Use of electronic health record data mining for heart failure subtyping.

Data mining Ejection fraction Electronic health records HFmrEF HFpEF HFrEF Heart failure Text mining

Journal

BMC research notes
ISSN: 1756-0500
Titre abrégé: BMC Res Notes
Pays: England
ID NLM: 101462768

Informations de publication

Date de publication:
11 Sep 2023
Historique:
received: 14 10 2022
accepted: 22 08 2023
medline: 13 9 2023
pubmed: 12 9 2023
entrez: 12 9 2023
Statut: epublish

Résumé

To assess whether electronic health record (EHR) data text mining can be used to improve register-based heart failure (HF) subtyping. EHR data of 43,405 individuals from two Finnish hospital biobanks were mined for unstructured text mentions of ejection fraction (EF) and validated against clinical assessment in two sets of 100 randomly selected individuals. Structured laboratory data was then incorporated for a categorization by HF subtype (HF with mildly reduced EF, HFmrEF; HF with preserved EF, HFpEF; HF with reduced EF, HFrEF; and no HF). In 86% of the cases, the algorithm-identified EF belonged to the correct HF subtype range. Sensitivity, specificity, PPV and NPV of the algorithm were 94-100% for HFrEF, 85-100% for HFmrEF, and 96%, 67%, 53% and 98% for HFpEF. Survival analyses using the traditional diagnosis of HF were in concordance with the algorithm-based ones. Compared to healthy individuals, mortality increased from HFmrEF (hazard ratio [HR], 1.91; 95% confidence interval [CI], 1.24-2.95) to HFpEF (2.28; 1.80-2.88) to HFrEF group (2.63; 1.97-3.50) over a follow-up of 1.5 years. We conclude that quantitative EF data can be efficiently extracted from EHRs and used with laboratory data to subtype HF with reasonable accuracy, especially for HFrEF.

Identifiants

pubmed: 37697398
doi: 10.1186/s13104-023-06469-x
pii: 10.1186/s13104-023-06469-x
pmc: PMC10496250
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

208

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Matti A Vuori (MA)

Division of Medicine, University of Turku, Kiinamyllynkatu 10, Turku, FI-20520, Finland. makvuo@utu.fi.
Turku University Hospital, Kiinamyllynkatu 4-8, Box 52, Turku, FI-20521, Finland. makvuo@utu.fi.
Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Tukholmankatu 8, Helsinki, Finland. makvuo@utu.fi.

Tuomo Kiiskinen (T)

Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Tukholmankatu 8, Helsinki, Finland.

Niina Pitkänen (N)

Auria Biobank, Kiinamyllynkatu 10, PO Box 30, Turku, FI-20520, Finland.

Samu Kurki (S)

Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Tukholmankatu 8, Helsinki, Finland.
Auria Biobank, Kiinamyllynkatu 10, PO Box 30, Turku, FI-20520, Finland.

Hannele Laivuori (H)

Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Tukholmankatu 8, Helsinki, Finland.
Centre for Child, Adolescent, and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Department of Obstetrics and Gynecology, Tampere University Hospital, Tampere, Finland.

Tarja Laitinen (T)

Administration Center, Tampere University Hospital and University of Tampere, P.O. Box 2000, Tampere, 33521, Finland.

Sampo Mäntylahti (S)

Helsinki Biobank, Haartmaninkatu 3, Helsinki, 00290, Finland.

Aarno Palotie (A)

Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Tukholmankatu 8, Helsinki, Finland.
Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Tukholmankatu 8, Helsinki, Finland.

Teemu J Niiranen (TJ)

Division of Medicine, University of Turku, Kiinamyllynkatu 10, Turku, FI-20520, Finland.
Turku University Hospital, Kiinamyllynkatu 4-8, Box 52, Turku, FI-20521, Finland.
Department of Public Health Solutions, Finnish Institute for Health and Welfare, PO Box 30, Helsinki, FI-00271, Finland.

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