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首页> 外文期刊>European journal of pain : >The effect of electroacupuncture on opioid-like medication consumption by chronic pain patients: a pilot randomized controlled clinical trial.
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The effect of electroacupuncture on opioid-like medication consumption by chronic pain patients: a pilot randomized controlled clinical trial.

机译:电针对慢性疼痛患者服用阿片样药物的影响:一项随机对照临床试验。

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摘要

Opioid-like medications (OLM) are commonly used by patients with various types of chronic pain, but their long-term benefit is questionable. Electroacupuncture (EA) has been previously shown beneficial in reducing post-operative acute OLM consumption. In this pilot randomized controlled trial, the effect of EA on OLM usage and associated side effects in chronic pain patients was evaluated. After a two-week baseline assessment, participants using OLM for their non-malignant chronic pain were randomly assigned to receive either real EA (REA, n=17) or sham EA (SEA, n=18) treatment twice weekly for 6 weeks before entering a 12-week follow-up. Pain, OLM consumption and their side effects were recorded daily. Participants also completed the McGill Pain Questionnaire (MPQ), SF-36 and Beck Depression Inventory (BDI) at baseline, and at the 5th, 8th, 12th, 16th and 20th week. Nine participants withdrew during the treatment period with another three during the follow-up period. Intention to treat analysis was applied. At the end of treatment period, reductions of OLM consumption in REA and SEA were 39% and 25%, respectively (p=0.056), but this effect did not last more than 8 weeks after treatment. There was no difference between the two groups with respect to reduction of side effects and pain and the improvement of depression and quality of life. In conclusion, REA demonstrates promising short-term reduction of OLM for participants with chronic non-malignant pain, but such effect needs to be confirmed by trials with adequate sample sizes.
机译:类阿片类药物(OLM)通常用于患有各种类型的慢性疼痛的患者,但其长期获益值得怀疑。先前已证明电针(EA)有助于减少术后急性OLM消耗。在该试验性随机对照试验中,评估了EA对慢性疼痛患者的OLM使用率及相关副作用的影响。经过两周的基线评估后,随机分配使用OLM治疗非恶性慢性疼痛的参与者,每周两次,分别在6周前接受真正的EA(REA,n = 17)或假EA(SEA,n = 18)治疗。进行为期12周的随访。每天记录疼痛,OLM消耗及其副作用。参与者还在基线以及第5、8、12、16和20周时完成了麦吉尔疼痛问卷(MPQ),SF-36和贝克抑郁量表(BDI)。 9名参与者在治疗期间退出,其余3名在随访期间退出。应用了治疗分析意向。在治疗期结束时,REA和SEA中的OLM消耗量分别减少了39%和25%(p = 0.056),但这种作用在治疗后持续不超过8周。两组在减少副作用和疼痛以及改善抑郁和生活质量方面没有差异。总之,REA证明对患有慢性非恶性疼痛的参与者有希望在短期内降低OLM,但这种效果需要通过具有足够样本量的试验来证实。

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