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轻度急性缺血性脑卒中患者的脑白质病变严重程度与 1 年后的功能结局。

White matter lesion severity in mild acute ischemic stroke patients and functional outcome after 1 year.

机构信息

Center for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Campus Mitte, Charité Platz 1, D-10117 Berlin, Germany.

出版信息

Stroke. 2012 Nov;43(11):3046-51. doi: 10.1161/STROKEAHA.111.646554. Epub 2012 Aug 30.

Abstract

BACKGROUND AND PURPOSE

To determine if severity of visually assessed white matter disease is associated with disability after ischemic stroke.

METHODS

In this Berlin "Cream & Sugar" substudy, all first ischemic stroke patients who received magnetic resonance imaging and completed follow-up between January 2009 and December 2010, were enrolled. Severity of white matter disease was assessed on fluid-attenuated inversion recovery or T2-weighted sequences using the Wahlund and Fazekas visual scales. Functional outcome was assessed after 1 year using the modified Rankin Scale (follow-up [FU] modified Rankin Scale [mRS]).

RESULTS

Of 101 patients (37% female; median age, 67 years; interquartile range, 54-75; National Institutes of Health Stroke Scale score, 1; interquartile range, 0-2), median FU mRS was 1 (interquartile range, 0-2). Binary logistical regression adjusted for age (at 5-year intervals), acute National Institutes of Health Stroke Scale scores, fasting glucose, insulin, glycosylated hemoglobin, creatinine, C-reactive protein quartiles, waist circumference, and systolic blood pressure revealed that Fazekas scores of 2 and 3 independently associated with FU mRS (Fazekas score 2: adjusted odds ratio, 8.4; 95% confidence interval, 2.35-30.09; P=0.001; Fazekas score 3: adjusted odds ratio, 4.2; 95% confidence interval, 1.04-16.96; P=0.044). Wahlund scores>10 were significantly associated with FU mRS when fasting glucose levels were removed from the regression analysis (adjusted odds ratio, 12.17; 95% confidence interval, 1.91-77.54; P=0.008).

CONCLUSIONS

Severe white matter disease defined by standard criteria in acute ischemic stroke patients is associated with disability at 1 year and can be assessed quickly using visual rating scales.

CLINICAL TRIAL REGISTRATION INFORMATION

URLs: http://www.clinicaltrials.gov and https://eudract.ema.europa.eu. Unique identifiers: NCT 01378468 and 2009-010356-97.

摘要

背景与目的

确定视觉评估的脑白质病严重程度是否与缺血性卒中后残疾相关。

方法

本柏林“奶油与糖”子研究纳入了 2009 年 1 月至 2010 年 12 月间接受磁共振成像且完成随访的所有首发缺血性卒中患者。脑白质病严重程度采用液体衰减反转恢复或 T2 加权序列,通过 Wahlund 和 Fazekas 视觉量表进行评估。1 年后采用改良 Rankin 量表(随访改良 Rankin 量表[FU mRS])评估功能结局。

结果

共纳入 101 例患者(37%为女性;中位年龄 67 岁,四分位间距 54-75;美国国立卫生研究院卒中量表评分 1 分,四分位间距 0-2),中位 FU mRS 为 1 分(四分位间距 0-2)。经年龄(每 5 年为一个区间)、急性美国国立卫生研究院卒中量表评分、空腹血糖、胰岛素、糖化血红蛋白、肌酐、C-反应蛋白四分位数、腰围和收缩压校正的二元逻辑回归显示,Fazekas 评分 2 分和 3 分与 FU mRS 独立相关(Fazekas 评分 2 分:校正比值比,8.4;95%置信区间,2.35-30.09;P=0.001;Fazekas 评分 3 分:校正比值比,4.2;95%置信区间,1.04-16.96;P=0.044)。当从回归分析中去除空腹血糖水平时,Wahlund 评分>10 与 FU mRS 显著相关(校正比值比,12.17;95%置信区间,1.91-77.54;P=0.008)。

结论

在急性缺血性卒中患者中,采用标准标准定义的严重脑白质病与 1 年后的残疾相关,可通过视觉评分量表快速评估。

临床试验注册信息

网址:http://www.clinicaltrials.govhttps://eudract.ema.europa.eu。独特标识符:NCT 01378468 和 2009-010356-97。

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