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Role Diagnosis of jaundice, severity of liver disease. Diagnosis of hepatocellular damage. Follow progression of disease. Diagnosis of cholestasis, biliary obstruction Severity of chronic liver disease Assess severity of hepatic synthetic function Correlates well with alkaline phosphatase, can exclude bone disease Highly specific for cholestasis Higher sensitivity & specificity for liver injury
Aminotransferase: Alanine Aspartate Alkaline phosphatase Serum albumin Prothrombin time Serum glutamyltrans peptidase Serum 5 nucleotidase Serum bile acids
4-36 IU/L 8-33 IU/L 20-90 U/L 35-50 g/L 3.5-5.0 g/dL 12-15 s 5-40 U/L
Markers of Cholestasis
ALP liver and bone (placenta, kidneys, intestine
and WBC) Hepatic ALP present on surface of bile duct epithelia and accumulating bile salts increase its release from cell surface. Takes time for induction of enzyme levels so may not be first enzyme to rise half-life is 1 week. ALP isoenzymes: 5-NT or gamma GT may be necessary to evaluate the origin of ALP
Albumin
300-500 g in body fluids Synthesize 15 g/d Half life: 20 days 4% degraded daily
Prothrombin time
I, II, V, VII, IX, X, XII, XIII Half life < 24h Congenital, consumption, warfarin, Vitamin K deficiency, parenchymal liver disease Not sensitive but highly prognostic
Alcoholic steatonecrosis, hepatocellular disease, acetaminophen overdose
Summery