Test Code 18074 Ammonia
Purpose
Ammonia is elevated in the following conditions: liver disease, urinary tract infection with distention and stasis, Reye syndrome, inborn errors of metabolism including deficiency of enzymes in the urea cycle, HHH syndrome, some normal neonates, total parenteral nutrition, ureterosigmoidostomy, and sodium valproate therapy. Ammonia determination is indicated in neonates with neurological deterioration, subjects with lethargy and/or emesis not explained, and in patients with possible encephalopathy. Ammonia measurements are mainly of use in the diagnosis of urea cycle deficiencies (any neonate with unexplained nausea, vomiting, or neurological deterioration appearing after first feeding), and they play an important part in the detection of Reye syndrome. In Reye syndrome threefold increases in AST, ALT and plasma ammonia are required for diagnosis with/or the diagnostic liver biopsy findings.
Performing Laboratory
Copley Hospital
Methodology
Bichromatic Rate
Specimen Requirements
Specimen Type: Blood (Plasma)
Container/Tube: Light-Green Top
Specimen Volume: Full Tube
Specimen Minimum Volume: 2 mL
Collection Instructions:
1. Label specimen with patient’s full name, date of birth,
date & time of collection, and person collecting.
2. Collect sample on ice and transport to the laboratory immediately.
Reference Values
Normal: 9-30 µmol / L
Stability
Immediately separated plasma is stable for 3 hours at 2 - 8 degrees.
Day(s) Performed
Daily
Available STAT
Analytical Time: 1 Day
Aliases
NH3
Test Classification & CPT Coding
82140