Department of Paediatric Neurology, University Hospital Southampton National Health Service Foundation Trust, United Kingdom (J.S.).
Neurosciences and Mental Health Program, Hospital for Sick Children Research Institute, Toronto, Canada (M.S., N.D., S.P., S.M., T.D.).
Stroke. 2024 Nov;55(11):2622-2631. doi: 10.1161/STROKEAHA.124.046518. Epub 2024 Oct 28.
The impact of age-at-stroke on outcome following pediatric arterial ischemic stroke remains controversial. We studied the interaction of age-at-stroke and infarct location and extent with long-term neurological outcomes.
We conducted a longitudinal prospective outcome study of children with acute pediatric arterial ischemic stroke diagnosed from 1996 to 2016 at the Hospital for Sick Children, Toronto, Canada. Pediatric Stroke Outcome Measure scores were dichotomized as normal or abnormal (ie, mild, moderate, or severe). Outcomes were analyzed by age-at-stroke (newborn: birth to 28 days; early childhood: 29 days to 5 years; middle/late childhood: >5-18 years), and infarct location, based on each of the following: model 1: circulation (anterior/posterior); model 2: cortical versus subcortical involvement; and model 3: specific arterial territory, including infarct extent (small [<50% arterial territory] or large [≥50%]). Univariable and multivariable logistic regression models were fitted.
Among 285 children, the outcome at median 6.1 years was 43.5% abnormal. Controlling for infarct location, increasing age-at-stroke was associated with increasing abnormal outcome. Model 1 demonstrated that, compared with neonates, abnormal outcomes were increased in early childhood (adjusted odds ratio [aOR], 2.91 [95% CI, 1.24-7.05]) and more so in middle/late childhood (aOR, 4.46 [95% CI, 1.71-12.13]). Outcomes were worse for combined locations, including anterior+posterior (model 1: aOR, 15.4 [95% CI, 4.49-64.63]) and cortical+subcortical (model 2: aOR, 10.7 [95% CI, 3.88-32.74]). Abnormal outcomes were also increased for anterior circulation (model 1: aOR, 14.91 [95% CI, 5.29-54.21]) and subcortical locations (model 2: aOR, 4.36 [95% CI, 1.37-14.95]). Among individual arterial territories, outcomes were best for superior division middle cerebral artery (100% normal) and worst for lateral lenticulostriate artery infarcts (47.4% abnormal; model 3: aOR, 14.2 [95% CI, 3.5-67.6]).
Among survivors of pediatric stroke, abnormal long-term neurological outcome is increased with increasing age-at-stroke, supporting enhanced plasticity after focal injury to the newborn brain compared with older pediatric ages.
年龄对儿童动脉缺血性脑卒中(pediaric arterial ischemic stroke,pAIS)后结局的影响仍存在争议。我们研究了年龄与梗死部位和范围与长期神经结局之间的相互作用。
我们对 1996 年至 2016 年在加拿大安大略省多伦多 SickKids 医院诊断为急性儿童动脉缺血性脑卒中的患儿进行了一项前瞻性纵向结局研究。采用儿科脑卒中结局测量(Pediatric Stroke Outcome Measure,PSOM)评分将结局分为正常或异常(即轻度、中度或重度)。根据以下模型 1:循环(前/后);模型 2:皮质与皮质下受累;和模型 3:特定动脉区域,包括梗死范围(小[<50%动脉区域]或大[≥50%]),对年龄(新生儿:出生至 28 天;早期儿童:29 天至 5 岁;中/晚期儿童:>5-18 岁)和梗死部位进行分析。使用单变量和多变量逻辑回归模型进行拟合。
在 285 名患儿中,中位随访 6.1 年时的结局为 43.5%异常。控制梗死部位后,年龄越大,异常结局的发生风险越高。模型 1 显示,与新生儿相比,早期儿童的异常结局风险增加(调整优势比[aOR],2.91[95%置信区间,1.24-7.05]),中/晚期儿童的异常结局风险更高(aOR,4.46[95%置信区间,1.71-12.13])。联合部位的结局更差,包括前+后(模型 1:aOR,15.4[95%置信区间,4.49-64.63])和皮质+皮质下(模型 2:aOR,10.7[95%置信区间,3.88-32.74])。前循环(模型 1:aOR,14.91[95%置信区间,5.29-54.21])和皮质下部位(模型 2:aOR,4.36[95%置信区间,1.37-14.95])的异常结局风险也增加。在各个动脉区域中,大脑中动脉优势分支部(superior division middle cerebral artery)的结局最好(100%正常),外侧纹状体动脉梗死(lateral lenticulostriate artery infarcts)的结局最差(47.4%异常;模型 3:aOR,14.2[95%置信区间,3.5-67.6])。
在儿童脑卒中幸存者中,随着年龄的增长,长期神经结局异常的风险增加,支持新生儿大脑局灶性损伤后的神经可塑性增强,与较大儿童相比。