Department of Anesthesia, Stanford University School of Medicine, Stanford, CA 94305, USA.
Reg Anesth Pain Med. 2010 Nov-Dec;35(6):514-9. doi: 10.1097/AAP.0b013e3181faa107.
Tissue injury is associated with the local release of inflammatory and nociceptive mediators and the development of hyperalgesia. It is unclear whether interrupting neuronal signaling using regional anesthetic techniques at the time of the injury modifies local nociceptive and inflammatory processes. The aim of this study was to determine whether a peripheral nerve block at the time of tissue injury could modify the development of wound hyperalgesia and the local release of inflammatory and nociceptive mediators.
Twelve healthy volunteers participated in this controlled, crossover, randomized study. A femoral nerve block or a sham block was established before inducing an experimental UVB burn on the thigh. Twenty-four hours later, the interstitial wound fluid was sampled, and mechanical and heat pain thresholds were assessed. Wound fluid concentrations of an array of cytokines, chemokines, nerve growth factor, prostaglandin E2, and substance P were determined.
Skin inflammation was associated with the release of inflammatory and nociceptive mediators and resulted in significant tissue hyperalgesia (P < 0.001). However, the presence of a fully established peripheral nerve block at the time of tissue injury did not alter the development of hyperalgesia after regression of the block. Similarly, the presence of a peripheral nerve block did not modify the release of inflammatory or nociceptive mediators.
These findings suggest that a preemptive, single-shot peripheral nerve block minimally affects wound hyperalgesia and inflammation. Continuous nerve block techniques may be better suited to alter nociceptive and inflammatory events in wounds beyond the duration of the block.
组织损伤与局部释放炎症和伤害性介质以及痛觉过敏的发展有关。目前尚不清楚在损伤时使用区域麻醉技术中断神经元信号是否会改变局部伤害性和炎症过程。本研究旨在确定组织损伤时进行外周神经阻滞是否可以改变伤口痛觉过敏的发展和炎症及伤害性介质的局部释放。
12 名健康志愿者参与了这项对照、交叉、随机研究。在大腿上诱导实验性 UVB 烧伤之前,建立股神经阻滞或假阻滞。24 小时后,取样间质伤口液,并评估机械和热痛阈值。测定伤口液中细胞因子、趋化因子、神经生长因子、前列腺素 E2 和 P 物质的浓度。
皮肤炎症与炎症和伤害性介质的释放有关,并导致明显的组织痛觉过敏(P<0.001)。然而,在组织损伤时完全建立外周神经阻滞的情况下,在阻滞消退后,痛觉过敏的发展并没有改变。同样,外周神经阻滞的存在也没有改变炎症或伤害性介质的释放。
这些发现表明,单次外周神经阻滞预先阻断对伤口痛觉过敏和炎症的影响最小。连续神经阻滞技术可能更适合改变伤口中的伤害性和炎症事件,其作用时间超过阻滞时间。