Test Catalog

Test Id : FCDU7

Cannabinoids, Umbilical Cord Tissue

Test Catalog

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

If appropriate, confirmation testing will be performed at no additional charge.

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

Only orderable as a profile. For more information see FCDSU / Comprehensive Drug Screen, Umbilical Cord Tissue.

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

Cannabinoids, UC

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

If appropriate, confirmation testing will be performed at no additional charge.

Specimen Type
Describes the specimen type validated for testing

Tissue

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

Only orderable as a profile. For more information see FCDSU / Comprehensive Drug Screen, Umbilical Cord Tissue.

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

  All specimens will be evaluated by the processing and performing laboratories for test suitability.

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
Tissue Refrigerated (preferred) 7 days
Frozen 14 days

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

If appropriate, confirmation testing will be performed at no additional charge.

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

Refer to www.nmslabs.com/test-catalog.

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.

Only orderable as a profile. For more information see FCDSU / Comprehensive Drug Screen, Umbilical Cord Tissue.

 

Reporting limit determined each analysis.

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 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.

3 to 7 days

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

NMS Labs

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.

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
FCDU7 Cannabinoids, UC 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.
Z6179 Delta-9 Carboxy THC 97584-7
Z6180 Delta-9 THC 97586-2

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