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向父母告知囊性纤维化的诊断结果:一个过程,而非一次性事件。

Breaking the diagnosis of cystic fibrosis to parents: A process not a one-off event.

机构信息

Great Ormond Street Hospital for Children, London, UK.

出版信息

Paediatr Respir Rev. 2020 Sep;35:103-105. doi: 10.1016/j.prrv.2020.04.006. Epub 2020 Apr 17.

Abstract

Breaking the news to parents that their child has cystic fibrosis [CF] is most frequently given in the first few weeks of the baby's life as a result of newborn screening. This is optimal to reduce morbidity but can have a significant impact on the parents' mental wellbeing and the parent-child relationship. Parent feedback indicates that assimilating the diagnosis is not a one-off event but a process that takes time. CF professionals therefore need to be aware not only of how they communicate the diagnosis initially but also the ways in which families make sense of this throughout at least the following year. The parent-patient-team relationship is essential to good health outcomes. Key objectives of this paper are to enable: (1) understanding parental responses to the diagnosis which can indicate how well they are managing CF for their child, (2) improving the way in which the diagnosis is communicated and, (3) changing team management of CF in the early years to include parental collaboration to support better mental and physical outcomes.

摘要

向父母告知其孩子患有囊性纤维化(CF)的消息,通常是在婴儿生命的最初几周内,这是由于新生儿筛查的结果。这样做可以优化减少发病率的效果,但可能会对父母的身心健康和亲子关系产生重大影响。父母的反馈表明,接受诊断不是一次性事件,而是一个需要时间的过程。因此,CF 专业人员不仅需要了解他们最初如何传达诊断结果,还需要了解家庭在至少接下来的一年中如何理解这一诊断。父母-患者-团队关系对良好的健康结果至关重要。本文的主要目标是实现:(1)了解父母对诊断的反应,这可以表明他们对孩子 CF 的管理情况,(2)改善诊断的传达方式,以及(3)改变 CF 的团队管理方式,包括让父母参与合作,以支持更好的身心结果。

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