期刊文献+

西那卡塞治疗血透患者继发性甲状旁腺功能亢进的观察 被引量:5

Observation of Cinacalcet in the Treatment of Hemodialysis Patients with Secondary Hyperparathyroidism
下载PDF
导出
摘要 目的:观察西那卡塞治疗血透患者继发性甲状旁腺功能亢进的疗效与安全性。方法:30例血透合并继发性甲状旁腺功能亢进的患者随机分为对照组与观察组,对照组予骨化三醇治疗,观察组同时加用西那卡塞,观察比较两组治疗效果。结果:治疗后,两组患者的血清磷、i PTH较治疗前均显著下降。对照组的血钙较治疗前显著升高,观察组患者的血清磷、i PTH下降幅度显著高于对照组,差异均有统计学意义(P<0.05)。观察组治疗有效率92.9%,高于对照组的71.4%,差异均有统计学意义(P<0.05)。观察组不良反应发生率26.7%,与对照组的20.0%比较,差异无统计学意义(P>0.05)。结论:血透患者合并继发性甲状旁腺功能亢进,联用骨化三醇与西那卡塞治疗,效果确切,安全性良好。 Objective:To study the effect and safety of Cinacalcet in hemodialysis patients with secondary hyperparathyroidism(SHPT).Method:30 hemodialysis patients with SHPT were randomly divided into observation group and control group.Each group was given Calcitriol,besids,the observation group was extra given Cinacalcet.The effect of the two groups were observed.Result:After treatment,in each group,the level of phosphor and i PTH significantly declined.In control group,the calcium level increased.The levels of phosphor and i PTH in the observation group were lower than those in the control group,the differences were statistically significant(P0.05).The effective rate of the observation group was 92.9%,significantly higher than 71.4% of the control group,the difference was statistically significant(P0.05).The adverse reaction rate of the observation group was 26.7%,while the adverse reaction rate of the observation group was 20.0%.There was not statistically significant difference between the two groups(P0.05).Conclusion:For hemodialysis patients with SHPT,Cinacalcet combined with Calcitriol can increase effective rate and has high safety.
出处 《中外医学研究》 2016年第27期4-5,共2页 CHINESE AND FOREIGN MEDICAL RESEARCH
关键词 血液透析 西那卡塞 继发性甲状旁腺功能亢进 Hemodialysis Cinacalcet Secondary hyperparathyroidism
  • 相关文献

参考文献9

二级参考文献160

  • 1燕宇.西那卡塞的临床应用以及研究进展[J].中国血液净化,2012,11(8):460-463. 被引量:22
  • 2<活性维生素D的合理应用>专家协作组.活性维生素D在慢性肾脏病继发性甲旁亢中合理应用的专家共识(修订版)[J].中华肾脏病杂志,2005,21(11):698-699. 被引量:97
  • 3慢性肾脏病骨代谢及其疾病的临床实践指南——指南8 慢性肾脏病患者的维生素D治疗[J].中国血液净化,2006,5(5):275-280. 被引量:11
  • 4National Kidney Foundation.K/DOQI clinical practice guidelines for bonemetabolism and disease in chronic kidney disease[J].Am J Kidney Dis,2003,42(4 Suppl 3):S1-201.
  • 5Khan S.Vitamin D deficiency and secondary hyperparathyroidism amongpatients with chronic kidney disease[J].Am J Med Sci,2007,333(4):201-207.
  • 6Evenepoel P,Meijers B,Viaene L,et al.Fibroblast growth factor-23 inearly chronic kidney disease:additional support in favor of a phosphate-centric paradigm for the pathogenesis of secondary hyperparathyroidism[J].Clin J Am Soc Nephrol,2010,5(7):1268-1276.
  • 7Brown J M,Secinaro K,Williams J S,et al.Evaluating hormonalmechanisms of vitamin D receptor agonist therapy in diabetic kidneydisease:the VALIDATE-D study[J].BMC Endonr Disord,2013,13(1):33.
  • 8Gallieni M,Cozzolino M,Fallabrino G,et al.Vitamin D:physiology andpathophysiology[J].Int J Artif Organs,2009,32(2):87-94.
  • 9Cozzolino M,Pasho S,Fallabrino G,el al.Pathogenesis of secondaryhyperparathyroidism[J].Int J Artif Organs,2009,32(2):75-80.
  • 10Cozzolino M,Pasho S,Fallabrino G. Pathogenesis of secondary hyperparathyroidism[J].International Journal of Artificial Organs,2009.3275-3280.

共引文献161

同被引文献33

二级引证文献34

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部