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首页> 外文期刊>Journal of clinical nursing >“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
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“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

机译:“没有承认这对人们所做的事情”:患有关键先天性心脏缺陷的儿童父母心理健康的定性探索

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摘要

Aims and objectives The 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. Background Children 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. Design This article presents data from a qualitative study with 25 congenital heart defect parents ( n ?=?15) and providers ( n ?=?10). Methods Using thematic analysis, semi‐structured in‐depth interviews were transcribed and coded by the first and second author to identify major themes and subthemes. Results Results 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. Conclusions Parents 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 practice Suggestions for how the field of paediatric cardiology could begin to integrate mental health services into congenital heart defect treatment are provided.
机译:目的和目标本研究的目的是探讨育儿一个孩子具有关键先天性心脏缺陷的心理影响以及将心理服务融入儿科心脏病学关怀的可行性和可接受性。背景技术具有关键的先天性心脏缺陷的儿童是长期行为,社会和情绪困难的风险增加。数据表明,这种风险是部分归因于父母心理健康,这是先天性心脏缺损儿童的长期行为问题的更强烈预测因素,而不是疾病特异性和外科因素。因此,父母压力和心理健康是重要的干预目标,特别是在高风险家庭中。设计本文从25个先天性心脏缺陷父母(n?= 15)和提供者(n?=?10)中介绍了与25个先天性缺陷的定性学研究的数据。使用主题分析的方法,由第一和第二作者转录和编码了半结构化的深入访谈,以确定主要主题和亚主题。结果将采访结果分为四个主要主题:(i)育儿患有临界先天性心脏缺陷的儿童的心理影响,(ii)影响父母父母患有关键先天性心脏缺陷的心理影响的因素(iii)如何何时何时何时何地支持先天性心脏缺陷父母和(iv)将心理支持整合到先天性心脏缺陷护理中的可行性和可接受性。提供商和父母赞同心理健康处理将心理健康待遇融入常规先天性心脏缺陷护理,并确定了与实施前应考虑的可行性(例如,资金和空间)相关的几个实际问题。结论患有危急先天性心脏缺陷的儿童的父母需要获得精神卫生服务,并将这些服务融入常规儿科心脏病学护理是父母接受所需治疗的新颖和实用的方式。与临床实践相关建议的相关性如何开始将心理健康服务整合到先天性心脏缺陷治疗中。

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