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Dihydropyrimidine Dehydrogenase (DPYD)
Test Code13603
CPT Codes
81232
Physician Attestation of Informed Consent
This genetic test requires provider confirmation that patient informed consent has been received if the ordering provider is located in AK, AZ, DE, FL, GA, IA, MA, MN, MT, NV, NH, NJ, NY, OR, SC, SD, or VT or testing is performed in MA.
Preferred Specimen
3 mL whole blood collected in an EDTA (lavender-top) tube, K2 EDTA (pink-top) tube, or ACD (yellow-top) tube
Minimum Volume
1 mL
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Room temperature: 72 hours
Refrigerated: 7 days
Frozen: 30 days
Refrigerated: 7 days
Frozen: 30 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Plasma • Serum • Heparinized specimens • Frozen specimens in glass collection tubes
Methodology
Polymerase Chain Reaction/Fluorescence Monitoring
FDA Status
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.
Setup Schedule
Set up: Varies; Report available: 5-10 days
Clinical Significance
Predicts risk of dose-related toxicity to 5-FU therapy.

