脊髓刺激治疗带状疱疹后主干神经痛1例

J. Ahn, Seu-ryang Jang, Sang-Bok Lee, Young-Woo Kim, Tae-Kyu Lee
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引用次数: 0

摘要

带状疱疹后神经痛是一种经医学治疗的顽固性疼痛。然而,医学上难治性带状疱疹后神经痛的侵入性手术的实践指南尚不清楚,也不清楚是否适用于个别病例。在我们的研究中,脊髓刺激(SCS)对带状疱疹后神经痛患者的效果被描述为伴有持续疼痛的发作性疼痛的老年患者,这种疼痛通过口服和侵入性治疗难以控制。我们使用了一个SCS设备(Synergy2 IPG,型号7427;美敦力公司,明尼阿波利斯,MN)配备电极(1×8标准铅型号977A290;美敦力公司,明尼阿波利斯,明尼苏达州)。一根导线置于T12椎体的左下缘(脉宽60 ms,脉率20 Hz,振幅2.5 V),覆盖左侧10、11、12胸皮节的分布。与基线VAS相比,SCS后VAS下降至3-4,维持1周3-4,维持1个月3-4。6个月后,疼痛维持在4-5。吗啡的基线剂量为200毫克/天,在术后1个月和6个月后显著降低至120毫克/天和90毫克/天。治疗前加巴喷丁的剂量(1800毫克/天)。与基线剂量(1200毫克/天)相比,服用加巴喷丁(1200毫克/天)第一个月的加巴喷丁剂量没有显著减少。6个月后的摄入量也显著减少了900毫克/天。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Spinal Cord Stimulation for Patients with Post-Zoster Neuralgia on the Trunk: A Case Report
Post-zoster neuralgia is an intractable pain by medical treatment. However, practice guidelines for invasive procedures of medically intractable post-zoster neuralgia are unclear, and it is not clear to apply to individual cases. In our study, the effect of spinal cord stimulation (SCS) for patients with post-zoster neuralgia was described in old patients with episodic pain with constant pain, which have been poorly controlled with oral and invasive treatments. We used an SCS device (Synergy2 IPG, model 7427; Medtronic Inc, Minneapolis, MN) equipped with an electrode (1×8 standard Lead model 977A290; Medtronic Inc, Minneapolis, MN). One lead was placed in the left lower margin of the T12 vertebral body (pulse width 60 ms, pulse rate 20 Hz, amplitude 2.5 V) and it covered on the distribution to left 10, 11, 12 thoracic dermatomes. VAS decreased to 3-4 after SCS compared with baseline VAS and was sustained by 3-4 for 1 week and by 3-4 at 1 month. After 6 months, the pain remained at 4-5. In morphine consumption, the baseline doses were 200 mg/day that significantly reduced to 120 mg/day and 90 mg/day after 1-month and 6-months post-procedure. The dose of gabapentin (1,800 mg/day) before treatment. The dose of gabapentin in the first month did not significantly decrease in taking gabapentin (1,200 mg/day ) compared with the baseline dose (1,200 mg/day). Consumption after 6 months was also significantly reduced by 900 mg/day.
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