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Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma
Little is known about the impact of adrenocortical carcinoma (ACC) on health-related quality of life (HRQoL), and no disease-specific questionnaire exists. This qualitative study aimed to identify relevant domains of HRQoL for patients with ACC. In 2 focus group interviews, we discussed concerns reg...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174051/ https://www.ncbi.nlm.nih.gov/pubmed/32342024 http://dx.doi.org/10.1210/jendso/bvaa040 |
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author | Steenaard, Rebecca V Kremers, Marjolein N T Michon, Laura A Zijlstra, Myrte Haak, Harm R |
author_facet | Steenaard, Rebecca V Kremers, Marjolein N T Michon, Laura A Zijlstra, Myrte Haak, Harm R |
author_sort | Steenaard, Rebecca V |
collection | PubMed |
description | Little is known about the impact of adrenocortical carcinoma (ACC) on health-related quality of life (HRQoL), and no disease-specific questionnaire exists. This qualitative study aimed to identify relevant domains of HRQoL for patients with ACC. In 2 focus group interviews, we discussed concerns regarding living with ACC and its treatments. The first group consisted of 6 patients on mitotane therapy and their partners or relatives, the second group of 4 patients after surgery alone and their partners. Inductive qualitative content analysis was used to analyze the interviews. We identified 4 domains related to HRQoL in patients with ACC, namely physical complaints, mental consequences, social consequences, and functional limitations. For example, physical complaints included symptoms of the disease and side effects of mitotane therapy; mental consequences included feeling insecure and living from scan to scan; and functional limitations included daily activities and mobility. We further found that patients’ experiences with the health care system and health care professionals and partner perspectives influence HRQoL. In conclusion, ACC has a large impact on HRQoL in 4 domains. These results can be used to improve communication about HRQoL issues. We will use our findings to generate a disease-specific questionnaire to measure HRQoL in patients with ACC. |
format | Online Article Text |
id | pubmed-7174051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71740512020-04-27 Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma Steenaard, Rebecca V Kremers, Marjolein N T Michon, Laura A Zijlstra, Myrte Haak, Harm R J Endocr Soc Research Article Little is known about the impact of adrenocortical carcinoma (ACC) on health-related quality of life (HRQoL), and no disease-specific questionnaire exists. This qualitative study aimed to identify relevant domains of HRQoL for patients with ACC. In 2 focus group interviews, we discussed concerns regarding living with ACC and its treatments. The first group consisted of 6 patients on mitotane therapy and their partners or relatives, the second group of 4 patients after surgery alone and their partners. Inductive qualitative content analysis was used to analyze the interviews. We identified 4 domains related to HRQoL in patients with ACC, namely physical complaints, mental consequences, social consequences, and functional limitations. For example, physical complaints included symptoms of the disease and side effects of mitotane therapy; mental consequences included feeling insecure and living from scan to scan; and functional limitations included daily activities and mobility. We further found that patients’ experiences with the health care system and health care professionals and partner perspectives influence HRQoL. In conclusion, ACC has a large impact on HRQoL in 4 domains. These results can be used to improve communication about HRQoL issues. We will use our findings to generate a disease-specific questionnaire to measure HRQoL in patients with ACC. Oxford University Press 2020-04-01 /pmc/articles/PMC7174051/ /pubmed/32342024 http://dx.doi.org/10.1210/jendso/bvaa040 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Steenaard, Rebecca V Kremers, Marjolein N T Michon, Laura A Zijlstra, Myrte Haak, Harm R Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma |
title | Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma |
title_full | Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma |
title_fullStr | Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma |
title_full_unstemmed | Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma |
title_short | Patient and Partner Perspectives on Health-Related Quality of Life in Adrenocortical Carcinoma |
title_sort | patient and partner perspectives on health-related quality of life in adrenocortical carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174051/ https://www.ncbi.nlm.nih.gov/pubmed/32342024 http://dx.doi.org/10.1210/jendso/bvaa040 |
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