Evidence map›Paper›PMID 39606323›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Time-Series Deep Learning and Conformal Prediction for Improved Sepsis Diagnosis in Non-ICU Hospitalized Patients.

Shaunak Dalal, Ahad Khaleghi Ardabili, Anthony S Bonavia

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

5 · Who and what money

Authors and funding

3 authors.

Shaunak DalalDepartment of Anesthesiology and Perioperative Medicine, 500 University Dr, Hershey, 17033, PA, USA.
Ahad Khaleghi ArdabiliDepartment of Anesthesiology and Perioperative Medicine, 500 University Dr, Hershey, 17033, PA, USA.
Anthony S BonaviaDepartment of Anesthesiology and Perioperative Medicine, 500 University Dr, Hershey, 17033, PA, USA.ORCID 0000-0001-9596-001X

Funding

Integration of Immunologic Phenotyping with Computational Approaches to Predict Clinical Trajectory in Septic PatientsR35GM150695 · NIGMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Anthony S Bonavia · 2023 to 2026
$1.7M
NIGMS NIH HHS R35 GM150695
6 · The paper itself

Abstract

Purpose: Sepsis, a life-threatening condition from an uncontrolled immune response to infection, is a leading cause of in-hospital mortality. Early detection is crucial, yet traditional diagnostic methods, like SIRS and SOFA, often fail to identify sepsis in non-ICU settings where monitoring is less frequent. Recent machine learning (ML) models offer new possibilities but lack generalizability and suffer from high false alarm rates. Methods: We developed a deep learning (DL) model tailored for non-ICU environments, using MIMIC-IV data with a conformal prediction framework to handle uncertainty. The model was trained on 83,813 patients and validated with the eICU-CRD dataset to test performance across hospital settings. Results: Our model predicted sepsis at 24, 12, and 6 h before onset, achieving AUROCs of 0.96, 0.98, and 0.99, respectively. The conformal approach reduced false positives and improved specificity. External validation confirmed similar performance, with a 57% reduction in false alarms at the 6 h window, supporting practical use in low-monitoring environments. Conclusions: This DL-based model enables accurate, early sepsis prediction with minimal data, addressing key clinical challenges and potentially improving resource allocation in hospital settings by reducing unnecessary ICU admissions and enhancing timely interventions.

Indexed as

conformal predictiondeep learningdiagnosticssepsistime series

Identifiers

PMID39606323
PMCPMC11601686

What OpenQuestion holds

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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.