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保持所有选择的开放性:父母对预先医疗照护计划的态度。

Keeping all options open: Parents' approaches to advance care planning.

机构信息

Louis Dundas Centre for Children's Palliative Care, Institute of Child Health, University College London, London, UK.

Marie Curie Palliative Care Research Department, Division of Psychiatry, University College London, London, UK.

出版信息

Health Expect. 2017 Aug;20(4):675-684. doi: 10.1111/hex.12500. Epub 2016 Sep 26.

Abstract

BACKGROUND

Early engagement in advance care planning (ACP) is seen as fundamental for ensuring the highest standard of care for children and young people with a life-limiting condition (LLC). However, most families have little knowledge or experience of ACP.

OBJECTIVE

To investigate how parents of children and young people with LLCs approach and experience ACP.

METHODS

Open-ended, semi-structured interviews were conducted with parents of 18 children; nine children who were currently receiving palliative care services, and nine children who had received palliative care and died. Verbatim transcripts of audiotaped interviews were analysed following principles of grounded theory while acknowledging the use of deductive strategies, taking account of both the child's condition, and the timing and nature of decisions made.

RESULTS

Parents reported having discussions and making decisions about the place of care, place of death and the limitation of treatment. Most decisions were made relatively late in the illness and by parents who wished to keep their options open. Parents reported different levels of involvement in a range of decisions; many wished to be involved in decision making but did not always feel able to do so.

DISCUSSION

This study highlights that parents' approaches to decision making vary by the type of decision required. Their views may change over time, and it is important to allow them to keep their options open. We recommend that clinicians have regular discussions over the course of the illness in an effort to understand parents' approaches to particular decisions rather than to drive to closure prematurely.

摘要

背景

早期参与预先医疗照护计划(ACP)被视为确保患有绝症儿童和青少年获得最高标准护理的基础。然而,大多数家庭对 ACP 知之甚少或没有经验。

目的

调查患有绝症儿童和青少年的父母如何处理和体验 ACP。

方法

对 18 名儿童的父母进行了开放式、半结构化访谈;其中 9 名儿童正在接受姑息治疗服务,9 名儿童接受过姑息治疗并已死亡。在遵循扎根理论原则的同时,对录音采访的逐字记录进行了分析,同时承认使用演绎策略,既要考虑到孩子的病情,也要考虑到决策的时间和性质。

结果

父母报告了关于护理地点、死亡地点和治疗限制的讨论和决策。大多数决策是在疾病晚期做出的,是那些希望保留选择余地的父母做出的。父母报告了在一系列决策中不同程度的参与;许多人希望参与决策,但并不总是感到能够这样做。

讨论

这项研究强调,父母的决策方法因所需决策的类型而异。他们的观点可能会随着时间的推移而改变,重要的是要让他们保留选择的余地。我们建议临床医生在疾病过程中定期进行讨论,以努力了解父母对特定决策的方法,而不是过早地强行做出决定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0934/5512998/cf385e57588a/HEX-20-675-g001.jpg

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