Liver - function and decompensated liver disease Flashcards
Liver function
Removal of toxins and urea
Production of clotting factors
Production of proteins including albumin, CRP and complement
Breakdown of proteins into aminoacids/formation of aas
Handling cholesterol
Bile production - emulsifies fats for absorption (fat-sol vits: DEAK), allows excretion of bilirubin (from RBC breakdown)
Glyconeogenesis, glycogenolyisis, gluconeogenesis
Hormone production including ILGF, thrombopoeitin and angiotensinogen
Blood supply of liver
25% from hepatic artery
75% from portal vein (from stomach, spleen and intestine)
Symptoms of liver disease
Abdominal pain
Fever, rigors
Pruritis (cholestasis)
Arthritis/arthralgia (haemochromatosis, AIH, HBV)
Pigmentation (cholestasis, haemochromatosis)
Bloody diarrhoea (PSC - IBD)
Weight loss
SoB/emphysema (alpha-1-antitrypsin deficiency)
Dry eyes/mouth (PBC - sjogren’s)
Decompensated liver disease
More liver cell destruction than capacity for regeneration
Decrease functional capacity: sedative, drugs (fluclox, diclofenac, co-amox, amiodarone), alcohol, GI bleed
Increase demands of liver: infection, stress, GI bleed
DLD - presentation
Ascites Encephalopathy Coagulopathy Variceal bleeding Renal failure Death Often on background of chronic liver disease
DLD - criteria
One or more of: Bilirubin >30 Albumin <30 PT >15s Ascites Encephalopathy And a risk factor present (pre-existing CLD/cirrhosis, hx of alcohol abuse, paracetamol OD)
DLD - triggers
Infection (esp SBP) Drugs incl alcohol Bleeding (variceal) Biochemical abnormalities (K+, Na+, glucose) Cancer - HCC Other: surgery, constipation
DLD - investigations
Bloods: FBC, U+E, LFT, coag, glucose, AFP, Mg, Ca, Phos, cultures, lactate, ferritin, transferrin, caeruloplasmin, autoantibodies, Ig, hepatitis screen
Septic screen
US abdomen
Ascitic tap
DLD - management
Manage cause and complications GI bleed Withdrawal Encephalopathy protocol Increased PT - vit K Renal failure Infection