Carnitine, Free and Total (Includes Carnitine, Esterified)

Abbrev Code:CARN   
Order Code:LAB3357Order Name:Carnitine Free and Total
Methodology:Tandem mass spectrometry
CPT Codes: 82379 x1
Test Includes:Total carnitine, free carnitine, L. Carnitine free and total, and esterified (acyl) carnitine (calculation).
Turnaround Time:Specimens are sent to reference laboratory Mon-Sat; results are reported in 1-4 days.

For tests developed and validated by ARUP (previously referred to as Compliance Statement B, C or D). This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the U.S. Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Collection Instructions

Optimal Volume:1 mL
Minimum\Peds Volume:0.6 mL
Container:Green (sodium heparin, no gel) on ICE
Alternate Containers: Green (lithium heparin) on ICE, Red (no gel) on ICE
Causes for Rejection:Room temperature specimens. Refrigerated specimens greater than 12 hours old. Avoid hemolysis.

Processing and Shipping

Specimen Processing:Separate plasma from cells ASAP or within 2 hours of collection. Centrifuge and aliquot 0.5 mL, 0.2 mL minimum and freeze immediately.
Note: Storage at room temperature is unacceptable. Sample must be maintained at refrigerated temperature (up to 12 hours) or frozen (preferred).
Shipping Instructions:Ship on dry ice. CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.
Stability:12 hours refrigerated; 1 month frozen.
Test Performed at or Referral Lab Lab Sendouts  (ARUP)
Referral Lab number:80068


Reference Range:
Age Free
1-31 d 15-55 21-83 4-29 0.2-0.8
32 d - 12 mo 29-61 38-73 7-24 0.1-0.8
13 mo - 6 yr 25-55 35-90 4-36 0.1-0.8
7-20 yr 22-63 31-78 3-38 0.1-0.9
21 yr or older 25-60 34-86 5-29 0.1-1.0
 Acylcarnitine Quantitative Profile: Reports include age appropriate reference intervals and interpretation.
Use:Carnitine deficiency has been suggested as the primary cause of human lipid storage myopathy, including Carnitine deficiency (type 1 lipid storage myopathy), Carnitine-palmitoyltransferase (CPT) deficiency, and Pyruvate-decarboxylase deficiency. Deficiencies have also been reported in premature infants and in patients with cirrhosis, renal failure, and long-term nutritional therapy (TPN). Serum carnitine levels increase during attacks of myoglobinuria.

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