Digital health technology to support patient-centered shared decision making at point of care for juvenile idiopathic arthritis

Front Pediatr. 2024 Oct 25:12:1457538. doi: 10.3389/fped.2024.1457538. eCollection 2024.

Abstract

Despite availability of multiple FDA approved therapies, many children with juvenile idiopathic arthritis (JIA) suffer pain and disability due to uncontrolled disease. The term JIA includes a heterogeneous set of conditions unified by chronic inflammatory arthritis, collectively affecting 1:1,000 children. When reviewing treatment options with families the rheumatologist currently refers to the experience of the average patient in relatively small controlled clinical trials, to consensus-based treatment plans, or increasingly the choice is dictated by the formulary restrictions of insurance payers. The current paradigm for treatment selection does not incorporate real-world evidence of treatment effectiveness centered to the individual patients with whom decisions are to be made. Treatment decisions based on the evidence of the average patient are not optimized to reflect the unique clinical characteristics of an individual with JIA and their disease course, nor does it account for heterogeneous treatment effects. To guide treatment choices centered around each patient, we describe a novel concept of utilizing digital health technology to bring patient-centered information into shared decision-making discussions based on comparative effectiveness analysis of electronic health record or observational clinical registry data of patients with similar characteristics. The envisioned digital tool will organize and present data relevant to the individual patient and enable evidence-based individualized treatment decision making when used in a collaborative manner with the patient family and rheumatologist. Capabilities in digital health technology, data capturing, and analytical methodologies are ripe for this endeavor. This brings the concept of a learning health system directly to the point of care.

Keywords: clinical decision support system; digital health technology; juvenile idiopathic arthritis; learning network model; personalized medicine; registry analysis; shared decision making.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Funding for this project was received from AHRQ R21/R33 grant mechanism to Co-PIs, Esi M. Morgan, MD, MSCE and Bin Huang, PhD (PA-21-164). Additionally, Dr. Huang is recipient of funding from Cincinnati Children’s Innovation Fund. Preliminary aspects of the work were funded by an award from PCORI to Dr. Huang (ME-1408-19894).