Normal Blood Ammonia Levels
Normal blood ammonia concentrations are ≤35 μmol/L (≤60 μg/dL) in adults. 1
Age-Specific Normal Ranges
- For neonates aged 1-7 days: ≤110 μmol/L (≤154 μg/dL) 2
- For infants aged 8-14 days: <90 μmol/L (≤126 μg/dL) 2
- For individuals aged 15 days to adulthood: 16-53 μmol/L (22-74 μg/dL) 2
Clinical Significance of Ammonia Levels
- Hyperammonemia is defined as:
- Levels >200 μmol/L (341 μg/dL) are associated with poor neurological outcomes 1, 3
- Severe hyperammonemia (>400 μmol/L or 681 μg/dL) may require kidney replacement therapy in pediatric patients 2
Proper Sample Collection and Handling
Accurate ammonia measurement requires proper sample collection and handling:
- Collect blood from a free-flowing venous or arterial sample 2, 4
- Use lithium heparin or EDTA tubes 2
- Transport sample on ice immediately to the laboratory 2
- Process within 15 minutes of collection and analyze immediately 2, 4
- Collect from fasting patients when possible 2
- Avoid venous stasis (tourniquet, fist clenching) 2
- Clean skin thoroughly before collection 2
- Fill tube completely, secure lid, and homogenize by inversion 2
Common Pitfalls in Ammonia Measurement
- Sample hemolysis can falsely elevate results 2
- Delayed processing leads to falsely elevated levels 2, 4
- High lipemia and jaundice can interfere with measurement 2
- High-protein diet, smoking, exercise, and certain drugs can affect levels 2
- If delayed measurement is necessary, centrifuge at +4°C and freeze the supernatant at −70/−80°C 2
Clinical Context
- Ammonia levels alone should not be used to confirm hepatic encephalopathy, as levels may be elevated in cirrhotic patients without encephalopathy 2
- However, a normal ammonia value casts doubt on the diagnosis of hepatic encephalopathy 2
- Ammonia levels correlate with the severity/grade of hepatic encephalopathy and prognosis 2
- Elevated ammonia levels >100 μmol/L with family history of liver disease, neurological disorders, or severe neurological impairment should prompt investigation for inherited metabolic disorders 2