非致残性缺血性脑血管事件患者的病因学分型与转归的相关性
Correlation betw een the etiologic subtype and outcome in patients w ith non -disabling ischemic cerebrovascular events
摘要目的:探讨非致残性缺血性脑血管事件(non-disablingischemiccerebrovascularevents, NICE)患者的病因学分型与转归的相关性。方法前瞻性连续纳入发病7 d内住院的NICE患者并随访90 d。根据中国缺血性卒中分型(Chinese Ischemic Stroke Subclassification, CISS )标准对每例患者进行病因学分型。在发病后90 d时评价卒中复发和功能转归,转归良好定义为改良 Rankin 量表(modified Rankin Scale, mRS)评分0~2分。采用多变量logistic回归分析确定复发和转归不良的独立危险因素。结果共纳入162例NICE患者。根据CISS 标准分型,76例(46.9%)为大动脉粥样硬化(large artery atherosclerosis, LAA),54例(33.3%)为穿支动脉疾病(penetrating artery disease, PAD),15例(9.3%)为心源性卒中(cardiogenic stroke, CS ),11例(6.8%)病因未确定(undetermined etiology, UE),6例(3.7%)其他病因( other etiology, OE);90 d内共有30例(18.5%)复发卒中,90 d时42例(25.9%)转归不良。复发组糖尿病(46.7%对20.5%;χ2=8.885,P=0.003)、既往卒中或短暂性脑缺血发作史(46.7%对25.0%;χ2=5.572,P=0.018)以及 CS (20.0%对6.8%;Fisher 精确检验:P=0.036)患者比例显著高于未复发组,而PAD 患者比例(16.7%对37.1%;χ2=4.602,P=0.032)显著低于未复发组。多变量logistic回归分析显示,糖尿病[优势比( odds ratio, OR)2.137,95%可信区间(confidence interval, CI)1.359~4.187;P=0.004]和 CS (OR 5.236,95%CI 2.326~10.256;P<0.001)是NICE复发卒中的独立危险因素。转归不良组高血压(83.3%对61.7%;χ2=6.635,P=0.010)、糖尿病(40.5%对20.0%;χ2=6.900,P=0.009)、心房颤动(35.7%对14.2%;χ2=9.113,P=0.003)、CS(19.0%对5.8%;Fisher精确检验:P=0.017)患者比例显著高于转归良好组,而PAD患者比例(16.7%对39.2%;χ2=7.088,P=0.008)显著低于转归良好组。多变量logistic回归分析显示,糖尿病(OR 2.257,95%CI 1.209~3.687;P=0.010)、心房颤动(OR 3.137,95%CI 1.359~6.107;P=0.002)和CS(OR 6.123,95%CI 2.026~12.256;P<0.001)是NICE患者转归不良的独立危险因素。结论 CISS病因学分型与NICE患者的复发卒中和转归不良有关,可为NICE患者的复发和临床转归评估提供参考。
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abstractsObjectiveToinvestigatethecorrelationbetweentheetiologicsubtypeandoutcomein patients w ith non-disabling ischemic cerebrovascular events (NICE). Methods The consecutive patients w ith NICE admitted to hospital within 7 days after onset were enroled prospectively and folowed for 90 days. Etiologic subtypes w ere classified according to the Chinese Ischemic Stroke Subclassification (CISS). Good outcome w as defined as modified Rankin Scale score 0-2. Multivariate logistic regression analysis w as used to identify the independent risk factors for stroke recurrence and poor outcomes. Results A total of 162 patients with NICE were enroled. According to CISS, 76 (46.9%) were classified into large artery atherosclerosis (LAA), 54 (33.3%) into penetrating artery disease (PAD), 15 (9.3%) into cardiogenic stroke (CS), 11 (6.8%) into undetermined etiology (UE), and 6 (3.7%) into other etiology (OE). A total of 30 patients (18.5%) had recurrent stroke w ithin 90 days and 42 (25.9%) had poor outcomes. The proportions of patients w ith diabetes (46.7%vs.20.5%;χ2 =8.885, P=0.003), previous stroke or transient ischemic attack (46.7%vs.25.0%;χ2 =5.572, P=0.018), CS (20.0%vs.6.8%;Fisher exact test:P=0.036) in the stroke recurrence group w ere significantly higher than those in the non-stroke recurrence group, and the proportion of PAD patients in the stroke recurrence group w as significantly low er than that in the non -stroke recurrence group ( 16.7%vs.37.1%; χ2 =4.602, P=0.032 ). Multivariate logistic regression analysis show ed that diabetes (odds ratio [OR] 2.137, 95%confidence interval [CI] 1.359-4.187;P=0.004) and CS (OR 5.236, 95%CI 2.326-10.256; P<0.001) w ere the independent risk factors for recurrent stroke of NICE. The proportions of patients w ith hypertension ( 83.3%vs.61.7%; χ2 =6.635, P=0.010 ), diabetes (40.5%vs.20.0%;χ2 =6.900, P=0.009), atrial fibrilation (35.7%vs.14.2%;χ2 =9.113, P=0.003) and CS ( 19.0%vs.5.8%; Fisher exact test: P= 0.017 ) in the poor outcome group w ere significantly higher than those in the good outcome group, and the proportion of PAD patients ( 16.7%vs. 39.2%;χ2 =7.088, P=0.008) in the poor outcome group w as significantly low er than that in the good outcome group. Multivariate logistic regression analysis show ed that diabetes ( OR 2.257, 95%CI 1.209-3.687; P=0.010), atrial fibrilation (OR 3.137, 95%CI 1.359-6.107, P=0.002), and CS (OR 6.123, 95%CI 2.026-12.256, P<0.001) w ere the independent risk factors for poor outcomes in patient w ith NICE. Conclusions The etiologic subtype is associated w ith the poor outcomes and recurrent stroke, and can provide reference for recurrence and clinical outcome assessment in patients w ith NICE.
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