The use of transcutaneous electrical acupoint stimulation to reduce opioid consumption in patients undergoing off-pump CABG: a randomized controlled trial.

IF 2 3区 医学 Q2 ANESTHESIOLOGY Perioperative Medicine Pub Date : 2024-07-05 DOI:10.1186/s13741-024-00427-2
Hui Zhang, Lini Wang, Ziyu Zheng, Jiange Han, Lin Li, Wenlong Yao, Zhijian Li, Gang Luo, Baobao Gao, Jie Shen, Hailong Dong, Chong Lei
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Abstract

Background: High doses of long-acting opioids were used to facilitate off-pump coronary artery bypass grafting procedure, which may result in opioid-related adverse events after surgery. Transcutaneous electrical acupoint stimulation (TEAS) had been reported to be effective in reducing intraoperative opioids consumption during surgery. The aim of this study is to assess whether TEAS with difference acupoints can reduce the doses of opioid analgesics.

Methods: This was a multicenter, randomized, controlled, double-blind trial. Patients underwent off-pump coronary artery bypass grafting under general anesthesia were enrolled. Eligible patients were randomly and equally grouped into sham acupuncture group (n = 105), regional acupoints combination group (n = 105), or distal-proximal acupoints combination group (n = 105) using a centralized computer-generated randomization system. Transcutaneous electrical acupoint stimulation was applied for 30 min before anesthesia induction. The primary outcome was the doses of sufentanil during anesthesia. Secondary outcomes included the highest postoperative vasoactive-inotropic scores within 24 h, intraoperative propofol consumption, length of mechanical ventilation, duration of cardiac care unit and postoperative hospital stay, incidence of postoperative complications, and mortality within 30 days after surgery.

Results: Of the 315 randomized patients, 313 completed the trial. In the modified intention-to-treat analysis, the doses of sufentanil were 303.9 (10.8) μg in the distal-proximal acupoints group, significantly lower than the sham group, and the mean difference was - 34.9 (- 64.9 to - 4.9) μg, p = 0.023. The consumption of sufentanil was lower in distal-proximal group than regional group (303.9 vs. 339.5), and mean difference was - 35.5 (- 65.6 to - 5.5) μg, p = 0.020. The distal-proximal group showed 10% reduction in opioids consumption comparing to both regional and sham groups. Secondary outcomes were comparable among three groups.

Conclusion: Transcutaneous electrical acupoint stimulation with distal-proximal acupoints combination, compared to regional acupoints combination and sham acupuncture, significantly reduced sufentanil consumption in patients who underwent off-pump coronary artery bypass grafting surgery.

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使用经皮穴位电刺激减少接受非体外循环心脏移植术患者的阿片类药物用量:随机对照试验。
背景:高剂量的长效阿片类药物被用于非体外循环冠状动脉旁路移植术,这可能导致术后阿片类药物相关不良事件的发生。有报道称,经皮穴位电刺激(TEAS)可有效减少术中阿片类药物的用量。本研究旨在评估经皮穴位电刺激疗法是否能减少阿片类镇痛药的剂量:这是一项多中心、随机、对照、双盲试验。方法:这是一项多中心、随机对照、双盲试验,在全身麻醉下接受非体外循环冠状动脉旁路移植术的患者均被纳入其中。符合条件的患者被随机平均分为假针灸组(n = 105)、区域穴位组合组(n = 105)或远端-近端穴位组合组(n = 105)。麻醉诱导前经皮电穴位刺激 30 分钟。主要结果是麻醉期间舒芬太尼的剂量。次要结果包括术后 24 小时内血管活性-肌张力最高评分、术中异丙酚用量、机械通气时间、心脏监护室和术后住院时间、术后并发症发生率以及术后 30 天内死亡率:结果:在 315 名随机患者中,有 313 人完成了试验。在修改后的意向治疗分析中,远端-近端穴位组的舒芬太尼剂量为 303.9 (10.8) μg,显著低于假穴组,平均差异为 - 34.9 (- 64.9 to - 4.9) μg,P = 0.023。远端-近端组的舒芬太尼消耗量低于区域组(303.9 对 339.5),平均差异为 - 35.5(- 65.6 到 - 5.5)微克,P = 0.020。与区域组和假体组相比,远端-近端组的阿片类药物用量减少了 10%。三组的次要结果具有可比性:结论:经皮电穴位刺激远端-近端穴位组合与区域穴位组合和假针灸相比,能显著减少接受非体外循环冠状动脉旁路移植手术患者的舒芬太尼用量。
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3.80%
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审稿时长
10 weeks
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