Test Catalog

Test Id : ABIDR

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Antibody Identification, Blood and Serum

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Overview

Test Catalog

Useful For
Suggests clinical disorders or settings where the test may be helpful

Assessing positive pretransfusion antibody screens, transfusion reactions, hemolytic disease of the newborn, and autoimmune hemolytic anemias

 

This test is not useful for monitoring the efficacy of Rh-immune globulin administration.

 

This test is not useful for identifying antibodies detected only at 4 degrees C or only after extended room temperature incubation.

Reflex Tests
Lists tests that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial tests.

Test Id Reporting Name Available Separately Always Performed
DCTR Direct Antiglobulin Test (Poly) Yes No
SPAGR Special Red Cell Ag Typing Yes No
ABIDR Antibody Identification, RBC Yes No
DC3TR Direct Antiglobulin Test (C3) No No
DIGTR Direct Antiglobulin Test (IgG) No No
DATR Direct Antiglobulin Tst (Poly) No No
ABTIR Antibody Titer, RBC Yes No
STTX25 Antibody Elution No, (Bill Only) No
STTX31 Antibody Adsorption No, (Bill Only) No
STTX32 Red Cell Antigen Typing No, (Bill Only) No

Additional Tests
Lists tests that are always performed, at an additional charge, with the initial tests.

Test Id Reporting Name Available Separately Always Performed
STTX26 Antibody Panel No, (Bill Only) Yes

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

The following tests may be ordered and performed as needed for antibody identification: direct antiglobulin testing (polyspecific), including its reflex tests and special red cell antigen typing. Additional reflex charges will be added as needed for antibody elution, antibody adsorption, antibody panels, and special red cell antigen typings.

 

If certain antibodies are detected and the patient is known to be pregnant, an antibody titration will be performed at an additional charge.

Method Name
A short description of the method used to perform the test

Hemagglutination

NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test

Antibody Identification, RBC

Aliases
Lists additional common names for a test, as an aid in searching

ABIDR

Antibody Identification, RBC

Antibody Workup

Red Cell Antibody Identification

Antibody Panel

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

The following tests may be ordered and performed as needed for antibody identification: direct antiglobulin testing (polyspecific), including its reflex tests and special red cell antigen typing. Additional reflex charges will be added as needed for antibody elution, antibody adsorption, antibody panels, and special red cell antigen typings.

 

If certain antibodies are detected and the patient is known to be pregnant, an antibody titration will be performed at an additional charge.

Specimen Type
Describes the specimen type validated for testing

Varies

Shipping Instructions

Specimen must arrive within 72 hours of collection.

Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Both blood and serum are required.

 

Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

 

Specimen Type: Plasma/Blood

Collection Container/Tube: 6-mL Pink-top (EDTA)

Submission Container/Tube: Plastic vial

Specimen Volume:

3 mL of plasma

3 mL of red blood cells (RBC)

Collection Instructions:

1. Centrifuge and aliquot plasma into plastic vial.

2. Label specimen as EDTA plasma or EDTA RBC, as appropriate.

3. Send both tubes.

 

Specimen Type: Serum/Blood

Collection Container/Tube: 10-mL Red top

Submission Container/Tube: Plastic vial

Specimen Volume:

5 mL of serum

5 mL of RBC

Collection Instructions:

1. Centrifuge and aliquot serum into plastic vial.

2. Label specimen as serum or clotted RBC, as appropriate.

3. Send both tubes.

Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the testing laboratory. The minimum volume is sufficient for one attempt at testing.

Blood: 6 mL in EDTA

Pediatric: 2 mL of serum

Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected

Gross hemolysis OK

Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included

Specimen Type Temperature Time Special Container
Varies Ambient (preferred) 4 days
Refrigerated 4 days

Useful For
Suggests clinical disorders or settings where the test may be helpful

Assessing positive pretransfusion antibody screens, transfusion reactions, hemolytic disease of the newborn, and autoimmune hemolytic anemias

 

This test is not useful for monitoring the efficacy of Rh-immune globulin administration.

 

This test is not useful for identifying antibodies detected only at 4 degrees C or only after extended room temperature incubation.

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

The following tests may be ordered and performed as needed for antibody identification: direct antiglobulin testing (polyspecific), including its reflex tests and special red cell antigen typing. Additional reflex charges will be added as needed for antibody elution, antibody adsorption, antibody panels, and special red cell antigen typings.

 

If certain antibodies are detected and the patient is known to be pregnant, an antibody titration will be performed at an additional charge.

Clinical Information
Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

After exposure to foreign red blood cells (RBC) via transfusion or pregnancy, some people form antibodies that are capable of the destruction of transfused RBC or of fetal RBC in utero. It is important to identify the antibody specificity in order to assess the antibody's capability of causing clinical harm and, if necessary, to avoid the antigen on transfused RBC.

 

Autoantibodies react against the patient's own RBC as well as the majority of cells tested. Autoantibodies can be clinically benign or can hemolyze the patient's own RBC, such as in cold agglutinin disease or autoimmune hemolytic anemia.

Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Negative,

If positive, antibodies will be identified and corresponding special red cell antigen typing on patient’s red blood cells will be performed. 

Interpretation
Provides information to assist in interpretation of the test results

Specificity of alloantibodies will be stated.

 

The patient's red blood cells will be typed for absence of the corresponding antigens or as an aid to identification in complex cases.

 

A consultation service is offered, at no charge, regarding the clinical relevance of red cell antibodies.

Cautions
Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Recent administration of Rh-immune globulin may cause anti-D to be identified and appear falsely as an alloantibody.

Clinical Reference
Recommendations for in-depth reading of a clinical nature

Fung MK, Eder AF, Spitalnik SL, Westhoff CM. Technical Manual. 19th ed. AABB; 2017

Method Description
Describes how the test is performed and provides a method-specific reference

A panel of reagent type O erythrocytes, with known antigenic determinants and the patient's cells are tested with the patient's serum/plasma. This panel should yield a distinct pattern of agglutination or hemolysis that identifies the auto- or alloantibody specificity. Elution, absorption, neutralization, and other special techniques may be necessary to complete antibody identification.(Fung MK, Eder AF, Spitalnik SL, Westhoff CM. Technical Manual. 19th ed. AABB; 2017)

PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information

No

Day(s) Performed
Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.

Monday through Friday, Sunday

Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

1 to 5 days

Specimen Retention Time
Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

14 days

Performing Laboratory Location
Indicates the location of the laboratory that performs the test

Rochester

Fees :
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.

  • Authorized users can sign in to Test Prices for detailed fee information.
  • Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
  • Prospective clients should contact their account representative. For assistance, contact Customer Service.

Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

86870

86860-(if appropriate)

86886-(if appropriate)

86880 x 3 (if appropriate)

86905-(if appropriate)

86978-(if appropriate)

LOINC® Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test Id Test Order Name Order LOINC Value
ABIDR Antibody Identification, RBC 888-8
Result Id Test Result Name Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
ABDR1 Antibody Identification, RBC 888-8

Test Setup Resources

Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | Pdf

Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports