The following information was updated in the Lab Catalog.
All changes are for Corewell Health Laboratories West.
The following information was updated in the Lab Catalog.
All changes are for Corewell Health Laboratories West.
Effective Thursday, April 18, 2024, Corewell Health Laboratory will discontinue the send out test Hepatitis A IgG Antibody, Serum (Mayo Test ID: HAIGG). This test has been made obsolete by Mayo Clinic Laboratories. We recommend to our healthcare providers the following in-house testing:
1.Hepatitis A Total Antibody (LAB1230596): intended for the clinical laboratory diagnosis of acute or past hepatitis A virus infection in persons with signs or symptoms of hepatitis and in persons at increased risk for hepatitis A infection, to identify HAV susceptible individuals and to determine the presence of an antibody response to HAV in vaccine recipients.
2.Hepatitis A Antibody, IgM (LAB7980): intended for use as an aid in the laboratory diagnosis of an acute or recently acquired hepatitis A virus infection.
The following information was updated in the Lab Catalog.
The following information was updated in the Lab Catalog.
Effective December 20, 2023, Rheumatoid Factor, IgM, Quantitative will be replaced with Rheumatoid Factor.
The following information was updated in the Lab Catalog.
Please note that our lab catalog URL has been updated to reflect our new name: CorewellHealth.TestCatalog.org
Effective Wednesday, November 29, 2023, the in-house test, Pyruvic Acid, will be made inactive. Recommended alternative testing is Pyruvic Acid, Blood [LAB1231461] which is referred to Mayo Clinic Laboratories. Please review the lab catalog for information on new specimen requirements and updated reference range information. Due to the update in reference ranges, this may disrupt trending data.
The test Lactate/Pyruvate Ratio will also be inactivated with no alternative testing. If you require assistance with obtaining the ratio, please Contact Us.
Effective October 3, 2023, Corewell Health Laboratories will discontinue the Influenza Rapid and Respiratory Syncytial Virus (RSV) Rapid tests. These antigen tests are less sensitive than the nucleic acid amplification tests (NAAT; such as PCR) that are now the standard of care for diagnosing these respiratory viruses. Specimen collection remains unchanged with PCR testing available for nasopharyngeal and nasal swabs collected in a universal transport media (UTM) tube.
Discontinued:
• Influenza (Flu) A/B Rapid – Epic Code: LAB9240
• Influenza (Flu) A/B Rapid, Influenza A/B PCR if Negative – Epic Code: LAB2111530
• Respiratory Syncytial Virus (RSV) Rapid – Epic Code: LAB495
Replace with:
• Influenza (Flu) A/B PCR – Epic Code: LAB3255
• COVID-19, Influenza A/B, RSV PCR – Epic Code: LAB1230746