ARUP's Laboratory Test Directory
| 0080044: Amino Acids Quantitative, Urine |
| Patient History For Biochemical Genetics |   |   |
| Test Mnemonic: UAA QNT | |
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#ExistMethodology>
Methodology: Ion Exchange Chromatography
*ExistMethodology> #ExistPerformed> Performed: Mon-Fri *ExistPerformed> #ExistReported> Reported: 3-7 days *ExistReported> |
| Specimen Required: | |
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#ExistCollect>
Collect: Random urine. First-morning urine is preferred.
*ExistCollect> #ExistTransport> Transport: 10 mL aliquot from a well-mixed random urine, frozen. (Min: 2 mL) Submit specimen in an ARUP Standard Transport Tube. *ExistTransport> #ExistPedCollectTransport> Pediatric Collection/Transport: 3 mL aliquot from a well-mixed random urine, frozen. *ExistPedCollectTransport> #ExistRemarks> Remarks: CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered. As soon as possible after urine has been obtained, mix the collection well and freeze. Avoid dilute urine when possible. Clinical information is needed for appropriate interpretation. Additional required information includes age, gender, diet (e.g., TPN therapy), drug therapy, and family history. Biochemical Genetics Patient History Form is available on the ARUP Web site or by contacting ARUP Client Services. *ExistRemarks> #ExistStability> Stability: Ambient: Unacceptable; Refrigerated: 24 hours; Frozen: 1 month *ExistStability> |
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#ExistRefRangeTable>
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| Note: | |
| Common indications for urine amino acid testing include clinical situations such as: 1) acute life-threatening episode, 2) failure to thrive, 3) recurrent vomiting, 4) neurological deterioration, 5) hyperammonemia, 6) lethargy, 7) metabolic acidosis, 8) testing or following therapy for a specific inborn error of metabolism (PKU, MSUD, tyrosinemia, etc.), and 9) kidney stones. Listing of clinical information is particularly important for appropriate interpretation. |
| CPT Code(s): | |
| 82139 |