Literature DB >> 18754901

Parent and professional reports of the quality of life of children with cerebral palsy and associated intellectual impairment.

Melanie White-Koning1, Hélène Grandjean, Allan Colver, Catherine Arnaud.   

Abstract

To examine parent-professional agreement in proxy-reports of child quality of life (QoL) and the factors associated with low child QoL in children with cerebral palsy (CP) and associated intellectual impairment. Professional (teacher, therapist, or residential carer) and parent reports of QoL for 204 children (127 males, 77 females, mean age 10 y 4 mo [SD 1y 6mo]; range 8-12 y) with CP and IQ<or=70 were obtained in 2004 to 2005 in nine European regions, using the KIDSCREEN questionnaire. Parent-professional agreement was studied using correlation and mean differences; multilevel logistic regression was used to determine factors influencing QoL reports and agreement. The mean parent-reported scores of child QoL were significantly higher than the professional reports in the Psychological well-being domain and significantly lower for Social support. The average frequency of disagreement (parent-professional difference >0.5SD of scores) over all domains was 62%. High levels of stress in parenting negatively influenced parent reports of child QoL compared with professional reports, while child pain was associated with professionals rating lower than parents. Proxies do not always agree when reporting the QoL of children with severe disabilities. Parental well-being and child pain should be taken into account in the interpretation of QoL reports in such children.

Entities:  

Mesh:

Year:  2008        PMID: 18754901     DOI: 10.1111/j.1469-8749.2008.03026.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  16 in total

1.  Impact of Symptoms of Maternal Anxiety and Depression on Quality of Life of Children with Cerebral Palsy.

Authors:  Serhat Türkoğlu; Ayhan Bilgiç; Gözde Türkoğlu; Savaş Yilmaz
Journal:  Noro Psikiyatr Ars       Date:  2016-03-01       Impact factor: 1.339

2.  The effect of parental mental health on proxy reports of health-related quality of life in children with sickle cell disease.

Authors:  Julie A Panepinto; Raymond G Hoffmann; Nicholas M Pajewski
Journal:  Pediatr Blood Cancer       Date:  2010-10       Impact factor: 3.167

3.  The Quality of Life for Children with Autism Spectrum Disorder Scale: Factor Analysis, MIMIC Modeling, and Cut-Off Score Analysis.

Authors:  Laura C Chezan; Jin Liu; Erik Drasgow; Ruyi Ding; Alexandro Magana
Journal:  J Autism Dev Disord       Date:  2022-06-03

4.  Family quality of life: perceptions of parents of children with developmental disabilities in Bosnia and Herzegovina.

Authors:  Alma Dizdarevic; Haris Memisevic; Armin Osmanovic; Amila Mujezinovic
Journal:  Int J Dev Disabil       Date:  2020-04-23

5.  Quality of life related to clinical features in patients with Rett syndrome and their parents: a systematic review.

Authors:  Silvia Corchón; Irene Carrillo-López; Omar Cauli
Journal:  Metab Brain Dis       Date:  2018-09-16       Impact factor: 3.584

6.  A Psychometric Evaluation of the Quality of Life for Children with Autism Spectrum Disorder Scale.

Authors:  Laura C Chezan; Jin Liu; Judith M Cholewicki; Erik Drasgow; Ruyi Ding; Adam Warman
Journal:  J Autism Dev Disord       Date:  2021-05-07

7.  The proxy problem anatomized: child-parent disagreement in health related quality of life reports of chronically ill adolescents.

Authors:  Jane N T Sattoe; AnneLoes van Staa; Henriëtte A Moll
Journal:  Health Qual Life Outcomes       Date:  2012-01-25       Impact factor: 3.186

8.  Pain, motor function and health-related quality of life in children with cerebral palsy as reported by their physiotherapists.

Authors:  Marta Badia; Inmaculada Riquelme; Begoña Orgaz; Raquel Acevedo; Egmar Longo; Pedro Montoya
Journal:  BMC Pediatr       Date:  2014-07-27       Impact factor: 2.125

9.  Determinants of participation and quality of life of young adults with cerebral palsy: longitudinal approach and comparison with the general population - SPARCLE 3 study protocol.

Authors:  Catherine Arnaud; Carine Duffaut; Jérôme Fauconnier; Silke Schmidt; Kate Himmelmann; Marco Marcelli; Lindsay Pennington; Joaquim Alvarelhão; Chirine Cytera; Marion Rapp; Virginie Ehlinger; Ute Thyen
Journal:  BMC Neurol       Date:  2021-06-30       Impact factor: 2.474

10.  Caregiver-reported health-related quality of life of children with cerebral palsy and their families and its association with gross motor function: A South Indian study.

Authors:  S Surender; Vykuntaraju K Gowda; K S Sanjay; G V Basavaraja; Naveen Benakappa; Asha Benakappa
Journal:  J Neurosci Rural Pract       Date:  2016 Apr-Jun
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