机器人辅助岛叶立体脑电图在小儿耐药性癫痫中的应用:准确性和诊断价值。

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-11-01 Epub Date: 2024-09-05 DOI:10.1007/s00381-024-06571-w
A González-Crespo, F Brugada-Bellsolà, S Candela-Cantó, J Aparicio Calvo, J Rumià Arboix, J Hinojosa Bernal
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引用次数: 0

摘要

背景:众所周知,岛叶性癫痫是导致儿童耐药性癫痫(DRE)的原因之一。如果不在术前排除它,可能会导致癫痫手术治疗失败。非侵入性方法通常只能提供有关其存在的有限信息,在绝大多数情况下,侵入性方法是诊断这种疾病的必要手段。使用最多的是立体脑电图(SEEG)。我们报告了一系列接受岛叶 SEEG 检查以排除岛叶癫痫的 DRE 儿科患者:我们对 2016 年 4 月至 2022 年 9 月间接受 SEEG(包括岛叶电极)手术的儿科 DRE 患者进行了回顾性回顾。我们描述了使用的不同轨迹(正交或斜交)和手术技术。植入后,我们使用三种方法评估电极的精确度:入口点位置误差(EPLE)、目标点位置误差(TPLE)和目标偏差(TD)。我们还报告了该技术发生的并发症以及提供的诊断信息:共有 32 名 DRE 患者接受了 SEEG(包括岛叶电极)手术。共植入 401 个电极,其中 148 个(39.91%)指向岛叶。其中 112 个电极轨迹为正交,36 个为斜交。平均 EPLE 为 1.45 毫米,TPLE 为 1.88 毫米,TD 为 0.71 毫米。三名患者出现额部血肿,其中两人在术后核磁共振成像中确诊,一人需要手术,但没有后遗症。一名患者患有脑膜炎,经抗生素治疗后无永久性后遗症。9名患者(28.13%)的致痫区包括岛叶:结论:当非侵入性检测结果几乎没有可疑之处时,必须排除DRE患者的岛叶癫痫。这一点在儿童群体中尤为重要,因为儿童癫痫发作的半定性更为困难,癫痫控制失败会对神经认知发育和学术研究造成破坏性后果。鉴于其相关并发症发生率相对较低且具有潜在益处,我们应考虑扩大岛叶 SEEG 监测的纳入标准。
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Robot-assisted insular stereoelectroencephalography in pediatric drug-resistant epilepsy: accuracy and diagnostic value.

Background: Insular epilepsy is a well-known cause of drug-resistant epilepsy (DRE) in the pediatric population. It can be a source of surgical epilepsy treatment failures when not ruled out pre-operatively. Non-invasive methods often provide limited information about its existence, being the invasive methods necessary to diagnose it in the vast majority of cases. The most used is stereoelectroencephalography (SEEG). We report a series of DRE pediatric patients in which insular SEEG was performed to rule out insular epilepsy.

Method: We performed a retrospective review of pediatric DRE patients operated on SEEG including insular electrodes between April 2016 and September 2022. We described the different trajectories used (orthogonal or oblique) and surgical techniques. After implantation, we assessed electrodes' precision using three measures: entry point location error (EPLE), target point location error (TPLE), and target deviation (TD). We also reported complications that occurred with this technique as well as the diagnostic information provided.

Results: Overall, 32 DRE patients were operated on SEEG including insular electrodes. Four hundred one electrodes were implanted, 148 (39.91%) of whom were directed to the insula. One hundred twelve followed an orthogonal trajectory, and 36 were oblique. The mean EPLE was 1.45 mm, TPLE was 1.88 mm and TD was 0.71 mm. Three patients suffered from frontal hematoma, two of them diagnosed on post-operative MRI and one who required surgery, with no sequelae. One patient suffered from meningitis treated with antibiotics with no permanent sequelae. Nine patients (28.13%) had the insula included in the epileptogenic zone.

Conclusions: Insular epilepsy has to be ruled out in DRE patients when little suspicion is obtained after non-invasive testing. This is especially important in the pediatric population, in which seizure semiology is more difficult to characterize and failures to control epilepsy have devastating consequences in neurocognitive development and scholarship. Given its relative low rate of relevant complications and potential benefits, we should consider widening the inclusion criteria for insular SEEG monitoring.

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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
期刊最新文献
Correction: Imaging features of pediatric meningiomas: emphasis on unusual locations. Correction: Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Radiographic severity is associated with worse executive function in metopic craniosynostosis. Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Vaulting further: cranial vault expansion for craniocerebral disproportion without primary craniosynostosis.
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