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An Exploratory Human Laboratory Experiment Evaluating Vaporized Cannabis in the Treatment of Neuropathic Pain from Spinal Cord Injury and Disease

机译:评价蒸气蒸发治疗脊髓损伤和疾病引起的神经性疼痛的实验性人类实验室实验

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摘要

Using eight hour human laboratory experiments, we evaluated the analgesic efficacy of vaporized cannabis in patients with neuropathic pain related to injury or disease of the spinal cord, the majority of whom were experiencing pain despite traditional treatment. After obtaining baseline data, 42 participants underwent a standardized procedure for inhaling 4 puffs of vaporized cannabis containing either placebo, 2.9%, or 6.7% delta-9-tetrahydrocannabinol on three separate occasions. A second dosing occurred 3 hours later; participants chose to inhale 4 to 8 puffs. This flexible dosing was utilized to attempt to reduce the placebo effect. Using an 11-point numerical pain intensity rating scale as the primary outcome, a mixed effects linear regression model demonstrated a significant analgesic response for vaporized cannabis. When subjective and psychoactive side effects (e.g., good drug effect, feeling high, etc.) were added as covariates to the model, the reduction in pain intensity remained significant above and beyond any effect of these measures (all p<0.0004). Psychoactive and subjective effects were dose dependent. Measurement of neuropsychological performance proved challenging because of various disabilities in the population studied. As the two active doses did not significantly differ from each other in terms of analgesic potency, the lower dose appears to offer the best risk-benefit ratio in patients with neuropathic pain associated with injury or disease of the spinal cord.
机译:通过八小时的人体实验室实验,我们评估了汽化大麻在与脊髓损伤或疾病相关的神经性疼痛患者中的镇痛效果,尽管采用传统疗法,大多数患者仍感到疼痛。在获得基线数据之后,有42位参与者进行了标准化程序,分别在三个不同的场合吸入4口气化大麻,其中包含安慰剂,2.9%或6.7%的delta-9-四氢大麻酚。 3小时后进行第二次给药;参与者选择吸入4至8抽吸。利用这种灵活的剂量来尝试降低安慰剂的作用。使用11点疼痛强度数字评分量表作为主要结局,混合效应线性回归模型证明了汽化大麻具有明显的镇痛作用。当将主观和精神上的副作用(例如,良好的药物作用,感觉良好等)作为协变量添加到模型中时,疼痛强度的降低在这些措施的任何作用之上和之外仍然很明显(所有p <0.0004)。精神和主观效果与剂量有关。由于所研究人群的各种残疾,神经心理表现的测量被证明具有挑战性。由于两种有效剂量在止痛效果上没有显着差异,因此较低的剂量似乎在患有与脊髓损伤或疾病相关的神经性疼痛的患者中提供了最佳的风险效益比。

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