Department of Neurosurgery, Great Ormond Street Hospital, London, UK.
Developmental Neuroscience, Institute of Child Health, University College London, London, UK.
Dev Med Child Neurol. 2024 Feb;66(2):216-225. doi: 10.1111/dmcn.15727. Epub 2023 Aug 9.
To evaluate a lesion detection algorithm designed to detect focal cortical dysplasia (FCD) in children undergoing stereoelectroencephalography (SEEG) as part of their presurgical evaluation for drug-resistant epilepsy.
This was a prospective, single-arm, interventional study (Idea, Development, Exploration, Assessment, and Long-Term Follow-Up phase 1/2a). After routine SEEG planning, structural magnetic resonance imaging sequences were run through an FCD lesion detection algorithm to identify putative clusters. If the top three clusters were not already sampled, up to three additional SEEG electrodes were added. The primary outcome measure was the proportion of patients who had additional electrode contacts in the SEEG-defined seizure-onset zone (SOZ).
Twenty patients (median age 12 years, range 4-18 years) were enrolled, one of whom did not undergo SEEG. Additional electrode contacts were part of the SOZ in 1 out of 19 patients while 3 out of 19 patients had clusters that were part of the SOZ but they were already implanted. A total of 16 additional electrodes were implanted in nine patients and there were no adverse events from the additional electrodes.
We demonstrate early-stage prospective clinical validation of a machine learning lesion detection algorithm used to aid the identification of the SOZ in children undergoing SEEG. We share key lessons learnt from this evaluation and emphasize the importance of robust prospective evaluation before routine clinical adoption of such algorithms.
The focal cortical dysplasia detection algorithm collocated with the seizure-onset zone (SOZ) in 4 out of 19 patients. The algorithm changed the resection boundaries in 1 of 19 patients undergoing stereoelectroencephalography for drug-resistant epilepsy. The patient with an altered resection due to the algorithm was seizure-free 1 year after resective surgery. Overall, the algorithm did not increase the proportion of patients in whom SOZ was identified.
评估一种旨在检测儿童立体脑电图(SEEG)中局灶性皮质发育不良(FCD)的病灶检测算法,该算法是他们进行耐药性癫痫手术评估的一部分。
这是一项前瞻性、单臂、干预性研究(Idea、Development、Exploration、Assessment 和 Long-Term Follow-Up 阶段 1/2a)。在常规 SEEG 规划后,结构磁共振成像序列通过 FCD 病灶检测算法运行,以识别可能的簇。如果前三个簇未被采样,则最多添加三个额外的 SEEG 电极。主要的观察指标是在 SEEG 定义的发作起始区(SOZ)中添加额外电极接触的患者比例。
20 名患者(中位年龄 12 岁,范围 4-18 岁)入组,其中 1 名患者未进行 SEEG。在 19 名患者中,有 1 名患者的额外电极接触是 SOZ 的一部分,而 19 名患者中有 3 名患者的簇是 SOZ 的一部分,但已经植入。共有 9 名患者植入了 16 个额外电极,且无来自额外电极的不良事件。
我们展示了一种机器学习病灶检测算法的早期前瞻性临床验证,该算法用于辅助识别接受 SEEG 的儿童的 SOZ。我们分享了从该评估中获得的关键经验教训,并强调在常规临床采用此类算法之前进行强有力的前瞻性评估的重要性。
在 19 名接受耐药性癫痫立体脑电图检查的患者中,病灶检测算法与发作起始区(SOZ)共定位了 4 例。该算法改变了 19 名接受立体脑电图检查的患者中的 1 名患者的切除术边界。由于算法改变了切除术边界,该患者在手术后 1 年内无癫痫发作。总体而言,该算法并未增加识别 SOZ 的患者比例。