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Test ID: FA1AG
Alpha-1 Acid Glycoprotein, NEPH

Secondary ID A test code used for billing and in test definitions created prior to November 2011

90464

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

Yes

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

Nephelometry

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Alpha-1 Acid Glycoprotein, Neph

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

AIAG FORWARD
Alpha-1 Acid Glycoprotein, NEPH FORWARD
IAP, Serum FORWARD
Immunosuppressive Acidic Protein (IAP) FORWARD

Specimen Type Describes the specimen type needed for testing

Serum

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

Draw blood in a plain, red-top tube(s). (Serum gel tube is

acceptable.) Spin down and send 0.5 mL of serum refrigerated.

Specimen Minimum Volume Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.

0.2 mL

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

Specimens other than

Serum

Anticoagulants other than

NA

Hemolysis

NA

Thawing

NA

Lipemia

NA

Icteric

NA

 

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
SerumRefrigerated (preferred)
 Ambient 4 days
 Frozen 

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.

Reference Range:  36-126 mg/dL

 

Interpretive Criteria:

< 36 mg/dL  Decreased level

36-126 mg/dL  Normal level

> 126  Increased level

 

Decreased serum levels of alpha-1-acid glycoprotein may be found

in association with malnutrition, severe liver damage, and in women

using estrogen-related oral contraceptives. Increased serum levels

have been reported in conditions of acute and chronic inflammation,

including myocardial infarction, rheumatoid arthritis, systemic lupus

erythematosus, and malignancy.  Except for a difference in sialic acid

content, alpha-1-acid glycoprotein is identical to immunosuppressive

acidic protein (IAP).

 

Test Performed by

Focus Diagnostics

5785 Corporate Avenue

Cypress, CA   90630-4750

 

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

Varies

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

1 day

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

9 days

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

6 weeks

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

Focus Diagnositics, Inc.

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 Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

83883

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
Z0615Alpha-1 Acid Glycoprotein, NephIn Process