Treatment of Low Albumin
The primary treatment for low albumin is to identify and treat the underlying cause—not to administer intravenous albumin—with IV albumin reserved only for specific liver-related complications such as large-volume paracentesis, spontaneous bacterial peritonitis, and hepatorenal syndrome. 1
Understanding Why Albumin is Low
Before treating, you must determine the mechanism:
- Inflammation is the most common driver of hypoalbuminemia, not malnutrition, as inflammatory cytokines directly downregulate hepatic albumin synthesis even when protein and caloric intake are adequate 1, 2
- Albumin functions as a negative acute-phase reactant, meaning it drops during any inflammatory state 1, 2
- Other mechanisms include decreased synthesis (liver disease), increased losses (nephrotic syndrome, protein-losing enteropathy), hemodilution from fluid overload, and true malnutrition 1, 3, 2
Critical pitfall: Assuming low albumin equals malnutrition when inflammation may be the primary cause 1, 3, 2
Diagnostic Workup
Systematically assess the following 1:
- Inflammatory markers (CRP, ferritin) to identify inflammation as the driver 1, 2
- Urine albumin-to-creatinine ratio to detect nephrotic-range proteinuria 1
- Liver function tests to assess synthetic function 1
- Hydration status as overhydration dilutes albumin concentration 1, 3
- Nutritional assessment using validated tools (Subjective Global Assessment, MUST, Mini Nutritional Assessment)—not albumin itself—to evaluate for true malnutrition 2
Primary Management Strategy
Treat the Underlying Condition
This is the cornerstone of management 1, 3:
For liver disease:
- Treat the underlying liver disease and its complications 1
- Provide nutrition targets of 1.2-1.3 g/kg/day protein and 30-35 kcal/kg/day 1
- Use albumin infusion ONLY for specific indications (see below) 1
For nephrotic syndrome:
- Reduce proteinuria with disease-specific immunosuppression 1
- Albumin infusion is generally NOT indicated except in congenital nephrotic syndrome with symptomatic hypovolemia 1
For chronic kidney disease/dialysis:
- Target albumin ≥4.0 g/dL 1
- Provide 1.2 g/kg/day protein 1
- Monitor dialysis adequacy (Kt/V) 1
- Address multiple risk factors including infections, dental disease, pain, and polypharmacy 4
- Monitor albumin at least every 4 months, more frequently during acute illness or declining trends 1, 2
For inflammation:
- Address the inflammatory source (infection, autoimmune disease, malignancy) 1, 2
- Recognize that albumin will not normalize until inflammation resolves 2
For malnutrition (when confirmed):
- Provide adequate protein (1.2-1.3 g/kg/day) and calories (30-35 kcal/kg/day) 1
- In dialysis patients, target normalized protein nitrogen appearance (nPNA) ≥0.9 g/kg/day 2
- Consider folate and vitamin B12 supplementation in dialysis patients to prevent deficiency 5
When IV Albumin IS Indicated
Albumin infusion is appropriate ONLY in these specific liver-related scenarios 1, 6, 7:
- Large-volume paracentesis 1, 6
- Spontaneous bacterial peritonitis at diagnosis 1, 6
- Hepatorenal syndrome 1, 6
- Acute kidney injury in cirrhosis 6
The amount and schedule require refinement to avoid volume overload complications 6, 7
When IV Albumin is NOT Indicated
Do not administer albumin to "correct the number" without addressing underlying pathology 1:
- NOT indicated for nephrotic syndrome (except congenital with symptomatic hypovolemia) 1
- NOT recommended for dialysis patients to prevent or treat intradialytic hypotension 3
- NOT indicated solely to increase serum albumin levels 3
- Targeting specific albumin levels with repeated infusions outside approved indications increases pulmonary edema risk 1, 7
Critical Pitfalls to Avoid
- Assuming hypoalbuminemia equals malnutrition when inflammation is often the primary driver 1, 3, 2
- Administering albumin to "correct the number" without addressing underlying pathology 1
- Ignoring fluid status as overhydration dilutes albumin concentration 1, 3
- Using albumin as a nutritional marker when it primarily reflects inflammation in acute illness 1, 2
- Failing to recognize non-nutritional factors affecting albumin such as age, comorbidities, metabolic acidosis, and protein losses 1, 2
- Failing to recognize that albumin synthesis can be suppressed by catabolic illness even with adequate protein intake 2
Clinical Significance
The stakes are high: each 0.1 g/dL decrease in serum albumin increases death risk by 6% in dialysis patients, increases hospitalization days by 5%, and increases technique failure risk by 5% in peritoneal dialysis patients 2. A meta-analysis found that a 1.0 g/dL decrease in albumin increased odds of morbidity by 89% and mortality by 137% 3.