Evidence map›Paper›PMID 40533506›Full record

ArticlePediatric research2026

Machine learning model for daily prediction of pediatric sepsis using Phoenix criteria.

Daniela Chanci, Jocelyn R Grunwell, Alireza Rafiei, Stephanie R Brown, Michael J Ripple, Natalie R Bishop, Prakadeshwari Rajapreyar, Lisa M Lima, Rishikesan Kamaleswaran

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Article in Pediatric research, 2026. 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

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

7 citing papers in PubMed.

  1. Mortality risk prediction from dense PICU data from patients with suspected infection: data-derived physiological trajectories outperform expert assessments when temporal resolution is high.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2026
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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

9 authors.

Daniela Chanci *Department of Biomedical Engineering, Duke University, Durham, NC, USA. daniela.chanciarrubla@duke.edu.
Jocelyn R Grunwell *Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Alireza RafieiDepartment of Biomedical Informatics, Emory University, Atlanta, GA, USA.
Stephanie R BrownDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Michael J RippleDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Natalie R BishopDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Prakadeshwari RajapreyarDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Lisa M LimaDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Rishikesan KamaleswaranDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.

Funding

Airway Immune Response in Critically Ill Children-Precision Medicine in Children At Risk for Acute Respiratory Distress SyndromeK23HL151897 · NHLBI · EMORY UNIVERSITY · PI GRUNWELL, JOCELYN REBECCA · 2020 to 2024
$888k
NHLBI NIH HHS K23 HL151897
6 · The paper itself

Abstract

backgroundEarly sepsis diagnosis is essential for initiating prompt treatment, preventing the progression of organ failure, and improving the survival rate of critically ill children. The aim of this study was to develop and validate a machine learning sepsis prediction model for patients admitted to a pediatric intensive care unit (PICU) who met the Phoenix Sepsis Score Criteria using EMR data.

methodsData were obtained from two PICUs within the same healthcare system. Readily available variables were used to develop and validate machine learning models predicting the onset of sepsis in critically ill children.

resultsA total of 63,875 PICU encounters were included, of which there were 5248 who met the criteria for Phoenix Sepsis. We trained and tested 4 machine learning models using vital signs, laboratory tests, demographic data, medications, and organ dysfunction scores. The Categorical Boosting (CatBoost) model had the best performance with an AUROC of 0.98 (95% CI, 0.98-0.98), and an AUPRC of 0.83 (95% CI, 0.82-0.83).

conclusionsThe implementation of our model capable of predicting the onset of sepsis defined by the Phoenix Sepsis Score criteria may help clinicians recognize and manage children with sepsis more efficiently to reduce morbidity and mortality. IMPACT: Sepsis is a life-threatening condition with high rates of morbidity and mortality in children, especially in pediatric critical care units. However, there is no validated model using readily available variables in the electronic medical record data to identify critically ill patients with sepsis. The use of machine learning and electronic medical health records data to develop a predictive model can automate the identification of patients at high risk for sepsis-related organ dysfunction. The implementation of this tool can improve recognition of sepsis and prevent the progression of sepsis-related organ dysfunction leading to death.

Indexed as

Machine LearningSepsisAdolescentChildChild, PreschoolCritical IllnessElectronic Health RecordsFemaleHumansInfantInfant, NewbornIntensive Care Units, PediatricMaleOrgan Dysfunction ScoresRetrospective Studies

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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.