What is the use of albumin (human albumin) in patients with conditions such as liver disease, nephrotic syndrome, or malnutrition?

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What is Albumin Used For?

Albumin is a human-derived blood product used primarily for specific liver disease complications—including large-volume paracentesis, spontaneous bacterial peritonitis, hepatorenal syndrome, and sepsis-induced hypotension in cirrhosis—and should NOT be used routinely for hypoalbuminemia correction, nutritional support, or general volume resuscitation in critically ill patients. 1, 2, 3

Established Evidence-Based Indications

Liver Disease Complications (Strong Recommendations)

Large-Volume Paracentesis:

  • Administer albumin when removing >5L of ascitic fluid to prevent paracentesis-induced circulatory dysfunction 2, 4
  • This indication has moderate certainty of evidence and is strongly recommended by the American Association for the Study of Liver Diseases 2
  • The typical dose is 6-8 g of albumin per liter of ascitic fluid removed 5

Spontaneous Bacterial Peritonitis:

  • Give 1.5 g/kg at diagnosis and 1.0 g/kg on day 3 2, 4
  • This regimen reduces mortality and prevents hepatorenal syndrome with moderate certainty of evidence 2
  • This is one of the most strongly supported indications for albumin use 1, 3

Hepatorenal Syndrome:

  • Albumin is recommended as part of the treatment protocol for hepatorenal syndrome 1, 2
  • Used in combination with vasoconstrictors for type 1 hepatorenal syndrome 6

Sepsis-Induced Hypotension in Cirrhosis:

  • Use 5% albumin over normal saline in cirrhotic patients with sepsis-induced hypotension 2
  • A 2024 RCT demonstrated higher 1-week survival with albumin (43.5% vs 38.3%, p=0.03) 2
  • Albumin achieved higher rates of shock reversal compared to crystalloids 1

Hepatic Encephalopathy (Emerging Indication)

Acute Hepatic Encephalopathy:

  • Consider albumin 1.5 g/kg on day 1 followed by 1.0 g/kg on day 3, combined with lactulose 2, 4
  • Alternative regimen: 1.5 g/kg/day for up to 10 days with lactulose 4
  • Evidence shows 75% complete resolution with albumin-lactulose versus 53% with lactulose alone (p=0.03) 2, 4
  • Mortality was reduced (18% vs 32% at day 10, p=0.04) in one trial 1, 4
  • However, certainty of evidence is low to very low, and guidelines show uncertainty about this indication 1, 2

Other Accepted Indications

Therapeutic Plasmapheresis:

  • Albumin is indicated for fluid replacement during plasmapheresis with exchange of large volumes of plasma 7, 6

Cardiopulmonary Bypass:

  • Used in pump priming to achieve a hematocrit of 20% and plasma albumin concentration of 2.5 g/100 mL 5

Neonatal Hemolytic Disease:

  • Administer 1 g/kg body weight about 1 hour prior to exchange transfusion to bind free bilirubin and reduce kernicterus risk 5

What Albumin is NOT Used For (Strong Recommendations Against)

Do NOT use albumin for:

  • Hypoalbuminemia correction alone - The American Thoracic Society explicitly recommends against this (adjusted OR 0.98,95% CI 0.71-1.33 for benefit) 1, 2, 3
  • Nutritional support - Albumin is not a source of protein nutrition in malnutrition, malabsorption, or protein-losing enteropathies 5, 7
  • Chronic nephrosis - Infused albumin is promptly excreted by the kidneys with no relief of chronic edema 5
  • First-line volume replacement in critically ill patients - Balanced crystalloids (lactated Ringer's) are preferred for initial resuscitation 1, 2, 3
  • Routine use in cardiovascular surgery, kidney replacement therapy, or neonatal/pediatric critical care 3

Physiologic Properties and Mechanism of Action

Oncotic Effects:

  • Each 20 mL of 25% albumin (Plasbumin-25) supplies the oncotic equivalent of approximately 100 mL citrated plasma 5
  • When administered intravenously, 20 mL of 25% albumin draws approximately 70 mL of fluid from extravascular tissues into circulation within 15 minutes 5
  • This increases total blood volume and reduces hemoconcentration and whole blood viscosity 5

Non-Oncotic Properties:

  • Albumin is produced exclusively by the liver and serves as a transport protein 1, 8
  • It binds multiple substances including fatty acids, bilirubin, thyroid hormone, and drugs 1, 8
  • Albumin has immunomodulatory, endothelial stabilization, and antioxidant effects 9, 8
  • In advanced cirrhosis, albumin quality is decreased due to oxidative stress and proinflammatory states 9, 10

Critical Safety Considerations and Adverse Effects

Monitor Closely for Volume Overload:

  • Patients with cirrhosis have increased capillary permeability and are at higher risk for pulmonary edema 1, 4
  • More severe or life-threatening serious adverse events were reported in albumin-treated patients, primarily pulmonary edema 1, 4
  • The ATTIRE trial showed significantly higher rates of pulmonary edema and fluid overload when targeting specific albumin levels 1

Immediately discontinue albumin if:

  • Pulmonary edema develops 2
  • Respiratory distress or declining oxygen saturation occurs 2

Other Potential Adverse Effects:

  • Hypotension 3
  • Hemodilution requiring RBC transfusion 3
  • Anaphylaxis 3
  • Allergic and transfusion reactions 9
  • Peripheral gangrene from dilution of natural anticoagulants 3

Practical Algorithm for Albumin Administration

Step 1: Identify the Specific Indication

  • Large-volume paracentesis (>5L removed) 2
  • Spontaneous bacterial peritonitis (at diagnosis) 2
  • Hepatorenal syndrome 1, 2
  • Sepsis-induced hypotension in cirrhosis 2
  • Consider for acute hepatic encephalopathy (with caution due to low certainty) 2, 4

Step 2: Assess Contraindications

  • Evaluate cardiac function for risk of volume overload 2
  • Assess pulmonary function and baseline respiratory status 2
  • Avoid in patients with significant cardiac or pulmonary compromise 4

Step 3: Administer Appropriate Dose

  • Large-volume paracentesis: 6-8 g per liter of ascitic fluid removed 5
  • Spontaneous bacterial peritonitis: 1.5 g/kg at diagnosis, 1.0 g/kg on day 3 2, 4
  • Acute hepatic encephalopathy: 1.5 g/kg day 1, then 1.0 g/kg day 3 (or 1.5 g/kg/day for up to 10 days) 2, 4
  • Sepsis-induced hypotension: Use 5% albumin for resuscitation 2

Step 4: Monitor During and After Administration

  • Use echocardiography to guide fluid management 2
  • Watch for respiratory distress or declining oxygen saturation 2
  • Monitor for signs of volume overload 2
  • Discontinue immediately if pulmonary edema develops 2

Common Pitfalls to Avoid

Do not target specific serum albumin levels in hospitalized patients with decompensated cirrhosis - The ATTIRE trial showed no benefit and increased pulmonary complications when targeting albumin levels of 3 g/dL 1

Do not use albumin as a substitute for addressing underlying causes of hypoalbuminemia - Treatment should focus on the underlying disease process (sepsis, liver disease, nephrotic syndrome, malnutrition) rather than simply correcting the albumin level 3

Do not use albumin for chronic conditions without evidence-based indications - In chronic cirrhosis with malabsorption or protein-losing enteropathies, albumin infusion as a source of protein nutrition is not justified 5

Consider cost and availability - Albumin is expensive (approximately $130/25g) and should be reserved for evidence-based indications 3, 9

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Albumin Administration in Chronic Liver Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Albumin Transfusions: Clinical Applications and Evidence

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Albumin Administration in Hepatic Encephalopathy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Hypoalbuminemia.

Internal and emergency medicine, 2012

Research

Albumin: a comprehensive review and practical guideline for clinical use.

European journal of clinical pharmacology, 2024

Research

Controversies regarding albumin therapy in cirrhosis.

Hepatology (Baltimore, Md.), 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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