Cystic Fibrosis Screen
Main Content
Test Code: 10458
CPT Code: 81220
Alternative Name(s): CF Mutation Screen,Cystic Fibrosis Mutation Screen,CFTR Screen,CF Carrier Screen,CF Screen,Cystic Fibrosis Carrier Screen
Methodology: Multiplex Polymerase Chain Reaction • Massively Parallel Sequencing
Clinical Significance: General screen for carrier status and assessment of CF risk. This test will identify approximately 90% of Cystic Fibrosis (CF) mutations in the Caucasian population, and 97% in the Ashkenazi Jewish population.
Test FAQ: https://education.questdiagnostics.com/faq/cfscreen
Supply: T02 - Lavender 4mL Blood Tube
Preferred Specimen: Whole Blood
Preferred Volume: 4mL
Collection Instructions: Please indicate the ethnicity of the patient.
Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship ambient immediately. Do not freeze. For prenatal diagnosis, please use test code 10226, Cystic Fibrosis DNA Analysis, Fetus.
Transport Container: EDTA Lavender-top 4mL tube
Transport Temperature: Room Temperature
Specimen Stability: Room Temperature: 8 days
Reject Criteria:
Specimens received frozen
For additional test, supply, or collection device information, please contact DLO's Customer Service at (800) 891-2917, option 2.
The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed.
CLIA