Department of Anesthesiology and Critical Care Medicine, Johns Hopkins Hospital, Baltimore, Maryland.
Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
J Pain. 2017 Dec;18(12):1468-1475. doi: 10.1016/j.jpain.2017.07.008. Epub 2017 Aug 10.
The long-term effects of opioids on sensitization processes are believed to be mediated through the N-methyl-D-aspartate receptor. Quantitative sensory testing (QST) changes observed after a ketamine infusion have been previously described but the effect that chronic opioids will have is not known. The results of this prospective randomized factorial trial compared the thermal QST changes observed after a .05 mg/kg ketamine infusion or a saline placebo in chronic pain subjects who were either opioid-naive or were chronically using opioids for chronic noncancer pain are presented. No baseline QST differences were noted between the 4 groups at baseline. Comparison of changes preinfusion with postinfusion QST measurements resulted in decreased average change in temporal summation response between opioid subjects who received a placebo compared with those who received a ketamine infusion (-5.22, SD = 9.96 vs 13.81, SD = 19.55; P = .004). Additionally, the average change in temporal summation was decreased among subjects who received a ketamine infusion and were not chronically using opioids compared with subjects who were using chronic opioids and received a placebo infusion (-1.91, SD = 13.25 vs 13.81, SD = 19.55; P = .007). The results indicate that low-dose ketamine infusions produce subtle changes in QST phenotypes that are modified by the chronic use of opioids. This illustrates the potential diagnostic and therapeutic value of ketamine in the setting of chronic opioid use.
The presented data further our understanding of modulation of sensory perception in the setting of chronic opioid use and the role of the N-methyl-D-aspartate receptor. The use of low-dose ketamine infusions may be useful for the treatment as well as diagnosis of opioid-related neuropathic conditions.
长期使用阿片类药物被认为通过 N-甲基-D-天冬氨酸受体对敏化过程产生影响。先前已经描述了氯胺酮输注后观察到的定量感觉测试 (QST) 变化,但尚不清楚慢性阿片类药物会产生什么影响。本前瞻性随机析因试验的结果比较了慢性疼痛受试者在接受 0.05mg/kg 氯胺酮输注或生理盐水安慰剂后观察到的热 QST 变化,这些受试者要么是阿片类药物初治者,要么是慢性使用阿片类药物治疗慢性非癌性疼痛。在基线时,4 组之间没有注意到 QST 基线差异。与输注前 QST 测量值相比,接受安慰剂的阿片类药物受试者的时间总和反应的平均变化与接受氯胺酮输注的受试者相比有所降低(-5.22,SD=9.96 与 13.81,SD=19.55;P=0.004)。此外,与接受安慰剂输注且未慢性使用阿片类药物的受试者相比,接受氯胺酮输注且正在使用慢性阿片类药物的受试者的时间总和平均变化减少(-1.91,SD=13.25 与 13.81,SD=19.55;P=0.007)。结果表明,低剂量氯胺酮输注会导致 QST 表型发生微妙变化,而慢性阿片类药物的使用会改变这些变化。这说明了氯胺酮在慢性阿片类药物使用环境中潜在的诊断和治疗价值。
所提供的数据进一步了解了慢性阿片类药物使用情况下的感觉感知调节以及 N-甲基-D-天冬氨酸受体的作用。使用低剂量氯胺酮输注可能对治疗和诊断阿片类药物相关的神经病变条件有用。