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慢性疼痛患者口服吗啡治疗1个月后的阿片类药物耐受性和痛觉过敏:一项初步前瞻性研究。

Opioid tolerance and hyperalgesia in chronic pain patients after one month of oral morphine therapy: a preliminary prospective study.

作者信息

Chu Larry F, Clark David J, Angst Martin S

机构信息

Department of Anesthesia, Stanford University School of Medicine, CA 94305, USA.

出版信息

J Pain. 2006 Jan;7(1):43-8. doi: 10.1016/j.jpain.2005.08.001.

DOI:10.1016/j.jpain.2005.08.001
PMID:16414554
Abstract

UNLABELLED

There is accumulating evidence that opioid therapy might not only be associated with the development of tolerance but also with an increased sensitivity to pain, a condition referred to as opioid-induced hyperalgesia (OIH). However, there are no prospective studies documenting the development of opioid tolerance or OIH in patients with chronic pain. This preliminary study in 6 patients with chronic low back pain prospectively evaluated the development of tolerance and OIH. Patients were assessed before and 1 month after initiating oral morphine therapy. The cold pressor test and experimental heat pain were used to measure pain sensitivity before and during a target-controlled infusion with the short-acting mu opioid agonist remifentanil. In the cold pressor test, all patients became hyperalgesic as well as tolerant after 1 month of oral morphine therapy. In a model of heat pain, patients exhibited no hyperalgesia, although tolerance could not be evaluated. These results provide the first prospective evidence for the development of analgesic tolerance and OIH by using experimental pain in patients with chronic back pain. This study also validated methodology for prospectively studying these phenomena in larger populations of pain patients.

PERSPECTIVE

Experimental evidence suggests that opioid tolerance and opioid-induced hyperalgesia might limit the clinical utility of opioids in controlling chronic pain. This study validates a pharmacologic approach to study these phenomena prospectively in chronic pain patients and suggests that both conditions do occur within 1 month of initiating opioid therapy.

摘要

未标注

越来越多的证据表明,阿片类药物治疗不仅可能与耐受性的产生有关,还与对疼痛的敏感性增加有关,这种情况被称为阿片类药物诱导的痛觉过敏(OIH)。然而,尚无前瞻性研究记录慢性疼痛患者中阿片类药物耐受性或OIH的发展情况。这项针对6例慢性下腰痛患者的初步研究前瞻性地评估了耐受性和OIH的发展情况。在开始口服吗啡治疗前及治疗1个月后对患者进行评估。在使用短效μ阿片类激动剂瑞芬太尼进行靶控输注之前和期间,采用冷加压试验和实验性热痛来测量疼痛敏感性。在冷加压试验中,所有患者在口服吗啡治疗1个月后均出现痛觉过敏和耐受性。在热痛模型中,患者未表现出痛觉过敏,尽管无法评估耐受性。这些结果首次提供了前瞻性证据,证明慢性背痛患者通过实验性疼痛会出现镇痛耐受性和OIH。本研究还验证了在更大规模疼痛患者群体中前瞻性研究这些现象的方法。

观点

实验证据表明,阿片类药物耐受性和阿片类药物诱导的痛觉过敏可能会限制阿片类药物在控制慢性疼痛方面的临床应用。本研究验证了一种在慢性疼痛患者中前瞻性研究这些现象的药理学方法,并表明这两种情况在开始阿片类药物治疗的1个月内确实会出现。

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