Amikacin Trough

Test Code
AMIKT


Alias/See Also
AMK, Amikin trough


Preferred Specimen
1.0 mL serum (0.5 mL minimum)


Instructions
Collect immediately prior to the next dose (within 30 minutes). Verify that the next dose has not yet been given. Deliver to the laboratory promptly.


Transport Container
No additive (red-top). SST also acceptable


Specimen Stability
Room temperature: 7 days, Refrigerated: 7 days, Frozen: 7 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Gross hemolysis


Limitations
Patient samples which contain kanamycin will cause significant elevation of amikacin results.


Reference Range
4.0 - 8.0 ug/mL


Clinical Significance
Monitoring Amikacin concentrations in serum is the most effective means of ensuring adequate therapy. Amikacin concentration in serum correlates better with antibacterial activity than does dosage. A standard dose of amikacin does not always yield a predictable serum level because the drug’s concentration also depends on the patient’s volume of distribution and on drug elimination. These factors are influenced by the mode of administration, the volume of extracellular fluid, renal function, and physiological changes during therapy. Patients with impaired renal function, dialysis patients, burn patients, and neonatal or elderly patients should be monitored closely. Exposure to high concentrations for a prolonged period may cause renal impairment or ototoxicity.




The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.