Aligning Concerns in Telecare: Three Concepts to Guide the Design of Patient-Centred E-Health

被引：29

作者：

Andersen T.O. ^{[1
]}

Bansler J.P. ^{[1
]}

Kensing F. ^{[1
]}

Moll J. ^{[1
]}

Mønsted T. ^{[2
]}

Nielsen K.D. ^{[3
]}

Nielsen O.W. ^{[4
]}

Petersen H.H. ^{[5
]}

Svendsen J.H. ^{[5
]}

机构：

[1] Department of Computer Science, University of Copenhagen, Copenhagen

[2] Department of Informatics, University of Oslo, Oslo

[3] Department of Philosophy, University of Twente, Enschede

[4] Department of Cardiology, Bispebjerg Hospital, University of Copenhagen, Copenhagen

[5] Department of Cardiology, The Heart Centre, Rigshospitalet, University of Copenhagen, Copenhagen

来源：

Computer Supported Cooperative Work (CSCW) | 2019年 / 28卷 / 6期

关键词：

Alignment of concerns; Medical phenomenology; Participatory design; Patient-centred e-health; Patient-clinician interaction; Patient-provider relationship;

D O I：

10.1007/s10606-018-9309-1

中图分类号：

学科分类号：

摘要：

The design of patient-centred e-health services embodies an inherent tension between the concerns of clinicians and those of patients. Clinicians’ concerns are related to professional issues to do with diagnosing and curing disease in accordance with accepted medical standards. In contrast, patients’ concerns typically relate to personal experience and quality of life issues. It is about their identity, their hopes, their fears and their need to maintain a meaningful life. This divergence of concerns presents a fundamental challenge for designers of patient-centred e-health services. We explore this challenge in the context of chronic illness and telecare. Based on insights from medical phenomenology as well as our own experience with designing an e-health service for patients with chronic heart disease, we emphasise the importance – and difficulty – of aligning the concerns of patients and clinicians. To deal with this, we propose a set of concepts for analysing concerns related to the design of e-health services: A concern is (1) meaningful if it is relevant and makes sense to both patients and clinicians, (2) actionable if clinicians or patients – at least in principle – are able to take appropriate action to deal with it, and (3) feasible if it is easy and convenient to do so within the organisational and social context. We conclude with a call for a more participatory and iterative approach to the design of patient-centred e-health services. © 2018, The Author(s).

引用

页码：1181 / 1214

页数：33

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