National Centre on Addiction and Doping, Istituto Superiore di Sanità, Rome, Italy.
Investigation, Crime and International Security, Università degli Studi Internazionali di Roma - UNINT, Rome, Italy.
J Pharm Biomed Anal. 2024 Jun 15;243:116084. doi: 10.1016/j.jpba.2024.116084. Epub 2024 Mar 2.
In 2019, Italian National Institute of Health established an external quality assessment program (EQA) to evaluate the performance of oral fluid testing for classical and new psychoactive substances by laboratories participating in the National Early Warning System collaborative centres. This report presents the results of four rounds between 2019 and 2023. Eleven oral fluid specimens, including 3 blank samples, were prepared by adding different classes of and new psychoactive drugs at known concentrations to pre-screened drug-free oral fluid. False-negative and false-positive results were calculated for the qualitative data evaluation. The quantitative evaluation measured the imprecision and accuracy of the results, in terms of coefficient of variation (CV%) and percent error (ERR%), respectively, with respect to a mean value obtained by reference laboratories. Z-score values were then calculated. Over the years, there has been a significant improvement in false-negative results (from 42.7% in the first year to 19.4% in the last year), but not in false-positive results (from 33.3% in the first year to 22.2% in the last one). In addition to the classic drugs of abuse (e.g. cocaine, amphetamine, methadone), the substances found in false positive samples belonged to the class of synthetic cannabinoids (e.g 5-fluoro CUMYL-PINACA and 5-fluoro-EDMB-PICA), synthetic opioids (e.g butyrylfentanyl) and tryptamines (e.g. 5-methoxy-N-methyl-N-isopropyltryptamine). The four rounds yielded a mean ERR% of approximately 22.1% and a mean CV% of around 41.5%. The participating laboratories demonstrated variable performances in relation to the class of analysed psychoactive substances, as evidenced by the calculated Z-scores. Between 25% and 60% of the reported results in all rounds should be considered satisfactory. EQA is a crucial element of laboratory quality management systems. It promotes continuous improvement and maintains high standards in the field of forensic and clinical drug testing.
2019 年,意大利国家卫生研究所建立了一个外部质量评估计划(EQA),以评估参与国家早期预警系统合作中心的实验室对口腔液中经典和新型精神活性物质的检测性能。本报告介绍了 2019 年至 2023 年期间进行的四轮评估结果。11 个口腔液样本,包括 3 个空白样本,是通过将不同类别的新型精神活性药物以已知浓度添加到预先筛选的无毒品口腔液中制备的。对定性数据评估计算了假阴性和假阳性结果。定量评估根据变异系数(CV%)和误差百分比(ERR%)分别测量结果的不精密度和准确度,相对于参考实验室获得的平均值。然后计算 Z 分数值。多年来,假阴性结果有了显著改善(从第一年的 42.7%降至最后一年的 19.4%),但假阳性结果没有改善(从第一年的 33.3%降至最后一年的 22.2%)。除了经典的滥用药物(如可卡因、苯丙胺、美沙酮)外,假阳性样本中还发现了属于合成大麻素(如 5-氟-CUMYL-PINACA 和 5-氟-EDMB-PICA)、合成阿片类药物(如丁酰芬太尼)和色胺类(如 5-甲氧基-N-甲基-N-异丙基色胺)的物质。四轮评估的平均 ERR%约为 22.1%,平均 CV%约为 41.5%。参与实验室在分析的精神活性物质类别方面表现出不同的性能,这一点可以从计算出的 Z 分数看出。在所有轮次中,25%至 60%的报告结果应被认为是令人满意的。EQA 是实验室质量管理体系的重要组成部分。它促进了不断改进,并在法医和临床药物检测领域保持了高标准。