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电针和曲马多对实验性止血带疼痛的影响。

The effect of electroacupuncture and tramadol on experimental tourniquet pain.

机构信息

Department of Complementary and Integrative Medicine, University of Duisburg-Essen, Essen, Germany.

出版信息

Acupunct Med. 2012 Mar;30(1):21-6. doi: 10.1136/acupmed-2011-010094.

Abstract

OBJECTIVES

The hypoalgesic effect of electroacupuncture (EA) was directly compared with the analgesic effect of pharmacological interventions using the submaximum effort tourniquet technique (SETT).

METHODS

125 healthy subjects (mean age 24.44±4.46 years; 62.4% female, 37.6% male) performed SETT at baseline and under one of five experimental conditions (n=25 per group): EA (2 Hz with burst pulses in alternating one-phase-square wave pulses; burst length 180 μs, burst frequency 80 Hz, stimulation time/pulse width 3 s), tramadol (50 mg), ibuprofen (400 mg), placebo pill or non-treatment control. EA was performed at LI4 and LI10 contralaterally with stimulation beginning 20 min before SETT and lasting throughout SETT. The pharmacological interventions were given in a double-blind design 1 h before the SETT assessment.

RESULTS

Subjects showed a hypoalgesic effect of the opiate and of the EA for subjective pain rating (EA p=0.0051; tramadol p=0.0299), and pain tolerance index (time/rating) (EA p=0.043; tramadol p=0.047) analysed using analysis of covariance. More subjects reached the strict time limit of 30 min (analysed by logistic regression and adjusted OR as a post-hoc analysis) under EA compared with most other experimental conditions. Only EA and tramadol were not significantly different (95% Wald confidence limits: non-treatment control vs EA 0.011 to 0.542; placebo pill vs EA 0.009 to 0.438; ibuprofen vs EA 0.021 to 0.766; tramadol vs EA 0.065 to 1.436).

CONCLUSION

In a laboratory setting, an EA procedure was as effective as a single dose of an orally administered opiate in reducing experimentally induced ischaemic pain.

摘要

目的

用电针(EA)的镇痛作用与使用次大努力止血带技术(SETT)的药物干预的镇痛作用进行直接比较。

方法

125 名健康受试者(平均年龄 24.44±4.46 岁;62.4%为女性,37.6%为男性)在基线和以下五种实验条件下进行 SETT(每组 25 名):EA(2 Hz 与单相方波脉冲交替的爆发脉冲;爆发长度 180 μs,爆发频率 80 Hz,刺激时间/脉冲宽度 3 s)、曲马多、布洛芬、安慰剂丸或非治疗对照。EA 在 LI4 和 LI10 处进行对侧刺激,在 SETT 前 20 分钟开始,持续整个 SETT。药物干预以双盲设计在 SETT 评估前 1 小时进行。

结果

使用协方差分析,受试者对主观疼痛评分(EA p=0.0051;曲马多 p=0.0299)和疼痛耐受指数(时间/评分)(EA p=0.043;曲马多 p=0.047)表现出阿片类药物和 EA 的镇痛作用。与大多数其他实验条件相比,更多的受试者在 EA 下达到了严格的 30 分钟时间限制(通过逻辑回归和事后分析调整的优势比进行分析)。只有 EA 和曲马多没有显著差异(95% Wald 置信区间:非治疗对照 vs EA 0.011 至 0.542;安慰剂丸 vs EA 0.009 至 0.438;布洛芬 vs EA 0.021 至 0.766;曲马多 vs EA 0.065 至 1.436)。

结论

在实验室环境中,EA 程序与单次口服阿片类药物一样有效,可减少实验性缺血性疼痛。

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