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Cardiovascular
Jaundice
Differentials
Most Common Causes:
Choledocholithiasis
Hepatitis B/C
Alcoholic hepatitis
Other Causes:
Malignancy: Pancreatic/hepatocellular carcinoma, cholangiocarcinoma
PBC/PSC: Common differentials in GPA
Drugs/Toxins
NASH
Haemochromatosis
Gilbert’s Syndrome
Haemolysis
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History
Pale stools / dark urine
Previous abdominal surgeries
IV drug use / travel to Hep B endemic regions / previous Hep B immunisations
Herbal medications, recreational drugs use
Abdominal pain
Prolonged excessive alcohol intake
Unexplained weight loss
Pallor, splenomegaly, personal/family history of haemolytic disorders
Fever (cholangitis)
Skin pigmentation changes / family history of haemochromatosis
Jaundice during periods of fasting or infections (Gilbert’s Syndrome)
Jaundice
Differentials
Most Common Causes
Choledocholithiasis (stones in the common bile duct)
Hepatitis B/C (infectious)
Alcoholic Hepatitis
Other Causes
Malignancy: Pancreatic cancer, hepatocellular carcinoma (HCC), cholangiocarcinoma
Autoimmune Cholangiopathies: Primary Biliary Cholangitis (PBC), Primary Sclerosing Cholangitis (PSC)
Drugs/Toxins: e.g. paracetamol overdose, methotrexate, herbal supplements
Non-Alcoholic Steatohepatitis (NASH)
Haemochromatosis (iron overload)
Gilbert’s Syndrome (benign unconjugated hyperbilirubinaemia)
Haemolysis (increased bilirubin production)
History
Symptoms & Signs to Elicit
Colour of Stool & Urine
Pale (acholic) stools and dark urine typical of obstructive or cholestatic jaundice
Previous Abdominal Surgeries
Risk of bile duct strictures or altered anatomy
Possible Infectious Risks
IV drug use (Hepatitis B/C)
Travel to high-prevalence regions
Past immunisations for hepatitis B
Medications/Exposures
Herbal medications, recreational drugs
Hepatotoxic drugs (anti-TB meds, certain antibiotics, etc.)
Abdominal Pain
Right upper quadrant pain (cholelithiasis, choledocholithiasis)
Epigastric pain radiating to the back (pancreatitis or pancreatic malignancy)
Alcohol Intake
Chronic heavy use can cause alcoholic hepatitis/cirrhosis
Weight Loss
Potential malignancy (pancreatic, HCC, cholangiocarcinoma)
Haemolysis Signs
Pallor (anaemia), splenomegaly, personal/family history of haemolytic disorders
Fever/Chills
Suggests ascending cholangitis if obstructive symptoms
Skin Pigmentation Changes
Haemochromatosis (bronze diabetes), family history
Intermittent Mild Jaundice
Triggered by fasting/infections → Gilbert’s Syndrome (mild unconjugated bilirubin elevation)
Interpretation of Jaundice
Pre-Hepatic: Haemolysis → unconjugated hyperbilirubinaemia
Hepatic: Hepatitis (viral, alcoholic, autoimmune), NASH, drug-induced → conjugated/unconjugated mix
Post-Hepatic: Obstruction (choledocholithiasis, malignancy, strictures) → predominantly conjugated hyperbilirubinaemia, dark urine, pale stool, pruritus
Key Investigations
LFTs (bilirubin fractions, ALP, GGT, ALT, AST)
Coagulation profile (INR) if severe liver impairment suspected
Viral serologies (Hep A/B/C, EBV if indicated)
Abdominal ultrasound (biliary tract dilation, gallstones, masses)
CT/MRI or ERCP/MRCP if uncertain aetiology or suspected obstruction
Iron studies (for haemochromatosis)
Autoimmune markers (ANA, ASMA) if autoimmune hepatitis or PBC/PSC suspected
Haemolysis markers (FBC, LDH, haptoglobin, reticulocyte count)
Genetic testing (Gilbert’s, haemochromatosis) if indicated
Management
Dependent on Aetiology
Choledocholithiasis: ERCP ± stone extraction
Hepatitis (B/C): Antiviral therapy guided by viral load, genotype, liver status
Alcoholic Hepatitis: Abstinence from alcohol, supportive care, consider corticosteroids if severe
Malignancy: Surgical resection if possible, chemotherapy, or palliative stenting for biliary obstruction
PBC/PSC: Ursodeoxycholic acid, potential transplant evaluation in advanced disease
Drug-Induced: Discontinue offending agent; supportive treatment
Haemolysis: Treat underlying cause, e.g. RBC transfusion if severe anaemia, manage triggers for haemolytic episodes
Gilbert’s Syndrome: Reassure, usually benign
General Measures
Optimise nutrition, correct vitamin deficiencies (e.g., fat-soluble vitamins in cholestatic disease)
Assess for pruritus → Cholestyramine or rifampicin can help if cholestatic
Monitor for complications: varices in cirrhosis, coagulopathy, encephalopathy
Lifestyle: Abstinence from alcohol if hepatic disease, healthy weight, adequate hydration
Notes
Always exclude obstructive causes (choledocholithiasis, cholangiocarcinoma) if conjugated hyperbilirubinaemia.
Chronic viral hepatitis needs specialist referral if advanced fibrosis, or for antiviral therapy.
Screen for hepatocellular carcinoma (HCC) in cirrhotic patients via 6-monthly ultrasound ± alpha-fetoprotein.
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