Interpreting LFTs – Practical Ward Guide for Junior Doctors
Abnormal LFTs are extremely common in hospital.
Most are:
- mild
- incidental
- non-urgent
But occasionally they signal:
- obstruction
- acute hepatitis
- decompensated cirrhosis
- liver failure
Your job is to:
Recognise the pattern
Decide if it’s dangerous
Act appropriately
Not memorise long lists of causes.
✅ First principle
Never read LFTs number by number.
Always ask:
What pattern is this?
Because management depends on the pattern, not the exact value.
There are only three patterns you need to recognise.
✅ Step 1 – Know what each test actually represents
Before interpreting, understand what they mean clinically.
ALT / AST → hepatocellular injury
Leak out when liver cells are damaged.
Think:
👉 inflammation or cell injury
Examples:
- hepatitis
- alcohol
- fatty liver
- drugs
ALP (± GGT) → cholestasis / obstruction
Raised when bile flow is blocked.
Think:
👉 bile duct problem
Examples:
- gallstones
- cholangitis
- PSC/PBC
- tumour
Bilirubin → excretion problem
Raised when:
- obstruction
- liver dysfunction
- haemolysis
Think:
👉 jaundice severity
Albumin & INR → liver function (most important)
Reflect how well the liver is working.
Think:
👉 severity, not diagnosis
If abnormal → patient may be sick.
✅ Step 2 – Identify the pattern
This is the key step.
🟡 Hepatocellular pattern (ALT predominant)
Labs:
ALT/AST ↑↑
ALP normal or mild
Think:
Liver inflammation/injury
Common real-life causes:
- MASLD
- alcohol
- viral hepatitis
- drugs (antibiotics, statins, paracetamol)
- autoimmune hepatitis
- ischaemic hepatitis
What to do:
👉 blood tests + history
(not urgent imaging usually)
🟢 Cholestatic pattern (ALP predominant)
Labs:
ALP ↑↑
ALT mild
Think:
Bile duct obstruction
Common causes:
- gallstones
- cholangitis
- malignancy
- PSC/PBC
- drug cholestasis
What to do:
👉 ultrasound first
Imaging is more important than blood tests here.
🔴 Synthetic dysfunction pattern
Labs:
Low albumin
High INR
± bilirubin
Think:
Liver failing
Causes:
- cirrhosis
- acute liver failure
- severe hepatitis
- sepsis
What to do:
👉 escalate early
This is the dangerous group.
✅ Step 3 – Add the clinical story
LFTs never interpreted in isolation.
Always combine with:
- symptoms
- observations
- alcohol history
- medications
- metabolic risk
- infection risk
Pattern + history = diagnosis
✅ Practical ward examples (how to think fast)
Scenario 1
ALT 550, ALP 120
→ hepatocellular
→ think hepatitis/drug/alcohol
Scenario 2
ALP 600, jaundice, fever
→ cholestatic
→ think cholangitis
→ urgent imaging + antibiotics
Scenario 3
AST > ALT (2:1), alcohol history
→ alcohol-related
Scenario 4
Low albumin, INR 2.0, ascites
→ decompensated cirrhosis
→ escalate
Scenario 5
Mild ALT 70 in obese diabetic
→ likely MASLD
→ outpatient management
✅ Red flags you must not miss
Escalate urgently if:
- confusion / encephalopathy
- INR rising
- jaundice + sepsis
- hypotension
- severe pain
- very high ALT (>1000)
- known cirrhosis deteriorating
These are not routine LFT abnormalities.
❌ Common junior mistakes
- Reading numbers individually
- Over-investigating mild ALT rises
- Missing synthetic failure
- Forgetting medication history
- Not imaging cholestasis
- Referring everyone to gastro
Most abnormal LFTs are benign.
A few are dangerous.
Learn to tell the difference.
✅ Simple ward algorithm
When you see abnormal LFTs:
- Is the patient sick?
- ALT or ALP predominant?
- Any synthetic dysfunction?
- Blood tests or imaging?
- Urgent or routine referral?
That’s it.
✅ Take-home concept
ALT = inflammation
ALP = obstruction
INR/albumin = severity
If you recognise those three ideas, you can interpret 90% of LFTs safely.
