Bush Donna M
Division of Workplace Programs, Substance Abuse and Mental Health Services Administration, US Department of Health and Human Services, One Choke Cherry Road, Room 2-1033, Rockville, MD 20857, USA.
Forensic Sci Int. 2008 Jan 30;174(2-3):111-9. doi: 10.1016/j.forsciint.2007.03.008. Epub 2007 Apr 16.
The U.S. Department of Health and Human Services (HHS) drug testing standards were published in 1988 and revised in 1994, 1998, and 2004. In 2004, significant revisions defining, standardizing, and requiring specimen validity testing on Federal employee donor urine specimens were included. In a separate notice, HHS proposed to establish scientific and technical guidelines for the Federal Workplace Drug Testing Program to: (1) permit laboratory testing of hair, oral fluid, and sweat patch specimens in addition to urine specimens for marijuana, cocaine, phencyclidine, opiates (with focus on heroin), and amphetamines [including methylenedioxymethamphetamine (MDMA), methylenedioxyethamphetamine (MDEA), methylenedioxyamphetamine (MDA)]; (2) permit use of on-site point of collection test (POCT) devices to test urine and oral fluid at collection sites; (3) permit use of instrumented initial test (screening only) facilities [IITF] to quickly identify negative specimens; and (4) add training requirement for collectors, on-site testers, and MROs. This proposal was published in the Federal Register on 13 April 2004, with a 90-day public comment period. The Substance Abuse and Mental Health Services Administration, HHS, reviewed those comments and is preparing the Final Notice that will define the requirements for such testing, including: specimen collection procedures, custody and control procedures that ensure donor specimen identity and integrity, testing facility, initial and confirmatory test cutoff concentrations, analytical testing methods, result review and reporting, evaluation of alternative medical explanations for presence of drug or metabolite in the donor's specimen, and laboratory certification issues. Voluntary pilot performance testing (PT) programs for each specimen type are on-going since April 2000 to determine how to prepare PT materials for specimens other than urine to evaluate laboratories' ability to routinely achieve accuracy and precision required. Certification programs will be developed using the current urine drug testing National Laboratory Certification Program model. The addition of accurate and reliable workplace drug testing using hair, oral fluid, and sweat patch specimens will complement urine drug testing, and aid in combating industries devoted to suborning drug testing through adulteration, substitution, and dilution. For example, hair testing may detect chronic drug use for up to 90 days and be useful in pre-employment situations; oral fluid testing may detect drug use in past hours and be useful in post-accident situations; sweat patch testing may be useful in follow-up drug testing and treatment programs; POCTs and IITFs may be most useful for quickly identifying specimens that are negative for drugs and indicate that the specimen is valid.
美国卫生与公众服务部(HHS)的药物检测标准于1988年发布,并在1994年、1998年和2004年进行了修订。2004年的修订内容包括对联邦雇员尿液样本进行定义、标准化并要求进行样本有效性检测。在另一则通知中,HHS提议为联邦工作场所药物检测计划制定科学和技术指南,以:(1)除尿液样本外,允许对毛发、口腔液和汗液贴片样本进行实验室检测,检测药物包括大麻、可卡因、苯环己哌啶、阿片类药物(重点是海洛因)和苯丙胺类药物[包括亚甲基二氧甲基苯丙胺(摇头丸)、亚甲基二氧乙基苯丙胺(MDEA)、亚甲基二氧苯丙胺(MDA)];(2)允许在采集地点使用现场即时检测(POCT)设备检测尿液和口腔液;(3)允许使用仪器化初始检测(仅筛查)设施[IITF]快速识别阴性样本;(4)增加对采集人员、现场检测人员和医学复查官的培训要求。该提议于2004年4月13日在《联邦公报》上发布,有90天的公众意见征询期。HHS的药物滥用和精神健康服务管理局对这些意见进行了审查,并正在准备最终通知,该通知将定义此类检测的要求,包括:样本采集程序、确保捐赠者样本身份和完整性的保管和控制程序、检测设施、初始和确认检测的截断浓度、分析检测方法、结果审查和报告、对捐赠者样本中药物或代谢物存在的替代医学解释的评估以及实验室认证问题。自2000年4月以来,针对每种样本类型的自愿性试点性能检测(PT)计划一直在进行,以确定如何为尿液以外的样本准备PT材料,以评估实验室常规达到所需准确性和精密度的能力。将使用当前的尿液药物检测国家实验室认证计划模式来制定认证计划。增加使用毛发、口腔液和汗液贴片样本进行准确可靠的工作场所药物检测,将补充尿液药物检测,并有助于打击通过掺假、替代和稀释来唆使药物检测的行业。例如,毛发检测可能检测出长达90天的长期药物使用情况,在入职前情况中很有用;口腔液检测可能检测出过去几小时内的药物使用情况,在事故后情况中很有用;汗液贴片检测在后续药物检测和治疗计划中可能很有用;POCT和IITF对于快速识别药物阴性样本并表明样本有效的作用可能最大。