Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments

Abstract Duchenne muscular dystrophy (DMD) is an inherited X-linked neuromuscular disorder. A number of questionnaires are available to assess quality of life in DMD, but there are concerns about their validity. This systematic review aimed to appraise critically the content and structural validity...

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Main Authors: Philip A. Powell, Jill Carlton, Helen Buckley Woods, Paolo Mazzone
Format: Article
Language:English
Published: BMC 2020-08-01
Series:Health and Quality of Life Outcomes
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12955-020-01511-z
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spelling doaj-f6b585a0e0bc4897a499114e1ce485d12020-11-25T02:58:14ZengBMCHealth and Quality of Life Outcomes1477-75252020-08-0118112610.1186/s12955-020-01511-zMeasuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instrumentsPhilip A. Powell0Jill Carlton1Helen Buckley Woods2Paolo Mazzone3School of Health and Related Research, University of SheffieldSchool of Health and Related Research, University of SheffieldSchool of Health and Related Research, University of SheffieldSchool of Health and Related Research, University of SheffieldAbstract Duchenne muscular dystrophy (DMD) is an inherited X-linked neuromuscular disorder. A number of questionnaires are available to assess quality of life in DMD, but there are concerns about their validity. This systematic review aimed to appraise critically the content and structural validity of quality of life instruments for DMD. Five databases (EMBASE, MEDLINE, CINAHL, PsycINFO, and Cochrane Library) were searched, with supplementary searches in Google Scholar. We included articles with evidence on the content and/or structural validity of quality of life instruments in DMD, and/or instrument development. Evidence was evaluated against the Consensus-based Standards for the selection of health Measurement INstruments (COSMIN) criteria. Fifty five articles featured a questionnaire assessing quality of life in DMD. Forty instruments were extracted and 26 underwent assessment. Forty-one articles contained evidence on content or structural validity (including 37 development papers). Most instruments demonstrated low quality evidence and unsatisfactory or inconsistent validity in DMD, with the majority not featuring direct validation studies in this population. Only KIDSCREEN received an adequate rating for instrument design and a satisfactory result for content validity based on its development, yet, like the majority of PROMs, the measure has not been directly validated for use in DMD. Further research is needed on the validity of quality of life instruments in DMD, including content and structural validity studies in this population.http://link.springer.com/article/10.1186/s12955-020-01511-zContent validityDuchenne muscular dystrophyPatient reported outcome measuresQuality of lifeStructural validity
collection DOAJ
language English
format Article
sources DOAJ
author Philip A. Powell
Jill Carlton
Helen Buckley Woods
Paolo Mazzone
spellingShingle Philip A. Powell
Jill Carlton
Helen Buckley Woods
Paolo Mazzone
Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
Health and Quality of Life Outcomes
Content validity
Duchenne muscular dystrophy
Patient reported outcome measures
Quality of life
Structural validity
author_facet Philip A. Powell
Jill Carlton
Helen Buckley Woods
Paolo Mazzone
author_sort Philip A. Powell
title Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
title_short Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
title_full Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
title_fullStr Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
title_full_unstemmed Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
title_sort measuring quality of life in duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments
publisher BMC
series Health and Quality of Life Outcomes
issn 1477-7525
publishDate 2020-08-01
description Abstract Duchenne muscular dystrophy (DMD) is an inherited X-linked neuromuscular disorder. A number of questionnaires are available to assess quality of life in DMD, but there are concerns about their validity. This systematic review aimed to appraise critically the content and structural validity of quality of life instruments for DMD. Five databases (EMBASE, MEDLINE, CINAHL, PsycINFO, and Cochrane Library) were searched, with supplementary searches in Google Scholar. We included articles with evidence on the content and/or structural validity of quality of life instruments in DMD, and/or instrument development. Evidence was evaluated against the Consensus-based Standards for the selection of health Measurement INstruments (COSMIN) criteria. Fifty five articles featured a questionnaire assessing quality of life in DMD. Forty instruments were extracted and 26 underwent assessment. Forty-one articles contained evidence on content or structural validity (including 37 development papers). Most instruments demonstrated low quality evidence and unsatisfactory or inconsistent validity in DMD, with the majority not featuring direct validation studies in this population. Only KIDSCREEN received an adequate rating for instrument design and a satisfactory result for content validity based on its development, yet, like the majority of PROMs, the measure has not been directly validated for use in DMD. Further research is needed on the validity of quality of life instruments in DMD, including content and structural validity studies in this population.
topic Content validity
Duchenne muscular dystrophy
Patient reported outcome measures
Quality of life
Structural validity
url http://link.springer.com/article/10.1186/s12955-020-01511-z
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