Executive summary
Abnormal liver blood tests are common and often incidental. A high-yield approach is pattern-based (hepatocellular vs cholestatic vs isolated bilirubin) + risk factor assessment + a core aetiology screen when abnormalities persist or are clinically significant.
- Hepatocellular: ALT/AST predominant (e.g., NAFLD/MASLD, alcohol, viral hepatitis, drug-induced).
- Cholestatic: ALP (± GGT) predominant (e.g., biliary obstruction, PBC, PSC, infiltrative disease).
- Isolated bilirubin: consider Gilbert syndrome, haemolysis, fasting, or early hepatobiliary disease.
Step 1 – confirm and contextualise (often overlooked)
- Symptoms: jaundice, pruritus, RUQ pain, weight loss, fevers, fatigue, easy bruising, confusion (encephalopathy).
- Drugs/supplements: statins, antibiotics, antiepileptics, herbal products, anabolic steroids; check timing vs onset.
- Alcohol: quantify units, pattern, binges; look for AST:ALT ratio >2 (suggestive but not diagnostic of alcohol-related injury).
- Metabolic risk: BMI/waist, T2D, dyslipidaemia (NAFLD/MASLD is common).
- Exposure: viral hepatitis risk, travel, transfusion history, IVDU, sexual exposure.
Repeat timing: if mild elevation (<2× ULN) with a plausible transient trigger (e.g., intercurrent illness, new medicine) you can repeat in 4–12 weeks with safety-netting. Persistently abnormal results should trigger structured investigation.
Step 2 – core primary care liver screen (practical panel)
- Bloods: FBC, INR, albumin, bilirubin, ALT/AST, ALP, GGT.
- Viral hepatitis: HBsAg, anti-HBc, anti-HCV (then PCR if positive) where risk/clinical suspicion.
- Autoimmune: AMA (PBC), ANA/SMA, IgG (autoimmune hepatitis) if pattern suggests.
- Iron overload: ferritin + transferrin saturation (haemochromatosis).
- Causes to remember: coeliac disease (especially with transaminitis), thyroid disease, muscle injury (check CK if very high AST).
- Ultrasound if persistent abnormalities, cholestatic pattern, or suspected fatty liver/structural disease (local pathways vary).
Step 3 – fibrosis risk + referral thresholds
- Fibrosis risk in NAFLD/MASLD: consider non-invasive scores such as FIB-4 (age, AST, ALT, platelets) and/or local elastography pathways.
- Urgent referral / same-day: jaundice with systemic illness, suspected acute liver failure (INR rising, encephalopathy), very high transaminases with severe symptoms, biliary obstruction with cholangitis features (Charcot triad).
- Specialist referral: persistent unexplained LFT derangement, cholestatic pattern with positive AMA, hepatitis markers positive, abnormal synthetic function (INR/albumin), imaging abnormalities, or high fibrosis risk.
Rule of thumb: “abnormal numbers + abnormal function” (INR/albumin/platelets) = escalate.
FAQ
Transparency
This page is an educational, clinician-written summary of publicly available NICE guidance intended for trained healthcare professionals. It uses original wording (not copied text) and should be used alongside the full NICE source, local pathways, and clinical judgement. Doses provided are for general reference; always check the BNF/SPC.