What is the recommended workup for a patient with suspected cirrhosis?

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Workup for Suspected Cirrhosis

Begin with a comprehensive hepatic function panel, complete blood count, renal function tests, and abdominal ultrasound, followed immediately by transient elastography and etiologic testing to confirm diagnosis and assess severity. 1, 2

Initial Laboratory Evaluation

Obtain the following tests immediately when cirrhosis is suspected:

  • Hepatic function panel: Bilirubin (total and conjugated), AST, ALT, alkaline phosphatase, GGT, albumin, and PT/INR 1
  • Complete blood count with differential: Thrombocytopenia (platelet count <150,000/µL) suggests portal hypertension and advanced disease 1
  • Renal function tests: Creatinine and BUN are essential for MELD score calculation and detecting hepatorenal syndrome 1
  • Serum electrolytes: Sodium is critical for MELD-Na scoring and detecting hyponatremia, an independent predictor of mortality 3

Key laboratory patterns to recognize:

  • AST/ALT ratio >1 typically indicates cirrhosis rather than acute hepatitis 1
  • Elevated conjugated bilirubin indicates advanced disease or biliary obstruction 1
  • Prolonged PT/INR reflects impaired hepatic synthetic function and is critical for Child-Pugh and MELD scoring 1
  • Low albumin (<3.5 g/dL) indicates impaired synthetic function and poor prognosis 1

Etiologic Workup

Perform these tests to identify the underlying cause:

  • Viral hepatitis panel: HBsAg, hepatitis B core antibody (total and IgM), hepatitis B surface antibody, and HCV antibody with reflex viral load if positive 1, 4
  • Iron studies: Ferritin and transferrin saturation to screen for hemochromatosis 1, 5
  • Autoimmune markers: ANA, anti-smooth muscle antibody, anti-mitochondrial antibody if etiology unclear 1
  • Alpha-1 antitrypsin level: Particularly in younger patients or those with emphysema 1
  • Ceruloplasmin: For Wilson disease screening, especially in patients under age 40 1

Initial Imaging Studies

Abdominal ultrasound is mandatory as the first-line imaging test:

  • Assess liver morphology for nodular surface (86% sensitive on undersurface, 53% on superior surface), right lobe atrophy, caudate lobe hypertrophy 1, 2
  • Detect ascites and measure spleen size 2
  • Screen for hepatocellular carcinoma 2
  • Evaluate portal vein diameter (>13 mm suggests portal hypertension) and identify collateral vessels 2
  • Rule out biliary obstruction with 71-97% specificity 1

Ultrasound has 65-95% sensitivity and 98% positive predictive value for detecting cirrhosis. 1

Non-Invasive Fibrosis Assessment

Transient elastography (FibroScan) should be performed next:

  • Liver stiffness <6.4 kPa: Rules out advanced fibrosis 1
  • Liver stiffness ≥15 kPa: Confirms compensated advanced chronic liver disease/cirrhosis 1, 2
  • Liver stiffness 12.5 kPa: Recommended cutoff by AGA for detecting cirrhosis in alcoholic liver disease, prioritizing sensitivity over specificity to avoid missing cases 3

Calculate non-invasive fibrosis scores using initial laboratory values:

  • APRI score: (AST/upper limit normal) × 100 / platelet count 1
  • FIB-4 score: (Age × AST) / (platelet count × √ALT) 1

Severity Assessment and Prognostication

Calculate prognostic scores immediately:

  • Child-Pugh score: Uses bilirubin, albumin, INR, ascites grade, and encephalopathy grade; Class C (score 10-15) carries >33% one-year mortality 2
  • MELD score: Uses bilirubin, INR, and creatinine; scores range 6-40 with 3-month survival from 90% to 7% respectively 2
  • MELD-Na score: Incorporates sodium for improved prognostic accuracy 3

Screening for Complications

If ascites is present or develops:

  • Perform diagnostic paracentesis immediately in all patients with new-onset grade 2 or 3 ascites or any hospitalized patient with cirrhosis 3, 2
  • Ascitic fluid analysis: Cell count with differential (neutrophils >250/µL diagnoses spontaneous bacterial peritonitis), total protein, albumin, and bedside inoculation of 10 mL into blood culture bottles 3
  • Calculate serum-ascites albumin gradient (SAAG): SAAG ≥1.1 g/dL confirms portal hypertension as the cause 3

Variceal screening:

  • Upper endoscopy is recommended for all patients with newly diagnosed cirrhosis unless low-risk criteria are met (platelets >150,000/µL AND liver stiffness <20 kPa) 1, 4

Hepatocellular carcinoma screening:

  • Abdominal ultrasound with serum AFP every 6 months for all patients with established cirrhosis 1, 2

Advanced Imaging When Indicated

  • MRI with MRCP: Consider if ultrasound is negative but clinical suspicion remains high, particularly for cholestatic diseases (primary sclerosing cholangitis, primary biliary cholangitis) 1
  • MR elastography: Most accurate imaging modality for diagnosing and staging hepatic fibrosis when available 2
  • Multiphasic CT or MRI: When hepatocellular carcinoma is suspected based on screening ultrasound 1

Monitoring Schedule for Established Cirrhosis

Compensated cirrhosis:

  • Liver function tests, CBC, and prognostic scores every 6 months 1, 6
  • Ultrasound with AFP for HCC screening every 6 months 1, 2
  • Upper endoscopy for variceal surveillance per initial findings 1

Decompensated cirrhosis:

  • Liver function tests every 1-3 months 1
  • More frequent monitoring based on specific complications 1

Immediate Referral Indications

Refer to gastroenterology/hepatology urgently when:

  • Any decompensation event occurs (ascites, variceal bleeding, hepatic encephalopathy) 2
  • MELD score ≥15 2, 6
  • Refractory ascites develops 2
  • Hepatocellular carcinoma is detected 2
  • Child-Pugh Class C cirrhosis 2

Critical Clinical Pitfalls to Avoid

Do not delay diagnosis based on normal or mildly elevated transaminases: Patients with established cirrhosis frequently have near-normal ALT/AST levels; persistent abnormalities over 3-6 months warrant full evaluation even if only mildly elevated 1, 2

Do not rely solely on conventional imaging for early cirrhosis: Morphological changes on CT, MRI, or ultrasound may not appear until very advanced stages 2

Never delay diagnostic paracentesis in hospitalized patients with ascites: SBP can present without typical symptoms, and mortality increases 10% for every hour's delay in initiating antibiotics in septic patients 3

Avoid NSAIDs in all cirrhotic patients: They reduce urinary sodium excretion, worsen ascites, and can precipitate acute kidney injury 2

Do not use age and sex-normative values for liver enzymes: Avoid high thresholds (>1.5-2× upper limit of normal) that delay diagnosis 1

References

Guideline

Laboratory Tests for Cirrhosis Diagnosis and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Evaluation for Liver Cirrhosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Initial Workup for New Cirrhosis Diagnosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Cirrhosis: Diagnosis and Management.

American family physician, 2019

Research

Liver Disease: Cirrhosis.

FP essentials, 2021

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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