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Mayo Test Catalog, (Sorted By Test Name) - Mayo Medical ...

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AFC<br />

80334<br />

AMOBS<br />

8325<br />

correlate with poor clinical response. Thus, therapeutic monitoring to ensure that the blood level is<br />

within the therapeutic window is critical to accomplish successful treatment with this drug. Like<br />

amitriptyline, nortriptyline can cause major cardiac toxicity when the concentration is in excess of 300<br />

ng/mL, characterized by QRS widening leading to ventricular tachycardia and asystole. In some<br />

patients, toxicity may manifest at lower concentrations.<br />

Useful For: Monitoring serum concentration during therapy Evaluating potential toxicity The test may<br />

also be useful to evaluate patient compliance<br />

Interpretation: Most individuals display optimal response to amitriptyline when combined serum<br />

levels of amitriptyline and nortriptyline are between 80 and 200 ng/mL. Risk of toxicity is increased with<br />

combined levels > or =300 ng/mL. Most individuals display optimal response to nortriptyline with serum<br />

levels between 70 and 170 ng/mL. Risk of toxicity is increased with nortriptyline levels > or =300 ng/mL.<br />

Some individuals may respond well outside of these ranges, or may display toxicity within the therapeutic<br />

range, thus interpretation should include clinical evaluation. Therapeutic ranges are based on specimens<br />

drawn at trough (ie, immediately before the next dose).<br />

Reference Values:<br />

AMITRIPTYLINE AND NORTRIPTYLINE<br />

Total therapeutic concentration: 80-200 ng/mL<br />

Total toxic concentration: > or =300 ng/mL<br />

NORTRIPTYLINE ONLY<br />

Therapeutic concentration: 70-170 ng/mL<br />

Toxic concentration: > or =300 ng/mL<br />

Note: Therapeutic ranges are for specimens drawn at trough (ie, immediately before next scheduled<br />

dose). Levels may be elevated in non-trough specimens.<br />

Clinical References: 1. Wille SM, Cooreman SG, Neels HM, Lambert WE: Relevant issues in the<br />

monitoring and the toxicology of antidepressants. Crit Rev Clin Lab Sci 2008;45(1):25-89 2. Thanacoody<br />

HK, Thomas SH: Antidepressant poisoning. Clin Med 2003;3(2):114-118 3. Baumann P, Hiemke C,<br />

Ulrich S, et al: The AGNP-TDM expert group consensus guidelines: therapeutic drug monitoring in<br />

psychiatry. Pharmacopsychiatry 2004;37(6):243-265<br />

Amniotic Fluid Culture for Genetic <strong>Test</strong>ing<br />

Clinical Information: Fetal cells obtained by amniocentesis (amniocytes) are used for a wide range<br />

of laboratory tests. Prior to testing, the cells may need to be cultured to obtain adequate numbers of<br />

amniocytes.<br />

Useful For: Producing amniocyte cultures that can be used for genetic analysis Once confluent flasks<br />

are established, the amniocyte cultures are sent to other laboratories, either within <strong>Mayo</strong> Clinic or to<br />

external sites, based on the specific testing requested.<br />

Reference Values:<br />

Not applicable<br />

Clinical References: Barch MJ, Knutsen T, Spurbeck JL: In The AGT Cytogenetics Laboratory<br />

Manual. 3rd edition, 1997<br />

Amobarbital, Serum<br />

Clinical Information: Amobarbital is an intermediate-acting barbiturate with hypnotic properties<br />

used in short-term treatment of insomnia and to reduce anxiety and provide sedation preoperatively. (1, 2)<br />

Amobarbital is administered by intravenous infusion or intramuscular injection. The duration of its<br />

hypnotic effect is about 6 to 8 hours. The drug distributes throughout the body, with a volume of<br />

distribution of 0.9 to 1.4 L/kg, and about 59% of a dose is bound to plasma proteins. Metabolism takes<br />

place in the liver primarily via hepatic microsomal enzymes. Its half-life is about 15 to 40 hours (mean: 25<br />

Current as of January 3, 2013 2:22 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong>Laboratories.com Page 122

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