What is the recommended dose of albumin for a patient with decompensated cirrhosis?

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Last updated: December 18, 2025View editorial policy

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Albumin Dosing in Decompensated Cirrhosis

For decompensated cirrhosis patients, albumin dosing depends critically on the specific clinical scenario: administer 1 g/kg (maximum 100 g) on day 1 followed by 1 g/kg on day 3 for spontaneous bacterial peritonitis; 1 g/kg (maximum 100 g) on day 1 followed by 20-40 g/day for hepatorenal syndrome-AKI when combined with vasoconstrictors; 6-8 g per liter of ascites removed for large-volume paracentesis >5L; and 1 g/kg (maximum 100 g) for 2 consecutive days as a volume challenge for AKI stage >1A without obvious cause. 1

Clinical Context-Specific Dosing Algorithm

For Spontaneous Bacterial Peritonitis (SBP)

  • Administer 1.5 g/kg within 6 hours of diagnosis, followed by 1.0 g/kg on day 3 2, 1
  • This regimen reduces type 1 hepatorenal syndrome incidence from 30% to 10% and mortality from 29% to 10% compared to antibiotics alone 2
  • Particularly beneficial when baseline serum bilirubin ≥68 µmol/L (4 mg/dl) OR creatinine ≥88 µmol/L (1 mg/dl) 2
  • Patients with bilirubin <68 µmol/L AND creatinine <88 µmol/L have very low HRS risk (0-7%), making albumin potentially unnecessary 2

For Hepatorenal Syndrome-AKI (HRS-AKI)

  • Initial loading: 1 g/kg body weight (maximum 100 g) on day 1 1
  • Maintenance: 20-40 g/day intravenously in combination with vasoconstrictors (typically terlipressin) 2, 1
  • Continue treatment until complete response (serum creatinine <1.5 mg/dl) or for maximum 14 days 2, 1
  • Start vasoconstrictors promptly—higher baseline creatinine correlates with treatment failure 3
  • Screen for cardiovascular disease before initiating terlipressin, as cardiovascular complications occur in up to 45% of patients 1

For Acute Kidney Injury (AKI) Without Specific Cause

  • When AKI stage >1A occurs without obvious precipitating factors, give 1 g/kg (maximum 100 g) for 2 consecutive days after withdrawing diuretics 2, 1
  • If HRS-AKI Stage 2 or greater is subsequently diagnosed, transition to 20-40 g/day with vasoconstrictors 1
  • The optimal dose for survival benefit in ARF is 87.5 g, with doses above 100 g associated with worse outcomes due to fluid overload 4

For Large-Volume Paracentesis

  • Administer 6-8 g of albumin per liter of ascites removed 1, 5
  • Only indicated when >5 liters are removed 1, 5
  • Give albumin after the paracentesis procedure is completed 1

For Sepsis-Induced Hypotension

  • Use 5% albumin solution over normal saline 5
  • A 2024 RCT demonstrated higher 1-week survival with albumin (43.5% vs 38.3%, p=0.03) 5, 3

Critical Dosing Thresholds and Safety

Maximum Safe Dose

  • Do not exceed 87.5-100 g in the initial loading period 4
  • Doses above this threshold are associated with increased mortality and complications from fluid overload 4
  • Use 20% or 25% albumin solution for all indications 1

Monitoring for Volume Overload

  • Monitor central venous pressure to prevent circulatory overload, though CVP is inaccurate for assessing cardiac output in cirrhosis 2
  • Use transthoracic echocardiography at bedside to evaluate volume status and cardiac function 3
  • Watch for respiratory distress or declining oxygen saturation during administration 5
  • Immediately discontinue if pulmonary edema develops 5
  • Length of stay and critical care requirements increase in a dose-dependent manner with albumin 4

Common Pitfalls to Avoid

Do NOT Use Albumin For:

  • Uncomplicated ascites without AKI, SBP, or large-volume paracentesis 1
  • Routine volume resuscitation in critically ill cirrhotic patients—use balanced crystalloids (lactated Ringer's) instead 1, 5
  • Treatment of hypoalbuminemia alone—correcting low albumin levels without specific complications does not improve outcomes 5
  • Infections other than SBP 1
  • Small-volume paracentesis (≤5 liters) 1

Key Clinical Considerations

  • Albumin alone is ineffective for HRS-AKI—must be combined with vasoconstrictors 3
  • Beta-blockers should be stopped when AKI develops, though data are controversial 2
  • Discontinue all diuretics immediately when AKI is diagnosed 2
  • Each 1 mg/dL reduction in creatinine with treatment reduces mortality risk by 27% 3
  • The ATTIRE trial showed maintaining elevated albumin levels long-term increased pulmonary edema rates without improving composite outcomes 5, 3

Practical Administration Details

Preparation and Delivery

  • Administer intravenously using 20% or 25% albumin solution 1
  • For continuous therapy with vasoconstrictors, mean dose is 20-40 g/day 2, 1
  • Terlipressin can be given by continuous IV infusion at 2 mg/day (lower adverse effects) or IV boluses 0.5-1 mg every 4-6 h, increased to maximum 2 mg every 4-6 h if creatinine reduction <25% 2

Response Assessment

  • Complete response: serum creatinine below 1.5 mg/dl 2
  • Partial response: decrease of creatinine ≥50% with final value still >1.5 mg/dl 2
  • Response rates to terlipressin plus albumin range from 64-76%, with complete response in 46-56% 2

References

Guideline

Albumin Regimen for Acute Decompensated Liver Cirrhosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Manejo de Pacientes con Cirrosis Hepática y Falla Renal Aguda

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Albumin Administration in Chronic Liver Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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