Quality of Life and Mental Health in Mothers and Fathers Caring for Children and Adolescents with Rare Diseases Requiring Long-Term Mechanical Ventilation

Author:

Boettcher JohannesORCID,Denecke Jonas,Barkmann Claus,Wiegand-Grefe Silke

Abstract

(1) Parents caring for children and adolescents with rare diseases fear the long-term progression of the child’s disease and the loss of their parental role. The aim of this study was to examine the quality of life, mental health and associated protective factors of mothers and fathers caring for children with rare diseases requiring mechanical long-term ventilation. (2) In a cross-sectional design, data on quality of life, mental health, coping mechanisms, social support and family functioning from n = 75 affected families were collected using standardized psychometric questionnaires. (3) Mothers compared to fathers were significantly more impaired in their quality of life and mental health. Protective factors significantly associated with the respective outcomes for mothers were coping mechanisms, social support and family functioning, whereas for fathers solely the latter was found to be significant. Multiple regression analyses showed that family functioning may be the most important predictor of quality of life and mental health. (4) The results support the need for family-oriented care in parents of children with rare diseases. To reach optimal efficiency, health care providers should not only screen parents for psychosocial impairment but also provide interventions that consider gender-specific differences in psychological health.

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health

Reference41 articles.

1. European Commission Rare Diseases. European Commission, European Unionhttp://europa.eu.int/comm/health/ph_threats/non_com/rare_diseases_en.htm

2. EURORDIS Rare Diseases: Understanding this Public Health Priorityhttp://beta.eurordis.org/IMG/pdf/princeps_document-EN.pdf

3. The supportive care needs of parents with a child with a rare disease: results of an online survey

4. Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database

5. Australian families living with rare disease: experiences of diagnosis, health services use and needs for psychosocial support

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