| Term 
 
        | most metabolically complex organ 
 hepatocytes perform liver's metabolic functions:
 formation and excretion of bile
 regulation of carbohydrate homeostasis
 lipid synthesis and secretion of plasma lipoproteins
 control of cholesterol metabolism
 formation of serum albumin, clotting factors, enzymes, urea, and numerous other proteins
 metabolism and detoxification of medications and other foreign substances
 storing glycogen, iron, vitamins, and minterals
 |  | Definition 
 
        | metabolic functions of the liver |  | 
        |  | 
        
        | Term 
 
        | endocrine and exocrine functions 
 3 major functions:
 to secrete fluid containing digestive enzymes into the duodenum
 to secrete the hormones insulin and glucagon, which help to regulate sugar levels in the blood stream
 to secrete into the duodenum the large quantities of sodium bicarbonate needed to neutralize the acid coming from the stomach
 |  | Definition 
 
        | metabolic functions of the pancreas |  | 
        |  | 
        
        | Term 
 
        | primary function = store and concentrate bile 
 bile = bile salts, bilirubin, phospholipids, cholesterol, bicarbonate, and water
 
 bile emulsifies fat and fat-dependent vitamins (DEAK) to promote absorption of food
 
 food enters the duodenum -> cholecystokinin is released -> stimulates contraction of the gallbladder and common bile duct -> bile secretion
 |  | Definition 
 
        | metabolic functions of the gallbladder |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | inflammation of the gallbladder |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | back up of bile in the liver |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | cholelithiasis cholecystitis
 cholestasis
 |  | Definition 
 
        | common disorders of the gallbladder |  | 
        |  | 
        
        | Term 
 
        | fatigue, weakness nausea, poor appetite, weight loss
 abdominal pain and distention
 fever
 steatorrhea - loose, fatty stool
 |  | Definition 
 
        | general symtpoms associated with hepatobiliary dysfunction |  | 
        |  | 
        
        | Term 
 
        | spider angioas - spiderlike blood vessels on face and chest (usually NOT on the lower extremities) 
 palmar erythema - red palms
 
 pruritis - itching
 
 clubbing
 |  | Definition 
 
        | skin manifestations associated with hepatobiliary dysfunction |  | 
        |  | 
        
        | Term 
 
        | anemia leukopenia
 THROMBOCYTOPENIA
 COAGULOPATHY
 |  | Definition 
 
        | blood abnormalities associated with hepatobiliary dysfunction |  | 
        |  | 
        
        | Term 
 
        | increased amylase increased lipase
 |  | Definition 
 
        | laboratory tests that indicate pancreatic injury |  | 
        |  | 
        
        | Term 
 
        | increased aminotransferases (AST and ALT) increased lactate dehydrogenase (LDH)
 |  | Definition 
 
        | laboratory tests that indicate liver injury |  | 
        |  | 
        
        | Term 
 
        | increase in unconjugatd bilirubin and conjugated bilirubin 
 increase in alkaline phosphatase
 
 increase in gamma-glutamyl transpeptidase
 |  | Definition 
 
        | laboratory tests that indicate cholestasis |  | 
        |  | 
        
        | Term 
 
        | increased PT/INR decreased serum albumin
 |  | Definition 
 
        | laboratory tests that indicate hepatic synthetic incapacity |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | laboratory test that indicates hepatic encephalopathy |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | enzyme used to help digest carbohydrates INCREASED when the pancreas is diseased, injured, or inflamed
 non-specific alone:  use in combination with lipase and signs/symptoms
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | enzyme used to help trigger the breakdown of fat 
 INCREASED when the pancreas is diseased, injured, or inflamed
 
 non-specific alone:  use in combination with amylase and signs/symptoms
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | enzymes located in the cytoplasm of hepatocytes 
 aspartate transaminase (AST) and alanine transaminase (ALT) are INCREASED with hepatocellular injury
 |  | 
        |  | 
        
        | Term 
 
        | highest level (> 20 x) = acute viral, drug-induced, or ischemic 
 alcohol liver disease:  rarely ALT > 500 IU/L
 ratio of AST/ALT > 2 suggests alcoholic liver disease
 
 moderate elevation (100-300 IU/L) = chronic liver disease
 
 AST can be elevated in rhabdomyolysis, heart or brain tissue damage
 |  | Definition 
 
        | degree of aminotransferase elevation is helpful for suggesting what possible etiologies? |  | 
        |  | 
        
        | Term 
 
        | lactate dehydrogenase (LDH) |  | Definition 
 
        | enzyme found in almost all body tissues and release is INCREASED when cells are damaged or destroyed 
 inentitive for hepatocellular injury but sensitive for cancers involving the liver
 
 INCREASE also indicates hemolysis, MI, or pulmonary embolism
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | bile pigment 
 formed when the liver breaks down old red blood cells
 
 then removed from the body through the stool
 |  | 
        |  | 
        
        | Term 
 
        | bilirubin circulates int he blood in 2 forms: 
 1)  indirect (unconjugated) bilirubin
 insoluble in water
 changed into soluble (conjugated) bilirubin in the liver
 
 2)  direct (conjugated) bilirubin
 water soluble form created from indirect bilirubin by the liver
 release into bile and stored in the gallbladder before eventually being excreted in the stool
 |  | Definition 
 
        | indirect (unconjugated) bilirubin vs. direct (conjugated) bilirubin |  | 
        |  | 
        
        | Term 
 
        | excessive production -> hemolysis 
 immature enzyme system -> jaundice of newborn/prematurity
 
 inherited defects -> Gilbert syndrome, Crigler-Najjar syndrome
 |  | Definition 
 
        | what can cause an INCREASE in unconjugated (indirect) bilirubin? |  | 
        |  | 
        
        | Term 
 
        | impaired intrahepatic excretion: hepato cellular disease -> hepatitis, CIRRHOSIS, medications
 intrahepatic cholestasis -> pregnancy, medications
 congenital -> Dubin-Johnson syndrome, Rotor syndrome
 
 obstruction:
 extrahepatic -> calculus, stricture, neoplasm
 intrahepatic -> sclerosing cholangitis, CIRRHOSIS, neoplams
 |  | Definition 
 
        | what can cause an INCREASE in conjugated (direct) bilirubin? |  | 
        |  | 
        
        | Term 
 
        | alkaline phosphatase (ALP) |  | Definition 
 
        | cellular enzyme with high concentrations in the liver and bone 
 in the liver, found in cells that join to form bile ducts
 
 INCREASED when bile flow through the bile ducts is disrupted (OBSTRUCTION)
 |  | 
        |  | 
        
        | Term 
 
        | gamma-glutamyl transpeptidase (GGT) |  | Definition 
 
        | liver enzyme that is very sensitive to changes in liver function 
 levels correlate well with ALP
 INCREASE = biliary tract disease
 
 combination with ALP is sensitive and specific for biliary tract disease
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | liver's ability to synthesize vitamin K dependent clotting factors:  factors II (prothrombin), V, VII, and X 
 INCREASED (in absence of warfarin administration) indicates severe hepatocellular dysfunction and indicates progression to advanced cirrhosis
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | most abundant protein in the blood plasma 
 maintains oncotic pressure, nourishes tissues, and transports hormones, vitamins, drugs, and ions like Ca throughout the body
 
 synthesized in the liver and is extrememly sensitive to liver damage
 
 DECREASED with liver damage, kidney disease, malnutrition, alcoholism, inflammation, and shock
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | prduced by colonic bacteria and metabolism of glutamine 
 liver metabolizes it from urea
 
 level correlates poorly with severity of hepatic encephalopathy
 
 INCREASED with hepatic encephalopathy, high protein meals, GI bleeding, hypokalemia, or metabolic alkalosis
 |  | 
        |  | 
        
        | Term 
 
        | Child-Pugh Classification |  | Definition 
 
        | quantifies effects of cirrhotic processes 
 based on combination of clinical and laboratory data
 
 USE FOR DRUG-DOSING ADJUSTMENTS
 
 limitation = relies on subjective scoring for ascites and encephalopathy
 |  | 
        |  | 
        
        | Term 
 
        | Mayo End-Stage Liver Disease (MELD) |  | Definition 
 
        | the accepted classification system used by the United Network of Organ Sharing (UNOS) 
 USED IN THE ALLOCATION OF LIVERS FOR TRANSPLANT
 
 relies solely on objective data
 
 NOT currently used for medication dosing
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | test that measure liver injury |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tests that measure cholestasis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | test that measure the synthetic capacity of the liver |  | 
        |  |