Outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review

Abstract Background Generalised joint hypermobility (GJH) is highly prevalent among children and associated with symptoms in a fifth with the condition. This study aimed to synthesise outcome measures in interventional or prospective longitudinal studies of children with GJH and associated lower lim...

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Autores principales: Muhammad Maarj, Andrea Coda, Louise Tofts, Cylie Williams, Derek Santos, Verity Pacey
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Lenguaje:EN
Publicado: BMC 2021
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spelling oai:doaj.org-article:bbababe115d344ad8ff772ac73cbf9d62021-12-05T12:21:12ZOutcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review10.1186/s12887-021-03009-z1471-2431https://doaj.org/article/bbababe115d344ad8ff772ac73cbf9d62021-11-01T00:00:00Zhttps://doi.org/10.1186/s12887-021-03009-zhttps://doaj.org/toc/1471-2431Abstract Background Generalised joint hypermobility (GJH) is highly prevalent among children and associated with symptoms in a fifth with the condition. This study aimed to synthesise outcome measures in interventional or prospective longitudinal studies of children with GJH and associated lower limb symptoms. Methods Electronic searches of Medline, CINAHL and Embase databases from inception to 16th March 2020 were performed for studies of children with GJH and symptoms between 5 and 18 years reporting repeated outcome measures collected at least 4 weeks apart. Methodological quality of eligible studies were described using the Downs and Black checklist. Results Six studies comprising of five interventional, and one prospective observational study (total of 388 children) met the inclusion criteria. Interventional study durations were between 2 and 3 months, with up to 10 months post-intervention follow-up, while the observational study spanned 3 years. Three main constructs of pain, function and quality of life were reported as primary outcome measures using 20 different instruments. All but one measure was validated in paediatric populations, but not specifically for children with GJH and symptoms. One study assessed fatigue, reporting disabling fatigue to be associated with higher pain intensity. Conclusions There were no agreed sets of outcome measures used for children with GJH and symptoms. The standardisation of assessment tools across paediatric clinical trials is needed. Four constructs of pain, function, quality of life and fatigue are recommended to be included with agreed upon, validated, objective tools.Muhammad MaarjAndrea CodaLouise ToftsCylie WilliamsDerek SantosVerity PaceyBMCarticleFatigueOutcome measuresPaediatricsHypermobilityPainFunctionPediatricsRJ1-570ENBMC Pediatrics, Vol 21, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Fatigue
Outcome measures
Paediatrics
Hypermobility
Pain
Function
Pediatrics
RJ1-570
spellingShingle Fatigue
Outcome measures
Paediatrics
Hypermobility
Pain
Function
Pediatrics
RJ1-570
Muhammad Maarj
Andrea Coda
Louise Tofts
Cylie Williams
Derek Santos
Verity Pacey
Outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review
description Abstract Background Generalised joint hypermobility (GJH) is highly prevalent among children and associated with symptoms in a fifth with the condition. This study aimed to synthesise outcome measures in interventional or prospective longitudinal studies of children with GJH and associated lower limb symptoms. Methods Electronic searches of Medline, CINAHL and Embase databases from inception to 16th March 2020 were performed for studies of children with GJH and symptoms between 5 and 18 years reporting repeated outcome measures collected at least 4 weeks apart. Methodological quality of eligible studies were described using the Downs and Black checklist. Results Six studies comprising of five interventional, and one prospective observational study (total of 388 children) met the inclusion criteria. Interventional study durations were between 2 and 3 months, with up to 10 months post-intervention follow-up, while the observational study spanned 3 years. Three main constructs of pain, function and quality of life were reported as primary outcome measures using 20 different instruments. All but one measure was validated in paediatric populations, but not specifically for children with GJH and symptoms. One study assessed fatigue, reporting disabling fatigue to be associated with higher pain intensity. Conclusions There were no agreed sets of outcome measures used for children with GJH and symptoms. The standardisation of assessment tools across paediatric clinical trials is needed. Four constructs of pain, function, quality of life and fatigue are recommended to be included with agreed upon, validated, objective tools.
format article
author Muhammad Maarj
Andrea Coda
Louise Tofts
Cylie Williams
Derek Santos
Verity Pacey
author_facet Muhammad Maarj
Andrea Coda
Louise Tofts
Cylie Williams
Derek Santos
Verity Pacey
author_sort Muhammad Maarj
title Outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review
title_short Outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review
title_full Outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review
title_fullStr Outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review
title_full_unstemmed Outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review
title_sort outcome measures for assessing change over time in studies of symptomatic children with hypermobility: a systematic review
publisher BMC
publishDate 2021
url https://doaj.org/article/bbababe115d344ad8ff772ac73cbf9d6
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