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耐药性早发性癫痫患儿癫痫手术转诊及评估的潜在延迟

Potential delays in referral and assessment for epilepsy surgery in children with drug-resistant, early-onset epilepsy.

作者信息

Prideaux Laura, Barton Sarah, Maixner Wirginia, Harvey A Simon

机构信息

Department of Paediatrics, The University of Melbourne, Parkville, VIC 3052, Australia.

Neurosciences, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia; Department of Neurology, The Royal Children's Hospital, Parkville, VIC 3052, Australia.

出版信息

Epilepsy Res. 2018 Jul;143:20-26. doi: 10.1016/j.eplepsyres.2018.04.001. Epub 2018 Apr 3.

Abstract

OBJECTIVE

To study potential delays in epilepsy surgery in children with drug-resistant epilepsy (DRE) of early-onset.

METHODS

Medical records were reviewed from 87 children with DRE and seizure onset before age 3 years who underwent epilepsy surgery between 2006 and 2015. Information was obtained about each child's epilepsy, treatment and specific time points in management. Time intervals along diagnostic, investigative, treatment and referral pathways were calculated.

RESULTS

Median ages at seizure onset, when seen in the epilepsy surgery program and surgery were 5.9 (IQR 10), 19 (IQR 29) and 36 (IQR 67) months; the median delay from seizure onset to surgery was 30 (IQR 67) months. Most children were promptly diagnosed, treated, investigated and seen by a pediatric neurologist. Focal abnormalities were reported on initial EEGs and MRIs in most children, and DRE developed within a median of 6.3 months from commencement of medication. There were median durations of 6.2 months between seeing a neurologist and being seen in the epilepsy surgery program, and then 6.1 months in determining surgical candidacy. Median durations from potential indications for a surgical evaluation to agreed surgical candidacy were 10 (DRE), 12 (focal MRI) and 17 (focal EEG) months. Children received a median of six antiepileptic drugs prior to surgery. Median interval from agreed surgical candidacy to surgery was only 3 months. There were longer durations from seizure onset to surgery in children needing PET (p = 0.001) and in children with seizure-free periods (p < 0.001), and shorter durations in children with a history of infantile spasms (p = 0.01).

SIGNIFICANCE

Delays in referral of children for epilepsy surgery are reported. Delays in assessment may be specific to centralized children's hospitals in public health systems.

摘要

目的

研究早发性耐药性癫痫(DRE)患儿癫痫手术可能存在的延迟情况。

方法

回顾了2006年至2015年间接受癫痫手术的87例DRE且癫痫发作始于3岁前的患儿的病历。获取了每个患儿的癫痫、治疗及管理中的特定时间点的信息。计算了诊断、检查、治疗及转诊路径中的时间间隔。

结果

癫痫发作、进入癫痫手术项目及手术时的中位年龄分别为5.9(四分位间距10)、19(四分位间距29)和36(四分位间距67)个月;从癫痫发作到手术的中位延迟时间为30(四分位间距67)个月。大多数患儿得到了及时诊断、治疗、检查,并由儿科神经科医生诊治。大多数患儿初次脑电图和磁共振成像(MRI)检查报告有局灶性异常,且从开始用药起,中位6.3个月发展为DRE。从看神经科医生到进入癫痫手术项目的中位时间为6.2个月,然后确定手术候选资格的时间为6.1个月。从手术评估的潜在指征到确定手术候选资格的中位时间分别为10(DRE)、12(局灶性MRI)和17(局灶性脑电图)个月。患儿术前接受抗癫痫药物的中位数量为六种。从确定手术候选资格到手术的中位间隔仅为3个月。需要正电子发射断层扫描(PET)的患儿及有癫痫发作间期的患儿从癫痫发作到手术的时间更长(p = 0.001),有婴儿痉挛病史的患儿时间更短(p = 0.01)。

意义

报告了儿童癫痫手术转诊的延迟情况。评估延迟可能是公共卫生系统中集中式儿童医院所特有的。

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