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Test Code LIDOC Lidocaine, Serum

Reporting Name

Lidocaine, S

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Useful For

Assessing optimal lidocaine dosing during the acute management of ventricular arrhythmias following myocardial infarction or during cardiac manipulation such as surgery

 

Assessing potential lidocaine toxicity


Specimen Required


Supplies: Sarstedt Aliquot Tube 5 mL (T914)

Collection Container/Tube: Red top (serum gel/SST are not acceptable)

Submission Container/Tube: Plastic vial

Specimen Volume: 0.5 mL Serum

Collection Instructions: Within 2 hours of collection, centrifuge and aliquot serum into a plastic vial.


Specimen Minimum Volume

Serum: 0.25 mL

Specimen Type

Serum Red

Specimen Stability Information

Specimen Type Temperature Time
Serum Red Refrigerated (preferred) 14 days
  Ambient  14 days
  Frozen  14 days

Day(s) Performed

Monday through Saturday

Reference Values

Therapeutic: 1.5-5.0 mcg/mL

Critical value: >6.0 mcg/mL

Method Name

Enzyme-Multiplied Immunoassay Technique (EMIT)

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

80176

LOINC Code Information

Test ID Test Order Name Order LOINC Value
LID Lidocaine, S 3714-3

 

Result ID Test Result Name Result LOINC Value
8382 Lidocaine, S 3714-3

Forms

If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:

-Cardiovascular Test Request (T724)

-Therapeutics Test Request (T831)

Report Available

Same day/1 to 2 days