Newborn Screening Program
NEWBORN GENETIC SCREENING PROGRAM
New Mexico Newborn Screening Program (NMNBSP) requires that all babies born in New Mexico receive screening for certain genetic, metabolic, hemoglobin and endocrine disorders. The New Mexico Newborn Screening Program offers screening for 27 disorders. The NMNBSP provides services to over 28,000 babies and their families annually. Currently the State of New Mexico mandates two newborn screens be collected on every newborn born in NM.
New Mexico Newborn Screening Program continues to partner with Mountain States Genetic Network and has also contracted with Oregon State Public Health Laboratory for expanded screening.
New Mexico Newborn Screening Program PowerPoint Presentation
WHY WE SCREEN
Babies with these conditions appear normal at birth. It is only with time that the conditions affects the baby’s brain or physical development or causes other medical problems. By then the damage may be permanent. Early diagnosis and treatment can result in normal growth and development and can reduce morbidity and mortality.
FOR PROVIDERS AND HOSPITALS
FORMS / FEES
TO ORDER BLOOD SPOT KITS
Contact: Eliza Garcia
Children's Medical Service
(505) 476-8856 or 476-8868 or 1-877-890-4692.
Allow at least 3-5 shipping days for delivery of forms
NOTE: The State of New Mexico mandates two tests.
Double Kits $ 89.00
- Double kits are 2-part filter paper bloodspot forms.
- The forms are bar coded in order to link the first form with the second form.
- Second bloodspot form is not to be used as a first bloodspot for another client.
- Parents need to be rigorously instructed on the importance of bringing the second bloodspot form with them to their first newborns appointment or lab visit.
Single Kits $25.00
- Single kits are provided free when Oregon State Public Health Laboratory requests another sample.
- Single kits may be used when the form is lost or when parents forget to bring it for their first pediatric or lab appointment. The lab or physician will have to purchase single kit bloodspot forms for $25.00 each. In the event a second form is not available for the second screen, in order to ensure a child receives testing, the family may be referred to the public health nurse at the local Public Health Office.
If a nurse is not available, contact a CMS social worker at the same office or Carla Ortiz, RN, NM Newborn Screening Program Nurse Consultant at 505-476-8858 or 1-877-890-4692.
NEWBORN SCREENING FOLLOW-UP SERVICES
- Children’s Medical Services (CMS) Newborn Screening program provides programmatic follow-up of all children diagnosed on newborn screening to age 21.
- Children’s Medical Services (CMS) provides clinical long-term follow-up for children that have been identified with a genetic/metabolic, endocrine, and hemoglobin disorder. Children are followed to the age of 21.
- CMS has almost 60 medical social workers and in 32 health offices throughout the state. Medical Social Workers and Family Infant Toddler Social workers provide service coordination for children and youth with special health care needs.
- CMS has 2 Registered Nurses in the Newborn Screening Program
- New Mexico Newborn Screening Program has an established relationship with the UNM Department of Pediatrics at the UNM Health Science Center/Children’s Hospital
- CMS has an Adult Cystic Fibrosis Program and provides some adult metabolic disease services
- Contact information: NBS Genetic nurse consultant 476-8858, Program Manager 476-8857
Material and Resources
Websites
- Oregon State Public Health Laboratory
- Mountain State Genetic Network
- March of Dimes Birth Defects Foundation
- National Newborn Screening and Genetic Resource
- Save Babies Through Screening Foundation
- www.savebabies.org