# Validation of CURB-65, CRB-65, NEWS2, qSOFA, and 4C scores for predicting mortality in COVID-19 patients across seven emergency Departments in Colombia

**Authors:** Sandra Liliana Valderrama-Beltrán, Juliana Cuervo-Rojas, Martín Rondón, Samuel Martinez-Vernaza, Ilich Herbert De La Hoz Siegler, Alfonso J. Rodriguez-Morales, Alejandra Cañas-Arboleda, Oscar Muñoz, Mónica Padilla, María Lucía Mesa-Rubio, José Antonio Rojas, Juan Sebastián Bravo Ojeda, Jaime Villa, Julio Alberto Chacón Sarmiento, Sandra Patiño, Roberto Tarud Ayub, Claudia Aristizábal, Paola Rengifo, Ginna Tambini, Silvia Bertagnolio, Janet Diaz, Ludovic Reveiz, Carlos Álvarez-Moreno

PMC · DOI: 10.3389/fmed.2026.1738978 · Frontiers in Medicine · 2026-02-18

## TL;DR

This study compares five risk scores for predicting 30-day mortality in COVID-19 patients in Colombia, finding that the 4C model performs best but needs recalibration.

## Contribution

The study provides an external validation of five mortality prediction models in a Latin American context, emphasizing the 4C model's superior performance after recalibration.

## Key findings

- The 4C Mortality Score had the highest discrimination (AUC 0.71) for predicting 30-day mortality in COVID-19 patients.
- Recalibration improved the 4C model's calibration, achieving an observed-to-expected ratio of 1.
- Other models like CURB-65, CRB-65, NEWS2, and qSOFA performed poorly in predicting mortality.

## Abstract

Accurate risk stratification is essential for guiding hospitalization decisions in COVID-19. We evaluated the performance of CURB-65, CRB-65, NEWS2, qSOFA, and the 4C Mortality Score in predicting 30-day mortality among patients presenting to the emergency department with COVID-19.

We conducted an external validation study using an ambispective cohort of COVID-19 patients who presented to emergency departments of seven high-complexity hospitals in Colombia between March 2020 and September 2021. We assessed discrimination using the area under the receiver operating characteristic curve (AUC) and calibration using the GiViTI belt, the observed-to-expected (O/E) ratio, and the calibration intercept and slope. Decision curve analysis and net benefit were used to evaluate clinical utility. The 4C model underwent logistic recalibration.

Among 7,973 patients included, 30-day mortality was 11.3%. The 4C model showed the highest discrimination (AUC 0.71, 95% CI 0.70–0.73) and clinical utility, but poor calibration. NEWS2, CURB-65, CRB-65, and qSOFA performed poorly across all performance metrics. After recalibration, the 4C model achieved an O/E ratio of 1 and showed a modest improvement in discrimination. Decision curve analysis confirmed its utility for guiding hospitalization decisions at a ≥4% mortality risk threshold.

The 4C Mortality Score outperformed other models in predicting COVID-19 mortality. Its use in emergency settings alongside clinical judgment can enhance risk stratification, guide hospitalization decisions, and optimize resource allocation. Recalibration and decision analysis are essential for its clinical applicability. Further validation with contemporary data is essential to ensure its transportability across epidemiological settings.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Human immunodeficiency virus (HIV) infection (MESH:D015658), Infectious Diseases (MESH:D003141), sepsis (MESH:D018805), CAP (MESH:D003147), Coma (MESH:D003128), cardiac disease (MESH:D006331), dementia (MESH:D003704), COVID-19 (MESH:D000086382), cardiovascular disease (MESH:D002318), connective tissue disease (MESH:D003240), Mortality (MESH:D003643), hypertension (MESH:D006973), acute respiratory distress syndrome (MESH:D012128), hypoxemia (MESH:D000860), HIV/AIDS (MESH:D016263), MR (MESH:D008944), obesity (MESH:D009765), Sepsis-related] Organ Failure (MESH:D009102), hypoxemic (MESH:D012131), Confusion (MESH:D003221), pneumonia (MESH:D011014), malignancy (MESH:D009369), diabetes (MESH:D003920), chronic kidney disease (MESH:D051436), asthma (MESH:D001249), liver disease (MESH:D008107), neurological conditions (MESH:D019636), respiratory disease (MESH:D012140)
- **Chemicals:** urea (MESH:D014508), Dexamethasone (MESH:D003907), CURB (-), mercury (MESH:D008628), Oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Gammacoronavirus (genus) [taxon 694013]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12956637/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956637/full.md

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Source: https://tomesphere.com/paper/PMC12956637