Literature DB >> 28326571

Family-centred service: differences in what parents of children with cerebral palsy rate important.

M Terwiel1, M W Alsem1,2, R C Siebes1, K Bieleman1,3, M Verhoef1,4, M Ketelaar1.   

Abstract

BACKGROUND: A family-centred approach to services of children with disabilities is widely accepted as the foundational approach to service delivery in paediatric health care. The 56 items of the Measure of Processes of Care questionnaire (MPOC-56) all reflect elements of family-centred service. In this study, we investigated which elements of family-centred service are rated important by parents of children with cerebral palsy by adding a question on importance to each item of the MPOC-56 (MPOC-56-I).
METHODS: In total, 175 parents of children with cerebral palsy completed the MPOC-56-I. For each MPOC item, parents were asked to rate the importance on a 5-point scale ranging from 0 (not important at all) up to and including 4 (very important). We used Spearman's rank correlation coefficient to further explore the variation in parents' importance ratings.
RESULTS: Parents' importance ratings of the MPOC-56 items varied. The percentage of parents rating an item important (importance rating 3 or 4) varied between 43.8% and 96.8%. The percentage of parents rating an item unimportant (rating 0 or 1) varied between 0.0% and 20.3%, and the percentage of parents rating an item neutral (rating 2) varied between 3.0% and 36.0%. Most diverse importance ratings were found for five items concerning the provision of general information. Three correlations between these items and child and parent characteristics were found. Six items were rated important by almost all (≥95%) parents. These items concern elements of specific information about the child, co-ordinated and comprehensive care for child and family and enabling and partnership.
CONCLUSIONS: Parents rate the importance of family-centred services for their situation in various ways. These findings endorse that family-centred services should recognize the uniqueness of families and should be tailored to what parents find important.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  MPOC-56; cerebral palsy; children; family-centred service; importance ratings; parents

Mesh:

Year:  2017        PMID: 28326571     DOI: 10.1111/cch.12460

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  5 in total

1.  Development of an inventory of goals using the International Classification of Functioning, Disability and Health in a population of non-ambulatory children and adolescents with cerebral palsy treated with botulinum toxin A.

Authors:  Linda Nguyen; Ronit Mesterman; Jan Willem Gorter
Journal:  BMC Pediatr       Date:  2018-01-04       Impact factor: 2.125

2.  Determinants of caregiver satisfaction with child neurodevelopmental assessment in neuropaediatric clinics.

Authors:  Katarina Smejda Kjærandsen; Per Håkan Brøndbo; Marianne Berg Halvorsen
Journal:  BMC Health Serv Res       Date:  2021-02-12       Impact factor: 2.655

3.  Caregivers' Feeding Experiences and Support of Their Child with Cerebral Palsy.

Authors:  Christine Taylor; Ariana C Kong; Jann Foster; Nadia Badawi; Iona Novak
Journal:  J Child Fam Stud       Date:  2021-10-04

4.  Play-based groups for children with cerebral palsy and their parents: A qualitative interview study about the impact on mothers' well-being.

Authors:  Kirsten R Prest; Aleksandra J Borek; Anne-Marie R Boylan
Journal:  Child Care Health Dev       Date:  2022-02-01       Impact factor: 2.943

Review 5.  Coaching approaches in early intervention and paediatric rehabilitation.

Authors:  Schirin Akhbari Ziegler; Mijna Hadders-Algra
Journal:  Dev Med Child Neurol       Date:  2020-02-17       Impact factor: 5.449

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.