Albumin Administration: Key Considerations
Albumin should NOT be used routinely in most critically ill patients for volume replacement or to correct hypoalbuminemia, but IS indicated for specific cirrhosis complications including large-volume paracentesis (>5L), spontaneous bacterial peritonitis, and hepatorenal syndrome. 1
When Albumin IS Indicated
Cirrhosis-Related Indications (Strong Evidence)
Large-Volume Paracentesis (>5L)
- Administer 8 g of albumin per liter of ascites removed after the procedure is completed 2
- This prevents paracentesis-induced circulatory dysfunction 1
- Doses exceeding 87.5 g (>4×100 mL of 20% albumin) may worsen outcomes due to fluid overload 2
Spontaneous Bacterial Peritonitis
- Give 1.5 g/kg within 6 hours of diagnosis, followed by 1.0 g/kg on day 3 2
- This reduces kidney impairment and mortality 2
Hepatorenal Syndrome
- Albumin is uniformly administered in treatment protocols, though specific dosing varies 1
Other FDA-Approved Indications
Emergency hypovolemic shock (when hyperoncotic 25% albumin is used, it expands plasma volume 3-4 times the infused volume) 3
Cardiopulmonary bypass (to achieve hematocrit of 20% and plasma albumin of 2.5 g/dL) 3
Neonatal hemolytic disease (1 g/kg given 1 hour prior to exchange transfusion to bind bilirubin) 3
When Albumin Is NOT Recommended
Critical Care Settings (Moderate to High Quality Evidence)
Do NOT use albumin for:
- First-line volume replacement in critically ill adults (excluding burns/ARDS) 1
- Correcting hypoalbuminemia alone 1, 4
- Thermal injuries or ARDS for volume replacement 1
- Mobilizing extravascular fluid with diuretics 1
Pediatric and Neonatal Populations
Do NOT use albumin for:
- Preterm neonates with respiratory distress and low albumin 1
- Preterm neonates requiring volume replacement 1
- Pediatric cardiovascular surgery (priming or volume replacement) 1
Other Settings
Do NOT use albumin for:
- Intradialytic hypotension or improving ultrafiltration during dialysis 1
- Cardiovascular surgery in adults 1, 2
- Chronic nephrosis (albumin is promptly excreted with no benefit) 3
- Protein nutrition in malabsorption, cirrhosis, or malnutrition 3
Critical Safety Considerations
Monitoring Requirements
Fluid overload is the primary risk, particularly in cirrhotic patients receiving higher doses or rapid administration 2
Monitor carefully for:
- Circulatory overload (mandatory monitoring per FDA labeling) 3
- Rising serum creatinine during infusion 2
- Rapid blood pressure increases that may unmask previously controlled bleeding 3
Dehydration Precautions
If using 25% hyperoncotic albumin in dehydrated patients:
- Must give with or followed by crystalloid fluids 3
- Alternatively, use 5% iso-oncotic albumin instead 3
Additional Adverse Effects
Documented complications include:
- Hypotension 1, 4
- Hemodilution requiring RBC transfusion 1, 4
- Anaphylaxis 1, 4
- Peripheral gangrene from dilution of natural anticoagulants 1, 4
Dosing Considerations
Concentration Selection
25% albumin (hyperoncotic):
- Expands plasma volume 3-4 times the infused volume 3
- Used for oncotic deficits, not simple volume replacement 3
- Requires adequate hydration or concurrent crystalloids 3
5% albumin (iso-oncotic):
Administration Timing
For spontaneous bacterial peritonitis: Within 6 hours of diagnosis 2
For large-volume paracentesis: After procedure completion 2
For cardiac surgery (in research protocols): Administered on ICU arrival and continued for 15 hours 2
Common Pitfalls to Avoid
Do not use albumin to "correct" low albumin levels - treat the underlying cause instead (malnutrition, inflammation, capillary leak) 4
Do not exceed 2 g/kg total dose in the absence of active bleeding 3
Do not mix with protein hydrolysates, amino acid solutions, or alcohol-containing solutions 3
In hemorrhage, supplement albumin with whole blood transfusion to treat relative anemia from hemodilution 3
Cost and Resource Considerations
Albumin costs approximately $130 per 25g (US warehouse acquisition cost), making it substantially more expensive than crystalloids 1
This high cost, combined with limited evidence of benefit in most settings, supports restricting use to well-defined indications 1, 5