Normandie Univ, Caen, France.
Psychopharmacology (Berl). 2013 Jul;228(2):309-20. doi: 10.1007/s00213-013-3035-7. Epub 2013 Mar 9.
Some recent pharmacoepidemiological studies revealed an elevated risk of driving accidents after opioid analgesics uses. Among analgesics, codeine is often associated with paracetamol in numerous pharmaceutical specialties.
The objective of this study was to evaluate the dose-effect relationship of three usual therapeutic doses of codeine/paracetamol on driving ability, psychomotor performance, subjective alertness, in link with blood concentrations in healthy young volunteers.
Driving performance, responses to psychomotor vigilance tests, and scales reflecting alertness were evaluated during the morning after drug intake in a double-blind, randomized, placebo-controlled study. Sixteen healthy volunteers (23.4 ± 2.7 years old, 8 men and 8 women) participated in this balanced, cross-over study. Three doses of codeine/paracetamol (20/400, 40/800, 60/1200 mg) were evaluated against placebo. Two blood samples were collected, 1 and 4 h after drug intake. In serum, codeine and morphine concentrations were determined in serum using high-performance liquid chromatography electrospray ionization-tandem mass spectrometry, and paracetamol concentrations using fluorescence polarization immunoassay.
Driving and psychomotor performance were not affected by any of the three codeine/paracetamol doses. However, significant, though modest, correlations were observed between the driving parameters and both morphine and codeine blood concentrations.
This study did not reveal any significant impairment in performance due to the three therapeutic doses used in healthy young volunteers. However, the relationships between drug blood concentration and behavioral measures suggest that an inter-subject variability in blood concentration may influence the power of the observed drug effect.
一些最近的药物流行病学研究显示,在使用阿片类镇痛药后,驾驶事故的风险增加。在镇痛药中,可待因通常与许多药物制剂中的对乙酰氨基酚联合使用。
本研究旨在评估三种常用治疗剂量的可待因/对乙酰氨基酚对驾驶能力、精神运动表现和主观警觉性的剂量-效应关系,并与健康年轻志愿者的血液浓度相关联。
在一项双盲、随机、安慰剂对照研究中,在药物摄入后的清晨评估驾驶表现、对精神运动警戒测试的反应以及反映警觉性的量表。16 名健康志愿者(23.4±2.7 岁,8 名男性和 8 名女性)参与了这项平衡、交叉研究。评估了三种可待因/对乙酰氨基酚剂量(20/400、40/800、60/1200mg)与安慰剂相比的效果。在药物摄入后 1 小时和 4 小时采集了两份血样。使用高效液相色谱-电喷雾串联质谱法测定血清中可待因和吗啡浓度,荧光偏振免疫分析法测定血清中对乙酰氨基酚浓度。
三种可待因/对乙酰氨基酚剂量均未影响驾驶和精神运动表现。然而,驾驶参数与吗啡和可待因的血液浓度之间存在显著的、但适度的相关性。
本研究未发现健康年轻志愿者使用三种治疗剂量会导致任何显著的表现受损。然而,药物血液浓度与行为测量之间的关系表明,个体间血液浓度的变异性可能会影响观察到的药物效应的强度。