Quality Metrics and Health Care Utilization for Adult Patients with Sickle Cell Disease
Author:
Funder
Mid-Atlantic Permanente Medical Group
Kaiser Permanente Mid-Atlantic States Community Benefits Program
Johns Hopkins Medicine
Publisher
Elsevier BV
Subject
General Medicine
Reference16 articles.
1. Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: the last 40 years;Chaturvedi;Am J Hematol,2016
2. Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members;Yawn;JAMA,2014
3. Recent treatment guidelines for managing adult patients with sickle cell disease: challenges in access to care, social issues, and adherence;Adams-Graves;Expert Rev Hematol,2016
4. Caring for the adult with sickle cell disease: results of a multidisciplinary pilot program;Artz;J Natl Med Assoc,2010
5. Development of a new adult sickle cell disease center within an academic cancer center: impact on hospital utilization patterns and care quality;Andemariam;J Racial Ethn Health Disparities,2016
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2. Assessing barriers and facilitators to transition in sickle cell disease care prior to implementation of a formalized program;Pediatric Blood & Cancer;2023-01-08
3. Patient Perspectives of Sickle Cell Management in the Emergency Department;Critical Care Nursing Quarterly;2021-04
4. Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects;Blood Advances;2020-08-12
5. Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review;International Journal of General Medicine;2020-07
Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review
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