Oral citicoline in acute ischemic stroke -: An individual patient data pooling analysis of clinical trials

被引:146
作者
Dávalos, A
Castillo, J
Alvarez-Sabín, J
Secades, JJ
Mercadal, J
López, S
Cobo, E
Warach, S
Sherman, D
Clark, WM
Lozano, R
机构
[1] Hosp Univ Girona Doctor Josep Trueta, Dept Neurol, Girona 17007, Spain
[2] Hosp Clin Univ, Dept Neurol, Santiago De Compostela, Spain
[3] Hosp Gen Valle Hebron, Dept Neurol, Barcelona, Spain
[4] Grp Ferrer SA, Dept Med, Barcelona, Spain
[5] Univ Politecn Cataluna, Dept Stat & Operat Res, Barcelona, Spain
[6] NINDS, NIH, Bethesda, MD 20892 USA
[7] Univ Texas, Hlth Sci Ctr, Dept Med, San Antonio, TX 78284 USA
[8] Oregon Hlth & Sci Univ, Oregon Stroke Ctr, Portland, OR 97201 USA
关键词
cytidine diphosphate choline; neuroprotection; stroke; acute; ischemic;
D O I
10.1161/01.STR.0000038691.03334.71
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-No single neuroprotective agent has been shown to influence outcome after acute stroke. Citicoline has been studied worldwide in many clinical trials with positive findings, but only 1 trial has obtained significant results in the primary efficacy variables. Our objective was to evaluate the effects of oral citicoline in patients with acute ischemic stroke by a data pooling analysis of clinical trials. The primary efficacy end point chosen was the common evaluation of recovery, combining National Institutes of Health Stroke Scale less than or equal to1, modified Rankin Scale score less than or equal to1, and Barthel Index less than or equal to95 at 3 months using the generalized estimating equations analysis. Methods-A systematic search of all prospective, randomized, placebo-controlled, double-blind clinical trials with oral citicoline (MEDLINE, Cochrane, and Ferrer Group bibliographic databases) was undertaken. Individual patient data were extracted from each study and pooled in a single data file. The main inclusion criteria included compatible neuroimaging with ischemic stroke, National Institutes of Health Stroke Scale greater than or equal to8, and prior modified Rankin Scale score less than or equal to1. Four clinical trials using various doses of oral citicoline (500, 1000, and 2000 mg) were identified. Results-Of 1652 randomized patients, 1372 fulfilled the inclusion criteria (583 received placebo, 789 received citicoline). Recovery at 3 months was 25.2% in citicoline-treated patients and 20.2% in placebo-treated patients (odds ratio [OR], 1.33; 95% CI, 1.10 to 1.62; P=0.0034). The dose showing the largest difference with placebo was 2000 mg, with 27.9% of patients achieving recovery (OR, 1.38; 95% CI, 1.10 to 1.72; P=0.0043). The overall safety of citicoline was similar to placebo. Conclusions-Treatment with oral citicoline within the first 24 hours after onset in patients with moderate to severe stroke increases the probability of complete recovery at 3 months.
引用
收藏
页码:2850 / 2857
页数:8
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