“…Distilling multiple clinical and biochemical measures into a practical model that can be used at the bedside for each decision interval remains a challenge. Previous predictive models for ALF in adults and children have included clinical and biochemical measures that are objective (e.g, INR, bilirubin, ammonia, age) or subjective (e.g., jaundice, encephalopathy) at the time of admission to hospital, the highest recorded or “peak” value(13, 14), or combinations of these data elements(2, 15–17). Measures obtained only at admission are limited by their inability to account for disease progression or improvement during the ensuing days.…”