Treatment for Hyperphosphatemia (7.3 mg/dL) in Tumor Lysis Syndrome
For a patient with tumor lysis syndrome and hyperphosphatemia of 7.3 mg/dL, aggressive hydration through a central venous access, aluminum hydroxide (50-100 mg/kg/day divided in 4 doses), and rasburicase administration are the recommended treatments. 1
Initial Management Algorithm
Immediate Interventions:
- Establish central venous access
- Initiate aggressive IV hydration (target urine output: 100 mL/hour in adults)
- Administer rasburicase (0.2 mg/kg/day as a 30-minute infusion)
Phosphate-Specific Management:
- Administer aluminum hydroxide 50-100 mg/kg/day divided in 4 doses (orally or via nasogastric tube)
- Monitor serum phosphate levels every 4-6 hours initially
Associated Electrolyte Management:
- Monitor for hypocalcemia (treat only if symptomatic with calcium gluconate 50-100 mg/kg)
- Address hyperkalemia if present (see algorithm below)
Detailed Approach to Hyperphosphatemia in TLS
Hydration Strategy
Aggressive hydration is the cornerstone of TLS management. The Haematologica consensus guidelines recommend:
- Starting hydration at least 48 hours before tumor-specific therapy when possible
- Maintaining urine output at minimum 100 mL/hour in adults
- Using loop diuretics if needed to maintain urine output (except in patients with obstructive uropathy or hypovolemia) 1
Phosphate Binding
For hyperphosphatemia of 7.3 mg/dL (which exceeds the mild threshold of <1.62 mmol/L), aluminum hydroxide is indicated:
- Dosage: 50-100 mg/kg/day divided in 4 doses
- Administration: Oral or via nasogastric tube 1
Hypouricemic Therapy
Rasburicase is essential in TLS management:
- Rapidly reduces uric acid levels (97.3% of patients reach target uric acid levels within 24 hours)
- Prevents uric acid nephropathy
- Allows earlier administration of chemotherapy if needed 1, 2
Management of Associated Electrolyte Abnormalities
Hypocalcemia
- Asymptomatic hypocalcemia: No treatment required
- Symptomatic (tetany, seizures): Calcium gluconate 50-100 mg/kg as a single dose, cautiously repeated if necessary 1
Hyperkalemia
- Mild (<6 mmol/L): Hydration, loop diuretics, sodium polystyrene 1 g/kg (oral or enema)
- Severe (≥6 mmol/L): Add rapid insulin (0.1 units/kg) plus 25% dextrose (2 mL/kg), calcium carbonate (100-200 mg/kg/dose), and sodium bicarbonate
- Continuous ECG monitoring is essential 1
Indications for Dialysis
Consider hemodialysis when:
- Severe hyperphosphatemia persists despite medical management
- Acute kidney injury is worsening
- Severe electrolyte abnormalities are unresponsive to medical therapy
- Fluid overload is present
Hemodialysis is highly effective for removing phosphate and uric acid (clearance approximately 70-100 mL/min) 1, 3
Monitoring Parameters
- Serum electrolytes (phosphorus, calcium, potassium) every 4-6 hours initially
- Renal function (creatinine, BUN) at least twice daily
- Urine output hourly
- ECG monitoring in patients with significant hyperkalemia
Pitfalls and Caveats
Calcium administration: Avoid routine calcium supplementation for asymptomatic hypocalcemia as it may promote calcium phosphate precipitation in tissues when phosphate levels are high 1
Phosphate binders: Calcium-based phosphate binders should be avoided in TLS as they may worsen calcium-phosphate product and increase risk of tissue deposition 3
Acidosis management: Address metabolic acidosis (pH 7.3) with bicarbonate therapy, especially if hyperkalemia is present, to help stabilize myocardial cell membranes 1
Early intervention: Delay in treating hyperphosphatemia can lead to acute kidney injury from calcium phosphate deposition in renal tubules, worsening the overall TLS picture 1, 3
By following this structured approach to hyperphosphatemia management in TLS, you can effectively reduce phosphate levels while addressing other metabolic derangements, ultimately improving patient outcomes and reducing mortality.