Department of Internal Medicine, Medical School, University of Ioannina , Ioannina , Greece.
Curr Med Res Opin. 2014 Jan;30(1):109-12. doi: 10.1185/03007995.2013.841667. Epub 2013 Oct 9.
In patients with kidney dysfunction hyperphosphatemia is more evident as renal failure progresses. It is related to increased FGF-23 levels, secondary hyperparathyroidism, and accelerated progressive vascular calcification. In CKD patients advanced coronary artery calcification is strongly associated with future cardiovascular events, cardiovascular death, and all-cause mortality. Apart from the above, phosphate per se is suspected as a causal risk factor for CKD progression. Keeping serum phosphorus within the target values are linked to improvement in life expectancy. A low phosphate diet, an efficient dialysis removal of phosphate load, and the administration of phosphate binders are the main recommended steps to control hyperphosphatemia. Calcium-based phosphate binders can lead to a positive calcium balance, hypercalcaemia, parathyroid gland suppression, adynamic bone disease, and coronary artery and aortic calcification. On the other hand Sevelamer hydrochloride and Lanthanum carbonate has been shown to be effective, safe and useful therapeutic tools for hyperphosphatemia. When prescribe pharmacological agents, one must take into account the large increase in health-care expenditure and the choice of phosphate binder should be individualized.
在肾功能不全的患者中,随着肾功能衰竭的进展,高磷血症更为明显。这与 FGF-23 水平升高、继发性甲状旁腺功能亢进和血管钙化加速进展有关。在 CKD 患者中,冠状动脉钙化程度越严重,与未来心血管事件、心血管死亡和全因死亡率的相关性越强。除此之外,磷本身被怀疑是 CKD 进展的一个因果危险因素。将血清磷控制在目标值内与延长预期寿命有关。低磷饮食、高效透析清除磷负荷以及使用磷结合剂是控制高磷血症的主要推荐措施。钙基磷结合剂可导致正钙平衡、高钙血症、甲状旁腺抑制、动力性骨病和冠状动脉及主动脉钙化。另一方面,盐酸司维拉姆和碳酸镧已被证明是治疗高磷血症的有效、安全和有用的治疗工具。在开处方时,必须考虑到医疗费用的大幅增加,并且应该个体化选择磷结合剂。