What is the recommended protocol for albumin 20% (human albumin) infusion?

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Albumin 20% Infusion Protocol

Albumin 20% should be administered according to specific clinical indications with dosing protocols that vary by condition, primarily for cirrhosis-related complications including large-volume paracentesis (8g/L of ascites removed), spontaneous bacterial peritonitis (1.5g/kg then 1g/kg on day 3), and hypovolemic shock, but should NOT be used routinely for general volume resuscitation or hypoalbuminemia correction alone. 1, 2

Evidence-Based Indications and Dosing Protocols

Large-Volume Paracentesis

  • Administer 8g albumin per liter of ascites removed when >5L is drained 1, 2, 3
  • Infuse after paracentesis is completed using 20% or 25% albumin solution 1, 2
  • This prevents post-paracentesis circulatory dysfunction and subsequent renal impairment 1, 2

Spontaneous Bacterial Peritonitis (SBP)

  • For patients with increased or rising serum creatinine:
    • 1.5g albumin/kg within 6 hours of diagnosis 1, 2
    • Followed by 1g/kg on day 3 1, 2
  • Use estimated dry weight for dosing calculations (though this can be challenging in cirrhotic patients) 1, 2
  • This protocol reduces renal dysfunction risk by 72% and mortality by 47% 1, 2
  • Caution: Doses exceeding 87.5g (>4×100mL of 20% albumin) may be associated with worse outcomes due to fluid overload 1

Hypovolemic Shock

  • Albumin 20% is hyperoncotic and expands plasma volume by 3-4 times the infused volume by recruiting interstitial fluid 3, 4
  • Total dose should not exceed 2g/kg body weight in the absence of active bleeding 3
  • The patient must be normally hydrated interstitially or have interstitial edema; if dehydrated, additional crystalloids are required 3
  • Maximum plasma volume expansion occurs approximately 20 minutes after completing the infusion 4, 5

Burn Therapy

  • Beyond 24 hours post-burn, albumin 20% can maintain plasma colloid osmotic pressure after initial crystalloid resuscitation 3

Infusion Rate Considerations

Fast vs. Slow Administration

  • Fast infusion (30 minutes) provides 69% larger plasma volume expansion during the first 2 hours compared to slow infusion (120 minutes) 5
  • The intravascular half-life of albumin is longer with fast infusion (8.0h vs 6.3h) 5
  • No disadvantages were found with the higher infusion rate in healthy volunteers 5
  • For clinical protocols being studied: 100mL of 20% albumin every 12 hours for 4 days in community-acquired pneumonia 1

Critical Safety Considerations

Fluid Overload Risk

  • Monitor closely for pulmonary complications, particularly in critically ill patients 6
  • In a trial comparing 20% albumin to plasmalyte in cirrhotic patients with sepsis, albumin had to be discontinued in 22% of patients due to adverse effects (primarily pulmonary complications) 6
  • Fluid overload has been reported in prospective studies of albumin in cirrhosis patients with infection 1

Retention and Capillary Leak

  • In septic patients, only 68.5% of infused albumin remains intravascular at 4 hours (compared to 79% in healthy controls) 7
  • Serum albumin concentrations decrease significantly faster in septic patients than in healthy controls 7
  • The recruited interstitial fluid amounts to approximately 3.4mL for each infused mL of 20% albumin 4

Situations Where Albumin 20% is NOT Recommended

The International Collaboration for Transfusion Medicine Guidelines explicitly advises against albumin use in: 1

  • Routine volume resuscitation in critically ill neonatal, pediatric, or adult patients
  • Intradialytic hypotension
  • Routine cardiovascular surgery
  • Treatment of hypoalbuminemia alone in hospitalized cirrhotic patients
  • Extraperitoneal infections in cirrhosis

Specific Contraindications from FDA Labeling

  • Chronic nephrosis (albumin is promptly excreted with no relief of edema) 3
  • Chronic cirrhosis, malabsorption, protein-losing enteropathies as a source of protein nutrition 3

Monitoring Requirements

Hemodynamic Monitoring

  • Monitor mean arterial pressure (MAP) - target >65 mmHg in septic shock 6
  • Track arterial lactate clearance as a marker of tissue perfusion 6
  • Observe for signs of circulatory overload throughout infusion 3

Laboratory Monitoring

  • Serial serum albumin levels to guide ongoing dosing 8
  • Renal function (creatinine) particularly in SBP patients 1, 2
  • Hematocrit for hemodilution assessment 7

Common Pitfalls to Avoid

  1. Do not use albumin to "correct" low serum albumin levels alone - this is not evidence-based and wastes resources 1, 2
  2. Avoid excessive dosing in SBP - doses >87.5g may cause fluid overload 1
  3. Do not assume albumin improves survival in all septic patients - the ALPS trial showed no 28-day mortality benefit despite faster hemodynamic improvement 6
  4. Monitor for pulmonary edema closely - this is the most common reason for treatment discontinuation 6
  5. Ensure adequate interstitial hydration before using 20% albumin for shock, or use 5% albumin instead 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Appropriate Indications for Albumin Infusion

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Recruitment of extravascular fluid by hyperoncotic albumin.

Acta anaesthesiologica Scandinavica, 2018

Research

Administration of Albumin Solution Increases Serum Levels of Albumin in Patients With Chronic Liver Failure in a Single-Arm Feasibility Trial.

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2018

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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