What is Non-Alcoholic Fatty Liver Disease (NAFLD)?
Liver steatosis (fat buildup) usually caused by lifestyle habits unrelated to alcoholic consumption.
What are some risk factors for NAFLD?
BMI >35, DM, Metabolic Syndrome.
What is a cirrhotic liver?
Irreversible scarred liver tissue caused by severe damage to the liver due to excessive alcohol consumption or other forms of liver disease.
What is ascites?
Accumulation of fluid in the peritoneal cavity, which dilutes albumin and decreases synthesis due to scarring, leading to edema.
What can ascites cause?
Can cause spontaneous bacterial peritonitis.
What are esophageal varices?
Enlarged and swollen veins at the lower end of the esophagus due to portal hypertension.
What is hepatic encephalopathy?
Central nervous system dysfunction resulting from liver disease, frequently associated with elevated ammonia levels.
What is the treatment for hepatic encephalopathy?
Treatment includes lactulose (causes diarrhea to remove nitrogen) and neomycin to destroy bacteria that produce ammonia.
What is the MNT for cirrhosis?
Very catabolic state requiring high calorie (25-35 kcal/kg) and protein (up to 1.5 g/kg).
What are common symptoms of cirrhosis?
Steatorrhea, ascites, and varices.
What is the MNT for pancreatitis?
Acute: NPO, progress to low fat diet/easily digested foods, early EN (within 48 hrs).
What is the MNT for chronic pancreatitis?
PO diet with pancreatic enzyme replacement therapy (PERT) with all meals and snacks, and MCT oil.
What is the MNT for spastic Cerebral Palsy?
High fiber/fluid, low calorie.
What is the MNT for athetoid (non-spastic) Cerebral Palsy?
High calorie, high protein, finger foods.
What is the MNT for galactosemia?
Galactose/lactose free diet, avoiding organ meats, dates, bell peppers, milk, whey/casein.
What is the MNT for urea cycle deficits?
Protein restrictions and special formula to adjust protein composition.
What is Phenylketonuria (PKU)?
An inherited disorder of protein metabolism leading to a toxic buildup of certain compounds.
What is the dietary management for PKU?
Low phenylalanine diet, no aspartame, supplement tyrosine, high carbohydrate, low protein.
What is glycogen storage disease?
A genetic disorder characterized by the inability to break down glycogen due to the lack of glucose 6-phosphatase.
What is the MNT for glycogen storage disease?
Consistent supply of glucose (dextrose infusion), raw cornstarch at regular intervals, small meals to maintain blood glucose.
What is Maple Syrup Urine Disease (MSUD)?
A genetic disorder characterized by the inability to metabolize branched-chain amino acids.
What is the MNT for MSUD?
Restrict BCAAs, adequate calories from carbohydrates and fat, small amounts of milk/gelatin for growth.
What is Addison’s disease and its MNT?
When adrenal glands do not produce enough cortisol; MNT includes high protein, frequent feedings, high salt.
What is Cushing’s disease and its MNT?
When adrenal glands produce too much cortisol; MNT includes low sodium for hypertension and blood glucose control.