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Evaluation of antihyperalgesic and analgesic effects of 35% nitrous oxide when combined with remifentanil

瑞芬太尼 医学 痛觉过敏 麻醉 止痛药 交叉研究 生理盐水 安慰剂 可视模拟标度 伤害 内科学 异丙酚 受体 替代医学 病理
作者
Andreas Wehrfritz,Marcus Bauer,N. Noel,Juan Fernando Ramirez‐Gil,Harald Ihmsen,Johannes Prottengeier,J. Schüttler,Baptiste Bessière
出处
期刊:European Journal of Anaesthesiology [Lippincott Williams & Wilkins]
卷期号:38 (12): 1230-1241 被引量:6
标识
DOI:10.1097/eja.0000000000001468
摘要

BACKGROUND Remifentanil is an effective drug in peri-operative pain therapy, but it can also induce and aggravate hyperalgesia. Supplemental administration of N 2 O may help to reduce remifentanil-induced hyperalgesia. OBJECTIVE To evaluate the effect of 35 and 50% N 2 O on hyperalgesia and pain after remifentanil infusion. DESIGN Single site, phase 1, double-blind, placebo-controlled, randomised crossover study. SETTING University Hospital, Germany from January 2012 to April 2012. PARTICIPANTS Twenty-one healthy male volunteers. INTERVENTIONS Transcutaneous electrical stimulation induced spontaneous acute pain and stable areas of hyperalgesia. Each volunteer underwent the following four sessions in a randomised order: 50 to 50% N 2 -O 2 and intravenous (i.v.) 0.9% saline infusion (placebo); 50 to 50% N 2 -O 2 and i.v. remifentanil infusion at 0.1 μg kg −1 min −1 (remifentanil); 35 to 15 to 50% N 2 O-N 2 -O 2 and i.v. remifentanil infusion at 0.1 μg kg −1 min −1 (tested drug) and 50 to 50% N 2 O-O 2 and i.v. remifentanil infusion at 0.1 μg kg −1 min −1 (gas active control). Gas mixtures were inhaled for 60 min; i.v. drugs were administered for 30 min. MAIN OUTCOME MEASURES Areas of pin-prick hyperalgesia, areas of touch-evoked allodynia and pain intensity on a visual analogue scale were assessed repeatedly for 160 min. RESULTS Data from 20 volunteers were analysed. There were significant treatment and treatment-by-time effects regarding areas of hyperalgesia ( P < 0.001). After the treatment period, the area of hyperalgesia was significantly reduced ( P < 0.001) in the tested drug and in the gas active control (30.6 ± 9.25 and 24.4 ± 7.3 cm 2 , respectively) compared with remifentanil (51.0 ± 17.0 cm 2 ). There was also a significant difference between the gas active control and the tested drug sessions ( P < 0.001). For the area of allodynia and pain rating, results were consistent with the results for hyperalgesia. CONCLUSIONS Administration of 35% N 2 O significantly reduced hyperalgesia, allodynia and pain intensity induced after remifentanil. It might therefore be suitable in peri-operative pain relief characterised by hyperalgesia and allodynia, such as postoperative pain, and may help to reduce opioid demand. TRIAL REGISTRATION EudraCT-No.: 2011-000966-37.
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