Assessing fitness to drive – proposal for a laboratory testing workflow tailored to the individual's case

IF 1.7 Q4 TOXICOLOGY
Katleen Van Uytfanghe , Hanne Van Beveren , Christophe P. Stove , Evy De Boosere
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引用次数: 0

Abstract

Aim

Violating the law on driving under the influence can lead to a forfeiture of the right to drive. Either before or after this temporary forfeiture the individual can be subject to an assessment of the fitness to drive. In Belgium, the latter can be executed by medical doctors. For what concerns the analytical tests executed during the assessments, there are no common procedures. This leads to differences in which tests are performed and in the associated costs for the individuals. Here we propose an analytical workflow, as followed in Ghent, which is tailored to the individual case.

Method

The individual is invited by the doctor for a medical assessment. During this assessment, the individual is questioned on his drinking behavior and on the use of drugs-of-abuse. Based on the background information that initially led to the invitation for the assessment and on the answers to the questions, a list of potential substances is drafted for which biological specimens will be tested. The biological specimens collected are urine, dried blood (collected via fingerprick) and a hair sample (maximum 5 cm is evaluated). If sample collection is not possible or refused, this is noted in the files. Samples are subject to different types of analysis: all urine samples are subject to a Nal Von Minden test and a screening based on liquid-chromatography high resolution mass-spectrometry (HRMS). If one of the screening methods indicates the presence of carboxy-THC, benzoylecgonine, amphetamines an/or opiates, the concentration is determined via other, independent, targeted MS-based methods. All dried whole blood samples are analyzed for their phosphatidylethanol 16: 0/18: 1 concentration (PEth). Hair samples are only tested for ethylglucuronide (hEtG) if PEth concentrations are below 270 ng/mL. Testing of hair for drugs-of-abuse is not performed when the urine tested positive for drugs of abuse. Hair testing for drugs (of abuse) is pursued in case of a negative urine test and if there are elements pointing at a (suspected) history of drug use.

Results

This workflow was evaluated based on 365 cases. In 56% of these, PEth and hEtG results were not in full agreement, which could be due to the differences in the window of detection. PEth has a shorter window of detection (several weeks) than hEtG (several months, depending on the length of the hair)–hence, if a subject recently changed drinking behavior, this would only be reflected in the PEth level. For example: 3 subjects with a PEth value < 20 ng/mL had hEtG ≥ 30 pg/mg. Based on the value of PEth these may have been considered fit to drive, but the hEtG level revealed excessive alcohol use in the months prior to testing.
A total of 163 samples was positive in the Nal Von Minden test. For the most commonly used drugs-of-abuse, this positive screening results could be confirmed by the HRMS screening and/or confirmatory targeted testing. Only for carboxy-THC, the positive Nal Von Minden test sometimes could not be confirmed (∼5% of cases)–for benzoylecgonine, on the other hand, the HRMS screening was positive in 8% of the samples that tested negative by the Nal Von Minden test, with cocaine use being confirmed via follow-up testing.

Conclusion

Performing the Nal Von Minden test in presence of the individual helps in opening a dialogue on substance use. The further cascade of screening and confirming the presence of biomarkers for drugs-of-abuse and ethanol intake allows an accurate picture of an individual's behavior, while limiting the number of hair analyses and targeted MS-based testing. This is beneficial for the efficiency of the testing process and minimizes the costs for the tested individuals.
评估适合驱动-建议实验室测试工作流程量身定制的个人情况
目的:违反酒后驾车的法律将被剥夺驾驶权。在此之前或之后的临时没收,个人可以受到一个健康的评估,以驱动。在比利时,后者可由医生执行。对于在评估期间执行的分析测试,没有共同的程序。这就导致了进行检测的方式和个人相关费用的差异。在这里,我们提出了一个分析工作流,如根特所示,它是针对个别情况量身定制的。方法由医生邀请个人进行医学评估。在这个评估中,个人被询问他的饮酒行为和滥用药物的使用情况。根据最初导致邀请进行评估的背景资料和对问题的回答,起草了一份将对生物标本进行测试的潜在物质清单。收集的生物标本包括尿液、干血(通过手指穿刺收集)和头发样本(评估最大5厘米)。如果样品收集不可能或被拒绝,将在文件中注明。样本需要进行不同类型的分析:所有尿液样本都需要进行Nal Von Minden测试和基于液相色谱-高分辨率质谱(HRMS)的筛选。如果其中一种筛选方法表明存在羧基四氢大麻酚、苯甲酰茶碱、安非他明和/或阿片类药物,则通过其他独立的靶向ms方法确定浓度。所有干燥的全血样本分析其磷脂酰乙醇16:0 / 18:1浓度(PEth)。头发样品只有在PEth浓度低于270 ng/mL时才检测乙基葡萄糖醛酸盐(hEtG)。当尿液药物滥用测试呈阳性时,不进行头发药物滥用测试。如果尿检呈阴性,并且有迹象表明(疑似)有药物使用史,则进行毛发测试以检测药物(滥用)。结果基于365例病例对该工作流程进行了评估。在其中的56%中,PEth和hEtG的结果不完全一致,这可能是由于检测窗口的差异。PEth的检测窗口(几周)比hEtG的检测窗口(几个月,取决于头发的长度)短,因此,如果一个受试者最近改变了饮酒行为,这只会反映在PEth水平上。例如:3个具有PEth值<;20 ng/mL hEtG≥30 pg/mg。根据PEth值,这些人可能被认为适合开车,但hEtG水平显示在测试前几个月过量饮酒。共有163个样本在Nal Von Minden测试中呈阳性。对于最常用的滥用药物,这种阳性筛查结果可以通过HRMS筛查和/或确证性靶向检测来证实。仅对于羧基四氢大麻酚,有时无法确认Nal Von Minden试验阳性(约5%的病例)-另一方面,对于苯甲酰lecgonine,在Nal Von Minden试验阴性的样本中,HRMS筛查在8%的样本中呈阳性,可卡因使用通过后续检测得到确认。结论在个体在场的情况下进行Nal Von Minden测试有助于开启关于药物使用的对话。进一步的筛选和确认药物滥用和酒精摄入的生物标志物的存在,可以准确地描绘个人行为,同时限制了头发分析和靶向ms测试的数量。这有利于提高测试过程的效率,并将被测试个体的成本降至最低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.90
自引率
33.30%
发文量
393
审稿时长
47 days
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