Department of Clinical Neurosciences, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Department of Functional Neurology and Epileptology, Hospices Civils de Lyon, Lyon 1 University Lyon Neuroscience Research Center, Institut National de la Santé et de la Recherche Médicale U1028/CNRS UMR 5292 Epilepsy Institute, Lyon, France.
Lancet Neurol. 2021 Dec;20(12):1038-1047. doi: 10.1016/S1474-4422(21)00300-8. Epub 2021 Oct 25.
Three neuromodulation therapies have been appropriately tested and approved in refractory focal epilepsies: vagus nerve stimulation (VNS), deep brain stimulation of the anterior nucleus of the thalamus (ANT-DBS), and closed-loop responsive neurostimulation of the epileptogenic zone or zones. These therapies are primarily palliative. Only a few individuals have achieved complete freedom from seizures for more than 12 months with these therapies, whereas more than half have benefited from long-term reduction in seizure frequency of more than 50%. Implantation-related adverse events primarily include infection and pain at the implant site. Intracranial haemorrhage is a frequent adverse event for ANT-DBS and responsive neurostimulation. Other stimulation-specific side-effects are observed with VNS and ANT-DBS. Biomarkers to predict response to neuromodulation therapies are not available, and high-level evidence to aid decision making about when and for whom these therapies should be preferred over other antiepileptic treatments is scant. Future studies are thus needed to address these shortfalls in knowledge, approve other forms of neuromodulation, and develop personalised closed-loop therapies with embedded machine learning. Until then, neuromodulation could be considered for individuals with intractable seizures, ideally after the possibility of curative surgical treatment has been carefully assessed and ruled out or judged less appropriate.
迷走神经刺激(VNS)、丘脑前核深部脑刺激(ANT-DBS)和致痫区或致痫区的闭环反应性神经刺激。这些疗法主要是姑息性的。只有少数人通过这些疗法实现了超过 12 个月的无癫痫发作完全自由,而超过一半的人受益于癫痫发作频率降低 50%以上。与植入相关的不良事件主要包括感染和植入部位疼痛。对于 ANT-DBS 和反应性神经刺激,颅内出血是一种常见的不良事件。VNS 和 ANT-DBS 还观察到其他刺激特异性副作用。目前尚无可预测神经调节治疗反应的生物标志物,也缺乏高级别的证据来帮助决策何时以及为何应优先选择这些疗法而不是其他抗癫痫治疗。因此,需要开展未来的研究来解决这些知识上的不足,批准其他形式的神经调节,并开发具有嵌入式机器学习的个性化闭环治疗。在此之前,可以考虑对难治性癫痫患者使用神经调节疗法,理想情况下,在仔细评估和排除治愈性手术治疗的可能性或认为不太合适之后。