首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Continuous epidural infusion of racemic methadone results in effective postoperative analgesia and low plasma concentrations.
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Continuous epidural infusion of racemic methadone results in effective postoperative analgesia and low plasma concentrations.

机译:连续硬膜外输注外消旋美沙酮可导致有效的术后镇痛和低血浆浓度。

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PURPOSE: To compare two protocols of epidural administration of racemic methadone for postoperative analgesia (continuous infusion and intermittent bolus), focussing on plasma concentration, analgesic efficacy and side effects. METHODS: Ninety patients undergoing abdominal or lower-limb surgery were randomly assigned to two groups in a prospective double-blind design. The continuous infusion patients (n=60) received initial doses of 3 to 6 mg followed by 6 to 12 mg by continuous infusion over 24 hr. The bolus administration patients (n=30) received repeated boluses of 3 to 6 mg of racemic methadone every eight hours. Pain intensity was assessed on a visual analog scale. Amount of supplementary analgesia was recorded, as was the incidence of side effects. Plasma methadone concentrations were determined by high performance liquid chromatography. Treatment was continued for 72 hr. RESULTS: Pain relief was good and comparable in both groups throughout the three days of treatment. No accumulation of plasma racemic methadone was observed in either group, although the concentrations were significantly higher in the bolus group. Miosis was significantly more frequent in the bolus group. CONCLUSION: Plasma methadone concentrations were significantly lower with continuous infusion. Plasma methadone accumulation, which is considered the main disadvantage for its purported influence on the incidence of side effects, did not occur at the doses used over the three days of treatment that we report.
机译:目的:比较两种外消旋美沙酮硬膜外给药用于术后镇痛的方法(连续输注和间歇推注),重点是血浆浓度,镇痛效果和副作用。方法:将90名接受腹部或下肢手术的患者按前瞻性双盲设计随机分为两组。连续输注患者(n = 60)接受初始剂量3至6 mg,然后在24小时内连续输注6至12 mg。推注给药的患者(n = 30)每8小时重复推注3至6 mg外消旋美沙酮。在视觉模拟量表上评估疼痛强度。记录辅助镇痛的数量,以及副作用的发生率。通过高效液相色谱法测定血浆美沙酮浓度。治疗持续72小时。结果:在整个治疗的三天中,两组患者的疼痛缓解良好且相当。两组均未观察到血浆外消旋美沙酮的蓄积,尽管浓注组的浓度显着较高。大剂量组的瞳孔缩小明显更为频繁。结论:连续输注血浆美沙酮浓度显着降低。在我们报告的三天治疗剂量中,并未发生血浆美沙酮积累(据称是其对副作用发生率的影响)的主要缺点。

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