Evidence map›Paper›PMID 42553473›Full record

ArticleHealth science reports2026

Predicting Outcomes of Traumatic Brain Injury Using Machine Learning Models Among Patients at Kilimanjaro Christian Medical Centre, Tanzania: A Registry-Based Cohort Study.

William Nkenguye, Edwin Joseph Shewiyo, João Vitor Perez De Souza, Timothy Antipas Peter, Alice Andongolile, Rosalia Njau, Baraka Moshi, Johnston George, Paige O'Leary, Catherine Staton and 4 more

Abstract read
In one paragraph

Article in Health science reports, 2026. 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

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

14 authors.

William NkenguyeDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.ORCID https://orcid.org/0000-0003-4322-7937
Edwin Joseph ShewiyoDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.ORCID https://orcid.org/0000-0002-2707-2720
João Vitor Perez De SouzaGlobal Emergency Medicine Innovation and Implementation (GEMINI) Research Centre, Duke Global Health Institute Duke University Durham North Carolina USA.
Timothy Antipas PeterDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.ORCID https://orcid.org/0000-0002-3112-1847
Alice AndongolileDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.ORCID https://orcid.org/0009-0005-7910-8237
Rosalia NjauDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.ORCID https://orcid.org/0009-0004-4116-7189
Baraka MoshiDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.ORCID https://orcid.org/0000-0002-2894-5132
Johnston GeorgeDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.
Paige O'LearyGlobal Emergency Medicine Innovation and Implementation (GEMINI) Research Centre, Duke Global Health Institute Duke University Durham North Carolina USA.
Catherine StatonGlobal Emergency Medicine Innovation and Implementation (GEMINI) Research Centre, Duke Global Health Institute Duke University Durham North Carolina USA.ORCID https://orcid.org/0000-0002-6468-2894
Blandina T MmbagaKilimanjaro Clinical Research Institute Moshi Tanzania.ORCID https://orcid.org/0000-0002-5550-1916
Francis M SakitaKilimanjaro Clinical Research Institute Moshi Tanzania.
João Ricardo Nickenig VissociGlobal Emergency Medicine Innovation and Implementation (GEMINI) Research Centre, Duke Global Health Institute Duke University Durham North Carolina USA.
Innocent B MboyaDepartment of Epidemiology and Biostatistics, School of Public Health KCMC University Moshi Tanzania.ORCID https://orcid.org/0000-0001-9861-5879

Funding

The TRECK Program: Trauma REsearch Capacity Building in Kilimanjaro, TanzaniaD43TW012205 · FIC · KILIMANJARO CHRISTIAN MEDICAL CENTRE · PI MMBAGA, BLANDINA THEOPHIL, STATON, CATHERINE ANN · 2021 to 2025
$1.5M
FIC NIH HHS D43 TW012205
6 · The paper itself

Abstract

Background: Traumatic brain injury (TBI) remains a major global health burden, disproportionately affecting low- and middle-income countries (LMICs) where access to neurocritical care is limited. Accurate and context-appropriate prognostic models are crucial to guide early clinical decision-making and optimize resource allocation in such settings. This study aims to develop and evaluate machine learning (ML) models for predicting TBI outcomes among adult patients using trauma registry data from Kilimanjaro Christian Medical Centre (KCMC), Tanzania. Methods: This retrospective cohort study utilized data from 4596 adult TBI patients recorded in the KCMC trauma registry between 2013 and 2024. The outcome was dichotomized Glasgow Outcome Scale (GOS): poor (1-3) versus good (4-5). Ten supervised ML algorithms, including Random Forest (RF), Decision Tree (DT), Logistic Regression, Support Vector Machine (SVM), and Artificial Neural Networks (ANN), were trained on 70% of the data after applying multiple imputation and synthetic minority Over-sampling Technique (SMOTE) to address missingness and class imbalance. Hyperparameter tuning was performed using 10-fold cross-validation. Model performance was assessed on a 30% test set using area under the ROC curve (AUC), accuracy, sensitivity, specificity, and predictive values. Results: Among the 4596 patients, 26.2% had poor outcomes. The RF and DT models achieved the highest AUCs of 0.83 and 0.82, respectively. RF also showed the highest accuracy (0.78) and strong positive predictive value (PPV = 0.87), while DT had the highest sensitivity for poor outcomes (84.5%). Predictors of poor outcomes included TBI severity, pupil non-reactivity, low oxygen saturation, lack of CT scan, alcohol use, and abnormal vital signs. Conclusion: ML models, particularly RF and DT, demonstrated strong predictive performance for TBI outcomes using routinely collected variables in a resource-limited LMIC setting. Their interpretability and reliance on admission-level data make them potential tools for real-time triage and risk stratification. Future research should focus on external validation and integration into clinical decision-support systems to support scaleup across similar settings.

Indexed as

emergency carelow‐ and middle‐income countriesmachine learningprognostic modelrisk predictionTanzaniatraumatic brain injury

Identifiers

PMID42553473
PMCPMC13434442

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LicenceCC BY-NC-ND
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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.