Trusted Resources: Evidence & Education
Scientific literature and patient education texts
Sickle cell disease in the emergency department
source: Hematology/Oncology Clinics of North America
year: 2017
authors: Lovett PB, Sule HP, Lopez BL
summary/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.
organization: Thomas Jefferson University & Hospitals, PhiladelphiaDOI: 10.1016/j.hoc.2017.08.009
read more full text
+myBinderRelated Content
-
Pfizer rare disease introduces Council for Change to further help SCD patientsFollowing a report earlier thi...
-
Sickle Cell Disease, More Than Just Pain: The Mediating Role of Psychological SymptomsObjectives: Perceived stress is associa...
-
Fondation Pierre FabreRecognized as a public utility since 199...
-
Colorado Sickle Cell Research and Treatment CenterColorado Sickle Cell Treatment and Resea...
-
Sickle Cell Disease and Cold Weather: Dos and Don’tsIn the United States today, one of every...
-
Flying doctor takes to the skies after sister’s deathOlamide Orekunrin was studying to become...
-
Yvonne Carroll, RN, JDYvonne M. Carroll, RN, JD is the Directo...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.