| FTA Drug
and Alcohol Regulation Updates Issue 16, page 2 |
FOR YOUR INFORMATION |
| Where To
Find?.....
49 CFR Part 653 ,
Prevention of Prohibited The information
presented on this page should be used to update Chapter 5 of the Implementation
Guidelines. |
Adulterant Use Up Quest Diagnostics, Inc. semi-annual Drug Testing Index (DTI) revealed a significant increase in adulteration rates over the last two years. The DTI reported that the adulteration rate for 1998 was 0.63 percent of the positive tests analyzed by Quest laboratories compared to 2.6 percent in 1999. The survey is based on over six million drug tests performed in 1999. Of the 650,000 federally mandated tests for safety-sensitive workers, 1998 test results revealed a 0.32 percent adulteration rate compared to a 4.06 percent in 1999. The adulterant testing process includes analyses for oxidizers such as bleach, nitrites and chromates (including pyridinium chlorochromate), interfering substances such as gluteraldehyde and acids, bases, and soaps. Substituted samples with low specific gravity and creatinine levels were also reported. Federally mandated testing agencies experienced a 3.2 percent positive rate for all testing categories compared to 4.6 percent for the Combined U.S. Workforce (Federal Safety-Sensitive and General Workforce). Of the federally mandated positive tests, 3.1 percent were adulterated by oxidizing agents, while 0.96 percent were substituted. Of the Combined U.S. Workforce, only 1.7 percent were adulterated and 0.81 percent were substituted. From this data it can be concluded that even though individuals in a federally mandated testing program are less likely to test positive, those that do are nearly twice as likely to adulterate or substitute a sample as those in the General Workforce. Last Seminar of the Year FTA will sponsor its last of four drug and alcohol regulatory seminars scheduled this year on October 31 - November 1, in Atlanta. The seminar will present the regulatory requirements, current interpretations, and other information necessary to facilitate grantees' self-assessment and compliance with the regulations. For further information or to register for the seminars, contact Jennifer Whalley of the Volpe Center National Transportation System Center at (617) 494-2686, or e-mail at Whalley@volpe.dot.gov. Federal Register Access The
U.S. Government Printing Office (USGPO) maintains an internet repository
of Response To Rx/OTC Drug Initiative Transit
systems have begun to develop new or enhance existing prescription and
over-the-counter (OTC) medication policies in response to the Dear
Colleague Letter sent to all grantees in May by Nuria Fernandez, Acting
Administrator of FTA. The programs are taking on different
characteristics depending on the unique nature of each system, but some
commonalities are beginning to emerge. Common Prescription/OTC
program components include the following: |