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Guiding Principles for Adolescent Web-Based Portal Access Policies: Interviews With Informatics Administrators
Bryan Sisk1,2, Alison L Antes1, Christine Bereitschaft2
1Bioethics Research Center, Department of Medicine, Washington University School of Medicine, St Louis, MO, United States.
Informatics leaders developed principles for adolescent patient portal access, balancing teen privacy with safety and legal needs. These guidelines help tailor policies for effective adolescent healthcare management.
Area of Science:
- Health Informatics
- Adolescent Health
- Patient Portals
Background:
- Web-based patient portals can empower adolescents in managing their health and autonomy.
- Developing portal access policies for adolescents involves balancing competing interests of administrators, patients, and parents.
Purpose of the Study:
- To assess informatics administrators' perspectives on guiding principles for web-based patient portal access policies in adolescent healthcare.
- To identify key considerations for creating effective and equitable portal access for young patients.
Main Methods:
- The study involved interviews with informatics administrators from US hospitals with at least 50 dedicated pediatric beds.
- A thematic analysis was conducted on the guiding principles for developing and implementing adolescent patient portal access policies.
Main Results:
- Sixty-five informatics leaders from 63 pediatric hospitals participated, representing diverse US healthcare systems.
- Nine guiding principles emerged, categorized into balancing confidentiality with care needs, simplicity with granularity, and collaboration/advocacy.
- Participants emphasized prioritizing adolescent health and safety within legal frameworks, though differing views on parental roles and specific implementations were noted.
Conclusions:
- Informatics administrators offer crucial principles for adolescent patient portal access policies, focusing on balancing confidentiality and utility.
- Policies must prioritize adolescent health and safety, adhering to legal requirements, with institutions determining practical enactment.
- Consensus among institutions and clinicians is vital for strengthening advocacy with electronic health record vendors and policymakers.
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