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Lidocaine, Serum/Plasma

Test ID: LIDOQ S

Test

Aliases/Synonyms

Xylocaine®

Method

Immunoassay

Report Includes

Lidocaine

Specimens

Avoid gel separator tubes; Serum; Plasma (heparin); Plasma (oxalate/fluoride); Plasma (EDTA)

Clinical Utility

Lidocaine direct injection or infusion is used in the emergency treatment of ventricular arrhythmias caused by acute myocardial infarction, open-heart surgery. It is also used for topical anesthesia administered as a gel or by injection. Lidocaine levels are monitored to assure adequate therapeutic levels are achieved and to avoid toxicity.

Test Location

Quest Diagnostics, California USA

Test Version

31-Jan-2023

Specimen

Specimens

Avoid gel separator tubes; Serum; Plasma (heparin); Plasma (oxalate/fluoride); Plasma (EDTA)

Collection Containers

Preferred

Serum (red top)

Acceptable

Plasma (heparin); Plasma (oxalate/fluoride); Plasma (EDTA)

Sample Volume

1.0 mL

Minimum Volume

0.2 mL

Specimen Comment

Avoid gel separator tubes.

Collection & Handling

Collection Instructions

Collect trough specimen within 1 hour prior to next dose.

Handling Information

Store and send frozen.

Stability

Ambient 5 days
Refrigerated 7 days
Frozen 30 days

Rejection Criteria

Other Gel-separator tube

Test Version

31-Jan-2023

Performance / Interpretation

Method

Immunoassay

Turnaround Time

6 days

Results

Name Units Reference Range Conversion Factor
Lidocaine mg/L
  • 1.5 - 5.0

Test Location

Quest Diagnostics, California USA

Test Version

31-Jan-2023

Interface / Setup

HL7 Interface Codes

Order Code Result Codes Units
LIDOQ S 63110LIDOCAINE mg/L

Test Version

31-Jan-2023