Sharing Patient-Controlled Real-World Data Through the Application of the Theory of Commons: Action Research Case Study

• Published in: Journal of medical Internet research 2021-01, Vol.23 (1), p.e16842-e16842
• Main Authors: Hager, Andreas, Lindblad, Staffan, Brommels, Mats, Salomonsson, Stina, Wannheden, Carolina
• Format: Article
• Language: English
• Subjects: Action control; Action research; Chronic illnesses; Conceptual models; Content analysis; Cystic fibrosis; Data Analysis; Health care management; Health information; Health Services Research - standards; Humans; Medical personnel; Medicin och hälsovetenskap; Morality; Original Paper; Patients; Personal control; Personal health; Privacy; Professionals; Property rights; Quality of care; Self care; Self determination; Specification; Stakeholders
• ISSN: 1438-8871; 1439-4456; 1438-8871
• DOI: 10.2196/16842

Technological advances have radically changed the opportunities for individuals with chronic conditions to practice self-care and to coproduce health care and research. Digital technologies enable patients to perform tasks traditionally carried out by health care professionals in a more convenient way, at lower costs, and without compromising quality. Patients may also share real-world data with other stakeholders to promote individual and population health. However, there is a need for legal frameworks that enable patient privacy and control in such sharing of real-world data. We believe that this need could be met by the conceptualization of patient-controlled real-world data as knowledge commons, which is a resource shared by a group of people. This study aimed to propose a conceptual model that describes how patient-controlled real-world data can be shared effectively in chronic care management, in a way that supports individual and population health, while respecting personal data privacy and control. An action research approach was used to develop a solution to enable patients, in a self-determined way, to share patient-controlled data to other settings. We chose the context of cystic fibrosis (CF) care in Sweden, where coproduction between patients, their families, and health care professionals is critical in the introduction of new drugs. The first author, who is a lawyer and parent of children with CF, was a driver in the change process. All coauthors collaborated in the analysis. We collected primary and secondary data reflecting changes during the time period from 2012 to 2020, and performed a qualitative content analysis guided by the knowledge commons framework. Through a series of changes, a national system for enabling patients to share patient-controlled real-world data to different stakeholders in CF care was implemented. The case analysis resulted in a conceptual model consisting of the following three knowledge commons arenas that contributed to patient-controlled real-world data collection, use, and sharing: (1) patient world arena involving the private sphere of patients and families; (2) clinical microsystem arena involving the professional sphere at frontline health care clinics; and (3) round table arena involving multiple stakeholders from different settings. Based on the specification of property rights, as presented in our model, the patient can keep control over personal health information and may grant use rights to other stake