Molina Vila Pablo, Sánchez Pérez Pilar, Garrigós Almerich Enrique, Peris Domingo Ana
Division of Nephrology, Hospital Francesc de Borja, Gandia, Spain.
Hemodial Int. 2008 Jan;12(1):73-9. doi: 10.1111/j.1542-4758.2008.00244.x.
The optimal dialysate calcium (Ca) concentration for hemodialysis (HD) patients is set at 2.5 mEq/L according to Kidney Disease Outcomes Quality Initiative (K-DOQI) guidelines. This recommendation is opinion-based and could negatively affect secondary hyperparathyroidism. Studies have suggested that a dialysate Ca of 3.0 mEq/L is a compromise between bone protection and cardiovascular risk. The aim of our study was to investigate the effect on bone metabolism parameters after increasing the dialysate Ca concentration from 2.5 to 3.0 mEq/L. The dialysate Ca concentration in our patients was increased from 2.5 to 3.0 mEq/L. Patients with hypercalcemia, normal-high Ca levels with a high Ca-Phosphorus product (Ca x P), excessively suppressed parathyroid hormone (PTH), or a past medical history of calciphylaxis were excluded. Twenty-two patients were studied over 20 weeks. Parathyroid hormone levels decreased significantly (442 +/- 254 vs. 255 +/- 226 pg/mL; p=0.000), without significant changes in serum Ca, P, and Ca x P levels at any sampling point. Better control of secondary hyperparathyroidism allowed us to decrease the paracalcitol dosage in 6 of the 12 patients who had been treated with this drug at the beginning of the study. Other potential factors involved in PTH secretion were not modified. A significant improvement in the rate of patients with 3 or more K-DOQI parameters within the target ranges (8 [36%] vs. 12 [55%]; p=0.026) was observed. In the absence of hypercalcemia or excessively suppressed PTH, an increase from 2.5 mEq to 3.0 mEq/L in dialysate Ca concentration resulted in better control of secondary hyperparathyroidism without affecting Ca, P, and Ca x P levels, thus enabling us to reduce the dosage of vitamin D metabolites.
根据《肾脏病预后质量倡议(K-DOQI)指南》,血液透析(HD)患者的最佳透析液钙(Ca)浓度设定为2.5 mEq/L。这一建议基于观点,可能会对继发性甲状旁腺功能亢进产生负面影响。研究表明,透析液钙浓度为3.0 mEq/L是在骨骼保护和心血管风险之间的一种折衷。我们研究的目的是调查将透析液钙浓度从2.5 mEq/L提高到3.0 mEq/L后对骨代谢参数的影响。我们患者的透析液钙浓度从2.5 mEq/L提高到了3.0 mEq/L。排除了高钙血症患者、钙磷乘积(Ca×P)处于正常高值水平且甲状旁腺激素(PTH)过度受抑制的患者,或有钙化防御病史的患者。对22例患者进行了为期20周的研究。甲状旁腺激素水平显著下降(442±254 vs. 255±226 pg/mL;p = 0.000),在任何采样点血清钙、磷和钙磷乘积水平均无显著变化。对继发性甲状旁腺功能亢进的更好控制使我们能够在研究开始时接受该药物治疗的12例患者中的6例中减少帕立骨化醇的剂量。其他参与PTH分泌的潜在因素未发生改变。观察到在目标范围内具有3个或更多K-DOQI参数的患者比例有显著改善(8例[36%] vs. 12例[55%];p = 0.026)。在没有高钙血症或PTH过度受抑制的情况下,透析液钙浓度从2.5 mEq/L增加到3.0 mEq/L可更好地控制继发性甲状旁腺功能亢进,而不影响钙、磷和钙磷乘积水平,从而使我们能够减少维生素D代谢物的剂量。