The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.21515/fullpdf
Reference12 articles.
1. Daily assessment of pain in adults with sickle cell disease;Smith;Ann Intern Med,2008
2. Medical care utilization and mortality in sickle cell disease: A population-based study;Shankar;Am J Hematol,2005
3. Hospitalization rates and costs of care of patients with sickle-cell anemia in the state of Maryland in the era of hydroxyurea;Lanzkron;Am J Hematol,2006
4. Utilization of the office, hospital and emergency department for adult sickle cell patients: A five-year study;Epstein;J Natl Med Assoc,2006
5. Epidemiologic analysis of an urban, public emergency department's frequent users;Mandelberg;Acad Emerg Med,2000
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1. Safety and efficacy of ketorolac continuous infusion for multimodal analgesia of vaso-occlusive crisis in patients with sickle cell disease;Orphanet Journal of Rare Diseases;2024-01-22
2. Comparing super-utilizers and lower-utilizers among commercial- and Medicare-insured adults with sickle cell disease;Blood Advances;2023-12-29
3. Psychiatric comorbidities in adults with sickle cell disease: A narrative review;British Journal of Haematology;2023-07-16
4. The Complex Association of Daily Opioid Dose with Visits for Pain in Sickle Cell Disease: Tolerance or Treatment-Refractory Pain?;Pain Medicine;2022-12-02
5. Chronic Pain;Hematology/Oncology Clinics of North America;2022-12
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