Literature DB >> 24417936

Factors related to the impact of chronically disabled children on their families.

Ibrahim Engin Simşek1, Suat Erel2, Tülay Tarsuslu Simşek3, Songül Atasavun Uysal4, Hilal Yakut5, Yavuz Yakut4, Fatma Uygur4.   

Abstract

BACKGROUND: This study to investigated the effects of chronically disabled children (CDC) on their families.
METHOD: The study included 655 CDD and their families from 45 cities located in Turkey representing the seven regions of the country. Sociodemographic characteristics, presence of mental retardation, primary care-giver, presence of social insurance, the number of other children and other family members living in the family, duration of the disorder, disabling conditions in the other children, time spent for care giving, and level of income were recorded. WeeFIM (Functional Independence for Children) and Impact on Family Scale (IPFAM) were administered to evaluate the level of functional independence and the overall burden on the families, respectively.
RESULTS: IPFAM and WeeFIM scores were not different between geographical regions (P > 0.05). Functional independence level of the child and the level of education of the mothers were significant contributors to the disruption of social relations subscale of IPFAM (P < 0.05). WeeFIM score, presence of mental retardation, and income were significant contributors to general impact subscale. WeeFIM, mothers' level of education, and income were significant factors for the financial support subscale (P < 0.05). WeeFIM score, presence of mental retardation, mothers' level of education, and income also were found to contribute to the total impact subscale scores (P < 0.05). None of the evaluated factors were found to contribute to coping subscale of IPFAM (P > 0.05).
CONCLUSION: Although some are expected, certain intriguing results, such as the impact of the mothers' literacy level, warrant further larger scale comprehensive studies to investigate the factors that contribute to the impact of CDC on their families. Also, policies that focus on family centered rehabilitation approaches should be encouraged in an effort to decrease the overall impact of CDC on families.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  caregiver; childhood disability; chronically disabled children; family impact; family-centered services

Mesh:

Year:  2013        PMID: 24417936     DOI: 10.1016/j.pediatrneurol.2013.11.012

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  3 in total

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Authors:  Tamryn van Aswegen; Hellen Myezwa; Joanne Potterton; Aimee Stewart
Journal:  S Afr J Physiother       Date:  2019-02-20

2.  The Burden of Primary Caregivers of Spinal Muscular Atrophy Patients and Their Needs.

Authors:  Ayça Evkaya Acar; Evrim Karadağ Saygı; Sena İmamoğlu; Gülten Öztürk; Olcay Ünver; Pınar Ergenekon; Yasemin Gökdemir; Gülnur Özel; Dilşad Türkdoğan
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3.  The Causal Factors Associated with the Loving Care of the Mothers of Children with Multiple Disabilities.

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  3 in total

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