Test Catalog

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.

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.

No

Reporting Name
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

Blood spots

Newborn Screen

Newborn Screening

Testing Algorithm
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

Whole blood

Specimen Minimum Volume
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

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

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.

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

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 Friday

Performing Laboratory Location
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.

  • 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.

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.

S3620

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
WINS Wisconsin Newborn Screen 54089-8
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.
113124 Wisconsin Newborn Screen No LOINC Needed
55323 PHENYLKETONURIA: Phenylalanine 29571-7
55324 MAPLE SYRUP URINE DISEASE: Leucine 38479-2
55325 HOMOCYSTINURIA: Methionine 63380-0
55326 CITRULLINEMIA/ASA: Citrulline 46733-2
55327 TYROSINEMIA Type I: Succinylacetone 46733-2
55328 TYROSINEMIA Type II and III: Tyrosine 46733-2
55329 HYPOTHYROIDISM: TSH 46762-1
55330 ADRENAL HYPERPLASIA: 17-OHP 46758-9
55331 CYSTIC FIBROSIS: Trypsinogen 46769-6
55332 HEMOGLOBINOPATHIES: Hgb Pattern 46740-7
55333 FATTY ACID OXIDATION: Acylcarnitine Prof 58088-6
55334 ORGANIC ACIDEMIAS: Acylcarnitine Profile 46733-2
55335 GALACTOSEMIA: GALT Activity 46737-3
55336 BIOTINIDASE DEF: Biotinidase Activity 46761-3
55337 SCID-IMMUNODEFICIENCY: TREC 62321-5
606121 SPINAL MUSCULAR ATROPHY: SMN1 92004-1

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