Alpha-1-Antitrypsin Quantitation
Label Mnemonic: | A1AT |
Epic code: | LAB927 |
Order form: | Laboratory Requisition |
Supply order: | Supply Order Form |
Billing: | Billing Policies |
CPT code: | 82103 |
Specimen(s):
Plasma
Collection Medium:
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Plasma Separator Tube 4.5 mL |
Alternate Collection Media:
Call laboratory for additional acceptable specimen collection
containers.
Minimum:
3 mL whole blood in light green top tube or ONE Microtainer®
Testing Schedule:
24 hrs/day, 7 days a week, including holidays.
Turn Around Time:
1 hour (upon receipt in laboratory)
Reference Range:
90-200 mg/dL
A1AT is an acute phase reactant, therefore any inflammatory process may result in transient elevations of the patient's A-1-AT level.
A1AT is an acute phase reactant, therefore any inflammatory process may result in transient elevations of the patient's A-1-AT level.
Test Limitations:
Criterion: Recovery within plus or minus 10% of initial values. Icterus: No significant interference up to an I index of 60 (approximate conjugated and unconjugated bilirubin concentration: 60 mg/dL). Hemolysis: No significant interference up to an H index of 1000 (approximate hemoglobin concentration: 1000 mg/dL). Lipemia (Intralipid): No significant interference up to an L index of 350 (approximate triglycerides concentration: 700 mg/dL). There is poor correlation between turbidity and triglycerides concentration. Rheumatoid factors less than 100 IU/mL do not interfere. No high dose hook effect is seen up to an alpha 1-antitrypsin concentration of 1200 mg/dL. Elevated estrogen levels (oral contraceptives; third trimester of pregnancy) give rise to false positive results. CRP and haptoglobin should therefore also be determined.* *Laurell CB, Kullander S, Thorell J. Effect of administration of a combined estrogen-progestin contraceptive on the level of individual plasma proteins. Scand J Lab Invest 1968;21:337-343.
Methodology:
Immunoturbidimetric
Sample Processing:
Centrifuge at a speed and time necessary to get barrier separation
of plasma/serum and cells within 1 hour of collection. Send specimen
in original tube. Do Not transfer to another tube.
Each sample must be labeled with at least TWO full patient identifiers (First/Last Name & DOB are sufficient for non-UIHC affiliated clients) to avoid sample rejection/delays.
Each sample must be labeled with at least TWO full patient identifiers (First/Last Name & DOB are sufficient for non-UIHC affiliated clients) to avoid sample rejection/delays.
Sample Storage:
Refrigerate.
All sample storage requirements are intended for delivery to UIHC within 24 hours of collection for testing. If samples won't arrive in this time period, please call the UIHC Core Lab for alternative storage/shipping instructions (319-356-3527).
All sample storage requirements are intended for delivery to UIHC within 24 hours of collection for testing. If samples won't arrive in this time period, please call the UIHC Core Lab for alternative storage/shipping instructions (319-356-3527).
Transport Instructions:
Place labeled specimen into zip-lock type biohazard bag; seal
bag.
Place completed requisition into outside pocket of bag.
Transport in cooler with refrigerated coolant packs.
Place completed requisition into outside pocket of bag.
Transport in cooler with refrigerated coolant packs.