Guella Adnane, Abduelkarem Abduelmula R, Hassanein Mohammed M
Senior Consultant Nephrologist, University Hospital Sharjah, Department of Nephrology, P.O. Box 72772 Sharjah, United Arab Emirates.
Pharmacy Practice and Pharmacotherapeutics Department, College of Pharmacy, The University of Sharjah, P.O. Box 27272, Sharjah, United Arab Emirates.
Pharm Pract (Granada). 2023 Jan-Mar;21(1):2773. doi: 10.18549/PharmPract.2023.1.2773. Epub 2022 Jan 5.
Different studies have shown that hemodialysis patients require higher doses of Vitamin D3 (VD3) than the general population to achieve satisfactory replenishment. This study aims to assess the safety of such practice and its benefits on some of the parameters of Chronic Kidney Disease- Mineral and Bone Disorder (CKD-MBD).
A single-center clinical trial assessing the benefits of high dose VD3 in hemodialysis patients. The dose of VD3 (300,000 IU) was administered orally and monthly from April to December 2020 (9 months) at the dialysis unit. The data analyzed were blood levels of calcium, phosphorus, alkaline phosphatase, 25(OH)D, 1,25(OH)2D and intact parathyroid hormone (iPTH) done every three months.
We could recruit a cohort of 23 patients. Blood levels of 25(OH)D increased significantly in 82.6% of the patients to above 30 ng/ml. A similar effect was observed with 1, 25(OH)2D levels. iPTH levels decreased significantly when levels of 25(OH)D exceeded 30ng/ml at the end of the nine months. Vitamin D serum levels were typically measured immediately before the next monthly dose was administered. Blood levels of calcium, phosphorus, and alkaline phosphatase were stable during the study period. No events of hypercalcemia were reported, and no patient discontinued the monthly VD3 supplementation.
Monthly administration of a high dose of VD3 over a long period of nine months in hemodialysis patients was found to be safe and beneficial in VD3 replenishment. It also allowed a significant decrease in iPTH levels. Further studies are warranted to identify the therapeutic target level of 25(OH)D in hemodialysis patients, allowing beneficial effects on iPTH.
不同研究表明,与普通人群相比,血液透析患者需要更高剂量的维生素D3(VD3)才能实现满意的补充。本研究旨在评估这种做法的安全性及其对慢性肾脏病 - 矿物质和骨异常(CKD - MBD)某些参数的益处。
一项单中心临床试验,评估高剂量VD3对血液透析患者的益处。2020年4月至12月(9个月)期间,在透析单元每月口服一次VD3(300,000国际单位)。分析的数据为每三个月检测一次的血钙、血磷、碱性磷酸酶、25(OH)D、1,25(OH)2D和完整甲状旁腺激素(iPTH)的血液水平。
我们招募了一组23名患者。82.6%的患者血液中25(OH)D水平显著升高至30 ng/ml以上。1,25(OH)2D水平也观察到类似效果。在9个月末,当25(OH)D水平超过30 ng/ml时,iPTH水平显著下降。维生素D血清水平通常在下一次每月剂量给药前立即测量。在研究期间,血钙、血磷和碱性磷酸酶的血液水平保持稳定。未报告高钙血症事件,也没有患者停止每月补充VD3。
在血液透析患者中,长期九个月每月给予高剂量VD3被发现对补充VD3是安全且有益的。它还能使iPTH水平显著降低。有必要进行进一步研究以确定血液透析患者中25(OH)D的治疗目标水平,从而对iPTH产生有益影响。