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尤瑞克林和巴曲酶治疗进展性脑梗死疗效观察 被引量:5

Urinary Kallidinogenase and Batroxobin Treatment of Progressive Cerebral Infarction
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摘要 目的:观察尤瑞克林和巴曲酶对进展性脑梗死的疗效。方法:进展性脑梗死患者94例,随机分为尤瑞克林组25例,巴曲酶组28例,联合组11例,对照组30例,均给予神经内科常规治疗,尤瑞克林组加用尤瑞克林,巴曲酶组加用巴曲酶,联合组同时加用尤瑞克林和巴曲酶。观察治疗14、28 d后神经功能缺损评分变化。结果:对照组于治疗14、28 d后神经功能缺损评分与治疗前比较无统计学差异。治疗14 d后尤瑞克林组显效率为12%,巴曲酶组为7.14%,联合组为27.27%,3组间无统计学差异。治疗28 d后尤瑞克林组显效率为36%,巴曲酶组为28.57%,联合组为45.45%,3组间无统计学差异。结论:尤瑞克林和巴曲酶对进展性脑梗死均有较好的疗效,联合应用疗效是否更佳还有待观察。 Objective:To observe the therapeutic effect of Urinary kallidinogenase in combination with batroxobin on progressive stroke.Methods:Ninety-four patients with progressive cerebral infarction were assigned into Urinary kallidinogenase group(25 cases),batroxobin group(28 cases),combined treatment group(11 cases) and control group(30 cases).All patients have been treated with the conventional neurological treatment.The neurological function was evaluated 14 days and 28 days after treatment.Results:There was no significant improvement of neurological function in control group 14 days and 28 days after the treatment.On 14 days after treatment,the efficiencys in Urinary kallidinogenase,batroxobin and combined groups were 12%,7.14% and 27.27%,without any difference among the groups.On 28 days,the efficiency of Urinary kallidinogenase group increased to 36%,but no significant difference was observed relative to 28.57% and 45.45% in the other two groups.Conclusion:Both Urinary kallidinogenase and batroxobin show effectiveness on progressive stroke.Whether the combined group has a better effect needs further studies.
作者 孙丰 林兴建
出处 《神经损伤与功能重建》 2010年第3期182-184,共3页 Neural Injury and Functional Reconstruction
关键词 尤瑞克林 巴曲酶 脑梗死 治疗 Urinary kallidinogenase batroxobin cerebral infarction treatment
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  • 1中华医学会全国第四届脑血管病学术会议.脑卒中患者临床神经功能缺损评分标准[J].中华神经科杂志,1996,:29-381,379.
  • 2中华医学会全国第二次脑血管病会议 脑血管病疗效评价标准.中华神经精神科杂志,1988,21(1):58-58.
  • 3Gautier JC.Stroke in Progression[J].Stroke(S0039-2499),1985,16(4):729-733.
  • 4李红云,纪晓军,裴海涛,丛志强.进展性缺血性卒中[J].国外医学(脑血管疾病分册),2005,13(2):132-135. 被引量:71
  • 5王泽颖,宋立公.进展性卒中的研究概况[J].中西医结合心脑血管病杂志,2005,3(6):527-528. 被引量:10
  • 6冯加纯.巴曲酶的临床研究现状[J].医学综述,2002,8(5):306-307. 被引量:12
  • 7吴萍嘉,赵瑛,余慧贞,翁中芳,姚景莉,王晋杨.巴曲酶治疗缺血性脑血管疾病[J].新药与临床,1996,15(1):26-28. 被引量:24
  • 8Leeb-Lundberg LM,Marceau F,Müller-EsterlW,et al.International Union of Pharmacology.XLV.Classification of the Kinin Receptor Family:from Molecular Mechanisms to Pathophysiological Consequences[J].Pharmacol Rev(S0031-6997),2005,57 (1):27-77.

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  • 1李小刚.2006年急性缺血性卒中溶栓治疗研究进展[J].中国卒中杂志,2007,2(2):140-144. 被引量:4
  • 2全国降纤酶临床再评价研究协作组.降纤酶治疗急性脑梗死临床再评价(Ⅱ)[J].中华神经科杂志,2005,38(1):11-16. 被引量:86
  • 3脑卒中患者临床神经功能缺损程度评分标准(1995)[J].中华神经科杂志,1996,29(6):381-383. 被引量:15752
  • 4Lee KY, Heo JH, Lee SI, et al. Rescue treatment with abciximab in acute ischemic stroke[J]. Neurology, 2001,56 ( 11 ): 1585 - 1587.
  • 5Spronk HM, Govers-Riemslag JW, ten Cate H. The blood coagulation system as a mo-lecular machine[J]. Bioessays, 2003,25 (12): 1220-1228.
  • 6Dahlback B. Blood coagulation[J]. Lancet, 2000,355(9215) :1627-1632.
  • 7Leeb-Lundberg LM, Marceau F, Maller-Es- terl W, et al. International union of pharma- cology. ⅩLⅤ. Classification of the kinin re- ceptor family, from molecular mechanisms to pathophysiological consequences [J]. Phar- macol Rev,2005,57(1) .27-77.
  • 8Lewis BE, Wallis DE, Leya F, et al. Ar- gatroban anticoagulation in patients with pa- tients with heparin-induced thrombocytope- nia[J]. Arch Intern Med, 2003, 163 (15): 1849-1856.
  • 9Birschel P, Ellul J, Barer D. Progressing stroke: towards an intemationally agreed definition [ J ]. Cerebrovase Dis, 2004,17 (2/3) :242 - 252.
  • 10Ali LK, Saver JL. The ischemic stroke patient who worsens : new assessment and ma agement approaches [ J ]. Rev Neur ol Dis, 2007,4 : 85-91.

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