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High frequency spinal cord stimulation for chronic back and leg pain

机译:慢性背部和腿部疼痛的高频脊髓刺激

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BackgroundHigh frequency stimulation (HFS) may provide pain relief without the paresthesias typical of traditional low-frequency Spinal cord stimulation (SCS).MethodsA consecutive single-center series of patients was retrospectively reviewed to evaluate safety and efficacy of HF10 therapy. In this 24-month study, 62 patients with variables pathologies (44 patients with back failure surgery syndrome (FBSS), 18 patients with chronic peripheral neuropathic pain in the lower limbs (NeppL) were included to be treated with HF10. Pain outcomes were compared from preoperative baseline and at the conclusion of each study period. Clinical features, outcomes and complications were reviewed.Results62 patients completed this study. All patients had a successful trial before the definitive implantation of a spinal cord stimulator at the low dorsal level. The mean follow-up period was 11?months, ranging from 6 to 24?months. 6 patients showed no change from baseline visual analogue scale (VAS) after permanent implant and 2 had improved during the trial but was aggravated after the permanent implant placement. At 1?month, 63% of implanted HF10 therapy subjects were responders and 77% at 6?months. The average baseline, trial and postoperative Visual Analogue Scale (VAS) was 8.1, 3.6 and 4.2 respectively. When compared to the baseline, the average reduction achieved during the VAS trial was 4.5 points, accounting for a 56% pain reduction. The long-term failure rate was 22%.ConclusionsThis study generated preliminary evidence showing improved VAS current pain scores in absence of paresthesias and increase patient satisfaction with HF10 spinal cord stimulation.
机译:背景高频刺激(HFS)可以在没有传统的低频脊髓刺激(SCs)的典型典型的情况下提供疼痛浮雕.Methodsa连续的单中心系列患者被回顾性审查,评估HF10治疗的安全性和功效。在这项24个月的研究中,包含62名可变性病理患者(44例背部失败手术综合征(FBSS),18名患有下肢慢性周围神经病疼痛(Neppl)的患者用HF10处理。比较疼痛结果从术前基线和每个研究期结束。审查了临床特征,结果和并发症。患者完成了这项研究。所有患者在低背水平处的脊髓刺激器的最终植入前均有成功的试验。平均值随访时间为11?月,从6到24个月出来的几个月。6名患者在永久植入物和2次改进后,在临时植入过程中有所改善但在永久植入物安置后,6名患者没有从基线视觉模拟量表(VAS)发生变化。 1?月,63%的植入的HF10疗法受试者是响应者,67%在6个月。平均基线,试验和术后视觉模拟量表(VAS)为8.1,3.6和4 .2分别。与基线相比,VAS试验期间达到的平均减少为4.5点,占减少56%的疼痛。长期失败率为22%.Clusionsthis研究产生的初步证据显示出在没有感觉子的情况下改善的VAS电流疼痛评分,并提高患者对HF10脊髓刺激的满意度。

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