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Usually symptomatic and severe (≥ 15 mg/dL [> 3.75 mmol/L)])
The neoplasm is clinically apparent in nearly all cases when hypercalcemia is detected
Occurs in 20–30% of patients with cancer
Common causes include
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Symptoms and signs can be subtle
More severe symptoms occur with higher levels of serum calcium and with a rapidly rising calcium level
Early symptoms typically include
Anorexia
Nausea
Fatigue
Constipation
Polyuria
Later findings may include
Hypercalcemia is caused by one of three mechanisms:
Systemic effects of tumor-released proteins
Direct osteolysis of bone by tumor
Vitamin D–mediated osteoabsorption
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Intravenous fluids with 0.9% saline at 100–300 mL/h to ensure rehydration with brisk urinary output of the often volume-depleted patient
Bisphosphonate should be given if kidney function is normal or only marginally impaired
Pamidronate, 60–90 mg intravenously over 2–4 hours
Zoledronic acid, 4 mg intravenously over 15 minutes
Ibandronate 2–4 mg intravenously over 2 hours
Once hypercalcemia is controlled, initiate treatment directed at the cancer, if possible
Other agents that can be used if hypercalcemia becomes refractory to bisphosphonates
Calcitonin, 4–8 international units/kg is given every 12 hours subcutaneously or intramuscularly
Denosumab, 120 mg subcutaneously weekly for 4 weeks, followed by monthly administration for long-term management
Corticosteroids (eg, low-dose dexamethasone, 40 mg intravenously weekly, or higher-dose dexamethasone, 40 mg intravenously daily on days 1–4, 9–12, and 17–20 each month) can be useful in patients with myeloma and lymphoma