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'Why Do They Need to Check Me?' Patient Participation Through eHealth and the Doctor-Patient Relationship: Qualitative Study

Authors :
Hanife Rexhepi
Christiane Grünloh
Åsa Cajander
Gunilla Myreteg
Source :
Journal of Medical Internet Research
Publication Year :
2018
Publisher :
JMIR Publications Inc., 2018.

Abstract

Background: Roles in the doctor-patient relationship are changing and patient participation in health care is increasingly emphasized. Electronic health (eHealth) services such as patient accessible electronic health records (PAEHRs) have been implemented to support patient participation. Little is known about practical use of PAEHR and its effect on roles of doctors and patients. Objective: This qualitative study aimed to investigate how physicians view the idea of patient participation, in particular in relation to the PAEHR system. Hereby, the paper aims to contribute to a deeper understanding of physicians' constructions of PAEHR, roles in the doctor-patient relationship, and levels and limits of involvement. Methods: A total of 12 semistructured interviews were conducted with physicians in different fields. Interviews were transcribed, translated, and a theoretically informed thematic analysis was performed. Results: Two important aspects were identified that are related to the doctor-patient relationship: roles and involvement. The physicians viewed their role as being the ones to take on the responsibility, determining treatment options, and to be someone who should be trusted. In relation to the patient's role, lack of skills (technical or regarding medical jargon), motives to read, and patients' characteristics were aspects identified in the interviews. Patients were often referred to as static entities disregarding their potential to develop skills and knowledge over time. Involvement captures aspects that support or hinder patients to take an active role in their care. Conclusions: Literature of at least two decades suggests an overall agreement that the paternalistic approach in health care is inappropriate, and a collaborative process with patients should be adopted. Although the physicians in this study stated that they, in principle, were in favor of patient participation, the analysis found little support in their descriptions of their daily practice that participation is actualized. As seen from the results, paternalistic practices are still present, even if professionals might not be aware of this. This can create a conflict between patients who strive to become more informed and their questions being interpreted as signs of critique and mistrust toward the physician. We thus believe that the full potential of PAEHRs is not reached yet and argue that the concept of patient empowerment is problematic as it triggers an interpretation of "power" in health care as a zero-sum, which is not helpful for the maintenance of the relationship between the actors. Patient involvement is often discussed merely in relation to decision making; however, this study emphasizes the need to include also sensemaking and learning activities. This would provide an alternative understanding of patients asking questions, not in terms of "monitoring the doctor" but to make sense of the situation. CC BY 4.0

Subjects

Subjects :
Male
020205 medical informatics
physicians
thematic analysis
02 engineering and technology
Telehealth
Medical Records
0302 clinical medicine
Health care
0202 electrical engineering, electronic engineering, information engineering
Electronic Health Records
030212 general & internal medicine
Doctor-Patient Relationship
skin and connective tissue diseases
Systemvetenskap, informationssystem och informatik
patient portal
Qualitative Research
learning
Computer Sciences
adult
Medical record
article
Patient portal
electronic health record
Telemedicine
doctor-patient relationship
medical records
Doctor–patient relationship
Female
patient participation
Information Systems
Patient Empowerment
Systemvetenskap, informationssystem och informatik med samhällsvetenskaplig inriktning
telehealth
Decision Making
education
Information Systems, Social aspects
Health Informatics
decision making
Patient Accessible Electronic Health Records
03 medical and health sciences
Human Aspects of ICT
personal health records
Nursing
Computer Systems
Physicians
eHealth
Humans
human
Patient participation
skill
Physician-Patient Relations
Original Paper
electronic patient record
business.industry
Personal Health Records
Ehealth Services For Patients
genetic transcription
Patient Portal
patient empowerment
semi structured interview
Self Care
monitoring
Datorsystem
Datavetenskap (datalogi)
eHealth services for patients
empowerment
patient accessible electronic health records
responsibility
sense organs
Patient Participation
Power, Psychological
business
qualitative research
Mänsklig interaktion med IKT
Qualitative research

Details

ISSN :
14388871
Volume :
20
Database :
OpenAIRE
Journal :
Journal of Medical Internet Research
Accession number :
edsair.doi.dedup.....cf2fc29106b7e404e4ba152c9aef7125