Cargando…
Measuring carer quality of life in Duchenne muscular dystrophy: a systematic review of the reliability and validity of self-report instruments using COSMIN
INTRODUCTION: Duchenne muscular dystrophy is a rare, progressive, life-limiting genetic neuromuscular condition that significantly impacts the quality of life of informal caregivers. Carer quality of life is measured using heterogeneous self-report scales, yet their suitability for Duchenne remains...
Autores principales: | Carlton, Jill, Powell, Philip A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977045/ https://www.ncbi.nlm.nih.gov/pubmed/35366897 http://dx.doi.org/10.1186/s12955-022-01964-4 |
Ejemplares similares
-
A review of quality of life themes in Duchenne muscular dystrophy for patients and carers
por: Uttley, Lesley, et al.
Publicado: (2018) -
Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
por: Powell, Philip A., et al.
Publicado: (2020) -
A comprehensive qualitative framework for health-related quality of life in Duchenne muscular dystrophy
por: Powell, Philip A., et al.
Publicado: (2022) -
Producing a preference-based quality of life measure for people with Duchenne muscular dystrophy: a mixed-methods study protocol
por: Powell, Philip A, et al.
Publicado: (2019) -
Reliability and validity of the Thai version of the Pediatric Quality of Life inventory™ 3.0 Duchenne Muscular Dystrophy module in Thai children with Duchenne Muscular Dystrophy
por: Thongsing, Apirada, et al.
Publicado: (2019)