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Repeated Intravenous Lidocaine Infusions for Patients with Fibromyalgia: Higher Doses of Lidocaine Have a Stronger and Longer-Lasting Effect on Pain Reduction

机译:对纤维肌痛患者的重复静脉内利多卡因输注:较高剂量的利多卡因对疼痛减少具有更强和更长的效果

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摘要

Objectives. To determine the effect of escalating doses of lidocaine infusion with or without added magnesium on pain levels and the duration of pain relief in patients with fibromyalgia (FM). Methods. A retrospective chart review of 74 patients diagnosed with FM who underwent at least three escalating doses of intravenous (IV) lidocaine infusions (5 mg/kg of body weight, 7.5 mg/kg, and 7.5 mg/kg of lidocaine + 2.5 g of magnesium sulfate) was conducted. Each patient's subjective impression of change in pain intensity and duration of pain relief after each treatment was recorded, along with an 11-point numeric rating scale (NRS) for pain intensity, immediately before and after each infusion. Results. Short-term lidocaine analgesia was evaluated by the reduction in NRS pain score according to the patients reported pre- (immediately before treatment) and post-treatment (immediately after treatment) values. There was a statistical difference in the NRS score reduction between doses 5 mg/kg and 7.5 mg/kg of lidocaine (P= 0.009). Long-term analgesia was evaluated at follow-up visits by the patient's subjective impression of change in pain intensity and duration of pain relief. There was a statistical difference in the percentage of pain relief and the mean duration of pain relief between the treatments with 5 mg/kg and 7.5 mg/kg of lidocaine (P = 0.007 and P = 0.003). Although there was a trend of greater response to magnesium sulfate as a beneficial adjunct to the lidocaine infusion, we were unable to find a statistically significant difference for any of the variables studied. Conclusions. This study demonstrated that escalating doses of IV lidocaine to 7.5 mg/kg safely and effectively reduced the pain with prolonged effect in a significant number of patients diagnosed with fibromyalgia. Larger, prospective clinical studies are required to confirm this finding.
机译:目标。确定增加利多卡因输注剂量并添加或不添加镁对纤维肌痛(FM)患者疼痛水平和疼痛缓解持续时间的影响。方法。对74例确诊为FM的患者进行回顾性图表回顾,这些患者接受了至少三次递增剂量的静脉注射利多卡因(5 mg/kg体重、7.5 mg/kg和7.5 mg/kg利多卡因+2.5 g硫酸镁)。记录每位患者在每次治疗后对疼痛强度变化和疼痛缓解持续时间的主观印象,以及每次输液前后疼痛强度的11分数字评分量表(NRS)。后果根据患者在治疗前(治疗前一刻)和治疗后(治疗后一刻)报告的数值,通过NRS疼痛评分的降低来评估短期利多卡因镇痛。5 mg/kg和7.5 mg/kg剂量的利多卡因在NRS评分降低方面存在统计学差异(P=0.009)。在随访时,通过患者对疼痛强度变化和疼痛缓解持续时间的主观印象来评估长期镇痛效果。5 mg/kg和7.5 mg/kg利多卡因治疗组的疼痛缓解百分比和疼痛缓解平均持续时间存在统计学差异(P=0.007和P=0.003)。虽然硫酸镁作为利多卡因输注的有益辅助物有更大的反应趋势,但我们无法找到任何研究变量的统计显著差异。结论。这项研究表明,在大量诊断为纤维肌痛的患者中,将静脉注射利多卡因的剂量增加到7.5 mg/kg安全有效地减轻了疼痛,并具有长期效果。需要更大规模的前瞻性临床研究来证实这一发现。

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