| Web: | mayocliniclabs.com |
|---|---|
| Email: | mcl@mayo.edu |
| Telephone: | 800-533-1710 |
| International: | +1 855-379-3115 |
| Values are valid only on day of printing | |
Test Id : WINS
Wisconsin Newborn Screen, Blood Spot
Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
This test is only orderable by MCHS Wisconsin sites. This test is performed by the Wisconsin State Laboratory of Hygiene.
When this test is ordered the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are automatically added. This test is collected on the Wisconsin State Laboratory of Hygiene collection card and the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are collected on the Mayo Clinic Laboratories blood spot card. The LDALD test is performed by the Biochemical Genetics Laboratory and reported separately from WINS. The SMNDX test is performed by the Genomics Laboratory Molecular and also reported separately from WINS. The Biochemical Genetics Laboratory is responsible for ensuring tests are completed on babies born at Mayo Clinic Health Systems Wisconsin sites and for transcribing test results into the SOFT computer system.
For information on LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies, see the individual Test IDs.
NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.
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
Lists a shorter or abbreviated version of the Published Name for a test
Wisconsin Newborn Screen
Aliases
Lists additional common names for a test, as an aid in searching
Lists additional common names for a test, as an aid in searching
Blood spots
Newborn Screen
Newborn Screening
Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
This test is only orderable by MCHS Wisconsin sites. This test is performed by the Wisconsin State Laboratory of Hygiene.
When this test is ordered the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are automatically added. This test is collected on the Wisconsin State Laboratory of Hygiene collection card and the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are collected on the Mayo Clinic Laboratories blood spot card. The LDALD test is performed by the Biochemical Genetics Laboratory and reported separately from WINS. The SMNDX test is performed by the Genomics Laboratory Molecular and also reported separately from WINS. The Biochemical Genetics Laboratory is responsible for ensuring tests are completed on babies born at Mayo Clinic Health Systems Wisconsin sites and for transcribing test results into the SOFT computer system.
For information on LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies, see the individual Test IDs.
Specimen Type
Describes the specimen type validated for testing
Describes the specimen type validated for testing
Whole blood
Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory
WINS: 4 blood spots
LDALD: 1 blood spot
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
Identifies specimen types and conditions that may cause the specimen to be rejected
| Blood spot; Shows serum rings; Insufficient specimen | Reject |
Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included
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 |
|---|---|---|---|
| Whole blood | Ambient (preferred) | 365 days | |
| Frozen | 365 days | ||
| Refrigerated | 365 days |
Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
This test is only orderable by MCHS Wisconsin sites. This test is performed by the Wisconsin State Laboratory of Hygiene.
When this test is ordered the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are automatically added. This test is collected on the Wisconsin State Laboratory of Hygiene collection card and the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are collected on the Mayo Clinic Laboratories blood spot card. The LDALD test is performed by the Biochemical Genetics Laboratory and reported separately from WINS. The SMNDX test is performed by the Genomics Laboratory Molecular and also reported separately from WINS. The Biochemical Genetics Laboratory is responsible for ensuring tests are completed on babies born at Mayo Clinic Health Systems Wisconsin sites and for transcribing test results into the SOFT computer system.
For information on LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies, see the individual Test IDs.
PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information
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.
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 Friday
Performing Laboratory Location
Indicates the location of the laboratory that performs the test
Indicates the location of the laboratory that performs the test
Rochester
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.
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.
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.
Not Applicable
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.
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.
CPT codes are provided by the performing laboratory.
S3620
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.
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.
Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.
Normal and Abnormal sample reports are provided as references for report appearance.
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.
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.