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Test Code C5DCU C5-DC Acylcarnitine, Quantitative, Random, Urine

Important Note

CMH Cerner Order: Ref Misc


Ordering Guidance


This second-tier test is used specifically to evaluate a newborn screening elevation of glutarylcarnitine and must not be ordered with either C4U / C4 Acylcarnitine, Quantitative, Random, Urine or C5OHU / C5-OH Acylcarnitine, Quantitative, Random, Urine.

 

For general screening for metabolic disorders, see OAU / Organic Acids Screen, Random, Urine; ACRN / Acylcarnitines, Quantitative, Plasma; and AAQP / Amino Acids, Quantitative, Plasma.



Necessary Information


Include patient's age, family history, clinical condition (asymptomatic or acute episode), diet, and drug therapy information.

Specimen Required


Patient Preparation: If clinically feasible, discontinue L-carnitine supplementation at least 72 hours before specimen collection.

Supplies: Urine Tubes, 10 mL (T068)

Collection Container/Tube: Clean, plastic urine collection container

Submission Container/Tube: Plastic, 10-mL urine tube

Specimen Volume: 5 mL

Collection Instructions:

1. Collect a random urine specimen.

2. Freeze specimen immediately.


Specimen Minimum Volume

1 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Urine Frozen (preferred) 7 days
  Refrigerated  24 hours
Children's Mercy Hospital Note:

CMH COLLECTION: 1mL urine in sterile cup

Useful For

Evaluation of patients with an abnormal newborn screen showing elevations of glutarylcarnitine

 

Diagnosis of glutaric aciduria type 1 deficiency

Reject Due To

  All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Day(s) Performed

Monday, Wednesday, Friday

Report Available

2 to 5 days

Reporting Name

C5-DC Acylcarnitine, QN, U

Reference Values

<1.54 millimoles/mole creatinine

Method Name

Flow Injection Analysis-Tandem Mass Spectrometry (FIA-MS/MS)

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

82017