期刊文献+

尤瑞克林联合胞二磷胆碱治疗急性前循环脑梗死的临床疗效 被引量:8

Clinical effect of urinary kallidinogenese compined with citicoline on treating acute carotisal cenebral infarction
下载PDF
导出
摘要 目的探讨尤瑞克林与胞二磷胆碱联合治疗急性前循环脑梗死的疗效和安全性。方法将64例急性前循环脑梗死患者在同时给予常规治疗的基础上随机分为单用胞二磷胆碱组和尤瑞克林与胞二磷胆碱联合治疗组,静脉滴注共14 d,观察两组患者治疗前和治疗后14 d神经功能缺损程度评分(neurological deficiency score,NDS)及日常生活活动量表(BI指数)评分的变化及不良反应。结果治疗后联合治疗组和单用胞二磷胆碱组患者NDS及日常生活活动量表评分与治疗前相比均有显著改善(P<0.01),联合治疗组改善程度与对照组相比差异有极显著性(P<0.01)。两组均未发现明显不良反应。结论尤瑞克林联合胞二磷胆碱治疗急性前循环脑梗死疗效优于单药治疗,且安全性好。 Aim To investigate the effect and safety of urinary kallidinogenase combined with citicoline in the treatment of acute carotisal cerebral infarction. Methods 64 cases with acute carotisal cerebral infarction were divided into two groups based on routine treatment randomly:citicoline group (n = 32 )and urinary, kallidinogenase combined with citicoline group (n = 32). citicoline group was treated with citicoline for 14 days and combined group was treated with citicoline 0. 175 g · d^-1 and urinary kallidinogenase 0.15PNA for 14 days. The neurological deficit scores (NDS) , BI index and adverse reactions were evaluated before and after the treatment, respectively. Results After the treatment, the scores of NDS and BI index were significantly decreased in two groups than those before the treatment (P 〈 0. 01 ) , and kallidinogenase combined with eitieoline group was much better than citicoline group. There was no obvious adverse reaction in two groups. Conclusion Kallidinogenase combined with citicoline shows better clinic effect and no more hemorrhagic risk than citicoline in the therapy of acute earotisal cerebral infarction.
出处 《安徽医药》 CAS 2009年第1期72-74,共3页 Anhui Medical and Pharmaceutical Journal
关键词 急性脑梗死 胞二磷胆碱 联合治疗 acute cerebral infarction citicoline combined treatment
  • 相关文献

参考文献10

  • 1屈志炜,苏丹,张丽英,吴俊芳,巫锦娣,王晓岩,谢永立.凯力康对大鼠局灶性脑缺血的实验研究[J].中国处方药,2005,4(11):73-75. 被引量:43
  • 2胡昌武,董少军,张新胜.尿激酶超早期静脉溶栓治疗急性脑梗死疗效观察[J].安徽医药,2005,9(11):816-816. 被引量:7
  • 3Onesmo. Structural studies of human urinary kallikrein (urokallikrein) [J]. Proc. Natl. Acad. Sci. ,1979,76(7) :3121 -5.
  • 4Lu HS. Human urinary kallikrein. Complete amino acid sequence and sites of glycosylation [J].Int J Pept Protein Res, 1989,33 (4) : 237 - 49.
  • 5Duncan J Campbell. The Kalllikrein-Ki-nin System in Humans[ J]. Clin Exp Pharnacol Physiol,2001,28 ( 12 ) : 1060 - 5.
  • 6Francois Marceau. The BI Receptors for Kinins[J].Pharmacoloical Reviews, 1998,50 (3) :357 - 86.
  • 7Simone Wagner. Activation of the tissue kallikrein-kinin system in stroke[J]. Jourrlal of the Neurological Seiences,2002,202( 1 - 2 ) : 75 - 6.
  • 8Fredrik LM. International Union of Pharmacology. Classification of the Kinin Receptor Family from molecular mechanisms to pathophysiological consequences [ J ]. Pharamaeol Rev, 200557 ( 1 ) : 27 - 77.
  • 9Emanueli C, Madeddu P. Angiogenesis therapy with human tissue kallikrein for the treatment of ischemic diseases [ J ]. Arch Mal Coeur,2004,97 : 679 - 87.
  • 10Chun-Fang Xia. Kallikrein gene transfer protects against ischemic stroke by promoting glialcell migration and inhibiting apoptosis[ J]. Hypertension 2004,43 ( 2 ) :452 - 9.

二级参考文献6

共引文献47

同被引文献80

引证文献8

二级引证文献100

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