Thompson Eric M, Wozniak Susan E, Roberts Colin M, Kao Amy, Anderson Valerie C, Selden Nathan R
Department of Neurological Surgery, Oregon Health & Science University, Portland, OR 97239, USA.
J Neurosurg Pediatr. 2012 Sep;10(3):200-5. doi: 10.3171/2012.5.PEDS11489. Epub 2012 Jul 6.
Vagus nerve stimulation (VNS) is approved by the FDA for the treatment of partial epilepsy in patients older than 12 years. Authors of the current study performed a large retrospective analysis and comparison of VNS outcomes in children with an age ≥ and < 12 years, including those with partial and generalized epilepsy.
A retrospective review of the records of pediatric patients (age < 18 years) who had undergone primary VNS system implantation between 2001 and 2010 by a single pediatric neurosurgeon was undertaken. Considered data included demographics, epilepsy type (partial vs generalized), seizure frequency, seizure duration, postictal period duration, and antiepileptic medication use.
One hundred forty-six patients (49% female) were followed up for a mean of 41 months after VNS implantation. Thirty-two percent of patients had partial epilepsy and 68% had generalized epilepsy. After VNS system implantation, seizure frequency was reduced in 91% of patients, seizure duration in 50%, postictal period in 49%, and antiepileptic medication use in 75%. There was no significant difference in age, sex, or duration of follow-up according to epilepsy type. Neither was there any significant difference in seizure frequency reduction, seizure duration, postictal period, medication use, overall clinical improvement, or improvement in quality of life based on an age ≥ or < 12 years or epilepsy type.
Vagus nerve stimulation reduced both seizure frequency and antiepileptic medication use in the majority of pediatric patients regardless of sex, age cohort, or epilepsy type. Vagus nerve stimulation also reduced seizure duration and postictal period in approximately half of the pediatric patients. Contrary to expectation, children with partial epilepsy do not benefit from VNS at higher rates than those with generalized epilepsy.
迷走神经刺激术(VNS)已获美国食品药品监督管理局(FDA)批准,用于治疗12岁以上患者的部分性癫痫。本研究的作者对年龄≥和<12岁的儿童患者进行了大规模回顾性分析和VNS治疗效果比较,包括部分性癫痫和全身性癫痫患者。
对2001年至2010年间由一名儿科神经外科医生进行原发性VNS系统植入的儿科患者(年龄<18岁)的记录进行回顾性研究。纳入的数据包括人口统计学资料、癫痫类型(部分性与全身性)、癫痫发作频率、发作持续时间、发作后时期持续时间以及抗癫痫药物使用情况。
146例患者(49%为女性)在VNS植入后平均随访41个月。32%的患者患有部分性癫痫,68%患有全身性癫痫。VNS系统植入后,91%的患者癫痫发作频率降低,50%的患者发作持续时间缩短,49%的患者发作后时期缩短,75%的患者抗癫痫药物使用减少。根据癫痫类型,在年龄、性别或随访时间方面无显著差异。基于年龄≥或<12岁或癫痫类型,在癫痫发作频率降低、发作持续时间、发作后时期、药物使用、总体临床改善或生活质量改善方面也无显著差异。
无论性别、年龄组或癫痫类型如何,迷走神经刺激术在大多数儿科患者中均降低了癫痫发作频率和抗癫痫药物的使用。迷走神经刺激术还使约一半的儿科患者发作持续时间和发作后时期缩短。与预期相反,部分性癫痫患儿从VNS中获益的比例并不高于全身性癫痫患儿。