Comparison of intermittent intravenous and oral calcitriol in the treatment of secondary hyperparathyroidism in chronic hemodialysis patients: a meta-analysis of randomized controlled trials

医学 继发性甲状旁腺功能亢进 骨化三醇 荟萃分析 随机对照试验 安慰剂 不利影响 内科学 血液透析 高磷血症 肾脏疾病 维生素D与神经学 甲状旁腺激素 病理 替代医学
作者
Haiyang Zhou,Chenggang Xu
出处
期刊:Clinical Nephrology [Dustri-Verlag]
卷期号:71 (03): 276-285 被引量:8
标识
DOI:10.5414/cnp71276
摘要

Controversy exists regarding the optimal route and mode of calcitriol administration in the treatment of secondary hyperparathyroidism (SHPT). The aim of this study is to compare the efficacy and adverse reaction of calcitriol in the same mode (intermittent) but different route (intravenous versus oral) in the treatment of SHPT.Electronic databases including Medline, Embase, Cochrane-controlled trials register, China Biological Medicine Disk (updated February 2008), and manual bibliographical searches were conducted. A meta-analysis of all randomized controlled trials (RCTs) comparing intermittent intravenous with intermittent oral calcitriol in the treatment of SHPT was performed.6 studies from 5 countries were finally considered for the meta-analysis, including a multicenter trial. The results of meta-analyses showed that there were no significant differences between the two routes in suppressing iPTH, AKP and rising Ca, P. In sensitivity analyses (baseline iPTH > or = 600 pg/ml, baseline iPTH < 600 pg/ml, and excluding the multicenter trial), the results were similar to those of the overall analyses. Results of the descriptive analysis showed that there were no significant differences between the two routes in the incidence of hypercalcemia and hyperphosphatemia.Our analysis indicated that there were no significant differences between intermittent intravenous and oral calcitriol in the treatment of SHPT, both in their efficacy and adverse reaction. Since the present studies had several limitations in methodological design and sample size, largescale and long-term comparisons of intermittent intravenous and oral treatment need to be done in a randomized, double-blind, placebo-controlled design to accurately evaluate their relative efficacy and safety.
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