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Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan
BACKGROUND: Gaucher disease (GD) is a rare, autosomal recessive lysosomal storage disorder that adversely affects life expectancy and health-related quality of life (HRQOL). Although HRQOL questionnaires are available for type 1 GD, they are not suitable for patients with the neuronopathic types 2 a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295096/ https://www.ncbi.nlm.nih.gov/pubmed/35854314 http://dx.doi.org/10.1186/s13023-022-02429-z |
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author | Koto, Yuta Narita, Aya Noto, Shinichi Ono, Midori Hamada, Anna Lissa Sakai, Norio |
author_facet | Koto, Yuta Narita, Aya Noto, Shinichi Ono, Midori Hamada, Anna Lissa Sakai, Norio |
author_sort | Koto, Yuta |
collection | PubMed |
description | BACKGROUND: Gaucher disease (GD) is a rare, autosomal recessive lysosomal storage disorder that adversely affects life expectancy and health-related quality of life (HRQOL). Although HRQOL questionnaires are available for type 1 GD, they are not suitable for patients with the neuronopathic types 2 and 3 GD who have neurological symptoms that develop during early childhood or adolescence. Here we report the development of a language-validated HRQOL questionnaire specifically for patients with neuronopathic types 2 and 3 GD in Japan, which is the first step toward HRQOL questionnaire provision for all types of GD in the future. METHODS: In February and March 2021, semi-structured interviews were conducted by the authors (supported by qualified interviewers) with patients and/or their caregivers (for patients < 16 years old) who were recruited from a Japanese patient association, the Association of Gaucher Disease Patients in Japan. Qualitative analysis of interview transcripts was used to identify major themes and key topics within those themes. Hierarchical cluster analysis and co-occurrence network analysis were performed to map relationships between commonly occurring words. The study is registered at the UMIN Clinical Trials Registry (https://www.umin.ac.jp/ctr/index.htm [UMIN000042872]). RESULTS: Three main themes emerged from qualitative analysis: treatment status, patient burden, and social support systems. Key topics within each theme included hearing impairment, visual impairment, difficulty swallowing, difficulty speaking, involuntary movement of extremities, epileptic seizures, and body aches (treatment status); anxiety about symptoms, difficulty with exercise and work, anxiety about continuing treatment, anxiety about going out, and tiredness from hospital visit or treatment (patient burden); and dissatisfaction about government service, lack of social support, and information exchange in the patient association (social support systems). Commonly used words and the relationships between words identified through the hierarchical cluster and co-occurrence network analyses supported these themes and topics. CONCLUSIONS: The themes and topics identified in this analysis were specific to patients with types 2 and 3 GD and will be used to inform the development of a HRQOL questionnaire specifically for patients with all GD types. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02429-z. |
format | Online Article Text |
id | pubmed-9295096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92950962022-07-19 Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan Koto, Yuta Narita, Aya Noto, Shinichi Ono, Midori Hamada, Anna Lissa Sakai, Norio Orphanet J Rare Dis Research BACKGROUND: Gaucher disease (GD) is a rare, autosomal recessive lysosomal storage disorder that adversely affects life expectancy and health-related quality of life (HRQOL). Although HRQOL questionnaires are available for type 1 GD, they are not suitable for patients with the neuronopathic types 2 and 3 GD who have neurological symptoms that develop during early childhood or adolescence. Here we report the development of a language-validated HRQOL questionnaire specifically for patients with neuronopathic types 2 and 3 GD in Japan, which is the first step toward HRQOL questionnaire provision for all types of GD in the future. METHODS: In February and March 2021, semi-structured interviews were conducted by the authors (supported by qualified interviewers) with patients and/or their caregivers (for patients < 16 years old) who were recruited from a Japanese patient association, the Association of Gaucher Disease Patients in Japan. Qualitative analysis of interview transcripts was used to identify major themes and key topics within those themes. Hierarchical cluster analysis and co-occurrence network analysis were performed to map relationships between commonly occurring words. The study is registered at the UMIN Clinical Trials Registry (https://www.umin.ac.jp/ctr/index.htm [UMIN000042872]). RESULTS: Three main themes emerged from qualitative analysis: treatment status, patient burden, and social support systems. Key topics within each theme included hearing impairment, visual impairment, difficulty swallowing, difficulty speaking, involuntary movement of extremities, epileptic seizures, and body aches (treatment status); anxiety about symptoms, difficulty with exercise and work, anxiety about continuing treatment, anxiety about going out, and tiredness from hospital visit or treatment (patient burden); and dissatisfaction about government service, lack of social support, and information exchange in the patient association (social support systems). Commonly used words and the relationships between words identified through the hierarchical cluster and co-occurrence network analyses supported these themes and topics. CONCLUSIONS: The themes and topics identified in this analysis were specific to patients with types 2 and 3 GD and will be used to inform the development of a HRQOL questionnaire specifically for patients with all GD types. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02429-z. BioMed Central 2022-07-19 /pmc/articles/PMC9295096/ /pubmed/35854314 http://dx.doi.org/10.1186/s13023-022-02429-z Text en © The Author(s) 2022 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Koto, Yuta Narita, Aya Noto, Shinichi Ono, Midori Hamada, Anna Lissa Sakai, Norio Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan |
title | Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan |
title_full | Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan |
title_fullStr | Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan |
title_full_unstemmed | Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan |
title_short | Qualitative analysis of patient interviews on the burden of neuronopathic Gaucher disease in Japan |
title_sort | qualitative analysis of patient interviews on the burden of neuronopathic gaucher disease in japan |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295096/ https://www.ncbi.nlm.nih.gov/pubmed/35854314 http://dx.doi.org/10.1186/s13023-022-02429-z |
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