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隐匿性卒中患儿无进展性动脉病变和卒中再发。

Lack of progressive arteriopathy and stroke recurrence among children with cryptogenic stroke.

机构信息

Neuropédiatrie, CHU Montpellier, Hôpital Gui de Chauliac, Montpellier, France.

出版信息

Neurology. 2012 Dec 11;79(24):2342-8; discussion 2346. doi: 10.1212/WNL.0b013e318278b629. Epub 2012 Nov 28.

DOI:10.1212/WNL.0b013e318278b629
PMID:23197751
Abstract

OBJECTIVE

We hypothesized that cryptogenic forms of arterial ischemic stroke (AIS) in children may present better outcomes than symptomatic ones.

METHODS

We conducted a single-centered retrospective cohort study using chart reviews of all inpatients aged 0.25-16 years and admitted for AIS or TIA between 1994 and 2007. Sixty-three consecutive children with AIS were divided into 2 stroke categories: first, AIS with an established cause, considered as symptomatic (S), and second, AIS only associated with risk factors, and considered as cryptogenic (C). AIS were further subclassified according to the CASCADE stroke classification system. We measured long-term outcome with 2 endpoints: recurrence rate and neurologic impairment score (NIS). We used univariate analysis to compare the clinical and radiologic characteristics of both groups.

RESULTS

AIS were cryptogenic in 28 patients (44%) and symptomatic in 35 (56%). Compared to patients in group S, patients in group C showed an absence of stroke recurrence under prolonged aspirin treatment (0% vs 30.3%; p < 0.01), a predominance of nonprogressive arteriopathies (p = 0.02), unilateral infarcts (p = 0.01), M1 segment stenosis (p = 0.02), and better stroke outcomes (mean NIS 2.7 vs 4.2; p = 0.04). Within group C, patients with post-varicella arteriopathy (PVA) had a profile comparable to that of patients with non-PVA strokes in terms of infarct topography, localization of vascular lesions, recurrence rate, and neurologic outcome.

CONCLUSION

Cryptogenic AIS during childhood is a homogeneous clinical and radiologic entity, likely reflecting similar underlying pathophysiologic mechanisms. Under early and prolonged treatment with aspirin, cryptogenic AIS does not recur.

摘要

目的

我们假设儿童隐源性动脉缺血性卒中(AIS)的表现可能优于症状性 AIS。

方法

我们进行了一项单中心回顾性队列研究,使用了 1994 年至 2007 年期间所有因 AIS 或 TIA 住院的 0.25-16 岁住院患者的病历回顾。63 例连续 AIS 患儿分为 2 个卒中亚组:首先,AIS 有明确病因,考虑为症状性(S),其次,AIS 仅与危险因素相关,考虑为隐源性(C)。AIS 进一步根据 CASCADE 卒中分类系统进行分类。我们用 2 个终点来衡量长期结果:复发率和神经功能缺损评分(NIS)。我们采用单变量分析比较两组的临床和影像学特征。

结果

28 例(44%)AIS 为隐源性,35 例(56%)为症状性。与 S 组患者相比,C 组患者在长期服用阿司匹林治疗下无卒中复发(0% vs 30.3%;p<0.01),非进行性血管病变更常见(p=0.02),单侧梗死(p=0.01),M1 段狭窄(p=0.02),且卒中结局更好(NIS 平均 2.7 vs 4.2;p=0.04)。在 C 组中,水痘后动脉炎(PVA)患者的梗死部位、血管病变定位、复发率和神经功能结局与非 PVA 卒中患者相似。

结论

儿童隐源性 AIS 是一种同质的临床和影像学实体,可能反映了相似的潜在病理生理机制。在早期和长期使用阿司匹林治疗下,隐源性 AIS 不会复发。

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