Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3571
Title: Longitudinal Study of Oropharyngeal Dysphagia in Preschool Children with Cerebral Palsy Presented as a poster to the American Academy of Cerebral Palsy and Developmental Medicine, October 21-24, 2015, Austin, TX
Authors: Benfer, K. A.
Ware, R. S.
Bell, K. L.
Weir, K. A.
Boyd, R. N.
Davies, P. S.
Issue Date: 2016
Source: 97, (4), 2016, p. 552-560
Pages: 552-560
Journal: Archives of Physical Medicine and Rehabilitation
Abstract: Objectives To determine changes in prevalence and severity of oropharyngeal dysphagia (OPD) in children with cerebral palsy (CP) and the relationship to health outcomes. Design Longitudinal cohort study. Setting Community and tertiary institutions. Participants Children (N=53, 33 boys) with a confirmed diagnosis of CP assessed first at 18 to 24 months (Assessment 1: mean age ± SD, 22.9±2.9mo corrected age; Gross Motor Function Classification System [GMFCS]: I, n=22; II, n=7; III, n=11; IV, n=5; V, n=8) and at 36 months (Assessment 2). Interventions Not applicable. Main Outcome Measures OPD was classified using the Dysphagia Disorders Survey (DDS) and signs suggestive of pharyngeal dysphagia. Nutritional status was measured using Z scores for weight, height, and body mass index (BMI). Gross motor skills were classified on GMFCS and motor type/distribution. Results Prevalence of OPD decreased from 62% to 59% between the ages of 18 to 24 months and 36 months. Thirty percent of children had an improvement in severity of OPD (greater than smallest detectable change), and 4% had worse OPD. Gross motor function was strongly associated with OPD at both assessments, on the DDS (Assessment 1: odds ratio [OR]=20.3, P=.011; Assessment 2: OR=28.9, P=.002), pharyngeal signs (Assessment 1: OR=10.6, P=.007; Assessment 2: OR=15.8, P=.003), and OPD severity (Assessment 1: β=6.1, P<.001; Assessment 2: β=5.5, P<.001). OPD at 18 to 24 months was related to health outcomes at 36 months: low Z scores for weight (adjusted β=1.2, P=.03) and BMI (adjusted β=1.1, P=.048), and increased parent stress (adjusted OR=1.1, P=.049). Conclusions Classification and severity of OPD remained relatively stable between 18 to 24 months and 36 months. Gross motor function was the best predictor of OPD. These findings contribute to developing more effective screening processes that consider critical developmental transitions that are anticipated to present challenges for children from each of the GMFCS levels.L6081077052016-02-10
2016-05-19
DOI: 10.1016/j.apmr.2015.11.016
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L608107705&from=exporthttp://dx.doi.org/10.1016/j.apmr.2015.11.016 |
Keywords: childhood disease;clinical assessment;cohort analysis;disease severity;dysphagia;female;Gross Motor Function Classification System;human;longitudinal study;major clinical study;male;body mass;nutritional status;oropharyngeal dysphagia;outcome assessment;parental stress;preschool child;prevalence;articlebody height;motor performance;body weight;cerebral palsy;child
Type: Article
Appears in Sites:Children's Health Queensland Publications

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