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Rethinking Care Models for Young Adults With Sickle Cell Disease

Bibliographic Data

ID15808463
AuthorsAlexander A Boucher (0000-0002-5392-1829, University of Minnesota Medical Center, corresponding author), Margaret Lyons (Brown University), Patrick T McGann (0000-0001-6198-4785, Lifespan)
Year2023
Volume4
Issue5
Pagese230877-e230877
Publication date2023-05-12
Open AccessYes
TypeARTICLE
VenueJAMA Health Forum (JOURNAL)
Journal identifiersISSN: 2689-0186 • E-ISSN: 2689-0186
PublisherAmerican Medical Association (PUBLISHER • US)
DOI10.1001/jamahealthforum.2023.0877
PMID37171796
OpenAlexW4376224230
LanguageEN
Citations received1
References cited10

This Viewpoint discusses developing new sickle cell disease adult care models to support specialized health care homes that are patient-focused and antiracist, rather than an approach focused mainly on financial incentives

Disease · Economic growth · Economics · Health care · Incentive · Intensive care medicine · Young adult · Adolescent and Pediatric Healthcare · Hemoglobinopathies and Related Disorders · Homelessness and Social Issues · Medicine · Psychology · Gerontology · Internal Medicine

  • The Predictive Influence of Self-Efficacy and Socioeconomic Factors on the Physical and Mental Health-Related Quality of Life of Adolescents and Young Adults with Sickle Cell Disease

    Open Access•Akinpelu Tomiwa•African Journal of Social…•2025

Citations per year1
Citation span2025 - 2025 (1)
Highly citedNo

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