Ammonia, Plasma

0020043
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Example Reports
High
Normal

Ordering Recommendation

Evaluate status of existing liver disease. Monitor treatment in patients with inborn errors of metabolism.

Mnemonic

AMMON

Methodology

Enzymatic

Performed

Sun-Sat

Reported

Within 24 hours

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation
Collect

Green (sodium or lithium heparin). Collect on ice.

Specimen Preparation

Separate plasma from cells and freeze within 15 minutes of draw time. Specimens need to be spun in a refrigerated centrifuge. Transfer 2 mL plasma to an ARUP Standard Transport Tube. (Min: 0.25 mL)

Storage/Transport Temperature

CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.

Unacceptable Conditions

Serum or blood. Non-frozen specimens. Specimens containing oxalate or citrate

Remarks
Stability

After separation from cells: Ambient: Unacceptable; Refrigerated: 2 hours; Frozen: 3 weeks (do not thaw)

Reference Interval

0-14 days: 95 µmol/L or less
15 days-6 years: 68 µmol/L or less
Greater than 6 years: 72 µmol/L or less

Interpretive Data



Compliance Category

FDA

Note

Hotline History

View Hotline History

 

Hotline History

Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
11/18/2019
X
X
N/A

CPT Codes

82140

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Components

Component Test Code* Component Chart Name LOINC
0020043 Ammonia, Plasma 16362-6
* 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

  • NH3
  • Plasma ammonia level
Ammonia, Plasma