Evidence map›Paper›PMID 41564435›Full record

ArticleBlood advances2026

High concordance of physician-attestation with manual data abstraction for sickle cell type: an ASH RC Data Hub study.

Alexis A Thompson, Ashima Singh, Donna S Neuberg, Amanda M Brandow, Allison A King, Sophie Lanzkron, Emily A Semmel, Sam Walters, Susan Rogers, Kathleen Torres and 1 more

Abstract read
In one paragraph

Article in Blood advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Alexis A ThompsonDivision of Hematology, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0003-4961-8103
Ashima SinghDivision of Hematology and Oncology, Department of Pediatrics, Medical College of Wisconsin, Pewaukee, WI.ORCID 0000-0002-1270-8132
Donna S NeubergDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA.
Amanda M BrandowDepartment of Pediatrics, Section of Hematology/Oncology/Bone Marrow Transplantation, Medical College of Wisconsin, Milwaukee, WI.
Allison A KingSchool of Medicine, Washington University, Clayton, MO.ORCID 0000-0002-1951-6176
Sophie LanzkronDivision of Hematology, Cardeza Foundation for Hematologic Research, Thomas Jefferson University, Philadelphia, PA.
Emily A SemmelASH Research Collaborative, Washington, DC.
Sam WaltersASH Research Collaborative, Washington, DC.ORCID 0000-0002-8853-3084
Susan RogersASH Research Collaborative, Washington, DC.
Kathleen TorresASH Research Collaborative, Washington, DC.
William A WoodDivision of Hematology, Department of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractSickle cell disease (SCD) is the most common inherited blood disorder in the United States. The American Society of Hematology Research Collaborative (ASH RC) has built an SCD Data Hub (DH) to facilitate research and quality improvement using real-world data. To our knowledge, we report here the first analyses from the DH, focusing on cohort demographics and accurate identification of SCD diagnosis type. DH sites have data use agreements with ASH RC to extract and transfer electronic health record (EHR) data at least quarterly. Principal investigators (PI) provided additional attestation of SCD diagnosis based on existing local data sources deemed sufficient by the PI. A random sample of 25 patients (per site) with a physician-attested diagnosis and at least 1 encounter in 2022 had SCD type and other variables manually abstracted by site personnel. Concordance was calculated as the percentage of cases with the same SCD type determined by the physician-attested and abstracted methods. Twenty DH sites have submitted data for 23 970 unique individuals with SCD. The median patient age was 23 years (range, birth to 75 years); 55.4% were female. Physician-attested SCD diagnosis types on 9484 patients from 13 sites were reported as HbSS (67.2%), HbSC (22.2%), HbSß0thalassemia (2.1%), HbSβ+thalassemia (6.1%), and HbS/other (2.4%). Physician-attested SCD type had 94% (233/248) concordance with manual chart abstraction. High concordance increases confidence in the validity of SCD DH data. Well-curated and transformed data on a large cohort of individuals with SCD will be leveraged to conduct observational studies and inform the design and feasibility of prospective interventional studies.

Indexed as

Anemia, Sickle CellData AccuracyData WarehousingElectronic Health RecordsPhysiciansAdolescentAdultAgedChildChild, PreschoolFemaleHumansInfantInfant, NewbornInformation DisseminationMale

Identifiers

PMID41564435
PMCPMC13094422

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.