Efficacy and Safety of Vinpocetine as Part of Treatment for Acute Cerebral Infarction: A Randomized, Open-Label, Controlled, Multicenter CAVIN (Chinese Assessment for Vinpocetine in Neurology) Trial

被引:29
作者
Zhang, Weiwei [1 ]
Huang, Yining [2 ]
Li, Ying [1 ]
Tan, Liming [3 ]
Nao, Jianfei [4 ]
Hu, Hongtao [5 ]
Zhang, Jingyu [6 ]
Li, Chen [7 ]
Kong, Yuenan [8 ]
Song, Yulin [9 ]
机构
[1] Beijing Mil Gen Hosp, Dept Neurol, Nanmencang 5,Dongsi St, Beijing 100700, Peoples R China
[2] Peking Univ, Hosp 1, 8 Xishiku St, Beijing 100034, Peoples R China
[3] Cent S Univ, Xiangya Hosp 2, 139 Renmin Rd Mid, Changsha, Hunan, Peoples R China
[4] China Med Univ, Shengjing Hosp, 36 Sanhao St, Shenyang 110004, Liaoning, Peoples R China
[5] Beijing Jishuitan Hosp, 31 East St, Beijing 100035, Peoples R China
[6] Harbin Med Univ, Hosp 4, 37 Yuyuan St, Harbin 150001, Heilongjiang, Peoples R China
[7] Tianjin Fifth Cent Hosp, 41 Zhejiang Rd, Tianjin 300450, Peoples R China
[8] Wuxi 2 Peoples Hosp, 68 Zhongshan Rd, Wuxi 214002, Jiangsu, Peoples R China
[9] Anshan Changda Hosp, 69 Changda St, Anshan, Liaoning, Peoples R China
关键词
ACUTE ISCHEMIC-STROKE; CEREBROVASCULAR DISEASES; DOUBLE-BLIND; CLINICAL-TRIAL; CITICOLINE; METAANALYSIS; THERAPY; INDEX;
D O I
10.1007/s40261-016-0415-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective The objective of this study was to evaluate the efficacy and safety of intravenous vinpocetine administration as part of a comprehensive treatment for acute cerebral infarction in a Chinese population. Methods 610 acute cerebral infarction patients were randomized into two groups: the vinpocetine group (469 patients) received cytidine disphosphate choline 0.4-0.5 g in combination with aspirin 75-100 mg or clopidogrel 75 mg once daily, plus vinpocetine 30 mg intravenously once daily for 7 days, while the control group (141 patients) received cytidine disphosphate choline 0.4-0.5 g in combination with aspirin 75-100 mg or clopidogrel 75 mg once daily for 7 days. Additionally, patients received medications for symptoms such as hypertension, hyperglycemia, hyperlipidemia, and intracranial hypertension when necessary. Mini-Mental State Examination (MMSE), National Institutes of Health Stroke Scale (NIHSS), modified Rankin Scale, and Barthel Index (BI) scores and transcranial doppler (TCD) were assessed at baseline, 7, 14, and 90 days after treatment. Adverse events (AEs) and abnormalities in blood, urine, liver, and kidney function were monitored. Results MMSE, NIHSS, and BI scores were significantly higher in the vinpocetine group than in the control group 90 days after treatment, indicating significantly improved cognitive skill, neurological function, and quality of life (QOL) in the vinpocetine group versus the control group. Importantly, such effects of vinpocetine were maintained over time. In addition, TCD monitoring showed significantly increased cerebral blood flow associated with vinpocetine versus control. No significant difference in safety was noted between the two groups. Conclusions When used as part of treatment for acute cerebral infarction, vinpocetine improves patients' cerebral blood flow, cognitive quality, neurological functions, and QOL. Vinpocetine could be an effective and safe component of treatment regimen for acute cerebral infarction.
引用
收藏
页码:697 / 704
页数:8
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