Sickle Cell Anemia DNA, Fetus Sickle DNA

Synonyms

Allscripts (AEHR) Order Name

Not Orderable

Sunrise Clinical Manager (SCM) Order Name

Sickle Cell Anemia DNA, Fetus

EPIC Order Name

Prenatal Sickle Cell Anemia Targeted Mutation Analysis

Clinical Info

Direct detection of hemoglobin A, S, and C. This test is most useful for prenatal diagnosis of an at-risk fetus. This test can also be used for diagnosis of a symptomatic patient or carrier testing for a healthy adult.

Specimen Type

Specimen Volume

Container

Sterile

Collection Instructions

Container/Tube:  Sterile leak-proof container
Specimen:
20 mL amniotic fluid collected in sterile transport tube, or
 30 mg direct chorionic villi, or
 20 mL amniotic fluid collected in each of two T-25 flasks, or
 20 mL cultured cells collected in each of two T-25 flasks
   Minimum Volume
10 mL amniotic fluid • 15 mg chorionic villi • 10 mL cultured cells
Transport Temperature: Room Temperature
Stability: Room temperature: 48 hours                 Refrigerated: Unacceptable                 Frozen: Unacceptable   
Collection Instructions
Amniotic fluid: Collect 10-20 cc of amniotic fluid in a sterile plastic container.
 
Chorionic Villus Sample (CVS): Collect 15-30 mg of chorionic villi in a sterile container. Add 2-3 mL of sterile saline or tissue culture medium.
 
Cultured Cells: Ship two 100% confluent T-25 flasks filled with growth media. Ship at room temperature. Do not refrigerate or freeze. Call lab for additional requirements for prenatal testing. Indicate source of cells: Amniotic Fluid (AF) or Chorionic Villus Sample (CVS).
 Please send  Maternal Cell Contamination Study, with this test. A separate tube of maternal blood (EDTA) must be drawn in order to rule out maternal contamination of the fetal sample       

Transport Instructions

Room Temperature

Specimen Stability

Room temperature: 48 hours                 Refrigerated: Unacceptable                 Frozen: Unacceptable   
Collection Instructions
Amniotic fluid: Collect 10-20 cc of amniotic fluid in a sterile plastic container.
 
Chorionic Villus Sam

Methodology

Polymerase Chain Reaction (PCR)
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Days Performed

Performing Laboratory

Quest Diagnostics' Nichols Institute, Inc. - Chantilly

CPT

81361
88235
 
LOINC Code: 21689-5

PDM

1759576

Result Interpretation

Forms