Chronic Liver Disease Flashcards
Liver Failure is ?
Often chronic and occurs over a long period and the presents as a sudden deterioration = acute on chronic
Presentation? Rx Factors and treatments to consider
Presentation:
- Swelling of feet and abdomen
- tiredness, nausea and weight loss
- jaundice, pruritis
- increased bruising
- Haematemesis/PR bleeding
- Sleep wake reversal, memory problems and confusion = encephalopathy
Risk Factors:
- Alcohol intake
- Past Hx of hepatitis or jaundice
- Hx of drugs, transfusions, tattoos
- Diabetes, cardiac failure, arthropathy, haemachromotoosis
Treatments to ask of:
- Nurtitional, alcohol cessation, avoidance of NSAIDs sedatives and opiates
- Medications - cholestrymine, ursodeoxycholic acid
- Fluid restriction
Examination:
General:
Jaundice, abdominal distension, muscle wasting
Hands:
Clubbing and leuconychia, palmar eythema, dupuytren’s contracture, tendon xanthoma
Arms:
hepatic flap, bruising, scratch marks, spider naevi, tattoos, needle marks
Face:
Cushingoid, parotid enlargement
EYE- xanthelesmata, Conj. pallor, KF rings
Chest:
gynaecomastia, loss of axillary hair, spider naevi
Abdo:
distension, striae, caput medusae, scars, hepato/splenomegaly, shifting dullness, bruit
Legs:
bruising, oedema
Causes of CLD
FIGCAT
Fatty Liver:
- Alcoholic
- Non-Alcoholic (NAFLD)
- DM, pregnancy, idiopathic
Infectious:
- Hepatitis
- A = acute, B + C = chronic
- EBV
- CMV
Genetic
- Hereditary haemachromotosis
- Wilson’s Disease
- Alpha-1-antitrypsin deficiency
Congestion
- Budd-chiari Syndrome (1 in 1M)
- RHF/CHF
Autoimmune
- Autoimmune Hepatitis (Ab against hepatocyte surface antigen)
- Primary biliary cirrhosis
- Primary sclerosing Cholangitis
Toxins/Drugs:
- Alcohol
- Paracetamol overdose
- Isoniazid, methotrexate, methyldopa, nitrofurantoin
Complications of CLD
PESCHARB
- Portal Hypertension
- Hepatic encephalopathy/cerebral oedema
- synthetic dysfunction - coagulopathy, hypoalbuminaemia and feminization
- Hepatocellular carcinoma
- spontaneous bacterial peritonitis (SBP)
- Hepatorenal syndrome (CLF CKD)
- Ascites
- Hypoglycaemia
Investigations for CLD?
Bedside
- Fluid Balance, weight
Bloods: (fkn everything)
- FBC, CRP (infection, GI bleed, leucopenia and thrombocytopenia suggest hypersplenism)
- Chem (urea synthesised in liver, Cr for HRS, Ammonia for encephalopathy)
- Glucose (?hypo)
- Coags (inc PT, APTT and thrombin time)
- LFTs (AST/ALT = hepatocellular, GGT/ALP = cholestatic picture. AST:ALT ratio > 2 suggests ALD)
LIVER SCREEN viral serology = hepB surface and core antigen, HepC antibody, HepA IgM, CMV and EBV autoantibodies =ANA - PSC =AMA = PBC, AIH =ASMA and ALKM1 = AIH Ferritin A-1-antitrypsin A-fetoprotein = HCC
Imaging
- Abdo USS +/- portal vein doppler (BC syndrome)
- Fibroscanning
- MRCP
Other
- ascitic tap
- liver biopsy
- paracetamol levels
- OGD
Grading Cirrhosis?
CHILD-PUGH SCORE
uses Encephalopathy, ascites, billirubin, albumin and prothrombin time/INR
5-6 mild = class A = 100% 1 year 7-9 moderate = class B = 80% 1 year 10-15 severe = Class C = 45% 1 year
NP management
low salt diet, fluid restrict
alcohol abstinence
optimise nutrition
P management
Treat Underlying cause:
- Hep B - SC PED interferon
- Hep C - oral ribavirin, weekly SC PEG interferon
- Haemochromotosis - venesection
- AIH - steroids
- NAFLD - weight loss, exercise, statin, VitE if not DM
Nutritional:
- NG feeding
- VitB
- Glucose infusion if hypo
Ascites:
- bed rest, fluid restrict, low salt
- Spironolactone - 100mg + frusemide if poor response
- Therapeutic paracentesis with albumin infusion
Varacies:
- B-blockers or variceal band ligation
SPB
- ABx - cefotaxime + metronidazole
- prophylaxis may be needed
Encephalopathy - remove precipitating factors = enemas + low protein diet - lorazepam for seizures - mannitol for cerebral oedema
Pruritis = cholestrymine
bleeding = VitK
Avoid - gentamicin, naltrexone, NSAIDs, sedatives
Invasive
- TIPSS (trans jugular intrahepatic portosystemic shunt)
- Liver transplant
Screening:
USS +/- alpha-fetoprotein ever 6 months to screen for HCC (especially if Hep B or Hep C)