Hasling C, Charles P, Mosekilde L
Am J Med. 1987 Feb 23;82(2A):51-4. doi: 10.1016/0002-9343(87)90487-6.
To evaluate the efficacy of intravenous etidronate disodium (etidronate) in controlling hypercalcemia of malignancy, 20 patients with known malignant disease and hypercalcemia were randomly assigned on a two-to-one basis to receive etidronate, 7.5 mg/kg of body weight, or placebo for three to five days. All patients received 3,000 ml of saline and 40 mg of furosemide per day. Eighteen patients completed the study. Eleven of 12 patients (92 percent) in the etidronate group attained normocalcemia, compared with two of six (33 percent) in the placebo group (p = 0.05). The etidronate group showed a greater decrease in the serum calcium level than did the placebo group (p less than 0.02). Renal calcium excretion decreased significantly in the etidronate group but not in the placebo group. Intravenous etidronate in combination with rehydration and furosemide constitutes a safe and effective alternative in the treatment of hypercalcemia of malignancy.
为评估静脉注射依替膦酸二钠(依替膦酸)控制恶性肿瘤高钙血症的疗效,将20例已知患有恶性疾病且伴有高钙血症的患者按2:1的比例随机分组,分别接受7.5mg/kg体重的依替膦酸或安慰剂治疗,为期三至五天。所有患者每天接受3000ml生理盐水和40mg呋塞米治疗。18例患者完成了研究。依替膦酸组12例患者中有11例(92%)血钙恢复正常,而安慰剂组6例患者中仅有2例(33%)血钙恢复正常(p = 0.05)。依替膦酸组血清钙水平的下降幅度大于安慰剂组(p < 0.02)。依替膦酸组肾钙排泄显著减少,而安慰剂组未出现这种情况。静脉注射依替膦酸联合补液和呋塞米是治疗恶性肿瘤高钙血症的一种安全有效的替代方法。