复发性和难治性急性髓性白血病及高危骨髓增生异常综合征患者对患者与医生就预后和未来进行沟通的看法。

IF 1.1 Q4 HEALTH CARE SCIENCES & SERVICES Palliative medicine reports Pub Date : 2024-01-19 eCollection Date: 2024-01-01 DOI:10.1089/pmr.2023.0064
Vinay Rao, Sarah Linsky, M Tish Knobf
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引用次数: 0

摘要

背景:急性髓性白血病(AML)和高危骨髓增生异常综合征(MDS)患者的疾病轨迹难以预测,预后的不确定性很高,这阻碍了患者与医生就预后以及患者在健康状况恶化时对未来的价值观和偏好进行交流。人们对患者的日常生活经历以及这种经历如何影响他们参与此类对话的意愿知之甚少:目的:探讨参与者对与疾病共存以及病人与医生就预后和未来进行交流的看法:这是一项采用半结构式访谈的定性研究:数据收集:对访谈内容进行逐字记录,并通过主题分析得出结论:在 14 名参与者中,平均年龄为 66 岁,79% 为男性,93% 为白人,已婚,患有急性髓细胞白血病。描述这段经历的总主题是:在不确定的迷雾中 "一天一天过"。不确定性是与临床医生预测预后的挑战有关的普遍看法。为了应对不确定性,大多数参与者试图关注当下,保持日常生活的正常。参与者重视患者与临床医生交流中的鼓励和积极态度,然而,大多数人并不愿意在健康状况恶化的情况下讨论预后和未来。值得注意的是,14 名参与者中有 7 人在访谈后三个月内去世:这些数据描述了R/R AML和高危MDS患者的独特视角,临床医生可以利用这些数据加强沟通策略。
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Perspectives of Patients With Relapsed and Refractory Acute Myeloid Leukemia and High-Risk Myelodysplastic Syndrome on Patient-Clinician Communication About Prognosis and the Future.

Background: Patients with acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS) experience unpredictable disease trajectories and high prognostic uncertainty, which serve as barriers to patient-clinician communication about prognosis and their values and preferences for the future in the event of worsening health. Little is known about patients' day-to-day lived experiences and how this shapes their willingness to engage in such conversations.

Objectives: To explore participant perspectives on living with their illness and patient-clinician communication about prognosis and the future.

Design: This is a qualitative study using semi-structured interviews.

Setting/subjects: Patients with relapsed and refractory (R/R) AML and high-risk MDS from a northeastern U.S. cancer center.

Data collection: Interviews were transcribed verbatim and thematic analysis was used to generate findings.

Results: Of the 14 participants, the mean age was 66 years, 79% were men, 93% were White, married, and had AML. The overarching theme that describes the experience was "Taking One Day at a Time" in a Fog of Uncertainty. Uncertainty was a universal perception related to the challenges for clinicians to predict prognosis. To cope with uncertainty, most participants tried to focus on the present and maintain normality in everyday life. Participants valued encouragement and positivity in patient-clinician communication, however, the majority were not ready to discuss prognosis and the future in the event of worsening health. Of note, 7 of 14 participants died within three months after the interview.

Conclusions: These data describe a unique perspective of patients with R/R AML and high-risk MDS that clinicians could use to enhance communication strategies.

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