Optimized identification of advanced chronic kidney disease and absence of kidney disease by combining different electronic health data resources and by applying machine learning strategies

GND
1219873985
Zugehörigkeit
Department of Clinical Chemistry and Laboratory Diagnostics and Integrated Biobank Jena (IBBJ), Jena University Hospital, 07747 Jena, Germany, christoph.weber@med.uni-jena.de
Weber, Christoph;
GND
121987325X
Zugehörigkeit
Department of Clinical Chemistry and Laboratory Diagnostics and Integrated Biobank Jena (IBBJ), Jena University Hospital, 07747 Jena, Germany, lena.marie.roeschke@uni-jena.de
Röschke, Lena;
GND
1219868736
Zugehörigkeit
Jena University Language & Information Engineering (JULIE) Lab, Friedrich Schiller University Jena, 07743 Jena, Germany, luise.modersohn@uni-jena.de
Modersohn, Luise;
ORCID
0000-0001-9889-162X
Zugehörigkeit
Jena University Language & Information Engineering (JULIE) Lab, Friedrich Schiller University Jena, 07743 Jena, Germany, christina.lohr@uni-jena.de
Lohr, Christina;
GND
1219872229
Zugehörigkeit
Jena University Language & Information Engineering (JULIE) Lab, Friedrich Schiller University Jena, 07743 Jena, Germany, tbs.kldtz@gmail.com
Kolditz, Tobias;
GND
1029524645
Zugehörigkeit
Jena University Language & Information Engineering (JULIE) Lab, Friedrich Schiller University Jena, 07743 Jena, Germany, udo.hahn@uni-jena.de
Hahn, Udo;
ORCID
0000-0001-8960-7316
Zugehörigkeit
Data Integration Center, Jena University Hospital, 07743 Jena, Germany, danny.ammon@med.uni-jena.de
Ammon, Danny;
GND
141147504
Zugehörigkeit
Department of Clinical Chemistry and Laboratory Diagnostics and Integrated Biobank Jena (IBBJ), Jena University Hospital, 07747 Jena, Germany, Boris.Betz@med.uni-jena.de
Betz, Boris;
GND
114935971
Zugehörigkeit
Department of Clinical Chemistry and Laboratory Diagnostics and Integrated Biobank Jena (IBBJ), Jena University Hospital, 07747 Jena, Germany, Michael.Kiehntopf@med.uni-jena.de
Kiehntopf, Michael

Automated identification of advanced chronic kidney disease (CKD ≥ III) and of no known kidney disease (NKD) can support both clinicians and researchers. We hypothesized that identification of CKD and NKD can be improved, by combining information from different electronic health record (EHR) resources, comprising laboratory values, discharge summaries and ICD-10 billing codes, compared to using each component alone. We included EHRs from 785 elderly multimorbid patients, hospitalized between 2010 and 2015, that were divided into a training and a test (n = 156) dataset. We used both the area under the receiver operating characteristic (AUROC) and under the precision-recall curve (AUCPR) with a 95% confidence interval for evaluation of different classification models. In the test dataset, the combination of EHR components as a simple classifier identified CKD ≥ III (AUROC 0.96[0.93–0.98]) and NKD (AUROC 0.94[0.91–0.97]) better than laboratory values (AUROC CKD 0.85[0.79–0.90], NKD 0.91[0.87–0.94]), discharge summaries (AUROC CKD 0.87[0.82–0.92], NKD 0.84[0.79–0.89]) or ICD-10 billing codes (AUROC CKD 0.85[0.80–0.91], NKD 0.77[0.72–0.83]) alone. Logistic regression and machine learning models improved recognition of CKD ≥ III compared to the simple classifier if only laboratory values were used (AUROC 0.96[0.92–0.99] vs. 0.86[0.81–0.91], p < 0.05) and improved recognition of NKD if information from previous hospital stays was used (AUROC 0.99[0.98–1.00] vs. 0.95[0.92–0.97]], p < 0.05). Depending on the availability of data, correct automated identification of CKD ≥ III and NKD from EHRs can be improved by generating classification models based on the combination of different EHR components.

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