A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.
||PROMETHEUS IBD sgi Diagnostic, S
||PROMETHEUS IBD sgi Diagnostic, B
A short description of the method used to perform the test
Enzyme Linked Immunosorbent Assay (ELISA), Immunofluorescence Assay (IFA), Chemiluminescent, Polymerase Chain Reaction (PCR), Nucleic Acid Probes
NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.
Lists a shorter or abbreviated version of the Published Name for a test
PROMETHEUS IBD sgi Diagnostic
Lists additional common names for a test, as an aid in searching
Describes the specimen type validated for testing
Whole Blood EDTA
Defines the optimal specimen required to perform the test and the preferred volume to complete testing
Requires both whole blood and serum
Note: Specimens must be shipped together
Note: Informed consent required from NYS clients
Collect 2 mL lavender top EDTA whole blood. Ship refrigerate.
Draw blood in a plain, red-top tube(s). (Serum gel tube is acceptable.) Spin down and send 2 mL of serum refrigerated.
Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory
Blood = 1 mL, Serum = 2 mL
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
| Hemolysis: || NA |
| Thawing: || Serum-Warm OK; Cold OK Whole blood-Warm reject; Cold Reject |
| Lipemia: || NA |
| Icterus: || NA |
| Other: || Both serum and EDTA whole blood required. |
Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included
Whole Blood EDTA
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.
Testing is complete. Final report has been sent to the referring laboratory.
Indicates whether the report includes an additional document with charts, images or other enriched information
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.
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.
3 to 12 days
Performing Laboratory Location
Indicates the location of the laboratory that performs the test
Prometheus Laboratories, Inc. Therapeutics and Diagnostics
Test Setup Resources
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.
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