Literature DB >> 26453412

The Parent Experience of Caring for a Child with Mitochondrial Disease.

Brenda A Senger1, Linda D Ward2, Celestina Barbosa-Leiker2, Ruth C Bindler2.   

Abstract

UNLABELLED: Mitochondrial disease is a spectrum of progressive genetic disorders resulting from dysfunctions of cellular metabolism in the mitochondria that greatly compromise the lives of affected individuals, who are often children.
PURPOSE: This study described the parent experiences unique to caring for a child with mitochondrial disease.
METHODS: Internet surveys were made available to parents of children with a known mitochondrial disease. Surveys included demographic items and two questionnaires: Parent Experience of Child Illness (PECI) and Pediatric Inventory for Parents (PIP). Descriptive data were collected and correlations calculated to determine relationships between the parent experience and stress.
RESULTS: The majority of participants (n=231) were mothers (95%) of children with mitochondrial disease around the age of 10 years (M=9.85). Elevated scores were found in parent adjustment illness-related concerns regarding Guilt and Worry (M=2.30, SD=.650), Sorrow and Anger (M=2.09, SD=.730), Long-term Uncertainty (M=2.56, SD=.690), and Emotional Resources (M=2.36, SD=.615). Scores indicated elevated feelings of stress in terms of both difficulty and frequency. Significant correlations (p<0.01) were found between parent illness-related concerns and parenting stress.
CONCLUSIONS: The results of this study suggest that parents of a child with mitochondrial disease feel a burden of responsibility that exceeds the typical caregiver role, see their child as fragile, and have concerns about their child's future. Identification of these concerns can assist nurses to better meet the needs of these parents and families.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Anger; Genetic diseases; Guilt; Mitochondrial diseases; Parent experience; Sorrow; Uncertainty; Worry

Mesh:

Year:  2015        PMID: 26453412     DOI: 10.1016/j.pedn.2015.08.007

Source DB:  PubMed          Journal:  J Pediatr Nurs        ISSN: 0882-5963            Impact factor:   2.145


  5 in total

Review 1.  Meta-Analysis: Caregiver and Youth Uncertainty in Pediatric Chronic Illness.

Authors:  Lauren Szulczewski; Larry L Mullins; Sarah L Bidwell; Angelica R Eddington; Ahna L H Pai
Journal:  J Pediatr Psychol       Date:  2017-05-01

2.  Gender Differences in Caring for Children with Genetic or Rare Diseases: A Mixed-Methods Study.

Authors:  Shao-Yin Chu; Chin-Chen Wen; Chun-Ying Weng
Journal:  Children (Basel)       Date:  2022-04-27

3.  Fear of disease progression in carriers of the m.3243A > G mutation.

Authors:  José A E Custers; Paul de Laat; Saskia Koene; Jan Smeitink; Mirian C H Janssen; Christianne Verhaak
Journal:  Orphanet J Rare Dis       Date:  2018-11-13       Impact factor: 4.123

4.  Blended cognitive behaviour therapy for children and adolescents with mitochondrial disease targeting fatigue (PowerMe): study protocol for a multiple baseline single case experiment.

Authors:  I L Klein; K F E van de Loo; T J Hoogeboom; M C H Janssen; J A M Smeitink; E van der Veer; C M Verhaak; J A E Custers
Journal:  Trials       Date:  2021-03-01       Impact factor: 2.279

5.  Psychological functioning in children suspected for mitochondrial disease: the need for care.

Authors:  Kim F E van de Loo; José A E Custers; Saskia Koene; Inge-Lot Klein; Mirian C H Janssen; Jan A M Smeitink; Christianne M Verhaak
Journal:  Orphanet J Rare Dis       Date:  2020-03-24       Impact factor: 4.123

  5 in total

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