Braun Kees P J, Rafay Mubeen F, Uiterwaal Cuno S P M, Pontigon Anne-Marie, DeVeber Gabrielle
Department of Child Neurology, Wilhelmina Children's Hospital, Rudolf Magnus Institute of Neuroscience, Utrecht, The Netherlands.
Stroke. 2007 Feb;38(2):298-302. doi: 10.1161/01.STR.0000254484.10680.c6. Epub 2006 Dec 28.
In children, early differentiation among various etiologies of arterial ischemic stroke (AIS) is important. Cerebral arteriopathy is a frequently identified cause of childhood stroke. Children with arteriopathies require a different therapeutic approach from children with AIS of nonarteriopathic origin. We aimed to investigate the association between temporal features of the onset of neurological symptoms and stroke etiology in children with AIS.
From a consecutive cohort of children (6 months to 18 years) with a confirmed diagnosis of AIS at one center, we selected all patients with transient cerebral arteriopathy (n=10), postvaricella angiopathy (n=20), dissection (n=8), cardio-embolic (n=8), and cryptogenic stroke (n=10). We retrospectively reviewed medical charts for mode of onset and classified the onset as either abrupt, reaching maximum severity of symptoms within 30 minutes, or nonabrupt, including a progressing, stuttering, or recurring course. We compared the mode of onset in patients with known cerebral arteriopathy to those with nonarteriopathic stroke using multivariate logistic regression modeling.
There were no significant differences for age, gender, location of infarction, seizures, and headache between the arteriopathic and nonarteriopathic group. Most children with nonarteriopathic AIS had an abrupt onset (72%), compared with 32% in children with arteriopathic stroke. With nonabrupt onset, the odds of having an arteriopathic etiology was 6.1 (95% CI, 1.6 to 22.8; P=0.007) after correction for possible confounders.
Mode of onset predicts etiological diagnosis of childhood AIS and may guide prioritization of ancillary investigations and choice of treatment. A nonabrupt onset of symptoms is associated with arteriopathic stroke, particularly with presumed inflammatory arteriopathies.
在儿童中,早期区分动脉缺血性卒中(AIS)的各种病因很重要。脑动脉病变是儿童卒中常见的病因。患有动脉病变的儿童需要与非动脉病变性AIS儿童采取不同的治疗方法。我们旨在研究AIS儿童神经症状发作的时间特征与卒中病因之间的关联。
从一个中心确诊为AIS的连续儿童队列(6个月至18岁)中,我们选取了所有患有短暂性脑动脉病变(n = 10)、水痘后血管病变(n = 20)、夹层动脉瘤(n = 8)、心源性栓塞(n = 8)和隐源性卒中(n = 10)的患者。我们回顾性分析病历以确定发病方式,并将发病分为急性(症状在30分钟内达到最大严重程度)或非急性(包括症状进展、间歇性发作或复发过程)。我们使用多变量逻辑回归模型比较已知脑动脉病变患者与非动脉病变性卒中患者的发病方式。
动脉病变组和非动脉病变组在年龄、性别、梗死部位、癫痫发作和头痛方面无显著差异。大多数非动脉病变性AIS儿童起病急性(72%),而动脉病变性卒中儿童为32%。在校正可能的混杂因素后,非急性起病时,动脉病变病因的几率为6.1(95%CI,1.6至22.8;P = 0.007)。
发病方式可预测儿童AIS的病因诊断,并可能指导辅助检查的优先级和治疗选择。症状非急性起病与动脉病变性卒中相关,尤其是与推测的炎症性动脉病变有关。