which is socially invisible. The degree and quality of pain cannot easily be measured, observed, or documented. Difficulties in communicating pain pose particular challenges when seeking diagnosis and support from health professionals. In this paper we explore the experiences and characterization of pain by thirteen Australian and thirteen French women with endometriosis. Data were collected through semi-structured interviews using a life-history approach to illness symptoms, diagnosis and treatment. We explore the experiences of women with endometriosis in two phases: from onset of symptoms to seeking advice from a clinician, and from first consulting a clinician to receiving a diagnosis. On average, initial pain symptoms were identified 2.1 years before consulting a health practitioner, after which women reported pain symptoms 8.5 years prior to diagnosis; that is, the time between consulting a clinician and receiving a diagnosis was almost four times the period between experiencing symptoms and consulting a doctor. Pain was often “made real” to doctors by findings consistent with endometriosis on ultrasound and MRI, mostly used in France, or laparoscopy, the predominant diagnostic tool in Australia. No woman described her practitioner using standardized pain assessment tools. Thus, the validation of pain relies largely on disease visibility and the clinician-classified degree of severity rather than self-reported grades of pain or impact on activities of daily living. The invisible and enigmatic pain of this chronic women's disease remains difficult to communicate to doctors, and the recognition of severe pain is often key to timely diagnostic procedures. Clinicians need to be more proactive about severe pain related to menstruation, taking into consideration women's individual circumstances, and maintain a high index of suspicion of underlying endometriosis as a condition characterized primarily by pain. Frontiers Media S.A. 2022-03-23 /pmc/articles/PMC8984272/ /pubmed/35400132 http://dx.doi.org/10.3389/fgwh.2022.765762 Text en Copyright © 2022 Ilschner, Neeman, Parker and Phillips. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Global Women's Health
Ilschner, Susanne
Neeman, Teresa
Parker, Melissa
Phillips, Christine
Communicating Endometriosis Pain in France and Australia: An Interview Study
title Communicating Endometriosis Pain in France and Australia: An Interview Study
title_full Communicating Endometriosis Pain in France and Australia: An Interview Study
title_fullStr Communicating Endometriosis Pain in France and Australia: An Interview Study
title_full_unstemmed Communicating Endometriosis Pain in France and Australia: An Interview Study
title_short Communicating Endometriosis Pain in France and Australia: An Interview Study
title_sort communicating endometriosis pain in france and australia: an interview study
topic Global Women's Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984272/
https://www.ncbi.nlm.nih.gov/pubmed/35400132
http://dx.doi.org/10.3389/fgwh.2022.765762
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