Evidence map›Paper›PMID 41322668›Full record

ArticleComputational and structural biotechnology journal2025

Design and validation of an automated healthcare-integrated biobanking algorithm for identification of advanced chronic kidney disease.

Claudia Fischer, Boris Betz, Johannes Stolp, Danny Ammon, André Scherag, Michael Kiehntopf

Abstract read
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Article in Computational and structural biotechnology journal, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Claudia FischerInstitute of Medical Statistics, Computer and Data Sciences (IMSID), Jena University Hospital - Friedrich Schiller University Jena, Jena, Germany.
Boris BetzDepartment of Clinical Chemistry and Laboratory Diagnostics and Integrated Biobank Jena (IBBJ), Jena University Hospital - Friedrich Schiller University Jena, Jena, Germany.
Johannes StolpDepartment of Clinical Chemistry and Laboratory Diagnostics and Integrated Biobank Jena (IBBJ), Jena University Hospital - Friedrich Schiller University Jena, Jena, Germany.
Danny AmmonData Integration Center, Jena University Hospital - Friedrich Schiller University Jena, Jena, Germany.
André ScheragInstitute of Medical Statistics, Computer and Data Sciences (IMSID), Jena University Hospital - Friedrich Schiller University Jena, Jena, Germany.
Michael KiehntopfDepartment of Clinical Chemistry and Laboratory Diagnostics and Integrated Biobank Jena (IBBJ), Jena University Hospital - Friedrich Schiller University Jena, Jena, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Healthcare-integrated biobanking (HIB) describes the collection of surplus samples from clinical routine and requires tailored algorithms for identification of adequate samples. However, identifying patients with specific conditions like chronic kidney disease (CKD) from heterogeneous real-world data remains challenging. This study develops and validates two HIB-specific algorithms for automated CKD identification based on electronic health records (EHR), enabling targeted sample collection and retrospective cohort assembly. Two logistic regression-based CKD algorithms were developed in an existing training cohort (n = 785) with high prevalence of CKD (48 %): the admissionHIB algorithm (based on laboratory values at admission) and the historyHIB algorithm (including additional previous hospital stays). The validation was carried out on patients of Jena University Hospital who gave informed consent to the Broad Consent of the Medical Informatics Initiative (MII) and were admitted between 01/2018 and 04/2020. The validation cohort was divided into a gold-standard cohort (n = 162) defined by manual chart review and a larger silver-standard cohort (n = 1075) generated using a validated algorithm from prior studies. The admissionHIB and historyHIB algorithms achieved F1-scores of 86 % and 91 %, respectively, in the training cohort. The validation cohort had a lower prevalence of CKD (approximately 12 %). Several automated review algorithms were evaluated in the gold-standard cohort, with the best-performing model (93 % recall, precision, and F1-score; 97 % accuracy) selected to generate the silver-standard cohort. Both HIB algorithms yielded F1-scores of 80 % (admissionHIB) and 78 % (historyHIB) in the gold-standard cohort, and 83 % and 80 %, respectively, in the silver-standard cohort. These findings demonstrate good performance of HIB-specific CKD algorithms across heterogeneous patient populations, establishing a reproducible framework combining real-world EHR data, patient consent infrastructure, and silver-standard validation.

Indexed as

Chronic kidney diseaseElectronic health records (EHR)Healthcare-integrated biobankingHIB algorithmsSilver-standard cohort

Identifiers

PMID41322668
PMCPMC12657308

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