Evidence map›Paper›PMID 39133661›Full record

ArticlePLOS digital health2024

Improving sepsis prediction in intensive care with SepsisAI: A clinical decision support system with a focus on minimizing false alarms.

Ankit Gupta, Ruchi Chauhan, Saravanan G, Ananth Shreekumar

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Article in PLOS digital health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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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

4 authors.

Ankit GuptaCenter for Innovation in Diagnostics, Siemens Healthcare Private Limited, Bangalore, India.ORCID https://orcid.org/0009-0002-0406-0716
Ruchi ChauhanCenter for Innovation in Diagnostics, Siemens Healthcare Private Limited, Bangalore, India.
Saravanan GCenter for Innovation in Diagnostics, Siemens Healthcare Private Limited, Bangalore, India.
Ananth ShreekumarCenter for Innovation in Diagnostics, Siemens Healthcare Private Limited, Bangalore, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prediction of sepsis using machine-learning approaches has recently gained traction. However, the lack of translation of these algorithms into clinical routine remains a major issue. Existing early sepsis detection methods are either based on the older definition of sepsis or do not accurately detect sepsis leading to the high frequency of false-positive alarms. This results in a well-known issue of clinicians' "alarm fatigue", leading to decreased responsiveness and identification, ultimately resulting in delayed clinical intervention. Hence, there is a fundamental, unmet need for a clinical decision system capable of accurate and timely sepsis diagnosis, running at the point of need. In this work, SepsisAI-a deep-learning algorithm based on long short-term memory (LSTM) networks was developed to predict the early onset of hospital-acquired sepsis in real-time for patients admitted to the ICU. The models are trained and validated with data from the PhysioNet Challenge, consisting of 40,336 patient data files from two healthcare systems: Beth Israel Deaconess Medical Center and Emory University Hospital. In the short term, the algorithm tracks frequently measured vital signs, sparsely available lab parameters, demographic features, and certain derived features for making predictions. A real-time alert system, which monitors the trajectory of the predictions, is developed on top of the deep-learning framework to minimize false alarms. On a balanced test dataset, the model achieves an AUROC, AUPRC, sensitivity, and specificity of 0.95, 0.96, 88.19%, and 96.75%, respectively at the patient level. In terms of lookahead time, the model issues a warning at a median of 6 hours (IQR 6 to 20 hours) and raises an alert at a median of 4 hours (IQR 2 to 5 hours) ahead of sepsis onset. Most importantly, the model achieves a false-alarm ratio of 3.18% for alerts, which is significantly less than other sepsis alarm systems. Additionally, on a disease prevalence-based test set, the algorithm reported similar outcomes with AUROC and AUPRC of 0.94 and 0.87, respectively, with sensitivity, and specificity of 97.05%, and 96.75%, respectively. The proposed algorithm might serve as a clinical decision support system to assist clinicians in the accurate and timely diagnosis of sepsis. With exceptionally high specificity and low false-alarm rate, this algorithm also helps mitigate the well-known issue of clinician alert fatigue arising from currently proposed sepsis alarm systems. Consequently, the algorithm partially addresses the challenges of successfully integrating machine-learning algorithms into routine clinical care.

Identifiers

PMID39133661
PMCPMC11318852

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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.