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患者及照料者对癌症治疗期间症状与生活质量管理决策支持的看法:对电子健康的启示

Patient and caregiver perspectives on decision support for symptom and quality of life management during cancer treatment: Implications for eHealth.

作者信息

Cooley Mary E, Nayak Manan M, Abrahm Janet L, Braun Ilana M, Rabin Michael S, Brzozowski Jane, Lathan Christopher, Berry Donna L

机构信息

Dana-Farber Cancer Institute, Boston, MA, USA.

Independent Clinical Informatics Consultant, Boston, MA, USA.

出版信息

Psychooncology. 2017 Aug;26(8):1105-1112. doi: 10.1002/pon.4442. Epub 2017 Jul 3.

Abstract

OBJECTIVES

Adequate symptom and quality-of-life (SQL) management is a priority during cancer treatment. eHealth is a timely way to enhance patient-engagement, facilitate communication, and improve health outcomes. The objectives of this study were to describe patient and caregivers' perspectives for providing, processing, and managing SQL data to enhance communication and identify desired components for decision support.

METHODS

Data were collected from 64 participants through questionnaires and focus groups. Analysis was conducted using NVivo. Open and axial coding was completed, grouping commonalities and large constructs into nodes to identify and synthesize themes.

RESULTS

Face-to-face meetings with clinicians were the prime time to communicate, and patients strove to understand treatment options and the effect on SQL by bringing caregivers to their visits, taking notes, tracking symptoms, and creating portable health records. Patients/caregivers struggled to self-manage their symptoms and were uncertain when to contact clinicians when experiencing uncontrolled symptoms. Most participants identified eHealth solutions for decision support. However, 38% of participants (n = 24) rarely used computers and identified non-eHealth options for decision support. Core components for both eHealth and non-eHealth systems were access to (1) cancer information, (2) medical records, (3) peer support, and (4) improved support and understanding on when to contact clinicians.

CONCLUSIONS

Patients were faced with an overwhelming amount of information and relied on their caregivers to help navigate the complexities of cancer care and self-manage SQL. Health technologies can provide informational support; however, decision support needs to span multiple venues to avoid increasing disparities caused by a digital divide.

摘要

目标

在癌症治疗期间,充分的症状和生活质量(SQL)管理是首要任务。电子健康是增强患者参与度、促进沟通并改善健康结果的适时方式。本研究的目的是描述患者和护理人员对于提供、处理和管理SQL数据以加强沟通的看法,并确定决策支持所需的组成部分。

方法

通过问卷调查和焦点小组从64名参与者收集数据。使用NVivo进行分析。完成开放式和轴心式编码,将共性和大的结构分组到节点中以识别和综合主题。

结果

与临床医生面对面的会议是沟通的主要时机,患者通过带护理人员就诊、做笔记、跟踪症状以及创建便携式健康记录,努力了解治疗选择及其对SQL的影响。患者/护理人员在自我管理症状方面存在困难,在症状无法控制时不确定何时联系临床医生。大多数参与者确定了用于决策支持的电子健康解决方案。然而,38%的参与者(n = 24)很少使用电脑,并确定了非电子健康的决策支持选项。电子健康和非电子健康系统的核心组成部分包括获取(1)癌症信息、(2)医疗记录、(3)同伴支持,以及(4)在何时联系临床医生方面得到更好的支持和理解。

结论

患者面临着大量信息,依赖护理人员帮助应对癌症护理的复杂性并自我管理SQL。健康技术可以提供信息支持;然而,决策支持需要跨越多个场所,以避免因数字鸿沟导致差距加大。

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