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Complication of treatment-associated tumor lysis of hematologic as well as rapidly proliferating malignancies
May be worsened by thiazide diuretic use
Rapid increase in serum uric acid can cause acute urate nephropathy from uric acid crystallization
To prevent urate nephropathy, serum uric acid must be reduced before chemotherapy
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Acute kidney injury
Hyperphosphatemia (associated symptoms include nausea, vomiting, anorexia, muscle cramps, tetany, and seizures)
Hyperkalemia (can cause arrhythmias and sudden death)
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At least two of the following criteria should be observed within a 24-hour period:
Uric acid ≥ 8 mg/dL (≥ 476 micromol/L)
Phosphate ≥ 4.5 mg/dL (≥ 1.45 mmol/L)
Potassium ≥ 6.0 mEq/L (≥ 6 mmol/L)
Corrected serum calcium ≤ 7 mg/dL (≤ 1.75 mmol/L)
25% increase from baseline for these parameters
A clinical diagnosis of tumor lysis syndrome includes meeting the laboratory criteria and at least one clinical criterion:
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Prevention is the most important factor in the management of tumor lysis syndrome
Aggressive hydration at least 24 hrs prior to chemotherapy as well as 24–48 hours after chemotherapy completion
If evidence of volume overload or inadequate urinary output develop
Allopurinol
Should be given to patients at moderate risk of developing tumor lysis syndrome (eg, those with intermediate-grade lymphomas and acute leukemias) before starting chemotherapy
Dose should be reduced in patients with impaired kidney function
Rasburicase
Should be given intravenously to patients at high risk for developing tumor lysis syndrome (eg, those with high-grade lymphomas or acute leukemias with markedly elevated white blood cell counts)
May also be considered for patients with baseline elevated uric acid who are being treated with venetoclax for chronic lymphocytic leukemia or in any patient in whom uric acid levels reach levels > 8 mg/dL despite treatment with allopurinol
Cannot be given to patients with known glucose 6-phosphate dehydrogenase (G6PD) deficiency or to pregnant or lactating women