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儿童结核性脑膜炎中阵发性交感神经亢进:一种新的关联。

Paroxysmal Sympathetic Hyperactivity in Childhood Tuberculous Meningitis: A New Association.

机构信息

Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.

Department of Radiology, Jay Prakash Narayan Apex Trauma Centre, All India Institute of Medical Sciences, New Delhi, India.

出版信息

J Child Neurol. 2024 Oct;39(11-12):403-408. doi: 10.1177/08830738241276234. Epub 2024 Sep 12.

Abstract

BACKGROUND

We sought to estimate the prevalence and clinical characteristics of paroxysmal sympathetic hyperactivity (PSH) in childhood tuberculous meningitis.

METHODS

Hospital records of children (6 months to 14 years) with tuberculous meningitis were retrospectively analyzed from September 2019 through January 2022. In September 2019, the first case of paroxysmal sympathetic hyperactivity in tuberculous meningitis was identified in our division. Since then, all admitted children with tuberculous meningitis have been screened for paroxysmal sympathetic hyperactivity using the Paroxysmal Sympathetic Hyperactivity Assessment Measure (PSH-AM). Paroxysmal sympathetic hyperactivity is suspected when any of the following are present: recurrence of fever after initial defervescence, episodic posturing, dystonia, or unexplained tachycardia. Outcome at 3 months was prospectively scored according to the Pediatric Cerebral Performance Category score.

RESULTS

Forty-one hospital records of children with tuberculous meningitis were analyzed, and 6 of them had paroxysmal sympathetic hyperactivity (probable paroxysmal sympathetic hyperactivity, 5/6; possible paroxysmal sympathetic hyperactivity, 1/6). Paroxysmal sympathetic hyperactivity appeared after a mean duration of 17 weeks (range: 12-25 weeks) from the diagnosis of tuberculous meningitis in 4 of 6 children and at 4 weeks in 2 of 6 children. Children with tuberculous meningitis who developed paroxysmal sympathetic hyperactivity were younger (median age: 5 years) compared with the nonparoxysmal sympathetic hyperactivity tuberculous meningitis cohort (median age: 10 years). A high proportion of children who developed paroxysmal sympathetic hyperactivity had hydrocephalus at presentation (5 of 6 [83.3%] vs 12 of 35 [34.3%],  = .035). Hospital stay was significantly prolonged in children with probable paroxysmal sympathetic hyperactivity (mean: 71.2 ± 26.8 days) compared with tuberculous meningitis without paroxysmal sympathetic hyperactivity (mean: 20.8 ± 11.6 days;  < .0001).

CONCLUSION

Paroxysmal sympathetic hyperactivity is a late complication of tuberculous meningitis observed in 14.6% cases and should be anticipated in children with reappearance of fever or neurologic worsening without any apparent cause.

摘要

背景

我们旨在评估儿童结核性脑膜炎中阵发性交感神经亢进症(PSH)的患病率和临床特征。

方法

我们回顾性分析了 2019 年 9 月至 2022 年 1 月期间我院收治的(6 个月至 14 岁)儿童结核性脑膜炎的住院病历。2019 年 9 月,我院首例结核性脑膜炎并发阵发性交感神经亢进症的病例被发现。此后,所有入院的结核性脑膜炎患儿均采用阵发性交感神经亢进评估量表(PSH-AM)筛查阵发性交感神经亢进症。当出现以下任何一种情况时,应怀疑发生阵发性交感神经亢进症:初始退热后再次发热、间歇性姿势异常、肌张力障碍或不明原因的心动过速。3 个月时的预后采用小儿脑功能分级(Pediatric Cerebral Performance Category score)进行前瞻性评分。

结果

分析了 41 例结核性脑膜炎患儿的住院病历,其中 6 例存在阵发性交感神经亢进症(可能的阵发性交感神经亢进症 5/6 例;可疑阵发性交感神经亢进症 1/6 例)。6 例患儿中,有 4 例在结核性脑膜炎确诊后 17 周(12-25 周)出现阵发性交感神经亢进,2 例在 4 周时出现。与无阵发性交感神经亢进的结核性脑膜炎患儿相比,发生阵发性交感神经亢进症的结核性脑膜炎患儿年龄更小(中位数:5 岁 vs 10 岁)。出现阵发性交感神经亢进症的患儿中,有较高比例在发病时存在脑积水(5/6[83.3%] vs 12/35[34.3%], = .035)。与无阵发性交感神经亢进的结核性脑膜炎患儿相比,可能的阵发性交感神经亢进症患儿的住院时间明显延长(平均:71.2 ± 26.8 天 vs 20.8 ± 11.6 天; < .0001)。

结论

阵发性交感神经亢进症是结核性脑膜炎的一种晚期并发症,约 14.6%的病例会出现这种并发症,应警惕发热再次出现或无明显原因的神经系统恶化的患儿。

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