NEWBORN SCREENING FOR SEVERE COMBINED IMMUNODEFICIENCY (SCID)
With the support of the Hawaii community-based SCID Task Force, the Hawaii Newborn Metabolic Screening Program Advisory Committee recommended the addition of SCID to the state newborn screening (NBS) panel. SCID is on the NBS panel as of March 1, 2015.
- More information about SCID
IMPLICATIONS FOR YOUR PRACTICE
- Severe Combined Immunodeficiency (SCID) is on the state newborn screening (NBS) panel as of March 1, 2015.
- NBS for SCID is a screening test. DO NOT base a diagnosis of SCID on a positive NBS result. Diagnosis of SCID needs to be confirmed with additional diagnostic tests and a Pediatric Immunologist evaluation. The Hawaii Newborn Screening Program can assist you with the coordination of the follow-up to confirm a diagnosis of SCID in the newborn.
- Families and infants diagnosed with SCID should receive immediate confirmatory testing and a Pediatric Immunologist evaluation with counseling.
- NBS does not detect all cases of SCID in newborns.
- SCID occurs once in every 54,000 births in the United States.
- SCID is a primary immune disorder. Common infections and vaccines are life-threatening without treatment.
- Long-term treatment is a bone marrow transplant or gene therapy.
- To ensure the babies born in Hawaii have access to the life-saving treatment options, a partnership between Kapi’olani Medical Center for Women and Children, the University of California at Los Angeles Mattel’s Children’s Hospital, and the Hawaii Department of Health has been created.
Hawaii follows the testing algorithm used by the Oregon State Public Health Laboratory (OSPHL), Hawaii’s contracted NBS laboratory. The algorithm involves initial T-cell receptor incision circles (TRECs) testing of the blood spot specimen routinely collected after birth ≥ 24 hours.
For additional information & questions, please contact:
Gwen Palmer, R.N., M.P.H.
Newborn Metabolic Screening Program
741 Sunset Avenue
Honolulu, HI 96816
Ph: (808) 733-9069
Fax: (808) 733-9071