Evidence map›Paper›PMID 40541283›Full record

Observational studyBMJ paediatrics open2025

Machine learning approaches to identify neonates and young children at risk for postdischarge mortality in Dar es Salaam, Tanzania and Monrovia, Liberia.

Chris A Rees, Rodrick Kisenge, Evance Godfrey, Readon C Ideh, Julia Kamara, Ye-Jeung G Coleman-Nekar, Abraham Samma, Hussein K Manji, Christopher R Sudfeld, Adrianna L Westbrook and 7 more

Abstract readObservational Study
In one paragraph

Observational study in BMJ paediatrics open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

17 authors.

Chris A ReesDivision of Pediatric Emergency Medicine, Emory University School of Medicine, Atlanta, Georgia, USA chrisrees2@gmail.com.ORCID http://orcid.org/0009-0005-7268-4346
Rodrick KisengeDepartment of Pediatrics and Child Health, Muhimbili University of Health and Allied Sciences, Dar es Salaam, United Republic of Tanzania.
Evance GodfreyMuhimbili National Hospital, Dar es Salaam, United Republic of Tanzania.
Readon C IdehDepartment of Pediatrics, John F. Kennedy Medical Center, Monrovia, Liberia.
Julia KamaraDepartment of Pediatrics, John F. Kennedy Medical Center, Monrovia, Liberia.
Ye-Jeung G Coleman-NekarDepartment of Pediatrics, John F. Kennedy Medical Center, Monrovia, Liberia.
Abraham SammaPediatrics and Child health, Muhimbili University of Health and Allied Sciences, Dar es Salaam, United Republic of Tanzania.
Hussein K ManjiDepartment of Emergency Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, United Republic of Tanzania.
Christopher R SudfeldDepartments of Nutrition and Global Health and Population, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Adrianna L WestbrookPediatrics Biostatistics Core, Department of Pediatrics, Emory University, Atlanta, Georgia, USA.
Michelle NiescierenkoDivision of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Claudia R MorrisDivision of Pediatric Emergency Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Todd A FlorinDivision of Emergency Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Cynthia G WhitneyGlobal Health Institute, Emory University, Atlanta, Georgia, USA.
Karim P ManjiDepartment of Pediatrics and Child Health, Muhimbili University of Health and Allied Sciences, Dar es Salaam, United Republic of Tanzania.
Christopher P DugganDepartments of Nutrition and Global Health and Population, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Rishikesan KamaleswaranDivision of Translational Biomedical Informatics, Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.

Funding

Implementing a Maternal health and PRegnancy Outcomes Vision for Everyone (IMPROVE)UL1TR002378 · NCATS · EMORY UNIVERSITY · PI Andres J Garcia, Elizabeth O. Ofili · 2017 to 2026
$92.1M
ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI STEVEN K. GRINSPOON · 1994 to 2026
$31.6M
Patient-Oriented Research in Arginine Deficiency SyndromesK24AT009893 · NCCIH · EMORY UNIVERSITY · PI Claudia R Morris · 2018 to 2026
$1.5M
Patient-oriented Research in Pediatric Diarrheal DiseasesK24DK104676 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI DUGGAN, CHRISTOPHER P · 2015 to 2019
$903k
Advancing Approaches to Identify Young Children at Risk for Post-Discharge MortalityK23HL173694 · NHLBI · EMORY UNIVERSITY · PI Christopher A. Rees · 2024 to 2026
$585k
NCATS NIH HHS UL1 TR002378NCCIH NIH HHS K24 AT009893NHLBI NIH HHS K23 HL173694NIDDK NIH HHS K24 DK104676NIDDK NIH HHS P30 DK040561
6 · The paper itself

Abstract

backgroundThe time after hospital discharge carries high rates of mortality in neonates and young children in sub-Saharan Africa. Previous work using logistic regression to develop risk assessment tools to identify those at risk for postdischarge mortality has yielded fair discriminatory value. Our objective was to determine if machine learning models would have greater discriminatory value to identify neonates and young children at risk for postdischarge mortality.

methodsWe conducted a planned secondary analysis of a prospective observational cohort at Muhimbili National Hospital in Dar es Salaam, Tanzania and John F. Kennedy Medical Center in Monrovia, Liberia. We enrolled neonates and young children near the time of discharge. The outcome was 60-day postdischarge mortality. We collected socioeconomic, demographic, clinical, and anthropometric data during hospital admission and used machine learning (ie, eXtreme Gradient Boosting (XGBoost), Hist-Gradient Boost, Support Vector Machine, Neural Network, and Random Forest) to develop risk assessment tools to identify: (1) neonates and (2) young children at risk for postdischarge mortality.

resultsA total of 2310 neonates and 1933 young children enrolled. Of these, 71 (3.1%) neonates and 67 (3.5%) young children died after hospital discharge. XGBoost, Hist Gradient Boost, and Neural Network models yielded the greatest discriminatory value (area under the receiver operating characteristic curves range: 0.94-0.99) and fewest features, which included six features for neonates and five for young children. Discharge against medical advice, low birth weight, and supplemental oxygen requirement during hospitalisation were predictive of postdischarge mortality in neonates. For young children, discharge against medical advice, pallor, and chronic medical problems were predictive of postdischarge mortality.

conclusionsOur parsimonious machine learning-based models had excellent discriminatory value to predict postdischarge mortality among neonates and young children. External validation of these tools is warranted to assist in the design of interventions to reduce postdischarge mortality in these vulnerable populations.

Indexed as

Infant MortalityMachine LearningPatient DischargeChild, PreschoolFemaleHumansInfantInfant, NewbornLiberiaMaleProspective StudiesRisk AssessmentTanzaniaInfantMachine LearningMortalityNeonatology

Identifiers

PMID40541283
PMCPMC12182169

What OpenQuestion holds

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Registered trials

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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.