Centre for Mental Health and Brain Sciences, Swinburne University of Technology, Hawthorn, VIC, Australia.
Institute for Breathing and Sleep (IBAS), Austin Health, Melbourne, VIC, Australia.
J Psychopharmacol. 2024 Mar;38(3):247-257. doi: 10.1177/02698811241229524. Epub 2024 Feb 8.
Despite increasing medical cannabis use, research has yet to establish whether and to what extent products containing delta-9-tetrahydrocannabinol (THC) impact driving performance among patients. Stable doses of prescribed cannabinoid products during long-term treatment may alleviate clinical symptoms affecting cognitive and psychomotor performance.
To examine the effects of open-label prescribed medical cannabis use on simulated driving performance among patients.
In a semi-naturalistic laboratory study, 40 adults (55% male) aged between 23 and 80 years, consumed their own prescribed medical cannabis product. Driving performance outcomes including standard deviation of lateral position (SDLP), the standard deviation of speed (SDS), mean speed and steering variability were evaluated using the Forum8 driving simulator at baseline (pre-dosing), 2.5 h and 5 -h (post-dosing). Perceived driving effort (PDE) was self-reported after each drive. Oral fluid and whole blood samples were collected at multiple timepoints and analysed for THC via liquid chromatography-mass spectrometry.
A significant main effect of time was observed for mean speed (p = 0.014) and PDE (p = 0.020), with patients displaying modest stabilisation of vehicle control, increased adherence to speed limits and reductions in PDE post-dosing, relative to baseline. SDLP (p = 0.015) and PDE (p = 0.043) were elevated for those who consumed oil relative to flower-based products. Detectable THC concentrations were observed in oral fluid at 6-h post-dosing (range = 0-24 ng/mL).
This semi-naturalistic study suggests that the consumption of medical cannabis containing THC (1.13-39.18 mg/dose) has a negligible impact on driving performance when used as prescribed.
尽管医用大麻的使用不断增加,但研究仍未确定含有Δ-9-四氢大麻酚(THC)的产品是否以及在何种程度上会影响患者的驾驶表现。长期治疗中使用稳定剂量的处方大麻素产品可能会缓解影响认知和运动表现的临床症状。
研究开处方的医用大麻使用对患者模拟驾驶表现的影响。
在一项半自然实验室研究中,40 名年龄在 23 至 80 岁之间的成年人(55%为男性)服用了自己的处方医用大麻产品。使用 Forum8 驾驶模拟器在基线(给药前)、2.5 小时和 5 小时(给药后)评估驾驶性能结果,包括横向位置标准差(SDLP)、速度标准差(SDS)、平均速度和转向变异性。每次驾驶后自我报告感知驾驶努力度(PDE)。在多个时间点采集口服液和全血样本,并通过液相色谱-质谱法分析 THC。
平均速度(p=0.014)和 PDE(p=0.020)存在显著的时间主效应,与基线相比,患者在给药后表现出对车辆控制的适度稳定,对限速的依从性增加,以及 PDE 降低。与花基产品相比,消耗油基产品时 SDLP(p=0.015)和 PDE(p=0.043)升高。在给药后 6 小时检测到口服液中的可检测 THC 浓度(范围为 0-24ng/mL)。
这项半自然研究表明,当按照规定使用时,含有 THC(1.13-39.18mg/剂量)的医用大麻对驾驶表现的影响可以忽略不计。