Liakina Tatjana, Bartley Andreas, Carstam Louise, Rydenhag Bertil, Nilsson Daniel
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Clinical Neurophysiology, Sahlgrenska University Hospital, Member of the ERN EpiCARE, Gothenburg, Sweden.
Acta Neurochir (Wien). 2025 Mar 17;167(1):75. doi: 10.1007/s00701-025-06489-5.
PURPOSE: Stereoelectroencephalography (SEEG) is the standard for invasive investigations in epilepsy surgery. Our aim was to investigate if similar precision and low complication rate can be achieved with optimized frameless navigation as with frame-based or dedicated stereotactic SEEG robot. METHODS: We compared five different implantation techniques assessing entry, target errors and complications in 53 SEEGs from 50 patients: Group 1 - surface registration and Vertek probe, Group 2 - rigid registration with conventional CT and Vertek probe, Group 3 - rigid registration and Vertek probe, Group 4 - rigid registration and Autoguide, Group 5 - rigid, sterile registration and Autoguide. Analysis was done using random effects linear modelling to calculate improvement in percent using Group 1 as a reference, p < 0.001 was considered significant. RESULTS: Mean patient age at implantation was 23 years (range 4-46 years) and mean number of implanted electrodes per patient were 11 (range 3-15). Accuracy data was available for 36 SEEG implantations (419 electrodes). The median entry/target errors were (mm): Group 1:4.6/4.3; Group 2:1.8/2.3; Group 3:0.9/1.5; Group 4:1.1/1.2; Group 5:0/0.7. Improvement of accuracy for entry error was 38% for Group 2 (p = 0.004), 47% for Group 3 (p < 0.001), 50% for Group 4 (p < 0.001), and 72% for Group 5 (p < 0.001). Improvement of accuracy for target error was 17% for Group 2 (p = 0.17), 22% for Group 3 (p < 0.001), 35% for Group 4 (p < 0.001), and 51% for Group 5 (p < 0.001). Complications (hemorrhage, edema, headache) occurred in 7/53 SEEGs, none of these led to permanent deficit. 40/53 investigations resulted in an epilepsy surgery procedure. CONCLUSION: High precision and low complication rate in SEEG implantation can be achieved with frameless navigation using rigid, sterile registration.
目的:立体定向脑电图(SEEG)是癫痫手术侵入性检查的标准。我们的目的是研究优化的无框架导航是否能像基于框架或专用立体定向SEEG机器人那样实现相似的精度和低并发症发生率。 方法:我们比较了五种不同的植入技术,评估了50例患者53次SEEG中的入路、靶点误差和并发症:第1组 - 表面配准和Vertek探头;第2组 - 使用传统CT进行刚性配准和Vertek探头;第3组 - 刚性配准和Vertek探头;第4组 - 刚性配准和自动导向仪;第5组 - 刚性、无菌配准和自动导向仪。使用随机效应线性模型进行分析,以第1组作为参考计算百分比改善情况,p < 0.001被认为具有统计学意义。 结果:植入时患者的平均年龄为23岁(范围4 - 46岁),每位患者植入电极的平均数量为11根(范围3 - 15根)。有36次SEEG植入(419根电极)的准确性数据可用。入路/靶点误差的中位数(毫米)为:第1组:4.6/4.3;第2组:1.8/2.3;第3组:0.9/1.5;第4组:1.1/1.2;第5组:0/0.7。第2组入路误差的准确性提高了38%(p = 0.004),第3组提高了47%(p < 0.001),第4组提高了50%(p < 0.001),第5组提高了72%(p < 0.001)。第2组靶点误差的准确性提高了17%(p = 0.17),第3组提高了22%(p < 0.001),第4组提高了35%(p < 0.001),第5组提高了51%(p < 0.001)。53次SEEG中有7次出现并发症(出血、水肿、头痛),这些均未导致永久性神经功能缺损。53次检查中有40次进行了癫痫手术。 结论:使用刚性、无菌配准的无框架导航可在SEEG植入中实现高精度和低并发症发生率。
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