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Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

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66 II. ASSESSMENT OF ADDICTIONINTERPRETATIONIn an ideal world, testing biological samples should lead to definitive answers.However, test results sometimes lead to more questions than answers. Adeptinterpretation <strong>of</strong> results will lead to improv<strong>ed</strong> clinical care or to more surety inconsultative cases. Interpretation depends on awareness <strong>of</strong> which test was us<strong>ed</strong>and its meaning to the situation.In most settings, the primary purpose <strong>of</strong> drug testing is to identify individualswho are using illegal or illicit drugs. Falsely accusing someone <strong>of</strong> using drugsis highly problematic and undermines the testing program. Similarly, not beingable to identify active drug users because <strong>of</strong> false-negative results renders a program<strong>of</strong> limit<strong>ed</strong> value. It does not deter use or identify users. This is so both forthe emergency room physician wondering if the agitat<strong>ed</strong> patient us<strong>ed</strong> PCP, andfor the consultant to the local college track team. For these situations, highlysensitive qualitative screening tests should be employ<strong>ed</strong>, even if this leads tosome false-positive results. On the other hand, definitive tests should have thehighest level <strong>of</strong> specificity: They should exclude as many true negatives as possible.For nonusers who are subject<strong>ed</strong> to drug testing, issues relat<strong>ed</strong> to falsepositiveresults are <strong>of</strong> great concern. Questions addressing which foods, prescrib<strong>ed</strong>m<strong>ed</strong>ications, dietary supplements, or potentially secondhand marijuanasmoke could result in a positive test are common, and some laboratories haverespond<strong>ed</strong> by raising the level requir<strong>ed</strong> in order to render a positive test result.With the proliferation <strong>of</strong> private laboratories and commercially manufactur<strong>ed</strong>kits, there has grown to be some interlaboratory variation in standardsand thresholds for results. The industry even has its own trade organization, theDrug and Alcohol Testing Industry Association (DATIA). The major concernin drug testing occurs with the reporting <strong>of</strong> laboratory results. Unlike NationalInstitute on Drug Abuse (NIDA)–certifi<strong>ed</strong> testing <strong>of</strong> the Standard Drug Panel(see Table 4.2), clinical drug testing for drugs <strong>of</strong> abuse currently has no standardtechnical criteria, no standard screening cut<strong>of</strong>fs for positive tests, no confirmationcut<strong>of</strong>fs, no chain-<strong>of</strong>-custody requirements, no blind pr<strong>of</strong>iciency submissionrequirements, and no certification programs. As a result, a sample testing posi-TABLE 4.2. “NIDA 5” or the DOT StandardDrug Panel 1990DrugCut<strong>of</strong>fs (ng/ml)Cocaine 300/150Cannabinoids 50/15PCP 25/25Opiates 2,000/2,000Amphetamines 1,000/500

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