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Measuring health-related quality of life in patients with rare disease
BACKGROUND: There has been a growing emphasis on health-related quality of life (HRQoL) as an important outcome in rare disease drug development, although its assessment may be useful outside the drug development context, including in clinical applications or natural history studies. Central to asse...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292508/ https://www.ncbi.nlm.nih.gov/pubmed/34283357 http://dx.doi.org/10.1186/s41687-021-00336-8 |
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author | Lenderking, William R. Anatchkova, Milena Pokrzywinski, Robin Skalicky, Anne Martin, Mona L. Gelhorn, Heather |
author_facet | Lenderking, William R. Anatchkova, Milena Pokrzywinski, Robin Skalicky, Anne Martin, Mona L. Gelhorn, Heather |
author_sort | Lenderking, William R. |
collection | PubMed |
description | BACKGROUND: There has been a growing emphasis on health-related quality of life (HRQoL) as an important outcome in rare disease drug development, although its assessment may be useful outside the drug development context, including in clinical applications or natural history studies. Central to assessing quality of life in health research is utilizing outcome measures that capture symptoms and impacts of the disease and treatment that are important and relevant to patients. Identifying and implementing valid and reliable tools to measure HRQoL in rare diseases poses unique challenges that often require creative solutions. MAIN BODY: In this commentary, we explore some of the challenges in HRQoL assessment in rare disease, propose solutions, and consider regulatory issues. Some of the solutions discussed entail the use of item banks, adapting existing measures from phenotypically similar disease contexts, use of multi-domain measurement indices, and adapting methods for assessing content validity of existing measures. Current regulatory considerations are discussed and resources outlined. CONCLUSION: Quality of life may be the most important endpoint for patients with rare diseases, and the challenges of valid assessment require effort and innovative thinking specific to each context to improve measurement and clinical outcomes. |
format | Online Article Text |
id | pubmed-8292508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-82925082021-08-05 Measuring health-related quality of life in patients with rare disease Lenderking, William R. Anatchkova, Milena Pokrzywinski, Robin Skalicky, Anne Martin, Mona L. Gelhorn, Heather J Patient Rep Outcomes Commentary BACKGROUND: There has been a growing emphasis on health-related quality of life (HRQoL) as an important outcome in rare disease drug development, although its assessment may be useful outside the drug development context, including in clinical applications or natural history studies. Central to assessing quality of life in health research is utilizing outcome measures that capture symptoms and impacts of the disease and treatment that are important and relevant to patients. Identifying and implementing valid and reliable tools to measure HRQoL in rare diseases poses unique challenges that often require creative solutions. MAIN BODY: In this commentary, we explore some of the challenges in HRQoL assessment in rare disease, propose solutions, and consider regulatory issues. Some of the solutions discussed entail the use of item banks, adapting existing measures from phenotypically similar disease contexts, use of multi-domain measurement indices, and adapting methods for assessing content validity of existing measures. Current regulatory considerations are discussed and resources outlined. CONCLUSION: Quality of life may be the most important endpoint for patients with rare diseases, and the challenges of valid assessment require effort and innovative thinking specific to each context to improve measurement and clinical outcomes. Springer International Publishing 2021-07-20 /pmc/articles/PMC8292508/ /pubmed/34283357 http://dx.doi.org/10.1186/s41687-021-00336-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Commentary Lenderking, William R. Anatchkova, Milena Pokrzywinski, Robin Skalicky, Anne Martin, Mona L. Gelhorn, Heather Measuring health-related quality of life in patients with rare disease |
title | Measuring health-related quality of life in patients with rare disease |
title_full | Measuring health-related quality of life in patients with rare disease |
title_fullStr | Measuring health-related quality of life in patients with rare disease |
title_full_unstemmed | Measuring health-related quality of life in patients with rare disease |
title_short | Measuring health-related quality of life in patients with rare disease |
title_sort | measuring health-related quality of life in patients with rare disease |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292508/ https://www.ncbi.nlm.nih.gov/pubmed/34283357 http://dx.doi.org/10.1186/s41687-021-00336-8 |
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