Literature DB >> 33155788

Family-centeredness of services for young children with Down syndrome: an observational study from Turkey

Emine Bahar Bingöler Pekcici1, Ezgi Özalp Akin1, Funda Akpinar1, Gamze Hayran1, Cansu Keleş1, Betül Yağbasan1, Nazmiye Kurşun2, İlgi Ertem1.   

Abstract

Background/aim: Physicians require information on the family centeredness of services for children with Down syndrome, one of the most frequently encountered disabilities in childhood. We aimed to determine the family-centeredness of services for young children with Down syndrome and using a bioecological theory framework we hypothesized that child, family and service-related factors would be associated with such services. Materials and methods: In a crosssectional design, children with Down syndrome seen at Ankara University Developmental Pediatrics Division (AUDPD) between February 2020 and June 2020 were included if they had received services in the community for at least 12 months. Mothers responded to the measure of process of care-20 (MPOC-20) used to measure family centeredness.
Results: All 65 eligible children were included; 57% were boys and median age was 25.0 (IQR: 18.5–38.0) months. The MPOC-20 subscale scores were highest for the “respectful and supportive care (RSC)” (median 6.0; IQR: 4.8–6.8) and lowest for the “providing specific information” (median 3.0; IQR: 4.4–6.5) subscales. On univariate analyses, maternal education <high school was associated with scores ≤4 on the RSC (OR = 6.75; 95%CI = 1.77–25.64) and “enabling and partnership” subscales (OR = 3.10; 95%CI = 1.06–9.05); income ≤ minimum wage (OR=3.94; 95%CI=1.10-14.02) was associated with scores ≤4 on the RSC. In the multivariate logistic regression model, maternal education ≤ high school was independently associated with RSC scores ≤4 (OR = 5.13; 95%CI = 1.26–20.84).
Conclusion: Our findings imply that limitations in family-centeredness of community service for young children with Down syndrome. Deficiencies of services particularly for children with less educated mothers need to be urgently resolved. This work is licensed under a Creative Commons Attribution 4.0 International License.

Entities:  

Keywords:  Down syndrome; children with special needs; disability; family-centered care; children with special needs; measure of process of care (MPOC)

Year:  2021        PMID: 33155788      PMCID: PMC7991864          DOI: 10.3906/sag-2009-76

Source DB:  PubMed          Journal:  Turk J Med Sci        ISSN: 1300-0144            Impact factor:   0.973


  33 in total

1.  Development of a measure of family-centred care for resource-poor South African settings: the experience of using a modified version of the MPOC-20.

Authors:  G M Saloojee; P R Rosenbaum; M S Westaway; A V Stewart
Journal:  Child Care Health Dev       Date:  2008-12-03       Impact factor: 2.508

Review 2.  Parents' Perception of Receiving Family-Centered Care for Their Children with Physical Disabilities: A Meta-Analysis.

Authors:  Nihad A Almasri; Mihee An; Robert J Palisano
Journal:  Phys Occup Ther Pediatr       Date:  2017-07-28       Impact factor: 2.360

3.  Parent perspectives on rehabilitation services for their children with disabilities: a mixed methods approach.

Authors:  Joseph Schreiber; Jennifer Benger; Joyce Salls; Gregory Marchetti; Lindsey Reed
Journal:  Phys Occup Ther Pediatr       Date:  2011-04-13       Impact factor: 2.360

4.  Brazilian versions of the Measure of Processes of Care-20 and Measure of Processes of Care-Service Providers: translation, cross-cultural adaptation and reliability.

Authors:  Ana Amélia Moraes Antunes; Sheyla Rossana Cavalcanti Furtado; Lívia de Castro Magalhães; Renata Noce Kirkwood; Daniela Virginia Vaz
Journal:  Braz J Phys Ther       Date:  2019-02-27       Impact factor: 3.377

5.  Evaluation of family-centred practices in the early intervention programmes for infants and young children in Singapore with Measure of Processes of Care for Service Providers and Measure of Beliefs about Participation in Family-Centred Service.

Authors:  H N Tang; W H Chong; W Goh; W P Chan; S Choo
Journal:  Child Care Health Dev       Date:  2011-06-13       Impact factor: 2.508

6.  Social support for diabetes illness management: supporting adolescents and caregivers.

Authors:  April Idalski Carcone; Deborah A Ellis; Arlene Weisz; Sylvie Naar-King
Journal:  J Dev Behav Pediatr       Date:  2011-10       Impact factor: 2.225

Review 7.  Evidence for family-centered care for children with special health care needs: a systematic review.

Authors:  Karen A Kuhlthau; Sheila Bloom; Jeanne Van Cleave; Alixandra A Knapp; Diane Romm; Kirsten Klatka; Charles J Homer; Paul W Newacheck; James M Perrin
Journal:  Acad Pediatr       Date:  2011 Mar-Apr       Impact factor: 3.107

8.  Evaluation of family-centred services from parents of Chinese children with cerebral palsy with the Measure of Processes of Care.

Authors:  M Wang; M A Petrini; Q Guan
Journal:  Child Care Health Dev       Date:  2014-07-31       Impact factor: 2.508

9.  Parental evaluation of processes of care in relation to the child, parent and family characteristics.

Authors:  Katja Groleger Sršen; Gaj Vidmar; Gregor Sočan; Anton Zupan
Journal:  Int J Rehabil Res       Date:  2014-09       Impact factor: 1.479

10.  Services and supports for young children with Down syndrome: parent and provider perspectives.

Authors:  J Marshall; J P Tanner; Y A Kozyr; R S Kirby
Journal:  Child Care Health Dev       Date:  2014-06-10       Impact factor: 2.508

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.