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青少年和青年癌症患者参与预先护理计划视频试点后的对话。

Adolescents and young adults with cancer conversations following participation in an advance care planning video pilot.

机构信息

Department of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA, 02215, USA.

Doctor of Medicine Program, Emory School of Medicine, Atlanta, GA, USA.

出版信息

Support Care Cancer. 2024 Feb 17;32(3):164. doi: 10.1007/s00520-024-08372-y.

Abstract

PURPOSE

Advance care planning (ACP) discussions can help adolescents and young adults (AYAs) communicate their preferences to their caregivers and clinical team, yet little is known about willingness to hold conversations, content, and evolution of care preferences. We aimed to assess change in care preferences and reasons for such changes over time and examine the reasons for engaging or not engaging in ACP discussions and content of these discussions among AYAs and their caregivers.

METHODS

We conducted a pilot randomized controlled trial of a novel video-based ACP tool among AYA patients aged 18-39 with advanced cancer and their caregivers. Participants were asked their care preferences at baseline, after viewing the video or hearing verbal description (post questionnaire), and again 3 months later. Three-month phone calls also queried if any ACP conversations occurred since the initial study visit. Study team notes from these phone calls were evaluated using content analysis.

RESULTS

Forty-five AYAs and 40 caregivers completed the 3-month follow-up. Nearly half of AYAs and caregivers changed their care preference from post questionnaire to 3-month follow-up. Increased reflection and learning on the topic (n = 45) prompted preference change, with participants often noting the nuanced and context-specific nature of these decisions (n = 20). Most AYAs (60%) and caregivers (65%) engaged in ACP conversation(s), often with a family member. Disease-related factors (n = 8), study participation (n = 8), and a desire for shared understanding (n = 6) were common reasons for initiating discussions. Barriers included disease status (n = 14) and timing (n = 12). ACP discussions focused on both specific wishes for treatment (n = 26) and general conversations about goals and values (n = 18).

CONCLUSION

AYAs and caregivers acknowledged the complexity of ACP decisions, identifying obstacles and aids for these discussions. Clinicians should support a personalized approach to ACP that captures these nuances, promoting ACP as an iterative, longitudinal, and collaborative process.

TRIAL REGISTRATION

This trial was registered 10/31/2019 with ClinicalTrials.gov (Identifier: NCT0414907).

摘要

目的

预先医疗照护计划(ACP)讨论可以帮助青少年和年轻成年人(AYAs)与他们的照护者和临床团队交流他们的偏好,但对于进行对话的意愿、内容以及护理偏好的演变知之甚少。我们旨在评估护理偏好的变化以及随时间推移发生此类变化的原因,并检查 AYAs 和他们的照护者进行 ACP 讨论的原因和这些讨论的内容。

方法

我们在一项针对患有晚期癌症的 18-39 岁 AYA 患者及其照护者的新型基于视频的 ACP 工具的试点随机对照试验中进行了此项研究。参与者在基线时、观看视频或听取口头描述后(问卷调查后)以及 3 个月后被要求表达他们的护理偏好。3 个月后的电话还询问了自首次研究访问以来是否进行了任何 ACP 对话。使用内容分析评估这些电话的研究团队记录。

结果

45 名 AYAs 和 40 名照护者完成了 3 个月的随访。近一半的 AYAs 和照护者从问卷调查后到 3 个月的随访期间改变了他们的护理偏好。增加对该主题的反思和学习(n=45)促使偏好发生变化,参与者经常注意到这些决定的细微差别和具体情况(n=20)。大多数 AYAs(60%)和照护者(65%)进行了 ACP 对话(通常与家庭成员进行)。常见的发起讨论的原因包括疾病相关因素(n=8)、研究参与(n=8)和渴望共同理解(n=6)。障碍包括疾病状况(n=14)和时间安排(n=12)。ACP 讨论侧重于治疗的具体意愿(n=26)和关于目标和价值观的一般对话(n=18)。

结论

AYAs 和照护者认识到 ACP 决策的复杂性,确定了这些讨论的障碍和辅助手段。临床医生应支持 ACP 的个性化方法,捕捉这些细微差别,将 ACP 作为一个迭代、纵向和协作的过程。

试验注册

这项试验于 2019 年 10 月 31 日在 ClinicalTrials.gov 注册(标识符:NCT0414907)。

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