Schlaeppi Janine-Ai, Schreen Raphael, Mija Raluca, Nowacki Andreas, Pollo Claudio, Seidel Kathleen
Department of Neurosurgery, Inselspital University Hospital Bern, University of Bern, Bern, Switzerland.
Department of Neurosurgery, Inselspital University Hospital Bern, University of Bern, Bern, Switzerland.
Neuromodulation. 2023 Jan;26(1):147-156. doi: 10.1016/j.neurom.2022.03.009. Epub 2022 May 20.
We aimed to demonstrate the feasibility of using motor evoked responses to intraoperative double-train stimulation to guide lead placement and matching of intraoperative contacts with postoperative electrode programming in spinal cord stimulation for pain performed under general anesthesia.
The study included a series of 20 consecutive patients with refractory pain operated on under general anesthesia. Either percutaneous or paddle leads were implanted and positioned according to the intraoperative mapping results. Neurophysiologic mapping was performed with a double-train stimulation paradigm (intertrain interval of 60 milliseconds, three to five cathodal pulses with 0.5-millisecond pulse duration, and within-train interstimulus intervals of 2-4 milliseconds). The sites where dorsal column responses of the targeted dermatomes were detected were considered optimal for lead placement (intraoperative best contacts). Following spinal cord stimulator (SCS) lead placement, blinded postoperative programming of electrode contacts was matched with the intraoperative best contacts and the pain-paresthesia overlap for the trial phase. A binominal test was used as a statistical method; pre- and postoperative numeric rating scale (NRS) after three months was obtained.
A total of 15 patients underwent spinal cord stimulation trial for intractable pain. Of these, ten patients (66%) had a successful trial and received permanent implants; one patient had a successful trial but was never intended to be implanted because of her poor health condition; four patients (26%) had an unsuccessful trial, leading to trial electrode explantation; and five patients had already had an implant with percutaneous leads and therefore underwent electrode revision, of whom four patients received paddle leads. In 18 of the 20 operated patients (90%), we found a match between the best intraoperative contacts and the postoperatively programmed contacts (significantly better than chance, p = 8.2 × 10). In 90% of the patients, a pain-paresthesia overlap of 100% was found. In the remaining two patients (10%), the postoperatively best programmed contacts were one contact away from the intraoperative neurophysiologic best contact. A mean preoperative NRS score of 8.2 (variance) and a mean follow-up NRS score after three months of 3.6 (variance) were obtained for all patients with implants.
In this proof-of-concept study, we were able to demonstrate that SCS lead placement using a double-train stimulation paradigm performed under general anesthesia is a safe and feasible technique, offering reliable prediction of contacts for postoperative programming and excellent pain-paresthesia coverage.
我们旨在证明在全身麻醉下进行脊髓刺激治疗疼痛时,利用术中双脉冲刺激的运动诱发电位来指导电极置入以及使术中触点与术后电极程控相匹配的可行性。
该研究纳入了连续20例在全身麻醉下接受手术的顽固性疼痛患者。根据术中映射结果植入并定位经皮或片状电极。采用双脉冲刺激模式进行神经生理学映射(双脉冲间隔60毫秒,三至五个阴极脉冲,脉冲持续时间0.5毫秒,脉冲内刺激间隔2 - 4毫秒)。检测到目标皮节背柱反应的部位被认为是电极置入的最佳位置(术中最佳触点)。在脊髓刺激器(SCS)电极置入后,对电极触点进行盲法术后程控,并使其与术中最佳触点以及试验阶段的疼痛 - 感觉异常重叠情况相匹配。采用二项检验作为统计方法;获取术前和术后三个月的数字疼痛评分量表(NRS)。
共有15例患者接受了脊髓刺激治疗顽固性疼痛的试验。其中,10例患者(66%)试验成功并接受了永久性植入;1例患者试验成功,但因健康状况不佳从未打算植入;4例患者(26%)试验失败,导致试验电极取出;5例患者已经植入了经皮电极,因此接受了电极翻修,其中4例患者接受了片状电极。在20例接受手术的患者中,有18例(90%)我们发现术中最佳触点与术后程控触点相匹配(显著优于随机情况,p = 8.2×10)。90%的患者疼痛 - 感觉异常重叠率为100%。在其余2例患者(10%)中,术后最佳程控触点与术中神经生理学最佳触点相差一个触点。所有植入患者术前NRS评分平均为8.2(方差),术后三个月随访NRS评分平均为3.6(方差)。
在这项概念验证研究中,我们能够证明在全身麻醉下使用双脉冲刺激模式进行SCS电极置入是一种安全可行的技术,可为术后程控提供可靠的触点预测,并实现出色的疼痛 - 感觉异常覆盖。