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Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease
BACKGROUND: It is now acknowledged that the input of patients in health outcome assessment is vital to understanding the impact of diseases and interventions for those diseases. This study is the first report of patient-reported outcome measures (PROM) in a large cohort of patients with type 1 Gauch...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556970/ https://www.ncbi.nlm.nih.gov/pubmed/33050940 http://dx.doi.org/10.1186/s13023-020-01544-z |
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author | Dinur, Tama Istaiti, Majdolen Frydman, Dafna Becker-Cohen, Michal Szer, Jeff Zimran, Ari Revel-Vilk, Shoshana |
author_facet | Dinur, Tama Istaiti, Majdolen Frydman, Dafna Becker-Cohen, Michal Szer, Jeff Zimran, Ari Revel-Vilk, Shoshana |
author_sort | Dinur, Tama |
collection | PubMed |
description | BACKGROUND: It is now acknowledged that the input of patients in health outcome assessment is vital to understanding the impact of diseases and interventions for those diseases. This study is the first report of patient-reported outcome measures (PROM) in a large cohort of patients with type 1 Gaucher disease (GD1) enabling us to study predictors of the reported outcomes. METHOD: The PROM was sent via a mobile phone survey to 405 adult patients with GD1. Demographics, clinical data, and treatment status were extracted from clinic charts. Age, sex, severity score index (SSI) at presentation and treatment status were used as variables to assess outcomes. RESULTS: A total of 192 patients with GD1 (111 females) responded (47.4% response rate), of whom 124 (64.5%) had received GD1-specific therapy. Around 40% of patients reported that GD had restricted their education/job and fun activities and were concerned about being emotional and financial burdens on others. Concerns regarding the risk of bone disease and Parkinson disease were also high (60%). The severity of GD1 (reflected by the need for GD1-specific therapy and a high SSI) was associated with GD1-related restrictions and concerns, fatigue, physical weakness, bone pain, and worry regarding the future. CONCLUSIONS: The use of GD1 specific PROM highlights personal problems that are not captured by traditional outcome parameters and that need to be addressed to improve health-related quality of life. Validated PROM should be included among the outcome measures in clinical practice and future prospective studies for patients with chronic and rare diseases. |
format | Online Article Text |
id | pubmed-7556970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75569702020-10-15 Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease Dinur, Tama Istaiti, Majdolen Frydman, Dafna Becker-Cohen, Michal Szer, Jeff Zimran, Ari Revel-Vilk, Shoshana Orphanet J Rare Dis Research BACKGROUND: It is now acknowledged that the input of patients in health outcome assessment is vital to understanding the impact of diseases and interventions for those diseases. This study is the first report of patient-reported outcome measures (PROM) in a large cohort of patients with type 1 Gaucher disease (GD1) enabling us to study predictors of the reported outcomes. METHOD: The PROM was sent via a mobile phone survey to 405 adult patients with GD1. Demographics, clinical data, and treatment status were extracted from clinic charts. Age, sex, severity score index (SSI) at presentation and treatment status were used as variables to assess outcomes. RESULTS: A total of 192 patients with GD1 (111 females) responded (47.4% response rate), of whom 124 (64.5%) had received GD1-specific therapy. Around 40% of patients reported that GD had restricted their education/job and fun activities and were concerned about being emotional and financial burdens on others. Concerns regarding the risk of bone disease and Parkinson disease were also high (60%). The severity of GD1 (reflected by the need for GD1-specific therapy and a high SSI) was associated with GD1-related restrictions and concerns, fatigue, physical weakness, bone pain, and worry regarding the future. CONCLUSIONS: The use of GD1 specific PROM highlights personal problems that are not captured by traditional outcome parameters and that need to be addressed to improve health-related quality of life. Validated PROM should be included among the outcome measures in clinical practice and future prospective studies for patients with chronic and rare diseases. BioMed Central 2020-10-13 /pmc/articles/PMC7556970/ /pubmed/33050940 http://dx.doi.org/10.1186/s13023-020-01544-z Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Dinur, Tama Istaiti, Majdolen Frydman, Dafna Becker-Cohen, Michal Szer, Jeff Zimran, Ari Revel-Vilk, Shoshana Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease |
title | Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease |
title_full | Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease |
title_fullStr | Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease |
title_full_unstemmed | Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease |
title_short | Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease |
title_sort | patient reported outcome measures in a large cohort of patients with type 1 gaucher disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556970/ https://www.ncbi.nlm.nih.gov/pubmed/33050940 http://dx.doi.org/10.1186/s13023-020-01544-z |
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