Method Name
A short description of the method used to perform the test
Direct Enzyme Immunoassay (EIA)
NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.
No
Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test
Growth Hormone Releasing Hormone
Aliases
Lists additional common names for a test, as an aid in searching
Growth Hormone-Releasing Hormone (IR-GH-RH)
FIRGH
Specimen Type
Describes the specimen type validated for testing
Serum
Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing
Patient Preparation: Patient should not be on any medications that may influence pituitary secretion.
Specimen Type: Serum
Collection Container/Tube: Red top or SST
Submission Container/Tube: Plastic vial
Specimen Volume: 3 mL
Collection Instructions:
1. Draw blood in a plain, red-top tube(s), serum-gel tube(s) is acceptable.
2. Separate immediately and send 3 mL of serum frozen 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
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
Hemolysis | Mild reject; Gross reject |
Lipemia | Mild reject; Gross reject |
Icterus | Mild reject; Gross reject |
Other | Specimens other than listed. Test is strict frozen |
Specimen Type |
Temperature |
Time |
Special Container |
Serum |
Frozen |
90 days |
|
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.
Levels of IR-GH-RH
Baseline ranges: 5 - 18 pg/mL
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 Regional Manager. 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 performed using a kit that has not been cleared or approved by the FDA and is designated as research use only.
The analytic performance characteristics of this test have been determined by Inter Science Institute. This test is not intended for diagnosis or patient management decisions without confirmation by other medically established means.
Test Id |
Test Order Name |
Order LOINC Value
|
FIRGH |
Growth Hormone Releasing Hormone |
14177-0 |
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.
|
Z0926 |
Growth Hormone Releasing Hormone |
14177-0 |