Identification of patients with hemoglobin SS/Sβ0 thalassemia disease and pain crises within electronic health records

Author:

Singh Ashima1,Mora Javier1,Panepinto Julie A.1

Affiliation:

1. Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI

Abstract

Key Points The algorithms have high sensitivity and specificity to identify patients with hemoglobin SS/Sβ0 thalassemia and acute care pain encounters. Codes conforming to common data model are provided to facilitate adoption of algorithms and standardize definitions for EHR-based research.

Publisher

American Society of Hematology

Subject

Hematology

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4. Acute care utilization and rehospitalizations for sickle cell disease;Brousseau;JAMA,2010

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