Rivat Cyril, Ballantyne Jane
Université de Montpellier, Montpellier, France, Institut des Neurosciences de Montpellier, INSERM U1051, Montpellier, France.
Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, USA.
Pain Rep. 2016 Sep 8;1(2):e570. doi: 10.1097/PR9.0000000000000570. eCollection 2016 Aug.
In the past 2 decades, opioids have been used increasingly for the treatment of persistent pain, and doses have tended to creep up. As basic science elucidates mechanisms of pain and analgesia, the cross talk between central pain and opioid actions becomes clearer.
We aimed to examine the published literature on basic science explaining pronociceptive opioid actions, and apply this knowledge to clinical observation.
We reviewed the existing literature on the pronociceptive actions of opioids, both preclinical and clinical studies.
Basic science provides a rationale for the clinical observation that opioids sometimes increase rather than decrease pain. Central sensitization (hyperalgesia) underlies pain chronification, but can also be produced by high dose and high potency opioids. Many of the same mechanisms account for both central pain and opioid hyperalgesia.
Newly revealed basic mechanisms suggest possible avenues for drug development and new drug therapies that could alter pain sensitization through endogenous and exogenous opioid mechanisms. Recent changes in practice such as the introduction of titration-to-effect for opioids have resulted in higher doses used in the clinic setting than ever seen previously. New basic science knowledge hints that these newer dosing practices may need to be reexamined. When pain worsens in a patient taking opioids, can we be assured that this is not because of the opioids, and can we alter this negative effect of opioids through different dosing strategies or new drug intervention?
在过去20年中,阿片类药物越来越多地用于治疗持续性疼痛,且剂量有逐渐增加的趋势。随着基础科学阐明疼痛和镇痛的机制,中枢性疼痛与阿片类药物作用之间的相互作用变得更加清晰。
我们旨在研究已发表的关于解释阿片类药物促伤害感受作用的基础科学文献,并将这些知识应用于临床观察。
我们回顾了关于阿片类药物促伤害感受作用的现有文献,包括临床前和临床研究。
基础科学为阿片类药物有时会增加而非减轻疼痛这一临床观察提供了理论依据。中枢敏化(痛觉过敏)是疼痛慢性化的基础,但也可由高剂量和高效力的阿片类药物引起。许多相同的机制既导致中枢性疼痛,也导致阿片类药物引起的痛觉过敏。
新揭示的基础机制为药物开发和新的药物治疗提供了可能的途径,这些药物治疗可以通过内源性和外源性阿片类药物机制改变疼痛敏化。最近的实践变化,如引入阿片类药物的滴定至有效剂量,导致临床环境中使用的剂量比以往任何时候都高。新的基础科学知识提示,这些新的给药方法可能需要重新审视。当服用阿片类药物的患者疼痛加重时,我们能否确定这不是阿片类药物所致,以及我们能否通过不同的给药策略或新的药物干预来改变阿片类药物的这种负面影响?