瑞芬太尼诱发的痛觉减退:现状。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-08-01 Epub Date: 2024-06-03 DOI:10.1097/ACO.0000000000001400
Alexander A Vitin, Talmage D Egan
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引用次数: 0

摘要

瑞芬太尼诱导的痛觉减退(RIH)是阿片类药物诱导的痛觉减退(OIH)综合征的一部分,似乎是由于突然停止以等于或超过 0.3 毫克/千克/分钟的速度连续输注瑞芬太尼所致。其复杂的发病机制仍未完全明了。不过,N-甲基-d-天冬氨酸受体系统的过度激活、脊髓下降促进和达吗啡素(一种κ-阿片配体)浓度的增加被普遍认为是可能的机制。目前已提出了几种预防和处理方法,如缓慢停止瑞芬太尼输注、添加丙泊酚、预处理或同时使用氯胺酮、丁丙诺啡、环氧化酶-2 抑制剂(非甾体抗炎药)、美沙酮、右美托咪定等。在临床和动物实验中,这些策略取得了不同程度的成功,许多策略仍在研究中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Remifentanil-induced hyperalgesia: the current state of affairs.

Remifentanil-induced hyperalgesia (RIH) is a part of a general opioid-induced hyperalgesia (OIH) syndrome, seemingly resulting from abrupt cessation of continuous remifentanil infusion at rates equal or exceeding 0.3 mcg/kg/min. The intricate mechanisms of its development are still not completely understood. However, hyperactivation of the N -methyl d -aspartate receptor system, descending spinal facilitation and increased concentration of dynorphin (a κ-opioid ligand) are commonly proposed as possible mechanisms. Several ways of prevention and management have been suggested, such as slow withdrawal of remifentanil infusion, the addition of propofol, pretreatment with or concomitant administration of ketamine, buprenorphine, cyclooxygenase-2 inhibitors (NSAIDs), methadone, dexmedetomidine. In clinical and animal studies, these strategies exhibited varying success, and many are still being investigated.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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