Recommendations for Toxicological Investigation of Drug-Impaired Driving and Motor Vehicle Fatalities-2017 Update

被引:55
|
作者
Logan, Barry K. [1 ,2 ]
D'Orazio, Amanda L. [1 ,3 ]
Mohr, Amanda L. A. [1 ]
Limoges, Jennifer F. [4 ]
Miles, Amy K. [5 ]
Scarneo, Colleen E. [6 ]
Kerrigan, Sarah [7 ]
Liddicoat, Laura J. [1 ]
Scott, Karen S. [3 ]
Huestis, Marilyn A. [2 ,8 ]
机构
[1] Fredr Rieders Family Fdn, Ctr Forens Sci Res & Educ, 2300 Stratford Ave, Willow Grove, PA 19090 USA
[2] NMS Labs, 3701 Welsh Rd, Willow Grove, PA 19090 USA
[3] Arcadia Univ, 450 S Easton Rd, Glenside, PA 19038 USA
[4] New York State Police Forens Invest Ctr, 1220 Washington Ave,Bldg 30, Albany, NY 12226 USA
[5] Wisconsin State Lab Hyg, 2601 Agr Dr,POB 7996, Madison, WI 53707 USA
[6] New Hampshire Dept Safety, Div State Police Forens Lab, 33 Hazen Dr, Concord, NH 03305 USA
[7] Sam Houston State Univ, 1003 Bowers Blvd, Huntsville, TX 77341 USA
[8] Univ Maryland, Sch Med, 655 W Baltimore St, Baltimore, MD 21201 USA
关键词
URINE;
D O I
10.1093/jat/bkx082
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This report describes the outcomes of a process undertaken to review and update the National Safety Council's Alcohol, Drugs and Impairment Division's recommendations for the toxicological investigation of suspected alcohol and drug-impaired driving cases and motor vehicle fatalities. The updates to the recommendations are made based on a survey of practices in laboratories in the USA and Canada performing testing in these cases, consideration of existing epidemiological crash and arrest data, current drug use patterns, and practical considerations of widely available technology platforms in laboratories performing this work. The final recommendations updates are derived from a consensus meeting of experts recruited from survey respondents and the membership of the National Safety Council's Alcohol, Drug and Impairment Division. The principal changes in this round of recommendations include removal of butalbital, phenobarbital, and phencyclidine from Tier I (mandatory) to Tier II (optional) due to changes in prevalence. In addition, buprenorphine, fentanyl, tramadol, and their metabolites were moved from Tier II to Tier I due to increased prevalence and concerns about their potential for causing impairment. In addition, screening and confirmatory cutoffs for the oral fluid scope were further refined. Other additions were made to the list of Tier II compounds including fentanyl analogs (e.g., acetylfentanyl, butyrylfentanyl, furanylfentanyl, etc), mitragynine, novel opioids (e.g., MT-45, U-47700), atypical antipsychotics, and novel benzodiazepines (e.g., clonazolam, flubromazolam, etc).
引用
收藏
页码:63 / 68
页数:6
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