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[慢性肾脏病中的矿物质与骨异常:药物治疗的批判性评估]

[Mineral and bone disorder in chronic kidney disease : Critical appraisal of pharmacotherapy].

作者信息

Brunkhorst R

机构信息

Innere Medizin und Nephrologie, Krankenhaus Oststadt, Podbielskistr. 380, 30659, Hannover, Deutschland,

出版信息

Internist (Berl). 2014 Mar;55(3):334-9. doi: 10.1007/s00108-014-3447-4.

DOI:10.1007/s00108-014-3447-4
PMID:24522558
Abstract

BACKGROUND

Mineral and bone disorder (MBD) in chronic kidney disease (CKD) is associated with increased cardiovascular calcification and mortality. Pharmacological interventions for MBD in CKD are characterized by inconsistent data and a wide spectrum of (sometimes costly) treatment options. The objective of this article is a guideline-oriented overview of the differential indications for pharmacotherapy considering cost-effectiveness.

CURRENT DATA

The serum phosphate concentration in patients with CKD stages 3-5 with a glomerular filtration rate (GFR) of < 45 ml/min should be kept within the normal range. Currently, under consideration of cost-effectiveness, calcium-containing phosphate binders and combinations of calcium acetate with magnesium carbonate are the preferred treatment options. Phosphate binders free of calcium are indicated in patients with high normal or elevated serum calcium levels. Low vitamin D concentrations in CKD stages 3-5 should be treated under consideration of serum calcium and parathyroid hormone (PTH) with calcidiol (25-cholecalciferol) and in dialysis patients (CKD 5D) with calcitriol (1,25 dihydroxycholecalciferol, activated vitamin D). In CKD the PTH levels should be kept in the range of 2-9-times the upper limit of normal levels. This is achieved by administration of phosphate binding drugs, activated vitamin D, calcimimetic compounds and parathyroidectomy. In CKD stages 3-5 patients metabolic acidosis with < 22 mmol/l serum bicarbonate should be treated with oral sodium bicarbonate.

CONCLUSION

In MBD of CKD patients an individualized pharmacotherapy which is closely guideline-oriented is required in order to achieve cost-effectiveness.

摘要

背景

慢性肾脏病(CKD)中的矿物质和骨代谢紊乱(MBD)与心血管钙化增加及死亡率升高相关。CKD中MBD的药物干预特点是数据不一致且有广泛的(有时成本高昂的)治疗选择。本文的目的是基于指南,对考虑成本效益的药物治疗的不同适应证进行概述。

当前数据

肾小球滤过率(GFR)<45 ml/min的CKD 3 - 5期患者的血清磷酸盐浓度应保持在正常范围内。目前,考虑到成本效益,含钙的磷酸盐结合剂以及醋酸钙与碳酸镁的组合是首选治疗方案。血清钙水平正常高值或升高的患者应使用无钙的磷酸盐结合剂。CKD 3 - 5期维生素D浓度低时,应根据血清钙和甲状旁腺激素(PTH)情况,使用骨化二醇(25 - 羟胆钙化醇)治疗,而透析患者(CKD 5D)则使用骨化三醇(1,25 - 二羟胆钙化醇,活性维生素D)治疗。在CKD中,PTH水平应保持在正常上限的2 - 9倍范围内。这可通过给予磷酸盐结合药物、活性维生素D、拟钙剂化合物以及甲状旁腺切除术来实现。CKD 3 - 5期患者血清碳酸氢盐<22 mmol/l的代谢性酸中毒应使用口服碳酸氢钠治疗。

结论

在CKD患者的MBD中,需要一种紧密遵循指南的个体化药物治疗,以实现成本效益。

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