Printable Test Catalog - OU Medicine

METHODOLOGY: Polymerase Chain Reaction (PCR)
CPT: 83891; 83894; 83898 x 10; 83904 x 10; 83912
[CFMUT] CYSTIC FIBROSIS MUTATION SCRN
SPECIMEN REQUIRED: Whole blood at room temperature
TUBE OR CONTAINER: Lavender (EDTA)
SPECIMEN VOLUME: 5 mL
MINIMUM VOLUME: 3 mL (adults)
1 mL (pediatrics)
TEST AVAILABILITY: Monday-Friday
TURNAROUND TIME: 7-10 days
REFERENCE RANGE: By report
METHODOLOGY: Polymerase Chain Reaction (PCR)
CPT: 83891; 83894; 83900, 83901 x 3; 83912
[CFPCR] CYSTIC FIBROSIS EXTENDED
SPECIMEN REQUIRED: Whole blood at room temperature or buccal
swab
TUBE OR CONTAINER: Lavender (EDTA), Yellow (ACD) or Buccal swab
SPECIAL HANDLING: A completed Cystic Fibrosis Screening
Questionnaire must accompany specimens
SPECIMEN VOLUME: 7 mL whole blood or buccal swab kit
MINIMUM VOLUME: 3 mL whole blood or two buccal swabs
TEST INCLUDES: Detection of 70 CF mutations
TEST AVAILABILITY: Daily
TURNAROUND TIME: 8-10 days
METHODOLOGY: Polymerase Chain Reaction (PCR)
CLINICAL USE: Expanded mutation panel of 70 mutations for CF
for diagnostic testing and for testing in those
persons whose family history or ethnicity require
testing for less common mutations
CPT: 83891; 83900; 83901 x 68; 83892 x 2; 83914 x 70; 83912
[CGD] CHRONIC GRANULOMATOUS DISEASE
SPECIMEN REQUIRED: Whole blood, buccal swab, amniotic fluid
or CVS at room temperature
TUBE OR CONTAINER: Lavender (EDTA), swab or T-25 flasks
SPECIMEN VOLUME: 5 mL or 2 T-25 flasks
MINIMUM VOLUME: 1 mL or 1 T-25 flasks
TURNAROUND TIME: 2-6 weeks
METHODOLOGY: Polymerase Chain Reaction (PCR)
CPT: 83891 x 2; 83892; 83894 x 4; 83898 x 2; 83904 x 2; 83912
[CH] CONGENITAL HYPERINSULINISM
SPECIMEN REQUIRED: Whole blood at room temperature
TUBE OR CONTAINER: Lavender (EDTA) or Yellow (ACD)
SPECIAL HANDLING: Blood samples should be submitted for proband
and both parents whenever possible
Specimen must arrive in laboratory by 1:30 pm
Monday through Thursday only