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阿片类药物剂量和治疗持续时间对标准化临床疼痛刺激感知的影响。

The effect of opioid dose and treatment duration on the perception of a painful standardized clinical stimulus.

作者信息

Cohen Steven P, Christo Paul J, Wang Shuxing, Chen Lucy, Stojanovic Milan P, Shields Cynthia H, Brummett Chad, Mao Jianren

机构信息

Department of Anesthesiology & Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, MD 21029, USA.

出版信息

Reg Anesth Pain Med. 2008 May-Jun;33(3):199-206. doi: 10.1016/j.rapm.2007.10.009.

Abstract

BACKGROUND AND OBJECTIVES

The concept of opioid-induced hyperalgesia has recently gained prominence as a contributing factor for opioid tolerance and long-term treatment failure. But whereas the preclinical data for this phenomenon are strong, the mixed clinical data derive primarily from experimental pain models conducted in volunteers and heroin addicts, and nonstandardized clinical stimuli, e.g., surgery. The primary objective of this study is to delineate the effect of opioid dose and treatment duration on pain intensity and unpleasantness ratings following a standardized clinical pain stimulus.

METHODS

Three hundred and fifty-five patients, on a steady regimen of analgesic medications and scheduled for an interventional procedure, received a standardized subcutaneous injection of lidocaine prior to a full dose of local anesthetic. Before and immediately following the injection, subjects were asked to rate pain and unpleasantness intensity on a 0 to 10 numerical rating scale. Subjects were stratified into 6 groups based on opioid dosage. A control group of 27 volunteers who had no pain and were taking no analgesics were also injected.

RESULTS

Both opioid dose and duration of treatment directly correlated with pain intensity and unpleasantness scores. Baseline pain intensity was also positively associated with both outcome variables. Gender was found to be associated with pain intensity and unpleasantness, with females scoring higher in both categories than males. Compared with patients not receiving opioid treatment, patients receiving opioid therapy were more likely to rate the standardized pain stimulus as being more unpleasant than painful.

CONCLUSIONS

The results of this study bolster preclinical and experimental pain models demonstrating enhanced pain perception in subjects receiving opioid therapy. This simple clinical model may provide a useful tool in examining opioid-induced hyperalgesia.

摘要

背景与目的

阿片类药物诱导的痛觉过敏这一概念近来作为阿片类药物耐受性和长期治疗失败的一个促成因素而备受关注。然而,尽管该现象的临床前数据确凿,但混杂的临床数据主要来自在志愿者和海洛因成瘾者身上进行的实验性疼痛模型,以及非标准化的临床刺激,如手术。本研究的主要目的是在标准化临床疼痛刺激后,描绘阿片类药物剂量和治疗持续时间对疼痛强度和不愉快程度评分的影响。

方法

355例正在接受稳定镇痛药物治疗且计划接受介入手术的患者,在给予全量局部麻醉药之前接受了标准化的利多卡因皮下注射。在注射前和注射后即刻,要求受试者在0至10的数字评分量表上对疼痛和不愉快程度进行评分。根据阿片类药物剂量将受试者分为6组。还对27名无疼痛且未服用镇痛药的志愿者组成的对照组进行了注射。

结果

阿片类药物剂量和治疗持续时间均与疼痛强度和不愉快程度评分直接相关。基线疼痛强度也与这两个结果变量呈正相关。发现性别与疼痛强度和不愉快程度有关,女性在这两个类别中的评分均高于男性。与未接受阿片类药物治疗的患者相比,接受阿片类药物治疗的患者更有可能将标准化疼痛刺激评为更不愉快而非更疼痛。

结论

本研究结果支持临床前和实验性疼痛模型,表明接受阿片类药物治疗的受试者疼痛感知增强。这个简单的临床模型可能为研究阿片类药物诱导的痛觉过敏提供一个有用的工具。

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