Test Code CENP Centromere Ab, IgG
Additional Codes
Meditech Order: CENTROAB
Panel Order:ENAE
Intended Use
EliA CENP is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to CENP in human serum and plasma (Li-heparin, EDTA) as an aid in the clinical diagnosis of scleroderma (CREST Syndrome) in conjunction with other laboratory and clinical findings. EliA CENP uses the EliA IgG methond on the Phadia 250 instrument.
Performing Lab
Boone Health Laboratory
Collection Method
Venous Collection
Container
Gold Serum Tube
Instructions/Special Handling
None
Preferred Specimen
Gold SST Serum Tube
Red Serum
Acceptable Specimes
- Plasma
- Lithium Heparin
- EDTA
Units
| EliA U/mL |
Reference Ranges
| <7 | Negative |
| >10 | Positive |
| 7-10 | Equivoval (recommend retesting after 8-12 weeks) |
| >240 | >240 EliA U/mL |
Critical Values
N/A
Reasons for Rejection
| Hemolysis | no hemolysis |
| Icterus | |
| Lipemia | no lipemia |
| Other | Contaminated specimen, QNS, Improperly labeled, Improper specimen type |
Specimen Stability
| Ambient (15-25°C) | 8 hours |
| Refrigerated (2-8°C) | 14 days |
| Frozen (-20°C) | 12months (only one freeze thaw cycle) |
Performance Information
| Days/Times Performed | Monday, Wednesday and Friday |
| Expected Turn around Time | 1-3 days |
| Methodology/Method Description | EliA IgG |
CPT Code(s)
83516