4.6 Article

There's no acknowledgement of what this does to people: A qualitative exploration of mental health among parents of children with critical congenital heart defects

期刊

JOURNAL OF CLINICAL NURSING
卷 27, 期 13-14, 页码 2785-2794

出版社

WILEY
DOI: 10.1111/jocn.14275

关键词

childhood illness; congenital heart disease; integrated care; mental health; parent

类别

资金

  1. Hellman Fellows Fund
  2. National Institute of Child Health and Human Development (NICHD) [R01HD084813, R01HD081188]

向作者/读者索取更多资源

Aims and objectivesThe purpose of this study was to explore the psychological impact of parenting a child with a critical congenital heart defect and the feasibility and acceptability of integrating psychological services into paediatric cardiology care. BackgroundChildren with critical congenital heart defect are at an increased risk for long-term behavioural, social and emotional difficulties. Data suggest that this risk is partially attributable to parental mental health, which is a stronger predictor of long-term behavioural problems in congenital heart defect children than disease-specific and surgical factors. Parental stress and mental health are thus important intervention targets, especially among high-risk families. DesignThis article presents data from a qualitative study with 25 congenital heart defect parents (n=15) and providers (n=10). MethodsUsing thematic analysis, semi-structured in-depth interviews were transcribed and coded by the first and second author to identify major themes and subthemes. ResultsResults of the interviews were organised into four major themes: (i) the psychological impact of parenting a child with critical congenital heart defect, (ii) factors that influence the psychological impact of parenting a child with critical congenital heart defect, (iii) how and when to psychologically support congenital heart defect parents and (iv) feasibility and acceptability of integrating psychological support into congenital heart defect care. Providers and parents endorsed the integration of mental health treatment into routine congenital heart defect care and identified several practical issues related to feasibility (e.g., funding and space) that should be considered prior to implementation. ConclusionsParents of children with critical congenital heart defect need access to mental health services, and integrating these services into routine paediatric cardiology care is a novel and practical way for parents to receive the treatment they need. Relevance to clinical practiceSuggestions for how the field of paediatric cardiology could begin to integrate mental health services into congenital heart defect treatment are provided.

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