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Deep learning-based prediction of Clostridioides difficile infection caused by antibiotics using longitudinal electronic health recordsopen access

Authors
Kim, JunmoKim, Joo SeongKim, Sae-HoonYoo, SooyoungLee, Jun KyuKim, Kwangsoo
Issue Date
Aug-2024
Publisher
NATURE PUBLISHING GROUP
Keywords
Prediction Models; Antibiotic Treatment; Clinical Settings; Electronic Health; Faecal Orals; Health Records; Hospital Acquired Infection; Learning Based Models; Oral Route; Risk Groups; Risk Score; Electronic Health Record; Antibiotic Agent; Adult; Age; Aged; Antibiotic Therapy; Area Under The Curve; Article; Body Temperature; Clostridium Difficile Infection; Comorbidity; Controlled Study; Deep Learning; Diagnostic Test Accuracy Study; Electronic Health Record; Female; Human; Laboratory Test; Longitudinal Study; Major Clinical Study; Male; Middle Aged; Patient Information; Platelet Count; Receiver Operating Characteristic; Sex; Vital Sign
Citation
Npj Digital Medicine, v.7, no.1, pp 1 - 10
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
Npj Digital Medicine
Volume
7
Number
1
Start Page
1
End Page
10
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/22975
DOI
10.1038/s41746-024-01215-4
ISSN
2398-6352
2398-6352
Abstract
Clostridioides difficile infection (CDI) is a major cause of antibiotic-associated diarrhea and colitis. It is recognized as one of the most significant hospital-acquired infections. Although CDI can develop severe complications and spores of Clostridioides difficile can be transmitted by the fecal-oral route, CDI is occasionally overlooked in clinical settings. Thus, it is necessary to monitor high CDI risk groups, particularly those undergoing antibiotic treatment, to prevent complications and spread. We developed and validated a deep learning-based model to predict the occurrence of CDI within 28 days after starting antibiotic treatment using longitudinal electronic health records. For each patient, timelines of vital signs and laboratory tests with a 35-day monitoring period and a patient information vector consisting of age, sex, comorbidities, and medications were constructed. Our model achieved the prediction performance with an area under the receiver operating characteristic curve of 0.952 (95% CI: 0.932-0.973) in internal validation and 0.972 (95% CI: 0.968-0.975) in external validation. Platelet count and body temperature emerged as the most important features. The risk score, the output value of the model, exhibited a consistent increase in the CDI group, while the risk score in the non-CDI group either maintained its initial value or decreased. Using our CDI prediction model, high-risk patients requiring symptom monitoring can be identified. This could help reduce the underdiagnosis of CDI, thereby decreasing transmission and preventing complications.
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