States Texas

Conditions Screened

Texas currently screens for 55 conditions

The Texas Program

Each state runs its program differently, for more detailed information please visit their website here.

Download Brochure

Here is a brochure for the state of Texas. Brochure>>

What Conditions are Screened For in Texas?

Hemoglobin Disorders

Contacts

Texas Department of State Health Services

Newborn Screening Laboratory

PO Box 149347, MC 1947

Austin, TX 78714-9347

Phone: 1-888-963-7111 ext. 7333

Fax: 512-776-7157

https://www.dshs.texas.gov/lab/newbornscreening.shtm


Texas Department of State Health Services

Newborn Screening Clinical Care Coordination 

PO Box 149347, MC 1918 

Austin, TX 78714-9347

Phone: 1-800-252-8023 ext. 3957

Fax: 512-776-7450

https://www.dshs.texas.gov/newborn-screening-program


Texas Department of State Health Services

Texas Early Hearing Detection and Intervention Program 

PO Box 149347, MC 1918 

Austin, TX 78714-9347

Phone: 1-800-252-8023 ext. 6616

Fax: 512-483-7417

https://www.dshs.texas.gov/texas-early-hearing-detection-intervention-tehdi


Newborn Screening Laboratory

Pawan Vohra

Phone: 512-776-7158

[email protected]


Clinical Care Coordination Program

Leslie McKenzie

Phone: 512-560-2513

[email protected]


Texas Early Hearing Detection and Intervention Program

Liz Sengler

Phone: 737-354-1893

[email protected]


Search Educational Resources

Looking for resources? Check out our Newborn Screening Education and Training Resource Center.

VIEW RESOURCES

About Newborn Screening in Texas

Program Overview:

The Texas Department of State Health Services (DSHS) Newborn Screening (NBS) Program consists of testing, two point-of service screenings, and clinical care coordination. DSHS Laboratory provides newborn screening services in support of the Texas NBS Program, which tests about 800,000 newborn specimens each year. Texas law requires the newborn screen to help find infants who may have one of the 55 disorders or medical conditions. 

The newborn screen requires a simple heel stick blood sample collected from newborns 24 to 48 hours after birth and another at 7 to 14 days of age, a minimum of 168 hours. If the NBS detects an infant with an abnormal result, the NBS Program's Clinical Care Coordination team initiates the process of follow-up with a health care provider for confirmatory testing. If it is determined that your child has a condition, treatment will begin as appropriate.

Early detection of these 55 disorders allows early treatment that can prevent serious complications, such as growth problems, developmental delays, deafness, blindness, intellectual disabilities, seizures, and early death. The sooner treatment begins, the greater the chances your child will live a healthier life. It is important that your doctor have a current phone number or address by which to reach you in case your newborn’s screen comes back with a possible positive result. If your doctor does reach out to you about the NBS results, respond immediately and follow all instructions as quickly as possible.

How is Newborn Screening Paid for in ­­Texas?

The NBS fee is $68.63 per specimen collection kit. Health care providers or facilities purchase the specimen collection kits, which include the cost of the testing for private pay or insurance covered patients.  DSHS provides specimen collection kits at no cost to the healthcare provider for those covered by Medicaid and Children’s Health Insurance Program (CHIP) and can also be used for anyone unable to pay for newborn screening. DSHS is reimbursed by Medicaid and CHIP for the testing performed on these kits. Inability to pay should not be a barrier to getting a newborn screened.

What two point-of-service screenings are conducted at the birthing facility?
Newborn Hearing Screening

Hearing loss can affect a child’s ability to develop communication, language, and social skills. All Texas newborns should receive a hearing screening before being discharged from the birth facility. The Texas Early Hearing Detection and Intervention (TEHDI) program certifies newborn hearing screening programs and oversees statewide achievement of Early Hearing Detection and Intervention (EHDI) goals that include screening for hearing loss before 1 month of age, diagnostic evaluation before 3 months of age, and enrollment in early childhood intervention (ECI) before 6 months of age, known as the 1-3-6 benchmarks. The earlier children with hearing differences are identified and enrolled in ECI and start getting services, the more likely they are to reach their full potential.

Critical Congenital Heart Disease (CCHD) Screening

CCHD screening is a point-of service screen to determine if an infant has a serious heart condition, usually requiring surgery. The screening is done at the birthing facility, and results are available in real time. This test uses a machine called a pulse oximeter to measure how much oxygen is in a baby’s blood at different areas of circulation: before blood gets to the heart and after it pumps out of the heart. If there’s a big difference in how much oxygen is present in those two areas, it could be a sign of a congenital heart defect or disease. There is no blood test involved. Currently, Texas Health and Safety Code requires that confirmed CCHD cases be reported to the Newborn Screening Program. The CCHD Toolkit, available on DSHS Newborn Screening Program – CCHD in Texas, was developed through the Texas Pulse Oximetry Project with support from the Newborn Screening Advisory Committee.

Policies and Resources

Opt-Out:

All newborns must participate in NBS unless a parent or guardian objects on religious grounds. The person who administers the screening must place a statement of refusal, signed by a parent or guardian, in the child's medical record.

Support for families:

One of the concerns many families have when they first learn their child has a condition detected by the NBS Program is the increase in health care costs. Texas has various laws and programs that are in place to help families gain access to affordable care for their loved ones with a condition identified through NBS.

All newborns who are diagnosed with one of these conditions will be referred to the Children and Youth with Special Health Care Needs Program (CYSHCN) where it will be determined if they are eligible for that program’s services. To be eligible, an individual must be under 21 years old and meet financial requirements. If a child has Cystic Fibrosis (CF), they will be eligible for services throughout their entire life. If a child is determined to be eligible, they may be provided with a special dietary formula, medications to help treat their condition, and other services. To see if your child qualifies, visit the CYSHCN website.

If Medicaid, Children and Youth with Special Health Care Needs (CYSHCN), CHIP or private insurance is not available to provide care for an individual with a condition, the NBS Benefits Program can provide limited assistance. To be eligible, the individual must have a condition detected by NBS or have an out-of-range newborn screen, be a Texas resident, have income within the guidelines and be able to provide documentation of all the requirements upon request. The Program will provide medical food, medications, vitamins and other testing and follow-up care at no cost or at a reduced cost to those approved for the program benefits. Funding will be limited to those with an income at or below 350% of the federal poverty income guideline who meet other program guidelines. 

Storage and Use of Dried Blood Spots:

For further information about the storage and use of dried blood spots, visit the Texas State Department of State Health Services website.

To see a copy of the blood spot card used in Texas click here.

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