Patient, Parent, and Oncologist Perspectives and Recommendations on the Right Way to Talk About Prognosis in Advanced Childhood Cancer.

IF 4.7 3区 医学 Q1 ONCOLOGY
Erica C Kaye, Harmony Farner, Shoshana Mehler, Kelly Bien, Nidhi Mali, Tara M Brinkman, Justin N Baker, Pamela Hinds, Jennifer W Mack
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引用次数: 0

Abstract

Purpose: Clear prognostic communication is associated with improvements in quality of life and suffering for children with advanced illness. Yet recent evidence demonstrates that pediatric oncologists often avoid, defer, or soften prognostic disclosure. We aimed to describe pediatric cancer shareholder perspectives on quality prognostic communication to inform design of an intervention to improve prognostic disclosure in advanced childhood cancer.

Methods: Semi-structured interviews were conducted with a purposeful sample of pediatric patients with cancer (n = 20), parents (n = 20), and oncologists (n = 20) representing six institutions across five states. Rapid analysis was performed using the National Cancer Institute core communication functions to organize domains of inquiry.

Results: Three main themes were endorsed by participants regarding the ideal timing of prognostic disclosure: early, ongoing, individualized. Although each group emphasized the need for an individualized approach, oncologists rarely elicited patient/parent preferences for prognostic communication and more commonly inferred what a patient/family wanted to hear. Participants described five key pillars for how to facilitate quality prognostic disclosure: conversation leadership, overall attendance, patient inclusion, location, and atmosphere. They also identified four themes around ideal prognostic content: range of information, use of numbers, population-level versus patient-specific information, and tone/delivery. Discordant recommendations between patients/parents and oncologists emerged for how much and what information to share.

Conclusion: Pediatric cancer shareholders advocated for diverse, and sometimes conflicting, approaches for prognostic disclosure. Although nearly all participants endorsed the importance of individualized prognostic disclosure, specific strategies to encourage or facilitate person-centered prognostic conversation are lacking. Future research will focus on collaboration with pediatric patients, parents, and oncologists to codesign a clinical intervention to improve prognostic communication for children with advanced cancer and their families.

晚期儿童癌症患者、家长和肿瘤学家对如何正确谈论预后的观点和建议。
目的:明确的预后告知与改善晚期患儿的生活质量和痛苦有关。然而,最近的证据表明,儿科肿瘤学家经常回避、推迟或弱化预后信息的披露。我们的目的是描述儿科癌症股东对优质预后沟通的看法,为设计干预措施提供信息,以改善晚期儿童癌症预后的披露:方法:我们对五个州六个机构的儿科癌症患者(20 人)、家长(20 人)和肿瘤专家(20 人)进行了半结构式访谈。采用国家癌症研究所的核心交流功能对调查领域进行了快速分析:结果:关于预后信息披露的理想时机,参与者认可三大主题:早期、持续、个性化。虽然每个小组都强调了个性化方法的必要性,但肿瘤学家很少询问患者/家长对预后信息交流的偏好,更多的是推断患者/家属想听到什么。与会者描述了如何促进高质量预后信息披露的五大支柱:谈话领导、整体出席情况、患者参与、地点和氛围。他们还围绕理想的预后内容确定了四个主题:信息范围、数字的使用、人群水平与患者特定信息的对比以及语气/表达。患者/家长和肿瘤学家对分享多少信息和什么信息的建议出现了分歧:小儿癌症股东主张采用不同的预后信息披露方法,有时甚至是相互冲突的。尽管几乎所有参与者都认可个体化预后信息披露的重要性,但仍缺乏鼓励或促进以人为本的预后对话的具体策略。未来的研究将侧重于与儿科患者、家长和肿瘤学家合作,共同设计一种临床干预措施,以改善晚期癌症患儿及其家人的预后沟通。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
7.50%
发文量
518
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