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Article

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

Blood advances - 12 Jun 2018

Singh Ashima, Mora Javier, Panepinto Julie A

Abstract excerpt

Electronic health records (EHRs) are a source of big data that provide opportunities for conducting population-based studies and creating learning health systems, especially for rare conditions such as sickle cell disease (SCD). The objective of our study is to validate algorithms for accurate identification of patients with hemoglobin (Hb) SS/Sβ0 thalassemia and acute care encounters for pain among SCD patients...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 29792312
DOI: 10.1182/bloodadvances.2018017541
PMCID: PMC5998922

Genes

SCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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