Test Catalog

Test Id : FANDR

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Androstenedione

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Overview

Test Catalog

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

Chromatography/Mass Spectrometry

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

Androstenedione

Specimen Type
Describes the specimen type validated for testing

Serum Red

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

Specimen Type: Serum

Container/Tube: Red Top

Specimen Volume: 1 mL

Collection Instructions: Draw blood in a plain red-top tube(s), serum gel tube(s) is not acceptable. Spin down and send 1 mL of serum refrigerated in a plastic vial.

Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory

0.25 mL

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

Hemolysis Mild OK; Gross reject
Other Serum separator tubes, glass tubes

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
Serum Red Refrigerated (preferred) 28 days
Ambient 14 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.

See Laboratory Report

 

Adult Males

 

18-30 years

50-220 ng/dL

31-50 years

40-190 ng/dL

51-60 years

50-220 ng/dL

 

Adult Females

 

Mid Follicular

51-213 ng/dL

Surge

73-230 ng/dL

Mid Luteal

73-184 ng/dL

Postmenopausal Phase

20-75 ng/dL

 

Pediatric

 

Premature Infants** (31-35 weeks)

<or=420 ng/dL

Term Infants**

<or=290 ng/dL

 

Age

Male (ng/dL)

Females (ng/dL

<30 days

Not established

Not established

1-11 months

<or=41

<or=41

1 year

<or=31

<or=35

2 years

<or=27

<or=34

3 years

<or=27

<or=38

4 years

<or=29

<or=42

5 years

<or=31

<or=45

6 years

<or=36

<or=45

7 years

<or=43

<or=48

8 years

<or=54

<or=57

9 years

<or=65

<or=77

10 years

10-77

15-111

11 years

12-90

24-149

12 years

14-106

32-182

13 years

17-124

37-205

14 years

19-139

42-221

15 years

21-154

46-238

16 years

24-172

50-252

17 years

27-192

53-265

 

Tanner Stages

 

II-III Males

17-82 ng/dL

II-III Females

43-180 ng/dL

IV-V males

57-150 ng/dL

IV-V Females

73-220 ng/dL

 

**Pediatric data from J Clin Endocrinol Metab.1991;73:674-686; J Clin Endocrinol Metab. 1989; 69:1133-1136.

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.

Sunday-Friday

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.

4 to 9 days

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

Quest Diagnostics Nichols Institute

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 was developed and its analytical performance characteristics have been determined by Quest Diagostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

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.

82157

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
FANDR Androstenedione Not Provided
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.
FANDR Androstenedione 1854-9

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

Test Update Resources

Change Type Effective Date
New Test 2028-02-28