“…With improvement in supportive therapy and LT, overall survival rates have increased to 62-83% (4,10,11). Diverse combinations of age, etiologies of ALF, onset and peak grade of hepatic encephalopathy (HE), biochemical tests [prothrombin time (PT), the international normalized ratio (INR), bilirubin, ammonia, and lactate], Pediatric End-Stage Liver Disease (PELD) score, several chemokines, cytokines, and reactive nitrogen oxide species have been evaluated to assess the prognosis of PALF (2,12,13). Applying King's College Hospital Criteria to children with PALF did not predict death, and the reported positive predictive value was only 33% (14).…”