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The Patient Should Have a Choice

Adults with Sickle Cell Disease Advise Integration of Telemedicine into the Comprehensive Sickle Cell Disease Care Model

Bibliographic Data

ID2073099
AuthorsLydia H Pecker (0000-0002-8371-9752, Johns Hopkins University, corresponding author), Elizabeth Ruvalcaba (0009-0001-2326-424X, Johns Hopkins University), Sophie Lanzkron (0000-0002-2878-0251, Johns Hopkins University), Michelle N Eakin (0000-0002-8587-8343, Johns Hopkins University)
Year2024
Volume11
Issue6
Pages3249-3259
Publication date2024-12-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueJournal of Racial and Ethnic Health Disparities (JOURNAL)
Journal identifiersISSN: 2196-8837 • E-ISSN: 2197-3792
PublisherSpringer Science and Business Media LLC (PUBLISHER)
DOI10.1007/s40615-023-01780-6
PMID37682425
OpenAlexW4386529522
LanguageEN
References cited32

Coronavirus disease 2019 (COVID-19 · Disease · Family medicine · Health care · Infectious disease (medical specialty · Medical emergency · Pandemic · Pathology · Population · Qualitative research · Telemedicine · Hemoglobinopathies and Related Disorders · HIV/AIDS Research and Interventions · Medicine · Syphilis Diagnosis and Treatment

  • Covid-19 and Health Care’s Digital Revolution

    Sirina Keesara, Andrea Jonas et al.•New England Journal of Medicine•2020

  • Thematic analysis.

    Braun, Victoria Clarke•APA Handbook of Research Methods…•2012

  • Consolidated criteria for reporting qualitative research (Coreq)

    A Jaure, A Tong et al.•International Journal for Quality…•2007

Citation velocityhistorical
Highly citedNo

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