When to administer albumin (human albumin) to patients?

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Last updated: November 17, 2025View editorial policy

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When to Administer Albumin

Albumin should be administered in patients with cirrhosis undergoing large-volume paracentesis (>5L), those with spontaneous bacterial peritonitis (especially with bilirubin >4 mg/dL or baseline AKI), and patients with hepatorenal syndrome in combination with vasoconstrictors. 1

Evidence-Based Indications for Albumin Administration

Strong Indications in Cirrhosis (High-Quality Evidence)

Large-Volume Paracentesis (>5L)

  • Administer albumin at 6-8 g per liter of ascites removed 1
  • In patients with acute-on-chronic liver failure (ACLF), give 6-8 g/L regardless of volume removed 1
  • Without albumin, 21% of patients develop AKI after daily 5-L paracenteses; zero patients developed AKI when albumin was given 1
  • This prevents post-paracentesis circulatory dysfunction and reduces activation of the renin-angiotensin-aldosterone system 1

Spontaneous Bacterial Peritonitis (SBP)

  • Give 1.5 g/kg on day 1 and 1.0 g/kg on day 3, in addition to antibiotics 1
  • Reduces AKI from 33% to 10% and mortality from 29% to 10% 1
  • Patients most likely to benefit: those with serum bilirubin >4 mg/dL and/or baseline AKI (creatinine >1.0 mg/dL and BUN >30 mg/dL) 1
  • Even lower doses (10 g/day for 3 days) showed benefit, reducing renal dysfunction from 20% to 7% and mortality from 40% to 27% 1
  • Albumin is superior to hydroxyethyl starch for improving systemic circulatory hemodynamics 1

Hepatorenal Syndrome

  • Administer 20-40 g/day during terlipressin treatment 1
  • Give 1 g/kg before initiating vasoconstrictor treatment 1
  • The combination of albumin plus vasoconstrictors is more effective than vasoconstrictors alone, though the specific albumin effect remains empirical 1

Conditional Indications (Moderate Evidence)

Hypovolemic Shock (Emergency Treatment)

  • Use 25% albumin (hyperoncotic) when oncotic deficits exist or in long-standing shock where treatment has been delayed 2
  • Expands plasma volume by 3-4 times the volume administered by withdrawing fluid from interstitial spaces 2
  • Total dose should not exceed 2 g/kg body weight in absence of active bleeding 2
  • Critical caveat: If patient is dehydrated, additional crystalloids must be given, or use 5% albumin instead 2

Burn Therapy

  • After the first 24 hours post-burn in patients with >30% total body surface area burns 2
  • Dose: 1-2 g/kg/day to maintain albumin levels >30 g/L 3
  • During first 24 hours, use large volumes of crystalloids instead 2

Cardiopulmonary Bypass

  • Use albumin and crystalloid in pump prime to achieve hematocrit of 20% and plasma albumin concentration of 2.5 g/100 mL 2

Neonatal Hemolytic Disease

  • Give 1 g/kg body weight approximately 1 hour prior to exchange transfusion to bind free bilirubin 2
  • Caution: Must be observed in hypervolemic infants 2

Where Albumin Should NOT Be Used

Critical Care Patients Without Specific Indications

  • Albumin is NOT suggested for first-line volume replacement or to increase serum albumin levels in general critically ill adults 1
  • Do not use for routine treatment of hypoalbuminemia 1

Infections Other Than SBP

  • Three RCTs and meta-analysis showed albumin does NOT reduce AKI or mortality in cirrhosis patients with non-SBP infections 1
  • Associated with MORE pulmonary edema 1

Chronic Conditions

  • NOT warranted in chronic nephrosis (promptly excreted by kidneys) 2
  • NOT justified in hypoproteinemic states from chronic cirrhosis, malabsorption, protein-losing enteropathies, pancreatic insufficiency, or undernutrition as protein nutrition 2

Intradialytic Hypotension

  • Guidelines suggest albumin should NOT be used routinely 1
  • Despite frequent use, minimal data support routine administration during kidney replacement therapy 4

Cardiovascular Surgery

  • Albumin should NOT be used routinely 1

Critical Safety Considerations

Fluid Overload Risk

  • Doses exceeding 87.5 g (>4×100 mL of 20% albumin) potentially associated with worse outcomes due to fluid overload 3
  • Pulmonary edema reported as adverse event, particularly with rapid administration 1, 2
  • Monitor hemodynamic response carefully and observe precautions against circulatory overload 2

Infusion Rate Guidelines

  • Hypovolemic patients can tolerate faster rates 3
  • Euvolemic patients should be limited to 2 mL/min (≈120 mL/hour for 25% albumin) 3
  • Avoid rapid infusion in patients with normal or elevated blood volumes (increases pulmonary edema risk) 3

Other Adverse Events

  • Hypotension/tachycardia, rigors, pyrexia, rash/pruritus, nausea/vomiting 1
  • Allergic and transfusion reactions, antibody formation, coagulation derangements 5

Common Pitfalls to Avoid

  • Do not use serum albumin levels alone to guide therapy; volume status is the critical determinant 3
  • Do not assume albumin corrects hypoalbuminemia long-term in chronic conditions 2
  • Do not mix with protein hydrolysates, amino acid solutions, or alcohol-containing solutions 2
  • Do not forget to supplement with crystalloids in dehydrated patients receiving hyperoncotic albumin 2
  • Do not extrapolate safety data from general ICU patients to those with traumatic brain injury (albumin associated with higher mortality in TBI) 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Albumin Infusion Guidance

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Intravenous Albumin for Mitigating Hypotension and Augmenting Ultrafiltration during Kidney Replacement Therapy.

Clinical journal of the American Society of Nephrology : CJASN, 2021

Research

Albumin is a blood product too - is it safe for all patients?

Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine, 2009

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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