Evidence map›Paper›PMID 36282970›Full record

ArticleDevelopmental medicine and child neurology2023

Development of social functioning in children with cerebral palsy: A longitudinal study.

Andrea Burgess, Leanne Sakzewski, Koa Whittingham, Jane Wotherspoon, Mark D Chatfield, Robert S Ware, Roslyn N Boyd

Abstract read
In one paragraph

Article in Developmental medicine and child neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Trial
  2. Therapeutic Effects of Metaverse Rehabilitation for Cerebral Palsy: A Randomized Controlled Trial.International journal of environmental research and public health · 2023
    Trial
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Andrea BurgessThe University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, Faculty of Medicine, Brisbane, Australia.ORCID 0000-0001-8697-5156
Leanne SakzewskiThe University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, Faculty of Medicine, Brisbane, Australia.ORCID 0000-0001-5395-544X
Koa WhittinghamThe University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, Faculty of Medicine, Brisbane, Australia.ORCID 0000-0002-5344-9907
Jane WotherspoonThe University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, Faculty of Medicine, Brisbane, Australia.ORCID 0000-0002-6893-7196
Mark D ChatfieldThe University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, Faculty of Medicine, Brisbane, Australia.
Robert S WareGriffith University, Menzies Health Institute Queensland, Brisbane, Australia.
Roslyn N BoydThe University of Queensland, Queensland Cerebral Palsy and Rehabilitation Research Centre, Child Health Research Centre, Faculty of Medicine, Brisbane, Australia.ORCID 0000-0002-4919-5975

Funding

National Health and Medical Research Council 1037220National Health and Medical Research Council 1077257National Health and Medical Research Council 1160694National Health and Medical Research Council 465128
6 · The paper itself

Abstract

aimTo describe the development of social function in children with cerebral palsy (CP) classified in all levels of the Communication Function Classification System (CFCS).

methodThis prospective, longitudinal population-based cohort study recruited children with CP born in Queensland, Australia. Social functioning was measured using the Pediatric Evaluation of Disability Inventory (PEDI) social function domain at 2 years, 2 years 6 months, 3 years, 4 years, and 5 years, and the PEDI Computer Adaptive Test (PEDI-CAT) social/cognitive domain at 8 to 12 years.

resultsSeventy-four children provided 356 observations. PEDI-CAT social/cognitive scaled scores at 8 to 12 years were (mean [SD] n) CFCS level I, 68.6 (2.7) 45; CFCS level II, 64.0 (3.4) 10; CFCS level III, 63.5 (3.7) 4; CFCS level IV, 56.8 (5.0) 9; CFCS level V, 47.2 (5.8) 6. Scores within expected range for age (not less than 2 SD below mean) at 8 to 12 years were achieved by 35 (78%) children in CFCS level I and four (14%) in CFCS levels II to V. Forty-nine per cent of children scored at least two standard deviations below the population mean on a proxy measure of fluid intelligence. Intellectual impairment was associated with lower PEDI-CAT social/cognitive scaled scores in univariable analysis (β = -8.3, 95% confidence interval - 10.91 to -5.63; p < 0.001) but had a smaller effect when modelled together with CFCS.

interpretationSocial function attained by 8 to 12 years of age was strongly related to level of communication function (CFCS). The small number of children classified in CFCS levels II to V necessitates caution when viewing these individual CFCS level trajectories. WHAT THIS PAPER ADDS: There is a strong relation between social functioning and Communication Function Classification System (CFCS) levels. At 8 to 12 years, 35 out of 45 children in CFCS level I met social functioning age expectations. Twenty-five out of 29 in CFCS levels II to V had social functioning below that expected for age. CFCS and age were more strongly associated with development of social functioning than Gross Motor Function Classification System or Manual Ability Classification System and age.

Indexed as

Cerebral PalsyChildCohort StudiesDisability EvaluationHumansLongitudinal StudiesProspective StudiesSocial Interaction

Identifiers

PMID36282970
PMCPMC10953437

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LicenceCC BY-NC-ND
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Registered trials

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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.