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Neuromodulation: Technology at the Neural Interface最新文献

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Maximal Analgesic Effect Attained by the Use of Objective Neurophysiological Measurements With Closed-Loop Spinal Cord Stimulation. 利用客观神经生理学测量闭环脊髓刺激达到最大镇痛效果
Pub Date : 2024-09-09 DOI: 10.1016/j.neurom.2024.07.003
Robert M Levy,Nagy A Mekhail,Leonardo Kapural,Christopher A Gilmore,Erika A Petersen,Johnathan H Goree,Jason E Pope,Shrif J Costandi,Jan Willem Kallewaard,Simon Thomson,Christopher Gilligan,Tariq AlFarra,Mustafa Y Broachwala,Harman Chopra,Corey W Hunter,Steven M Rosen,Kasra Amirdelfan,Steven M Falowski,Sean Li,James Scowcroft,Shivanand P Lad,Dawood Sayed,Ajay Antony,Timothy R Deer,Salim M Hayek,Maged N Guirguis,Ronald B Boeding,Aaron K Calodney,Brian Bruel,Patrick Buchanan,Nicole Soliday,Rui V Duarte,Angela Leitner,Peter S Staats
OBJECTIVESSpinal cord stimulation (SCS) has been challenged by the lack of neurophysiologic data to guide therapy optimization. Current SCS programming by trial-and-error results in suboptimal and variable therapeutic effects. A novel system with a physiologic closed-loop feedback mechanism using evoked-compound action potentials enables the optimization of physiologic neural dose by consistently and accurately activating spinal cord fibers. We aimed to identify neurophysiologic dose metrics and their ranges that resulted in clinically meaningful treatment responses.MATERIALS AND METHODSSubjects from 3 clinical studies (n = 180) with baseline back and leg pain ≥60 mm visual analog scale and physical function in the severe to crippled category were included. Maximal analgesic effect (MAE) was operationally defined as the greatest percent reduction in pain intensity or as the greatest cumulative responder score (minimal clinically important differences [MCIDs]) obtained within the first 3 months of SCS implant. The physiologic metrics that produced the MAE were analyzed.RESULTSWe showed that a neural dose regimen with a high neural dose accuracy of 2.8μV and dose ratio of 1.4 resulted in a profound clinical benefit to chronic pain patients (MAE of 79 ± 1% for pain reduction and 12.5 ± 0.4 MCIDs). No differences were observed for MAE or neurophysiological dose metrics between the trial phase and post-implant MAE visit.CONCLUSIONFor the first time, an evidence-based neural dose regimen is available for a neurostimulation intervention as a starting point to enable optimization of clinical benefit, monitoring of adherence, and management of the therapy.
目的 脊髓刺激(SCS)因缺乏神经生理学数据指导治疗优化而面临挑战。目前的脊髓刺激治疗方案是通过试验和错误来制定的,其结果是治疗效果不理想且不稳定。一种新型系统具有生理学闭环反馈机制,利用诱发复合动作电位,通过持续、准确地激活脊髓纤维来优化生理学神经剂量。我们的目标是确定神经生理学剂量指标及其范围,从而产生有临床意义的治疗反应。材料和方法纳入了 3 项临床研究的受试者(n = 180),这些受试者的基线腰腿痛视觉模拟量表≥60 毫米,身体功能属于严重至残废类别。最大镇痛效果(MAE)在操作上被定义为在植入 SCS 的前 3 个月内疼痛强度降低的最大百分比或最大累积应答者评分(最小临床重要差异 [MCID])。结果我们发现,神经剂量精确度为 2.8μV、剂量比为 1.4 的神经剂量方案为慢性疼痛患者带来了巨大的临床益处(疼痛减轻的 MAE 为 79 ± 1%,MCID 为 12.5 ± 0.4)。结论首次为神经刺激干预提供了循证神经剂量方案,作为优化临床获益、监测依从性和治疗管理的起点。
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Neuromodulation: Technology at the Neural Interface
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