RenalTwin: Diseño y validación de un gemelo digital para el modelado predictivo y la detección temprana de lesión renal aguda en pacientes críticos
DOI:
https://doi.org/10.67166/dygxgh35Palabras clave:
gemelo digital; lesión renal aguda; cuidados intensivos; modelado predictivo; medicina de precisión.Resumen
La lesión renal aguda (LRA) continúa siendo una complicación de alto impacto en las unidades de cuidados intensivos y su reconocimiento puede ocurrir después de que la alteración funcional ya se ha establecido. El objetivo fue diseñar y validar metodológicamente RenalTwin, un gemelo digital orientado al modelado predictivo y a la detección temprana de LRA en pacientes críticos. Se desarrolló un estudio cuantitativo, correlacional-descriptivo y de validación predictiva multicéntrica in silico con una cohorte sintética reproducible de 2.480 perfiles clínicos distribuidos en cuatro centros virtuales. El gemelo integró creatinina basal, diuresis, presión arterial media, lactato, Sequential Organ Failure Assessment (SOFA), soporte vasopresor, ventilación mecánica, sepsis, exposición nefrotóxica, nitrógeno ureico y variables demográficas. La cohorte se dividió en entrenamiento (60 %), calibración (20 %) y prueba (20 %); se estimaron área bajo la curva ROC (AUROC), área bajo la curva precisión-recall (AUPRC), sensibilidad, especificidad, valor predictivo, F1-score, Brier, calibración, t de Student pareada y tamaño del efecto d de Cohen. En prueba, RenalTwin alcanzó AUROC de 0,916 (IC95 % bootstrap aproximado: 0.890-0.941), AUPRC de 0,856 (IC95 %: 0.805-0.901), sensibilidad de 0,814, especificidad de 0,862, F1-score de 0,770 y Brier de 0,106. El adelanto temporal sintético de alerta fue de 14.3 horas respecto al criterio convencional, con diferencia estadísticamente significativa (p<0,001; d=3.42). Se concluye que la arquitectura propuesta muestra discriminación, calibración y utilidad potencial suficientes para justificar una validación prospectiva con datos clínicos reales. Los hallazgos no constituyen evidencia de eficacia clínica y deben interpretarse como una validación metodológica previa a implementación.
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Derechos de autor 2026 Christian Gustavo Masapanta Salazar (Autor/a)

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