Sickle Cell Disease in the Emergency Department.
Publication/Presentation Date
12-1-2017
Abstract
Acute painful episodes are the most common reason for emergency department visits among patients with sickle cell disease (SCD). Early and aggressive pain management is a priority. Emergency providers (EPs) must also diagnose other emergent diagnoses in patients with SCD and differentiate them from vaso-occlusive crisis. EPs should be aware of cognitive biases that may misdirect the diagnostic process. Administration of intravenous fluids should be used judiciously. Blood transfusion may be considered. Coordination of care with hematology is an important part of the effective emergency department and long-term management of patients with SCD.
Volume
31
Issue
6
First Page
1061
Last Page
1079
ISSN
1558-1977
Published In/Presented At
Lovett, P. B., Sule, H. P., & Lopez, B. L. (2017). Sickle Cell Disease in the Emergency Department. Hematology/oncology clinics of North America, 31(6), 1061–1079. https://doi.org/10.1016/j.hoc.2017.08.009
Disciplines
Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods
PubMedID
29078924
Department(s)
Administration and Leadership
Document Type
Article