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Sorted By Test Name - Mayo Medical Laboratories

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DABAR<br />

505335<br />

Urine<br />

Clinical Information: Amphetamines are sympathomimetic amines that stimulate central nervous<br />

system activity and, in part, suppress appetite. Phentermine, amphetamine, and methamphetamine are<br />

prescription drugs for weight loss. All of the other amphetamines are Class I (distribution prohibited)<br />

compounds. In addition to their medical use as anorectic drugs, they are used in the treatment of<br />

narcolepsy and minimal brain dysfunction. Because of their stimulant effects, the drugs are commonly<br />

sold illicitly and abused. Physiological symptoms associated with amphetamine overdose include elevated<br />

blood pressure, dilated pupils, hyperthermia, convulsions and acute psychosis.<br />

Useful For: Confirming drug abuse involving amphetamines such as amphetamine and<br />

methamphetamine, phentermine,, methylenediaoxyethylamphetamine (MDEA), and<br />

methylene-diaoxyethylamphetamine (MDA, a metabolite of MDMA and MDEA)<br />

Interpretation: The presence of amphetamines in urine concentrations >499 ng/mL is a strong<br />

indicator that the patient has used 1 of these drugs within the past 3 days. This test is very specific and<br />

does not produce a false-positive result when over-the-counter drugs are present in the specimen. This test<br />

will produce true-positive results for urine specimens collected from patients who are administered<br />

Adderall and Benzedrine (which contain amphetamine); Desoxyn and Vicks Inhaler (which contain<br />

methamphetamine); Selegiline (metabolizes to methamphetamine and amphetamine); and clobenzorex,<br />

famprofazone, fenethylline, fenproporex, and mefenorex (which are amphetamine pro-drugs).<br />

Reference Values:<br />

Negative<br />

EMIT cutoff concentration: 500 ng/mL<br />

Positives are reported with a quantitative GC/MS result.<br />

Clinical References: Baselt RC, Cravey RH: Disposition of Toxic Drugs and Chemicals in Man.<br />

Third edition. Chicago, Year Book <strong>Medical</strong> Publishers, 1989<br />

Drug of Abuse, Barbiturate Screen with GC-MS Confirmation,<br />

Urine<br />

Clinical Information: Barbiturates constitute a class of central nervous system depressants. They are<br />

classified on their duration of action. The duration of action is approximately 15 minutes for the<br />

short-acting types (eg, secobarbital and pentobarbital), and a day or more for the long-acting types (eg,<br />

phenobarbital). Short-acting barbiturates are usually excreted in the urine as metabolites, while the<br />

long-acting barbiturates appear primarily unchanged. Barbiturates were originally introduced as sleep<br />

inducers. Butalbital also is used to control severe headaches. Mephobarbital and phenobarbital are<br />

frequently used to control major motor (grand mal) seizures. These drugs are commonly abused as<br />

"downers" to induce sleep after an amphetamine- or cocaine-induced "high".<br />

Useful For: Screening and confirming drug abuse involving barbiturates such as amobarbital,<br />

butalbital, pentobarbital, phenobarbital, and secobarbital.<br />

Interpretation: The presence of barbiturate in urine at >300 ng/mL indicates use of one of these drugs.<br />

Most barbiturates are fast acting; their presence indicates use within the past 3 days. Phenobarbital,<br />

commonly used to control epilepsy, has a very long half-life. The presence of phenobarbital in urine<br />

indicates that the patient has used the drug sometime within the past 30 days.<br />

Reference Values:<br />

Negative<br />

Positives are reported with a quantitative GC-MS result.<br />

EMIT cutoff concentration: 200 ng/mL<br />

Clinical References: Baselt RC, Cravey RH: Disposition of Toxic Drugs and Chemicals In Man. 3rd<br />

edition. Chicago, IL Year Book <strong>Medical</strong> Publishers, 1989<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 634

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