The Spectrum of Intracranial Arteriopathies and Ischemic Strokes in Pediatric Tubercular Meningitis: A Tricentric Study From Eastern India

IF 3.2 3区 医学 Q2 CLINICAL NEUROLOGY
Dr. Suman Das MBBS, MD (Pediatric Medicine), DM (Neurology) (Assistant Professor) , Dr. Biman Kanti Ray MBBS, MD (Medicine), DM (Neurology) (Professor) , Dr. Madhumita Nandi MBBS, MD (Pediatric Medicine) (Professor) , Dr. Gobinda Mondal MBBS, MD (Pediatric Medicine) (Associate Professor) , Dr. Dilip Kumar Paul MBBS, MD (Pediatric Medicine) (Professor)
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引用次数: 0

Abstract

Introduction

Addressing the need to uniformly classify arteriopathies among patients with arterial ischemic stroke (AIS) due to tubercular meningitis (TBM), we used the Childhood AIS Standardised Classification and Diagnostic Evaluation (CASCADE) criteria.

Methods

This tri-centric prospective study included children aged 0.5-12 years with TBM and AIS. Magnetic resonance angiographies (MRAs) were done during admission and repeated 3 and 12 months after discharge. Arteriopathies were classified according to the primary CASCADE criteria. We used the modified Pediatric Alberta Stroke Programme Early Computed Tomography Score as an ordinal measure of infarct volume. The severity of arteriopathies was graded using the focal cerebral arteriopathy severity score (FCASS). The final outcomes were measured at the 12-month follow-up visit using the Pediatric Stroke Outcome Measure (PSOM).

Results

Out of 55 patients, 64% had MRA-evidenced arteriopathies and 84% had multiple infarcts. The middle cerebral (46%) and internal carotid arteries (22%) were most commonly affected. The basal ganglia (70%) and the cerebral cortex (61%) were most commonly infarcted. CASCADE categories included 3b (40%), 1d (38%), 2b (16%), 2c (5%), progressive (32%), and stable (44%) arteriopathies. Younger age, hypertrophic pachymeningitis, cortical infarcts, recurrent strokes, progressive arteriopathies, EEG abnormalities, and mortality were significantly higher among patients with MRA-proven arteriopathies. Patients with progressive arteriopathies had a significantly higher prevalence of hypertrophic pachymeningitis, cortical infarcts, and recurrent strokes. FCASS correlated positively with outcomes measured by the Pediatric Stroke Outcome Measure and modified Pediatric Alberta Stroke Programme Early Computed Tomography Score.

Conclusion

The CASCADE classification clarified the arteriopathy patterns, enabling us to correlate them with the characteristics of the infarcts. FCASS is useful to grade the arteriopathy severity and progression in TBM.

小儿结核性脑膜炎的颅内动脉病变和缺血性脑卒中谱系--来自印度东部的一项三中心研究。
简介:为了对结核性脑膜炎(TBM)导致的动脉缺血性卒中(AIS)患者的动脉疾病进行统一分类,我们采用了儿童 AIS 标准化分类和诊断评估(CASCADE)标准。入院时进行磁共振血管造影(MRA),出院后 3 个月和 12 个月复查。动脉病变根据 CASCADE 初级标准进行分类。我们使用改良的阿尔伯塔省儿科卒中项目早期计算机断层扫描评分作为梗死体积的序数测量方法。动脉病变的严重程度采用局灶性脑动脉病变严重程度评分(FCASS)进行分级。结果55名患者中,64%有MRA显示的动脉病变,84%有多发性梗死。大脑中动脉(46%)和颈内动脉(22%)最常受到影响。基底节(70%)和大脑皮层(61%)最常发生梗死。CASCADE类别包括3b(40%)、1d(38%)、2b(16%)、2c(5%)、进行性(32%)和稳定型(44%)动脉病变。在经 MRA 证实的动脉病变患者中,年龄较小、肥厚性桥脑膜炎、皮质梗死、复发性中风、进展性动脉病变、脑电图异常和死亡率明显较高。进行性动脉病变患者中,肥厚性脑积水、皮质梗死和复发性脑卒中的发病率明显更高。FCASS与小儿卒中预后测量(Pediatric Stroke Outcome Measure)和改良的小儿阿尔伯塔卒中计划早期计算机断层扫描评分(Pediatric Alberta Stroke Programme Early Computed Tomography Score)的结果呈正相关。FCASS有助于对TBM的动脉病变严重程度和进展情况进行分级。
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来源期刊
Pediatric neurology
Pediatric neurology 医学-临床神经学
CiteScore
4.80
自引率
2.60%
发文量
176
审稿时长
78 days
期刊介绍: Pediatric Neurology publishes timely peer-reviewed clinical and research articles covering all aspects of the developing nervous system. Pediatric Neurology features up-to-the-minute publication of the latest advances in the diagnosis, management, and treatment of pediatric neurologic disorders. The journal''s editor, E. Steve Roach, in conjunction with the team of Associate Editors, heads an internationally recognized editorial board, ensuring the most authoritative and extensive coverage of the field. Among the topics covered are: epilepsy, mitochondrial diseases, congenital malformations, chromosomopathies, peripheral neuropathies, perinatal and childhood stroke, cerebral palsy, as well as other diseases affecting the developing nervous system.
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