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Organization: | Alberta Precision Laboratories | ||||||||||
Message Alert: | PLEASE NOTE: This Test Directory is in an interim state and due to changes pertaining to the DynaLIFE transition, performing site for routing has not been updated. Please refer to Laboratory Information System for appropriate routing. | ||||||||||
Test Name/Synonym: | Direct Antiglobulin Test (DAT, Direct Coombs) | ||||||||||
Clinical Indications: | The DAT is useful in the diagnosis of autoimmune hemolytic anemia (AIHA), hemolytic disease of the newborn (HDN), red blood cell sensitization caused by drugs, and Investigation of transfusion reactions. For suspected transfusion reactions, see Transfusion Reaction Investigation | ||||||||||
Test Includes: | Patients greater than or equal to 4 months: Polyspecific and/or monospecific direct antiglobulin test (anti-human globulin and anti-complement testing). If polyspecific test is positive, monospecific testing with anti-IgG and anti-complement reagents is performed. Neonates (less than 4 months): Monospecific anti-IgG testing only | ||||||||||
Collection Alert: | Avoid hemolysis | ||||||||||
LABID (Connect Care): | LAB41779 | ||||||||||
Test Code: |
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Specimen Type: | Blood | ||||||||||
Specimen Source: | Venous, Arterial, Capillary | ||||||||||
Primary Container: | Lavender Top - EDTA | ||||||||||
Alternate Containers: |
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Minimum Collection Volume: | 1 mL 250 μL (Microcollection – neonates only) | ||||||||||
Specimen Collection Requirements: | For specimen collection and testing for DAT on cord blood, see Neonatal Evaluation (Cord) For specimen collection and testing for suspected transfusion reactions, see Transfusion Reaction Investigation | ||||||||||
Stability and Storage: | Refrigerated 1-60C and retain a minimum of 7 days | ||||||||||
Processing: | Do not centrifuge | ||||||||||
Method and Interpretation of Results: | A positive DAT result may indicate autoimmune hemolytic anemia, hemolytic transfusion reaction, hemolytic disease of the newborn or drug interactions. Clinical correlation and consultation is recommended if the patient’s clinical condition is suggestive of hemolysis. Patients with a positive DAT require serological crossmatch regardless of antibody screen result. | ||||||||||
Routine Turn Around Time: | Stat – performed within 90 minutes for ED patients, or 120 minutes for hospital patients if ordered at a testing site and required for transfusion. | ||||||||||
Testing Schedule: | Daily | ||||||||||
Reference Interval: | Negative | ||||||||||
Testing Area: | Transfusion Medicine | ||||||||||
Performing Site: |
*polyspecific testing only. Monospecific referred out | ||||||||||
Last Updated On: | Tuesday, August 11, 2020 |