Lidocaine

0090155
copy
 

Copy Utility


emailprint
Example Reports
High
In Range

Ordering Recommendation

Optimize drug therapy and monitor patient adherence.

Mnemonic

LIDO

Methodology

Immunoassay

Performed

Sun-Sat

Reported

Within 24 hours

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation

Draw specimens 12 hours after initiating therapy for arrhythmia prophylaxis, then every 24 hours thereafter.

Collect

Plain red. Also acceptable: green (sodium heparin).

Specimen Preparation

Separate serum from cells immediately. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Separator tubes.

Remarks
Stability

After separation from cells: Ambient: 1 week; Refrigerated: 1 week; Frozen: 1 month

Reference Interval

1.2-5.0 µg/mL
Toxic: greater than 9.0 µg/mL

Interpretive Data



Compliance Category

FDA

Note

Hotline History

N/A

CPT Codes

80176

Are you an ARUP Client? Click here for your pricing.

Components

Component Test Code* Component Chart Name LOINC
0090155 Lidocaine, Serum/Plasma 3714-3
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Xylocaine
Lidocaine