Evidence map›Paper›PMID 41867227›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Two-step deep-learning candidemia prediction model using two large time-sequence electronic health datasets.

Hisato Yoshida, Max W Adelman, Laila Rasmy, Francis Ifiora, Ziqian Xie, María Alejandra Pérez, Francisco Guerra, Hitoshi Yoshimura, Stephen L Jones, Cesar A Arias and 2 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Corrections and comments

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

12 authors.

Hisato YoshidaCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.ORCID 0000-0003-1468-1903
Max W AdelmanCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.
Laila RasmyMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX, USA.ORCID 0000-0002-2644-4908
Francis IfioraCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.
Ziqian XieMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX, USA.
María Alejandra PérezCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.
Francisco GuerraDivision of Infectious Diseases, Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA.
Hitoshi YoshimuraDepartment of Dentistry and Oral Surgery, Unit of Sensory and Locomotor Medicine, Division of Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Stephen L JonesCenter for Health Data Science and Analytics, Houston Methodist Hospital, Houston, TX, USA; Department of Surgery, Weill Cornell Medical College, New York, NY, USA.
Cesar A AriasCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.
Degui ZhiMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX, USA.ORCID 0000-0001-7754-1890
Masayuki NigoCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.

Funding

Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogenP01AI152999 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HAAG, ANTHONY · 2020 to 2025
$12.0M
VENOUS: A translational study of enterococcal bacteremiaR01AI148342 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2020 to 2024
$3.9M
The LiaFSR system and antimicrobial peptide resistance in enterococciR01AI134637 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Cesar Augusto Arias · 2018 to 2026
$3.7M
Deep Learning Based Pharmacokinetic Model for VancomycinR01AI175699 · NIAID · METHODIST HOSPITAL RESEARCH INSTITUTE · PI NIGO, MASAYUKI · 2023 to 2025
$2.4M
POR Program on Genomic Prediction of Antimicrobial Resistance in VREK24AI121296 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2016 to 2025
$1.5M
Pathogen and patient determinants of Candida gut colonization in critically ill patientsK23AI185174 · NIAID · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Max Wiener Adelman · 2024 to 2026
$582k
NIAID NIH HHS K23 AI185174NIAID NIH HHS K24 AI121296NIAID NIH HHS P01 AI152999NIAID NIH HHS R01 AI134637NIAID NIH HHS R01 AI148342NIAID NIH HHS R01 AI175699
6 · The paper itself

Abstract

Background: Candidemia is a rare but life-threatening bloodstream infection that remains difficult to predict using conventional risk stratification approaches, highlighting the need for improved predictive strategies. As a result, empiric antifungal therapy is often delayed even in high-risk patients. Methods: We developed a deep learning model (PyTorch_EHR) to predict 7-day candidemia risk by using electronic health record data from two large cohorts (Houston Methodist Hospital System [HMHS] and MIMIC-IV), including adult inpatients who underwent at least one blood culture. Model performance was compared with logistic regression (LR), LightGBM, and established intensive care unit candidemia scores. We further implemented a two-step prediction framework integrating candidemia and 30-day mortality risk models to inform empiric antifungal decision-making. Results: Among 213,404 and 107,507 patients in the HMHS and MIMIC-IV cohorts, candidemia occurred in fewer than 1% (851 [0.4%] and 634 [0.6%], respectively). PyTorch_EHR outperformed LR, LightGBM, and existing candidemia scores, particularly in terms of area under the precision-recall curve (AUPRC) in HMHS and MIMIC-IV. By integrating 30-day mortality risk, the two-step framework identified an additional 20 and 28 candidemia cases beyond the one-step model, increasing coverage to 61% (121/199) and 46% (68/147) in HMHS and MIMIC-IV, respectively. Many patients identified by the two-step framework had high mortality yet did not receive empiric antifungal therapy (61.1% HMHS; 82.6% MIMIC-IV). Conclusion: A two-step deep-learning framework integrating candidemia and mortality risk may support early identification of high-risk patients and facilitate timely empiric antifungal therapy. Prospective studies are warranted to confirm the findings.

Indexed as

blood cultureCandidemiadeep learningelectronic health recordempirical antifungal therapy

Identifiers

PMID41867227
PMCPMC13001403

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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.