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首页> 外文期刊>Neurologia medico-chirurgica. >Predictive Factors Associated with Pain Relief of Spinal Cord Stimulation for Central Post-stroke Pain
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Predictive Factors Associated with Pain Relief of Spinal Cord Stimulation for Central Post-stroke Pain

机译:与中风后中枢脊髓刺激疼痛缓解相关的预测因素

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The efficacy and predictive factors associated with successful spinal cord stimulation (SCS) for central post-stroke pain (CPSP) have yet to be definitively established. Thus, this study evaluated the rates of pain relief found after more than 12 months and the predictive factors associated with the success of SCS for CPSP. The degree of pain after SCS in 18 patients with CPSP was assessed using the Visual Analog Scale preoperatively, at 1, 6 and 12 months after surgery, and at the time of the last follow-up. After calculating the percentage of pain relief (PPR), patients were separated into two groups. The first group exhibited continuing PPR ≥30% at more than 12 months (effect group) while the second group exhibited successful/unsuccessful trials followed by decreasing PPR 30% within 12 months (no effect group). Pain relief for more than 12 months was achieved in eight out of 18 (44.4%) patients during the 67.3 ± 35.5 month follow-up period. Statistically significant differences were found for both the age and stroke location during comparisons of the preoperative characteristics between the two groups. There was a significantly younger mean age for the effect versus the no effect group. Patients with stoke in non-thalamus were significantly enriched in effect group compared with those with stoke in thalamus. Multivariable analysis using these two factors found no statistical differences, suggesting that these two factors might possibly exhibit the same behaviors for the SCS effect. These results suggest that SCS may be able to provide pain relief in young, non-thalamus stroke patients with CPSP.
机译:与成功的脊髓刺激(SCS)相关的中风后疼痛(CPSP)的疗效和预测因素尚未确定。因此,本研究评估了超过12个月后发现的疼痛缓解率以及与CPS的SCS成功相关的预测因素。术前,术后1、6和12个月以及最后一次随访时,使用Visual Analog Scale评估了18例CPSP患者SCS术后的疼痛程度。在计算缓解疼痛(PPR)的百分比后,将患者分为两组。第一组在超过12个月时表现出持续PPR≥30%(效果组),而第二组显示出成功/失败的试验,随后在12个月内将PPR降低至<30%(无效果组)。在67.3±35.5个月的随访期内,18名患者中有8名(44.4%)的疼痛缓解超过12个月。在比较两组的术前特征时,发现年龄和卒中位置在统计学上都有显着差异。与未治疗组相比,该治疗组的平均年龄明显年轻。与非丘脑中风患者相比,非丘脑中风患者明显丰富。使用这两个因素的多变量分析未发现统计学差异,表明这两个因素可能对SCS效应表现出相同的行为。这些结果表明,SCS可能能够减轻CPSP的年轻非丘脑中风患者的疼痛。

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