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Ammonia Level

Immunology & Autoimmune

Blood ammoniaNH3Plasma ammonia

Review status

Currently under review

Pending specialist review and validation.

What it shows

An ammonia level measures the amount of ammonia circulating in your blood. Ammonia is a natural byproduct formed when your body breaks down protein. A healthy liver converts ammonia into urea, which is then removed by the kidneys. When the liver cannot process ammonia efficiently, it can build up in the bloodstream.

This test is usually performed on a plasma sample taken from a vein. Because the result can be affected by how the specimen is handled, the sample is typically kept cold and processed quickly. Your care team interprets this test alongside your symptoms and other labs that assess liver function and overall metabolism.

Why it matters

Ammonia can affect how the brain works. When levels rise, people may experience confusion, sleepiness, irritability, or behavior changes. Clinicians often order this test when there are signs of liver problems, concern for hepatic encephalopathy, or when a newborn or child may have an inborn issue with processing nitrogen waste known as a urea cycle disorder.

Ammonia testing can also help guide care during flares of chronic liver disease, in unexplained vomiting or altered mental status, and when certain medicines might be contributing to symptoms. Knowing your level helps your team decide on next steps, which may include treating the underlying cause, adjusting medications, providing nutrition support, or repeating the test if collection issues are suspected.

Understanding your results

Your result is interpreted with your age, symptoms, physical exam, and other tests such as liver function panels and acid base measures. Because collection and handling can influence ammonia, an unexpected result is sometimes repeated to confirm it before making decisions.

If your level is higher than expected, your clinician may look for causes such as liver injury, a urea cycle disorder, bleeding into the gut, infection, dehydration, or medication effects. If your level appears appropriate for your situation, your symptoms may be due to other conditions. Your care team will discuss whether additional testing or treatment is needed and how urgently to act based on your overall clinical picture.

Reference ranges

080 umol/L
All sexes
0 days – 1 month
055 umol/L
All sexes
1 month – 18 years
950 umol/L
All sexes
18 years – 150 years

Reference intervals vary by laboratory, analyzer, methodology, population, and units. The ranges shown here are for education only. Always interpret your results against the reference interval printed on your own lab report.

Factors that could impact Ammonia Level

  • Specimen handling and timing

    Delayed processing, warm storage, prolonged tourniquet time, or vigorous fist clenching can falsely raise ammonia. Samples are best kept cold and processed quickly to reduce false elevations.

  • Medications and substances

    Valproate, salicylates, diuretics, chemotherapy agents, alcohol, and some anticonvulsants can increase ammonia. Therapies like lactulose or rifaximin may lower ammonia by reducing gut production.

  • Diet, exercise, and physiologic stress

    Recent strenuous exercise, a high protein meal, prolonged fasting, dehydration, or cigarette smoking can affect ammonia levels. Severe illness, fever, or seizures may also raise levels temporarily.

  • Liver, kidney, and metabolic conditions

    Cirrhosis, acute liver failure, portosystemic shunts, kidney dysfunction, and inherited urea cycle disorders can reduce ammonia clearance and cause elevations.

  • Age and special populations

    Newborns, especially those born early, can have higher values due to immature metabolism. Critically ill patients and those with gastrointestinal bleeding are also at higher risk of elevations.

2026

References

  1. McGill University Health Centre. (2014, September 25). Ammonia Level (Task CD 315910). Laboratory reference ranges.
  2. Vilstrup, H., Amodio, P., Bajaj, J., Cordoba, J., Ferenci, P., Mullen, K. D., Weissenborn, K., & Wong, P. (2014). Hepatic encephalopathy in chronic liver disease: 2014 practice guideline by the American Association for the Study of Liver Diseases and the European Association for the Study of the Liver. Hepatology, 60(2), 715-735. External link
  3. Häberle, J., Burlina, A., Chakrapani, A., Dixon, M., Karall, D., Lindner, M., Mandel, H., Martinelli, D., Pintos-Morell, G., Santer, R., Servais, A., Dionisi-Vici, C., Rubio, V., Walter, J., & the UCDC Consortium. (2019). Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision. Journal of Inherited Metabolic Disease, 42(6), 1192-1230. External link