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Sharko, Marianne

https://orcid.org/0000-0002-1103-7525

Mayo Clinic

Weill Cornell Medicine

Citations 3

Patient-Driven Sharing of Health Information: A National Effort to Advance Equitable Interoperability
Galvin, Hannah K. , Sharko, Marianne , Jafari, Mohammad, Mack, Serena, English, Abigail , Petersen, Carolyn , Petersen, Carolyn , Coughlin, Jeff, Grando, Adela

Applied Clinical Informatics | August 29, 2025 | Volume: 16 | Issue: 04 | Pages: 951-960

10.1055/a-2591-9129 Get It

AbstractThe goal of national interoperability is to improve care quality and decrease administrative burden and costs. Patients, providers, and other stakeholders are increasingly concerned that indiscriminate sharing of data may have deleterious, permanent consequences, as well as fail to provide granular control over the sharing of individual health data. Data segmentation and consent standards to date have been limited in scope and implementation, which has hindered efforts to scale data sharing preferences. Shift, an independent expert stakeholder task force, has been convened to mature standards, terminologies, and consensus-driven implementation guidance, which are prerequisites for more robust policy drivers needed to support nationwide sensitive data segmentation and consent capabilities. This paper describes Shift's framework and processes as means to advance equitable interoperability.
Equitable Interoperability Through Precise Control of Sensitive Health Information: An Emerging Pathway to Health Equity
Petersen, Carolyn , Galvin, Hannah K. , Lehmann, Christoph U. , Sharko, Marianne , Lehmann, Christoph U , Petersen, Carolyn

Annals of Internal Medicine | March 4, 2024 | Volume: 177 | Issue: 3 | Pages: 387-388

10.7326/m23-2876 Get It

Shifting into Action: from Data Segmentation to Equitable Interoperability for Adolescents (and Everyone Else)
Sarabu, Chethan , Sharko, Marianne , Petersen, Carolyn , Galvin, Hannah K. , Petersen, Carolyn

Applied Clinical Informatics | July 19, 2023 | Volume: 14 | Issue: 03 | Pages: 544-554

10.1055/s-0043-1769924 Get It

Abstract Background Technological improvements and, subsequently, the federal 21st Century Cures Act have resulted in increased access to and interoperability of electronic protected health information (ePHI). These not only have many benefits, but also have created unique challenges for privacy and confidentiality for adolescent patients. The inability to granularly protect sensitive data and a lack of standards have resulted in limited confidentiality protection and inequitable access to health information. Objectives This study aimed to understand the challenges to safe, equitable access, and interoperability of ePHI for adolescents and to identify strategies that have been developed, ongoing needs, and work in progress. Methods Shift, a national task force formalized in 2020, is a group of more than 200 expert stakeholder members working to improve functionality to standardize efforts to granularly identify and protect sensitive ePHI to promote equitable interoperability. Results Shift has created high-priority clinical use cases and organized challenges into the areas of Standards and Terminology; Usability and Implementation; and Ethics, Legal, and Policy. Conclusion Current technical standards and value sets of terminology for sensitive data have been immature and inconsistent. Shift, a national diverse working group of stakeholders, is addressing challenges inherent in the protection of privacy and confidentiality for adolescent patients. The diversity of expertise and perspectives has been essential to identify and address these challenges.