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Guidelines for Complications of Cancer Treatment Vol VIII Part B

Guidelines for Complications of Cancer Treatment Vol VIII Part B

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icarbonate and calcium should not be administered throughthe same line (level <strong>of</strong> evidence: V; grade <strong>of</strong>recommendation: D). Elevated potassium levels should beverified immediately with a second sample to rule out fictitioushyperkalemia from hemolysis during phlebotomy. Patient ECGand cardiac rhythm should be closely followed, along withevaluation <strong>of</strong> electrolyte levels. The above recommendationsare valid <strong>for</strong> adult patients (level <strong>of</strong> evidence: V; grade <strong>of</strong>recommendation: D).Management <strong>of</strong> HypocalcemiaFor asymptomatic pediatric patients, no intervention isrecommended (Table 6). Symptomatic patients may be treatedwith calcium gluconate 50 to 100 mg/kg IV, administeredslowly with EKG monitoring (Level <strong>of</strong> evidence: V; grade<strong>of</strong> recommendation: D). Care must be taken becauseincreased calcium might increase the risk <strong>of</strong> calcium phosphateprecipitation in the tissues and consequential obstructiveuropathy. The above recommendations are valid <strong>for</strong> adultpatients (level <strong>of</strong> evidence: V; grade <strong>of</strong> recommendation: D).Monitoring during treatment:Check laboratory and clinical TLS parameters 4 to 6 hoursafter the initial administration <strong>of</strong> chemotherapy. The TLSparameters consist <strong>of</strong> levels <strong>of</strong> uric acid, phosphate, potassium,creatinine, calcium, and LDH, as well as fluid input and urineoutput. For all patients, uric acid levels should be re-evaluated4 hours after administration <strong>of</strong> rasburicase and every 6 to 12hours thereafter until resolution <strong>of</strong> TLS, <strong>for</strong> example, untilnormalization <strong>of</strong> LDH levels (level <strong>of</strong> evidence: V; grade <strong>of</strong>recommendation: D).For adult intermediate-risk patients, patients should bemonitored <strong>for</strong> at least 24 hours after the completion <strong>of</strong>chemotherapy. For multiagent chemotherapeutic regimens in428

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