Fanara Benoît, Lambiel Silvia
Anesthesiology Department, Mont Blanc Regional Hospital, Sallanches-Chamonix, France.
Acupuncture Department, Clinic Dr. Benoît Fanara, Annecy-le-Vieux, Annecy, France.
Med Acupunct. 2019 Apr 1;31(2):103-108. doi: 10.1089/acu.2018.1327. Epub 2019 Apr 15.
Auricular acupuncture, through a combination of several points, can produce sedative and analgesic effects. The aim of this study was to compare the induction dose of propofol required to obtain a loss of response to verbal commands, with and without a preoperative combination of auricular points. This study involved American Society of Anesthesiologists physical status I and II patients, ages 18- 65, of either sex, having elective ambulatory surgery (digestive or gynecologic) under general anesthesia. The subjects were allocated to 2 groups: (1) patients treated by auricular acupuncture (group AA), compared with (2) patients not treated by auricular acupuncture (group NA). Propofol injection was initiated in each group, 10 mg, every 5 seconds, in order for the anesthetist to determine the minimum dose until there was a loss of response to verbal commands (the clinical hypnotic endpoint). At this point, the main outcome-the dose of propofol given-was noted. There were 32 patients in this study (16 in each group). Age, height, weight, and body mass index were similar in the groups ( ≥ 0.05). The required induction propofol dose was 17.7% lower in group AA than in group NA-a statistically significant difference ( ≤ 0.05). The mean induction dose indexed to weight was 2.18 mg/kg (range: 1.53-3.13 mg/kg) in group NA and 1.79 mg/kg (range: 1.12-2.11 mg/kg) in group AA. There were no complications. Auricular acupuncture is a method for stimulating the vagus nerve and parasympathetic nervous system. Preoperative auricular acupuncture enabled reductions of induction doses of propofol for general anesthesia without any clinically important side-effects.
耳针疗法通过多个穴位的组合,可产生镇静和镇痛效果。本研究的目的是比较在术前联合或不联合耳穴的情况下,获得对言语指令无反应所需的丙泊酚诱导剂量。本研究纳入了年龄在18至65岁之间、美国麻醉医师协会身体状况分级为Ⅰ级和Ⅱ级、男女不限、接受全身麻醉下择期门诊手术(消化或妇科)的患者。受试者被分为两组:(1)接受耳针治疗的患者(AA组),与(2)未接受耳针治疗的患者(NA组)。每组均以每5秒10毫克的速度开始注射丙泊酚,以便麻醉师确定直至对言语指令无反应(临床催眠终点)的最小剂量。此时,记录主要结局指标——给予的丙泊酚剂量。本研究共有32例患者(每组16例)。两组患者的年龄、身高、体重和体重指数相似(P≥0.05)。AA组所需的丙泊酚诱导剂量比NA组低17.7%——差异具有统计学意义(P≤0.05)。NA组以体重计算的平均诱导剂量为2.18毫克/千克(范围:1.53至3.13毫克/千克),AA组为1.79毫克/千克(范围:1.12至2.11毫克/千克)。未出现并发症。耳针疗法是一种刺激迷走神经和副交感神经系统的方法。术前耳针疗法可降低全身麻醉时丙泊酚的诱导剂量,且无任何具有临床意义的副作用。