Attie M F
University of Pennsylvania School of Medicine, Philadelphia.
Endocrinol Metab Clin North Am. 1989 Sep;18(3):807-28.
Severe hypercalcemia is a potentially life-threatening complication of several diseases. Most commonly it is caused by cancers that enhance bone resorption. Impaired renal calcium excretion resulting from a combination of volume contraction and calcium-induced renal injury (nephrocalcinosis) plays a critical role in the genesis and aggravation of hypercalcemia. Treatment of hypercalcemia is based on treating the underlying disease, restoring extracellular volume, correcting electrolyte deficiencies (potassium and magnesium), and reducing bone resorption. Several measures are available to reduce bone resorption, of which the most efficacious are the bisphosphonates and plicamycin (mithramycin). One of these agents in combination with volume expansion can reduce serum calcium concentrations to near normal in most patients within 3 to 6 days. Because of the delayed hypocalcemic action of these agents, they should be administered early. Calcitonin has a more modest hypocalcemic action than the bisphosphonates or plicamycin but has a more rapid effect. Combining calcitonin with plicamycin or a bisphosphonate can enhance the rate of decline of the serum calcium level. Bone resorption also can be reduced by getting patients out of bed to stand or walk. Glucocorticoids may be effective in patients with hypercalcemia associated with high levels of vitamin D, such as sarcoidosis, some lymphomas, or vitamin D intoxication. Patients with mild to moderate hypercalcemia may be asymptomatic. Therapy in these patients should be directed at the primary disease as well as at preventing complications that could raise the level of serum calcium. Efforts should be made to prevent volume contraction and prolonged bed rest. Sedatives and narcotic analgesics, by reducing activity and oral intake, can raise serum calcium levels. In the future it may be possible to predict which patients with cancer are likely to develop accelerated local tumor-mediated or humorally mediated osteolysis. For example, high circulating levels of PTH-like peptides in patients with lung cancer might suggest a greater risk of developing hypercalcemia. These patients could be monitored more closely by periodically measuring urinary calcium. Another prophylactic approach would be to treat patients at risk of developing hypercalcemia with drugs, such as the bisphosphonates, that inhibit bone resorption.
严重高钙血症是多种疾病潜在的危及生命的并发症。最常见的是由增强骨吸收的癌症引起。容量收缩和钙诱导的肾损伤(肾钙质沉着症)导致的肾钙排泄受损在高钙血症的发生和加重中起关键作用。高钙血症的治疗基于治疗基础疾病、恢复细胞外液量、纠正电解质缺乏(钾和镁)以及减少骨吸收。有多种措施可用于减少骨吸收,其中最有效的是双膦酸盐和普卡霉素(光辉霉素)。这些药物之一与扩容联合使用可使大多数患者的血清钙浓度在3至6天内降至接近正常水平。由于这些药物的降钙作用延迟,应尽早给药。降钙素的降钙作用比双膦酸盐或普卡霉素弱,但起效更快。将降钙素与普卡霉素或双膦酸盐联合使用可提高血清钙水平的下降速度。让患者下床站立或行走也可减少骨吸收。糖皮质激素对与高水平维生素D相关的高钙血症患者可能有效,如结节病、某些淋巴瘤或维生素D中毒。轻度至中度高钙血症患者可能无症状。这些患者的治疗应针对原发疾病以及预防可能升高血清钙水平的并发症。应努力预防容量收缩和长期卧床休息。镇静剂和麻醉性镇痛药通过减少活动和口服摄入量可升高血清钙水平。未来有可能预测哪些癌症患者可能发生加速的局部肿瘤介导或体液介导的骨溶解。例如,肺癌患者循环中高水平的甲状旁腺激素样肽可能提示发生高钙血症的风险更大。可通过定期测量尿钙对这些患者进行更密切的监测。另一种预防方法是用抑制骨吸收的药物,如双膦酸盐,治疗有发生高钙血症风险的患者。