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Patient perspectives on the impact of acromegaly: results from individual and group interviews

PURPOSE: Acromegaly is a chronic condition resulting from a growth hormone-secreting pituitary tumor that can substantially impact patients’ physical and emotional well-being. We sought to understand the impact of acromegaly on disease-related concerns and treatment choices from the patient perspect...

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Autores principales: Gurel, Michelle H, Bruening, Paul R, Rhodes, Christine, Lomax, Kathleen G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894135/
https://www.ncbi.nlm.nih.gov/pubmed/24453479
http://dx.doi.org/10.2147/PPA.S56740
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author Gurel, Michelle H
Bruening, Paul R
Rhodes, Christine
Lomax, Kathleen G
author_facet Gurel, Michelle H
Bruening, Paul R
Rhodes, Christine
Lomax, Kathleen G
author_sort Gurel, Michelle H
collection PubMed
description PURPOSE: Acromegaly is a chronic condition resulting from a growth hormone-secreting pituitary tumor that can substantially impact patients’ physical and emotional well-being. We sought to understand the impact of acromegaly on disease-related concerns and treatment choices from the patient perspective. The path to diagnosis, current disease management, interactions with the treating health care providers (HCPs), and support networks were also assessed. METHODS: Acromegaly patients were recruited primarily from a patient support group (Acromegaly Community). In Phase I, ten patients participated over the course of 5 days in a moderated online discussion board and they answered questions about their disease. In Phase II, a separate nine-patient cohort participated in face-to-face interviews conducted during an acromegaly patient conference. Data were summarized qualitatively by grouping similar answers and quotations. RESULTS: Nineteen acromegaly patients were recruited across the two cohorts, and both groups shared similar concerns. They demonstrated a notable interest in understanding their disease and its treatment. Patients were focused on the impact of the disease on their life, and they expressed a desire to get beyond reminders of their disease. The patients described long journeys to a correct diagnosis and relief at having a name for their condition. Many shared a sense of shock at needing pituitary surgery and felt unsatisfied by the treatment decision process, motivating them to discuss it with other patients. Patients not connected to a patient support group reported feeling helpless and lonely. Most patients shared a desire to improve their general knowledge about acromegaly to spare others their protracted diagnostic period. Patients also reported hesitancy in asking questions or sharing details about the disease’s impact on their lives with their HCPs. CONCLUSION: Acromegaly can be a life-changing diagnosis with profound, ongoing effects on patients’ lives. Patients struggle with many issues they fail to openly share with their HCPs, but may discuss these issues more easily with other acromegaly patients. Better collaboration between patients and care providers could lead to increased patient satisfaction.
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spelling pubmed-38941352014-01-17 Patient perspectives on the impact of acromegaly: results from individual and group interviews Gurel, Michelle H Bruening, Paul R Rhodes, Christine Lomax, Kathleen G Patient Prefer Adherence Original Research PURPOSE: Acromegaly is a chronic condition resulting from a growth hormone-secreting pituitary tumor that can substantially impact patients’ physical and emotional well-being. We sought to understand the impact of acromegaly on disease-related concerns and treatment choices from the patient perspective. The path to diagnosis, current disease management, interactions with the treating health care providers (HCPs), and support networks were also assessed. METHODS: Acromegaly patients were recruited primarily from a patient support group (Acromegaly Community). In Phase I, ten patients participated over the course of 5 days in a moderated online discussion board and they answered questions about their disease. In Phase II, a separate nine-patient cohort participated in face-to-face interviews conducted during an acromegaly patient conference. Data were summarized qualitatively by grouping similar answers and quotations. RESULTS: Nineteen acromegaly patients were recruited across the two cohorts, and both groups shared similar concerns. They demonstrated a notable interest in understanding their disease and its treatment. Patients were focused on the impact of the disease on their life, and they expressed a desire to get beyond reminders of their disease. The patients described long journeys to a correct diagnosis and relief at having a name for their condition. Many shared a sense of shock at needing pituitary surgery and felt unsatisfied by the treatment decision process, motivating them to discuss it with other patients. Patients not connected to a patient support group reported feeling helpless and lonely. Most patients shared a desire to improve their general knowledge about acromegaly to spare others their protracted diagnostic period. Patients also reported hesitancy in asking questions or sharing details about the disease’s impact on their lives with their HCPs. CONCLUSION: Acromegaly can be a life-changing diagnosis with profound, ongoing effects on patients’ lives. Patients struggle with many issues they fail to openly share with their HCPs, but may discuss these issues more easily with other acromegaly patients. Better collaboration between patients and care providers could lead to increased patient satisfaction. Dove Medical Press 2014-01-09 /pmc/articles/PMC3894135/ /pubmed/24453479 http://dx.doi.org/10.2147/PPA.S56740 Text en © 2014 Gurel et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Gurel, Michelle H
Bruening, Paul R
Rhodes, Christine
Lomax, Kathleen G
Patient perspectives on the impact of acromegaly: results from individual and group interviews
title Patient perspectives on the impact of acromegaly: results from individual and group interviews
title_full Patient perspectives on the impact of acromegaly: results from individual and group interviews
title_fullStr Patient perspectives on the impact of acromegaly: results from individual and group interviews
title_full_unstemmed Patient perspectives on the impact of acromegaly: results from individual and group interviews
title_short Patient perspectives on the impact of acromegaly: results from individual and group interviews
title_sort patient perspectives on the impact of acromegaly: results from individual and group interviews
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894135/
https://www.ncbi.nlm.nih.gov/pubmed/24453479
http://dx.doi.org/10.2147/PPA.S56740
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