“The Patient Should Have a Choice”: Adults with Sickle Cell Disease Advise Integration of Telemedicine into the Comprehensive Sickle Cell Disease Care Model
Author:
Funder
Patient-Centered Outcomes Research Institute
Publisher
Springer Science and Business Media LLC
Subject
Public Health, Environmental and Occupational Health,Health Policy,Sociology and Political Science,Anthropology,Health (social science)
Link
https://link.springer.com/content/pdf/10.1007/s40615-023-01780-6.pdf
Reference33 articles.
1. Kanter J, Smith WR, Desai PC, et al. Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects. Blood Adv. 2020;4:3804–13.
2. Woods K, Kutlar A, Grigsby RK, et al. Primary-care delivery for sickle cell patients in rural Georgia using telemedicine. Telemed J. 1998;4:353–61.
3. Keesara S, Jonas A, Schulman K. Covid-19 and health care’s digital revolution. New Engl J Med. 2020;382:e82.
4. Noisette ML, Phillips S, Schlenz AM, et al. Changes in care delivery for children with sickle cell anemia during the COVID-19 pandemic. J Pediatric Hematol Oncol. 2020;43:e1231–4.
5. Reeves SL, Patel PN, Madden B, et al. Telehealth use before and during the COVID-19 pandemic among children with sickle cell anemia. Telemed E-health. 2022;28:1166–71.
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