脊髓刺激治疗无反应患者的成功止痛:氯胺酮与脊髓刺激联合应用。

Successful pain relief in non-responders to spinal cord stimulation: the combined use of ketamine and spinal cord stimulation.

机构信息

Pain Management and Research Center, Department of Anesthesiology, Maastricht University Hospital, P. Debyelaan 25, PO Box 5800, 6202 AZ Maastricht, The Netherlands.

出版信息

Eur J Pain. 2011 Nov;15(10):1049.e1-9. doi: 10.1016/j.ejpain.2011.04.004. Epub 2011 May 11.

Abstract

Although spinal cord stimulation (SCS) is an established therapy for chronic neuropathic pain, still 30% of patients do not respond adequately to trial stimulation. These so called "non-responders" do not receive a permanent implantation for pain relief. The induction and maintenance of central sensitization plays a pivotal role in (chronic) neuropathic pain and is thought to be the resultant of the activation of the N-methyl-d-aspartate (NMDA) receptor in the dorsal horn. Blocking the NMDA receptor through the use of the non-competitive blocker ketamine has shown to attenuate neuropathic pain, although the undesirable side effects limit its use. The present study was performed to examine whether the combination of SCS with an individually determined sub-effective dose of intrathecal (i.t.) ketamine could convert non-responders into responders in rats with chronic neuropathic pain. Rats received a partial ligation of the sciatic nerve for the induction of neuropathic pain. Animals with tactile hypersensitivity to von Frey monofilaments (n=15) received 30 min of SCS. Non-responders to SCS (n=8) received their individually determined sub-effective i.t. dose of ketamine followed by 30 min of SCS. No side effects of the sub-effective dose of ketamine could be noted. The combined treatment of SCS and sub-effective dose of i.t. ketamine in non-responders resulted in a significant reduction of the withdrawal threshold in all previous non-responders to SCS, thereby converting them into responders to SCS.

摘要

虽然脊髓刺激 (SCS) 是治疗慢性神经性疼痛的一种既定疗法,但仍有 30%的患者对试验刺激反应不足。这些所谓的“无反应者”不会因缓解疼痛而接受永久性植入。中枢敏化的诱导和维持在(慢性)神经性疼痛中起着关键作用,被认为是背角中 N-甲基-D-天冬氨酸 (NMDA) 受体激活的结果。通过使用非竞争性阻滞剂氯胺酮阻断 NMDA 受体已被证明可以减轻神经性疼痛,但不理想的副作用限制了其使用。本研究旨在检查 SCS 与鞘内(i.t.)氯胺酮的个体确定亚有效剂量联合使用是否可以使慢性神经性疼痛大鼠中的无反应者转变为有反应者。大鼠接受坐骨神经部分结扎以诱导神经性疼痛。对 von Frey 单丝有触觉过敏的动物(n=15)接受 30 分钟 SCS。对 SCS 无反应者(n=8)接受其个体确定的亚有效 i.t. 剂量氯胺酮,随后接受 30 分钟 SCS。亚有效剂量氯胺酮没有副作用。SCS 和亚有效剂量 i.t. 氯胺酮联合治疗无反应者可显著降低所有先前 SCS 无反应者的退缩阈值,从而使他们对 SCS 有反应。

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