PLASMA AMMONIA TESTING

Testing for Hyperammonemia

Why, when, and how to test

Any unexplained change in consciousness, encephalopathy, or other neurological symptoms should prompt consideration of a plasma ammonia test.

This is important at any age, particularly in neonates whose clinical history does not match the severity of illness or whose illness remains unexplained.

CLINICAL PRIORITY

Acute hyperammonemia can be life threatening.

Prompt plasma ammonia testing is critical when symptoms cannot otherwise be explained.

DIFFERENT SYMPTOMS.
SAME TEST.
CHECK AMMONIA.

When Should Ammonia Be Checked?

Hyperammonemia may present in different ways across the lifespan. Unexplained neurological or behavioral changes should raise consideration of ammonia testing.

01

Altered Consciousness

Unexplained changes in alertness, responsiveness, or consciousness.

02

Encephalopathy

Acute or unexplained neurological deterioration or altered mental status.

03

Neurological Symptoms

Neurological symptoms that are unexplained or do not fit the expected clinical picture.

04

Unexplained Neonatal Illness

Especially when the clinical history does not match the severity of illness.

Proper Collection and Handling Matter

Problems with sampling, transport, and analysis can contribute to inaccurate results, including false positive plasma ammonia levels. Follow proper procedures when obtaining the sample.

1

Alert the Laboratory

Notify the laboratory of the incoming STAT ammonia order before the sample arrives.

STAT
2

Collect a Free Flowing Sample

Prepare to collect a free flowing venous or arterial blood sample. Do not use a tourniquet and keep the patient’s arm as relaxed as possible.

BLOOD DRAW
3

Use the Correct Specimen Tube

Collect the sample in a specimen tube, preferably prechilled, containing either lithium heparin or EDTA as an anticoagulant.

HEPARIN OR EDTA
4

Transport and Analyze Immediately

Place the sample on ice. Order the sample to be handled STAT, transported to the laboratory, separated within 15 minutes of the draw, and analyzed immediately.

ON ICE
!
DO NOT WAIT FOR RESULTS

Call a Metabolic Geneticist

Call a metabolic geneticist immediately to evaluate signs or symptoms that may suggest an inborn error of metabolism.

Individual inborn errors of metabolism are rare, but collectively these disorders are common.

EXPECTED LAB TURNAROUND < 1 hour

Do not wait for test results to call a metabolic geneticist.

Testing for Hyperammonemia The Essentials

Testing for Hyperammonemia: The Essentials

This downloadable brochure is designed for laboratory technicians, nurses, and other allied healthcare professionals.

It provides information about blood draw procedures, analysis of plasma ammonia results, and additional testing that may help differentiate among causes of hyperammonemia.

Download The Essentials PDF

Age Dependent Ammonia Reference Levels

Normal age dependent blood ammonia reference levels currently displayed on CheckAmmonia.com are shown below.

Premature Neonates
< 150
μmol/L
Term Neonates
< 100
μmol/L
Infants
< 40
μmol/L
Adults
11–32
μmol/L
Important: Individual laboratory reference levels may vary.
CHECK AMMONIA

When symptoms do not make sense, Check Ammonia.

Explore additional clinical and awareness resources in the Check Ammonia Toolkit.