A multicenter,randomized,double-blinded and placebo-controlled study of acute brain infarction treated by human urinary kallidinogenase

D. Ding, L. Chuan-zhen, M. Ding, Bing-hua Su, C. Feng
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引用次数: 18

Abstract

Objective To evaluate the efficacy and safety of a new drug,human urinary kallidinogenase,against acute brain infarction.Method A 15-center,randomized,double-blinded and 3:1 placebo-controlled study was carried out.Acute brain infarction within 48 hours of onset in the territory of the middle cerebral artery were indicated as subjects;kallidinogenase or placebo which was dissolved in 50 ml saline,was slowly injected intraveousely within 30 minutes daily for 3 weeks.The European Stroke Scale and Barthel Index were used to evaluate the neurological deficit and the activities of daily living(ADL),followed by a follow-up at the end of the third month.Results 446 patients were enrolled,who completed ITT analysis,including 330 in kallidinogenase group and 116 in placebo group,meanwhile 421 proceeded with PP analysis(311 and 110 respectively).There were no significant differences of the baseline data between the 2 groups.At the end of treatment,the ESS scores increased by 55.1%±33.0% and 44.7%±32.8% respectively in kallidinogenase group(KG)and placebo group(PG,P=0.0022),the difference being significant.PP analysis had similar results.As for ADL,follow-up 90 days after the treatment showed 374 cases followed,280 in KG and 94 in PG;1 died in PG,while none in KG.In KG,the cases whose BI≥50 were significantly more than those in PG(P=0.0228).Adverse events possibly or definitely attributable to the drug were observed in 27 cases(7.74%),mostly were mild,such as palpitation,flush,dizziness, nausea etc,without special management needed.Only 2 died which was confirmed not correlated to kallidinogenase,and another 2 cases of sudden blood pressure drop were observed.The blood pressure drop, quickly restoring soon after the withdrawal of kallidinogenase and use of hemopiesic drugs,was considered to be caused by the combination use of anti-hypertensive drug ACEI and quick infusion speed.Conclusion Kallidinogenase is efficacious for acute brain infarction in improving the neurological deficits,which is safe in clinical use.
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一项多中心、随机、双盲和安慰剂对照研究:人尿钾碱二酚原酶治疗急性脑梗死
目的评价新药人尿碱碱二原酶治疗急性脑梗死的疗效和安全性。方法采用15个中心、随机、双盲、3:1安慰剂对照研究。以发病后48小时内大脑中动脉区域急性脑梗死为研究对象,将碱碱二原酶或安慰剂溶解于50 ml生理盐水中,每天30分钟内缓慢静脉注射,连续3周。使用欧洲卒中量表和Barthel指数评估神经功能缺损和日常生活活动(ADL),并在第三个月末进行随访。结果共纳入446例患者,完成ITT分析,其中kallidinogenase组330例,安慰剂组116例,PP分析421例(分别为311例和110例)。两组患者基线数据无显著差异。治疗结束时,kallidinogenase组(KG)和安慰剂组(PG,P=0.0022) ESS评分分别提高55.1%±33.0%和44.7%±32.8%,差异有统计学意义。PP分析也有类似的结果。ADL治疗90天后随访374例,KG组280例,PG组94例,PG组1例死亡,KG组无死亡。KG组BI≥50的病例明显多于PG组(P=0.0228)。27例(7.74%)患者出现可能或肯定可归因于该药的不良事件,多为心悸、潮红、头晕、恶心等轻微不良事件,无需特殊处理。其中2例死亡,证实与钾碱二原酶无关,另有2例血压突然下降。停用碱二酚原酶及使用止血药物后血压迅速恢复,考虑与降压药ACEI联合使用及输液速度快有关。结论Kallidinogenase治疗急性脑梗死可有效改善神经功能缺损,临床应用安全。
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中华神经科杂志
中华神经科杂志 Medicine-Neurology (clinical)
CiteScore
0.70
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0.00%
发文量
6868
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