Evidence map›Paper›PMID 32122377›Full record

ReviewJournal of foot and ankle research2020

Walking and weakness in children: a narrative review of gait and functional ambulation in paediatric neuromuscular disease.

Rachel A Kennedy, Kate Carroll, Jennifer L McGinley, Kade L Paterson

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Journal of foot and ankle research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06666816 (Observational Study for the Identification of Fatigue and Gait Biomarkers in Populations With Neuromuscular Pathologies in the Clinical Context and Daily Life), which is not on this map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06666816 recruitingnot on this map

Observational Study for the Identification of Fatigue and Gait Biomarkers in Populations With Neuromuscular Pathologies in the Clinical Context and Daily Life

TypeobservationalSponsorIRCCS Eugenio MedeaRan2017 to 2026Enrolled120ConditionsMuscular Dystrophies, Myopathies, Spinal Muscular Atrophy (SMA), Charcot Marie Tooth DiseaseArmsinapplicable
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Rachel A KennedyDepartment of Neurology, The Royal Children's Hospital, Parkville, Vic, Australia. rachel.kennedy@rch.org.au.ORCID http://orcid.org/0000-0003-1805-6937
Kate CarrollDepartment of Neurology, The Royal Children's Hospital, Parkville, Vic, Australia.
Jennifer L McGinleyMurdoch Children's Research Institute, Parkville, Vic, Australia.
Kade L PatersonDepartment of Physiotherapy, The University of Melbourne, Parkville, Vic, Australia.
Royal Children's Hospital · AUThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWeakness is the primary impairment in paediatric neuromuscular diseases, impacting gait and gait-related functional activities in ambulant children affected by these rare and often degenerative diseases. Gait speed is an indicator of health and disability, yet gait is a complex, multi-faceted activity. Using the International Classification of Function, Health and Disability (ICF) model, assessment of gait and functional ambulation should consider the impairments, activity limitations and participation restrictions due to disease, and factors related to the environment and the individual person.

methodsThis narrative review involved a literature search of databases including Medline, Embase and Pubmed from 1946 to October 2019. Inclusion criteria included assessments of gait, endurance and ambulatory function in paediatric (0-18 years) neuromuscular diseases.

resultsFifty-two papers were identified reporting assessments of gait speed, timed function, endurance and ambulatory capacity, gait-related balance and qualitative descriptive assessments of gait function and effect of disease on gait and gait-related activities. Gait speed is an indicator of disability and children with neuromuscular disease walk slower than typically developing peers. Increasing disease severity and age were associated with slower walking in children with Duchenne muscular dystrophy and Charcot-Marie-Tooth disease. The six-minute walk test is used widely as a test of endurance and ambulatory capacity; six-minute walk distance was substantially reduced across all paediatric neuromuscular diseases. Endurance and ambulatory capacity was more limited in children with spinal muscular atrophy type 3, congenital muscular dystrophy and older boys with Duchenne muscular dystrophy. Only a few papers considered normalisation of gait parameters accounting for the effect on gait of height in heterogeneous groups of children and linear growth in longitudinal studies. Balance related to gait was considered in five papers, mainly in children with Charcot-Marie-Tooth disease. There was limited investigation of factors including distance requirements and terrain in children's typical environments and personal factors related to self-perception of disease effect on gait and gait-related function.

conclusionAssessments of gait and functional ambulation are important considerations in documenting disease progression and treatment efficacy in the clinical setting; and in clinical trials of disease-modifying agents and physiotherapeutic interventions in paediatric neuromuscular diseases. There is a need for expert consensus on core gait and functional ambulation assessments for use in clinical and research settings.

Indexed as

Mobility LimitationWalkingAdolescentCharcot-Marie-Tooth DiseaseChildChild, PreschoolDisease ProgressionFemaleGait AnalysisGait Disorders, NeurologicHumansInfantInfant, NewbornInternational Classification of Functioning, Disability and HealthMaleMuscular Dystrophy, DuchenneAssessmentCharcot-Marie-tooth diseaseDuchenne muscular dystrophyFunctional ambulationGaitMyopathyNeuromuscular diseasePaediatricSpinal muscular atrophyWeakness

Identifiers

PMID32122377
PMCPMC7052968
OpenAlexW3011289173

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.