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为长期疾病患者出院后自我管理支持设计未来的电子健康服务:定性访谈研究

Designing a Future eHealth Service for Posthospitalization Self-management Support in Long-term Illness: Qualitative Interview Study.

作者信息

Wathne Hege, Morken Ingvild Margreta, Storm Marianne, Husebø Anne Marie Lunde

机构信息

Department of Public Health, University of Stavanger, Faculty of Health Sciences, Stavanger, Norway.

Department of Quality and Health Technologies, University of Stavanger, Stavanger, Norway.

出版信息

JMIR Hum Factors. 2023 Feb 6;10:e39391. doi: 10.2196/39391.

Abstract

BACKGROUND

For patients with noncommunicable diseases (NCDs; eg, heart failure [HF] and colorectal cancer [CRC]), eHealth interventions could meet their posthospital discharge needs and strengthen their ability to self-manage. However, inconclusive evidence exists regarding how to design eHealth services to meet the complex needs of patients. To foster patient acceptability and ensure the successful development and implementation of eHealth solutions, it is beneficial to include different stakeholders (ie, patients and health care professionals) in the design and development phase of such services. The involvement of different stakeholders could contribute to ensuring feasible, acceptable, and usable solutions and that eHealth services are developed in response to users' supportive care needs when transitioning to home after hospitalization. This study is the first step of a larger complex intervention study aimed at meeting the postdischarge needs of 2 NCD populations.

OBJECTIVE

This study aimed to explore the perspectives of patients with HF and CRC and health care professionals on patient self-management needs following hospital discharge and investigate how a future nurse-assisted eHealth service could be best designed to foster patient acceptability, support self-management, and smooth the transition from hospital to home.

METHODS

A qualitative, explorative, and descriptive approach was used. We conducted 38 semistructured interviews with 10 patients with HF, 9 patients surgically treated for CRC with curative intent, 6 registered nurses recruited as nurse navigators of a planned eHealth service, and 13 general practitioners experienced in HF and CRC treatment and follow-up care. Patients were recruited conveniently from HF and CRC outpatient clinics, and the nurses were recruited from the cardiology and gastro-surgical departments at a university hospital in the southwest of Norway. The general practitioners were recruited from primary care in surrounding municipalities. Semistructured interview guides were used for data collection, and the data were analyzed using thematic analysis.

RESULTS

In total, 3 main themes were derived from the data analysis: expecting information, reassurance, and guidance when using eHealth for HF and CRC self-management; expecting eHealth to be comprehensible, supportive, and knowledge promoting; and recognizing both the advantages and disadvantages of eHealth for HF and CRC self-management. The data generated from this interview study depicted the diverse needs for self-management support of patients with CRC and HF after hospital discharge. In addition, valuable suggestions were identified regarding the design and content of the eHealth service. However, participants described both possible advantages and disadvantages of a remote eHealth service.

CONCLUSIONS

This study is the first step in the development of an eHealth service for posthospitalization self-management support for long-term illnesses. It concerns patients' supportive care needs and user requirements of an eHealth service. The findings of this study may add value to the planning and development of eHealth interventions for patients with NCDs.

摘要

背景

对于患有非传染性疾病(如心力衰竭[HF]和结直肠癌[CRC])的患者,电子健康干预措施可以满足他们出院后的需求,并增强他们的自我管理能力。然而,关于如何设计电子健康服务以满足患者的复杂需求,现有证据尚无定论。为了提高患者的接受度,并确保电子健康解决方案的成功开发和实施,在这类服务的设计和开发阶段纳入不同的利益相关者(即患者和医疗保健专业人员)是有益的。不同利益相关者的参与有助于确保解决方案可行、可接受且可用,并确保电子健康服务是为满足患者出院后回家过渡期间的支持性护理需求而开发的。本研究是一项更大规模复杂干预研究的第一步,该研究旨在满足两类非传染性疾病患者的出院后需求。

目的

本研究旨在探讨心力衰竭和结直肠癌患者以及医疗保健专业人员对出院后患者自我管理需求的看法,并调查未来护士辅助的电子健康服务如何才能得到最佳设计,以提高患者接受度、支持自我管理并顺利实现从医院到家庭的过渡。

方法

采用定性、探索性和描述性方法。我们对10名心力衰竭患者、9名接受了根治性手术治疗的结直肠癌患者、6名被招募为计划中的电子健康服务护士导航员的注册护士以及13名在心力衰竭和结直肠癌治疗及后续护理方面经验丰富的全科医生进行了38次半结构化访谈。患者从心力衰竭和结直肠癌门诊方便抽样招募,护士从挪威西南部一家大学医院的心脏病学和胃肠外科招募。全科医生从周边市镇的初级保健机构招募。使用半结构化访谈指南进行数据收集,并采用主题分析法对数据进行分析。

结果

数据分析共得出3个主要主题:在使用电子健康进行心力衰竭和结直肠癌自我管理时期望获得信息、安心和指导;期望电子健康易于理解、提供支持并促进知识获取;认识到电子健康在心力衰竭和结直肠癌自我管理中的优点和缺点。这项访谈研究产生的数据描绘了结直肠癌和心力衰竭患者出院后对自我管理支持的多样化需求。此外,还就电子健康服务的设计和内容提出了有价值的建议。然而,参与者描述了远程电子健康服务可能存在的优点和缺点。

结论

本研究是开发用于长期疾病出院后自我管理支持的电子健康服务的第一步。它涉及患者的支持性护理需求以及电子健康服务的用户要求。本研究结果可能会为非传染性疾病患者电子健康干预措施的规划和开发增添价值。

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