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. 2025 Jul 1;5(7):e0004606.
doi: 10.1371/journal.pgph.0004606. eCollection 2025.

Validation of a risk-prediction model for pediatric post-discharge mortality after hospital admission for infection in Rwanda: A prospective cohort study

Affiliations

Validation of a risk-prediction model for pediatric post-discharge mortality after hospital admission for infection in Rwanda: A prospective cohort study

Anneka Hooft et al. PLOS Glob Public Health. .

Abstract

Mortality following hospital discharge remains a significant threat to child health, particularly in resource-limited settings. The Smart Discharges risk-prediction models use simple clinical, socio-behavioral, and point-of-care lab test variables to successfully predict children at the highest risk of death after hospital admission for infection to guide a risk-based approach to post-discharge care. In Rwanda, we externally validated five models derived from the prior Smart Discharges Uganda studies in a new cohort of children ages 0 days to 60 months admitted for suspected sepsis at two hospitals. We evaluated model performance using metrics including area under the receiver operating characteristic curve (AUROC), Brier score, and test characteristics (e.g., sensitivity, specificity). Performance was visualized through ROC and gain curves and calibration plots. Of 1218 total children (n = 413, Kigali; n = 805, Ruhengeri), 1161 lived to discharge (95.3%) and 1123 of those completed 6-month follow-up (96.7%). The overall rate of post-discharge mortality was 4.8% (n = 58). All five prediction models tested achieved an area under the receiver-operating curve (AUROC) greater than 0.7 (range 0.706 - 0.738). Low outcome rates resulted in moderately wide confidence intervals. Model degradation ranged from 1.1% to 7.7%, as determined by the percent reduction in AUROC between the internal validation of the original Ugandan cohort and the external Rwandan cohort. Calibration plots showed good calibration for all models at predicted probabilities below 10%. There were too few outcomes to assess calibration among those at the highest predicted risk levels. Discrimination was good with minimal degradation of the model despite low outcome rates. Future work to assess model calibration among the highest risk groups is required to ensure models are broadly generalizable to all children with suspected sepsis in Rwanda and in similar, resource-limited settings.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Study flow chart stratified by age group.
Fig 2
Fig 2. Performance of the two prediction models for post-discharge mortality in Rwanda validation cohort for 0-6 month age group.
Fig 3
Fig 3. Performance of the three prediction models for post-discharge mortality in Rwanda validation cohort for the 6–60-month age group.

References

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