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首页> 外文期刊>The Pain Clinic >Does intravenous lidocaine reduce fibromyalgia pain?: A randomized, double-blind, placebo controlled cross-over study
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Does intravenous lidocaine reduce fibromyalgia pain?: A randomized, double-blind, placebo controlled cross-over study

机译:静脉注射利多卡因可减轻纤维肌痛吗?:一项随机,双盲,安慰剂对照的交叉研究

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摘要

Objective. To determine if intravenous lidocaine has an analgesic effect in fibromyalgia pain. Method. A randomized, double-blind, placebo controlled cross-over study of 75 consenting adult patients with pain due to fibromyalgia. Patients received either 48 ml placebo (0.9% saline) intravenously over 24 h or lidocaine 960 mg (48 ml 2% lidocaine) over a similar period. After 4 weeks the patients returned, those who initially received placebo were given lidocaine, those who initially received lidocaine given placebo, again intravenously over 24 h. Average pain was measured using a 0-10 cm visual analogue scale and recorded on a daily basis for the 4 week study period. Analgesic consumption as number of tablets taken was also recorded daily. Results. 63 patients provided results (44 female, 19 male) with an average age of 45 years and duration of fibromyalgia pain of 93 months. The average pre-treatment pain VAS score was 7.31 and did not change after placebo. After lidocaine infusion there was a significant fall to 6.5 (95% C.L. 5.81-7.19) during the first week, 6.6 (95% C.L. 5.85-7.33) after the second week, 6.6 (95% C.L. 5.88-7.36) after the third and 6.98 (95% C.L. 6.27-7.69) after the fourth week (p < 0.01). There was no change in analgesic consumption after either infusion. Side-effects were seen in 14 patients after lidocaine infusion and in 6 after placebo infusion. Eight patients got more than 50% reduction in pain scores with lidocaine while only one got similar relief after placebo infusion. Conclusion. Intravenous lidocaine produces analgesia in some patients with fibromyalgia, and the duration of this relief outlives both the infusion time and plasma half-life of the drug.
机译:目的。确定静脉注射利多卡因对纤维肌痛是否有镇痛作用。方法。一项随机,双盲,安慰剂对照的交叉研究,研究了75名同意的成年患者,因纤维肌痛而疼痛。患者在24小时内静脉接受48 ml安慰剂(0.9%生理盐水),或在相似时期接受960 mg利多卡因(48 ml 2%利多卡因)。 4周后患者返回,最初接受安慰剂的患者接受利多卡因治疗,最初接受利多卡因的患者接受安慰剂,在24小时内再次静脉注射。使用0-10厘米的视觉模拟量表测量平均疼痛,并在4周的研究期间每天记录一次。每天还记录镇痛剂的消耗量(服用药片的数量)。结果。 63例患者的结果(44例女性,19例男性)平均年龄为45岁,纤维肌痛持续时间为93个月。治疗前平均疼痛VAS评分为7.31,安慰剂后无变化。利多卡因输注后,第一周显着下降至6.5(95%CL 5.81-7.19),第二周为6.6(95%CL 5.85-7.33),第三周后为6.6(95%CL 5.88-7.36),第四周后为6.98(95%CL 6.27-7.69)(p <0.01)。两种输注后镇痛剂的用量没有变化。利多卡因输注后有14例患者出现了副作用,安慰剂输注后有6例出现了副作用。利多卡因使八名患者的疼痛评分降低了50%以上,而安慰剂输注后只有一例得到了类似的缓解。结论。静脉注射利多卡因会使某些纤维肌痛患者产生镇痛作用,这种缓解的持续时间超过了药物的输注时间和血浆半衰期。

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    《The Pain Clinic》 |2000年第3期|p.181-185|共5页
  • 作者

    McCleane Gary;

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