Updated: Aug. 12, 2026

Purpose and Overview

Much more than a PKU test 

Newborn screening (NBS) consists of a panel of tests done shortly after a baby is born. These tests check for serious health problems that may not be easy to see at first. If these problems are not found and treated early, they can cause serious health issues, delays in learning and growing, or even death. Early detection helps doctors start treatment right away. NBS can help your baby stay healthier in the future. Each year, newborn screening helps find treatable conditions in about 15,000 babies in the U.S. In South Carolina, newborn screening is required by law under SC Code of Laws Title 44.  

NBS consists of three main tests: 

  1. Blood Spot Test (Heel Prick Test) 
    • A healthcare provider pricks the newborn’s heel to collect a few drops of blood (within 24 - 48 hours of life).
    • The blood is placed on a special filter paper card and sent to the public health laboratory for analysis.
    • The laboratory screens for many conditions, including organic acid, fatty acid oxidation, amino acid, endocrine, hemoglobin, and others (e.g., cystic fibrosis, galactosemia, and more). See the complete list of conditions screened for using the blood spot test.
  2. Hearing Screening (First Sound) 
    • Hearing screening is done using Otoacoustic Emissions (OAE):
      • A tiny earphone plays soft sounds, and a microphone measures the ear’s response.
    • The test is painless, non-invasive, and takes just a few minutes.
    • Hearing tests can be performed while the baby is asleep. 
    • For babies delivered at a hospital, this screening is done before discharge.
    • For babies born outside of a hospital setting, screening is done by one month of age.
    • For more information, contact Tara Carroll: carroltp@dph.sc.gov, (803) 898-0708
  3. Pulse Oximetry Screening (for Critical Congenital Heart Defects - CCHDs) 
    • A small sensor is placed on the baby’s hand and foot to measure oxygen levels in the blood.
    • This test is performed at the hospital or birth facility when the baby is at least 24 hours of age and before discharge. 
    • Low oxygen levels may indicate a heart problem, requiring further tests.
    • Heart defects are the most common types of birth defects.
    • Babies born with these conditions are living longer and healthier lives, and data shows improved survival over time.
    • For more information, contact Heather Blackwell: blackwhr@dph.sc.gov, (803) 898-3885

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Newborn Screening Provider Responsibilities

Who This Applies To 

Physicians, Nurse Practitioners, Certified Nurse Midwives, Licensed Midwives, and Physician Assistants

Core Responsibilities

  • Collect specimens: The attending provider (or designee) must ensure newborn screening specimens are collected for every infant under their care.
  • Refusals: Neonatal Screening for Inborn Errors of Metabolism and Hemoglobinopathies, Sections 44-37-30 and 44-37-35 of the South Carolina Code of Laws requires: 
    • Every child born in South Carolina is required to have a newborn screen.
    • Parents/legal guardians may only exempt testing based on religious grounds and must sign a religious exemption/refusal form if they decline the newborn screen:
  • Confidentiality: Test information is confidential and may be released only to:

Parent and Caregiver Education

South Carolina Code of regulations 60-80 (formerly 61-80) requires hospitals, midwives, and other birthing facilities to educate parents and caregivers about newborn screening by:

Follow-Up and Communication

  • Notify families: Inform parents or legal guardians of all screening results, both normal and abnormal.
  • Repeat testing: If a specimen is unsatisfactory or a repeat test is required, collect and submit a new specimen as soon as possible.
  • Abnormal results:
    • Begin medical follow-up and diagnostic testing immediately.
    • Refer to pediatric specialists when needed. View the list of pediatric specialists (pdf). 
    • If prompt referral or treatment is not possible, notify the Newborn Screening follow-up team at (803) 898-3192
  • Reporting
    • List of Reportable Conditions (LORC)
    • Providers must report all results to the Newborn Screening follow-up team, whether the infant is diagnosed with a condition, cleared after confirmatory testing, or expired.
    • Reports must include the final diagnosis, treatment start date, and clarification if the initial result was a false positive or false negative.
      • How to report results:

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List of Newborn Screening Conditions Tested on the South Carolina Bloodspot Screening Panel

View condition-specific information sheets and additional details.

2,4 Dienoyl-CoA Reductase Deficiency (DE RED)Holocarboxylase Synthetase Deficiency (MCD)
2-Methyl-3-Hydroxybutyric Acidemia (2M3HBA)Homocystinuria (HCY)
2-Methylbutyrylglycinuria (2MBG) Hypermethioninemia (MET)
3-Hydroxy-3-Methylglutaric Aciduria (HMG)Isovaleric Acidemia (IVA)
3-Methylcrotonyl-CoA Carboxylase Deficiency (3-MCC)Krabbe Disease (globoid cell leukodystrophy)
3-Methylglutaconic Aciduria (3MGA)Long-Chain L-3 Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD)
Argininemia (ARG)Malonic Acidemia (MAL)
Argininosuccinic Aciduria (ASA)Maple Syrup Urine Disease (MSUD)
Benign Hyperphenylalaninemia (H-PHE)Medium/Short-Chain L-3 Hydroxyacyl-CoA Dehydrogenase Deficiency (M/SCHAD)
Beta-Ketothiolase Deficiency (BKT)Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
Biopterin Defect in Cofactor Biosynthesis (BIOPT-BS) Medium-Chain Ketoacyl-CoA Thiolase Deficiency (MCAT)
Biopterin Defect in Cofactor Regeneration (BIOPT-REG)Methylmalonic Acidemia (Cobalamin Conditions) (Cbl A,B)
Biotinidase Deficiency (BIOT)Methylmalonic Acidemia (Methylmalonyl-CoA Mutase Deficiency) (MUT)
Carnitine Acylcarnitine Translocase Deficiency (CACT)Methylmalonic Acidemia with Homocystinuria (Cbl C, D, F)
Carnitine Palmitoyl Transferase I Deficiency (CPT-IA)Mucopolysaccharidosis Type-I (MPS I)
Carnitine Palmitoyl Transferase Type II Deficiency (CPT-II)Mucopolysaccharidosis Type-II (MPS II)
Carnitine Uptake Defect (CUD) Primary Congenital Hypothyroidism (CH)
Citrullinemia, Type I (CIT)Propionic Acidemia (PROP)
Citrullinemia, Type II (CIT II)S, Beta-Thalassemia (Hb S/ßTh)
Classic Galactosemia (GALT)S, C Disease (Hb S/C)
Classic Phenylketonuria (PKU)Severe Combined Immunodeficiency (SCID)
Congenital Adrenal Hyperplasia (CAH)Sickle Cell Anemia (Hb SS)
Cystic Fibrosis (CF)Spinal Muscular Atrophy (SMA)
Fabry Disease (FD)T-cell related lymphocyte deficiencies
Galactoepimerase Deficiency (GALE)Trifunctional Protein Deficiency (TFP)
Galactokinase Deficiency (GALK) Tyrosinemia, Type I (TYR I)
Glutaric Acidemia, Type I (GA-1)Tyrosinemia, Type II (TYR II)
Glutaric Acidemia, Type II (GA-2)Tyrosinemia, Type III (TYR III)
Glycogen Storage Disease Type II (Pompe)Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)
Hemoglobinopathies (Var Hb)X-Linked Adrenoleukodystrophy (ALD)

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Screening Process and Timeline

Specimen Collection 

  • Collect the dried blood spot specimen 24–48 hours after birth. 
  • If the newborn is in a NICU or is critically ill, collect:
    • On admission if transfusion is expected or before transfer to a higher level of care.
    • At 24–48 hours of age, regardless of TPN status (and before transfusion, if possible).
    • Repeat at 28 days of age or at discharge for infants < 34 weeks or < 2000 g at birth, or if requested by the NBS follow-up program. 
  • Complete the DPH 1327 Blood Collection Card fully, accurately, and legibly.
    • Always fill each circle completely with a single large drop of blood. Allow specimens to dry flat for 3–4 hours and avoid contamination or layering.

Packaging and Transport

  • Ship specimens within 24 hours of collection; do not hold or batch specimens.
  • Use the newborn screening daily courier service (Sunday–Friday for birthing hospitals) or a fast overnight service (FedEx/UPS Priority) for pediatric offices, midwives, etc. 
  • Place dried cards in official NBS envelopes. Do not use staples, tape, or plastic bags.
  • Keep a daily shipping log: number of specimens, MRNs/names, courier, and time of pick-up.

Lab Analysis

  • Specimens are accessioned and tested at the SC Public Health Laboratory.
  • SC currently screens for 60 disorders, including metabolic, endocrine, hemoglobin, immunologic, and other genetic conditions. 
  • Certain abnormal results undergo second or third-tier confirmatory testing, either in-house or at partner labs (e.g., Greenwood Genetic Center, UCSF).   

Results Reporting

  • All results are posted to the DPH Newborn Screening eReports Portal.
  • Abnormal results are reviewed by the DPH laboratory follow-up team. Abnormal results are sent directly to providers for clinical follow-up. 
    • In the case of a critical test result, the primary healthcare provider listed on the newborn screening card will be directly contacted by the Newborn Screening Program. 
    • Normal results are not called to the provider and are available to providers through the secure eReports portal. 

Follow-Up

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Collection Guidelines

Heel Stick Technique

baby's foot with cross-hatching showing where it is safe to perform heel stick blood spot test


Only two sites are acceptable for collection:

  • The most medial portion of the plantar surface of the heel
  • The most lateral portion of the plantar surface of the heel

The following are unacceptable collection sites:

  • Swollen or previously punctured areas
  • The arch of the foot the curvature of the heel
  • Fingers
  • Earlobes

Filling Out the Form

Image
NBS Bloodspot Correction Card
  • Accurate information
  • Legible information
    • Print all information; no cursive writing.
    • Use black or blue ballpoint pens only. Do not use a pencil.
    • If an error occurs:
      • Place a single line through the mistake and add the collector’s initials.
      • Write the correct information in the available space if possible.
      • If errors are extensive or there is not enough space for corrections, include a note with the card and attach a new card to the original using a paperclip (do not use staples).
  • Missing information
    • Physician fields cannot be left blank or entered as “Unknown”
    • All dates and times are critical and needed for testing
      • Birth date and time
      • Collection date and time
      • Transfusion date and time (if applicable)

NICU Collection Protocol for Preterm, Low Birth Weight and Sick Infants

First Specimen

  • A specimen should be collected on admission if a blood transfusion is expected or if the infant is transferred to a higher level of care.
  • At 24–48 hours of age, a specimen should be collected regardless of TPN status, and before transfusion if possible.
    • Exception: If the TSH result is between 20 and 39, endocrinology recommends recollection at 2 weeks.

Second Specimen

A repeat specimen should be collected at 28 days of age or at discharge. This applies to:

  • Infants born at less than 34 weeks gestation or weighing less than 2000 grams at birth, regardless of the initial specimen results.
  • Infants with non-urgent abnormal results reported by the DPH NBS follow-up team.
  • Repeat as soon as possible for:  
    • Infants with urgent abnormal results reported by the DPH Newborn Screening follow-up team.
    • At the request of a specialist for a screening disorder.

For more information regarding the NICU Collection Protocol, please review the official departmental instructions in the South Carolina Newborn Screening Manual.

Infants Being Placed for Adoption

  • Patient name on form:
    • Use legal name at birth or adopted name.
    • If unknown: Last name = birth mother’s last name, First name = “Adoption” (e.g., “Smith, Adoption”).
  • If birth mother is not to be contacted:
    • Mother’s name fields = lawyer, adoption agency, or legal guardian.
    • Address & phone = lawyer, adoption agency, or legal guardian.
  • Always enter when known:
    • Physician contact information (complete name, address, and phone number).
    • Infant medical record number.

Entering all known information helps the Newborn Screening Program locate the infant, alerts legal guardian or adoption agency of abnormal/potentially life-threatening results, and ensures the infant receives timely medical care.

Age Matters

Any infant under a year old should be tested.

For infants over six months old, a modified testing panel is used. This panel includes:

  • Amino acid disorders
  • Biotinidase deficiency
  • Galactosemia
  • Hemoglobin disorders 
  • Spinal Muscular Atrophy (SMA)
  • Severe Combined Immunodeficiency (SCID) 
  • Cystic Fibrosis - DNA panel only (applies to all infants over 30 days old)

The PHL can also test specimens from older babies, children, and adults, for the monitoring of select amino acids (such as phenylalanine and tyrosine levels for known PKU patients) and hemoglobin disorders and traits (such as Sickle Cell Disease).

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Reporting Newborn Screening Follow-Up Results/Reporting a Diagnosed Case

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Accessing Test Results

Dried Blood Spot testing

Healthcare professionals can retrieve completed newborn screening lab reports online anytime via Specimen Gate® eReports. Specimen Gate® eReports is a secure web portal that gives the end user the ability to view, download, and/or print patient lab reports for infants under their care 24/7/365 for a period of 1 year (from date specimen received).

Hearing Screening

For information on a baby’s hearing screen results, contact:

Critical Congenital Heart Defects

For information on a baby’s heart screen results, contact:

Hemoglobin/Sickle Cell Test Results

The DPH Public Health Laboratory (PHL) can provide newborn Hemoglobin (Sickle Cell) screening results for individuals born in South Carolina. These results are required for NCAA athletic participation.

Patients Born in South Carolina

  • Patients born in South Carolina, or parents/legal guardians (if child is under 18), requesting results:
    • Option 1: Physician Request (Preferred & Fastest)
      • A healthcare provider may request newborn Hemoglobin (Sickle Cell) screening results on behalf of their patient.
      • Providers should submit requests on office letterhead using one of the following methods:
        • Fax: (803) 896-3862 (Attn: LIMS)
        • Encrypted email: NBSLab@dph.sc.gov 
          • Please include "DPH PHI" in the subject line. To send the email securely, follow your facility’s email encryption process.
      • Information needed for requests:
        • Child’s full name at birth
        • Date of birth
        • Mother’s full name at time of the child’s birth
        • Request for “Hemoglobin (Sickle Cell) screen results”
        • Contact name and phone number for the provider’s office
        • A completed DPH 1878 Form MUST be signed by the patient/requestor and received by the PHL with the request before any results can be released to the provider.  
      • Turnaround time: Results are faxed back to the provider as soon as possible, typically within 24–72 hours after all required documentation is received.
    • Option 2: Patient or Parent/Guardian Request
      • Individuals may request their own results directly from the Public Health Laboratory. 
      • For individuals 18 years or older:
        • Complete DPH 1623 - Authorization to Release Health Information:
        • Provide a copy of a valid government-issued photo ID.
        • Ensure the form includes:
          • Full name at birth
          • Date of birth
          • Mother’s full name at time of birth (written in the space below “Patient’s Name and Date of Birth”)
          • Request for "Hemoglobin (Sickle Cell) screen results”
      • For individuals under 18 years old:
        • A parent or legal guardian must complete and sign DPH 1623 - Authorization to Release Health Information:
        • A copy of the parent/guardian’s valid photo ID must be included.
        • Ensure the form includes:
          • Full name at birth
          • Date of birth
          • Mother’s full name at time of the child’s birth (written in the space below “Patient’s Name and Date of Birth”)
          • Request for “Hemoglobin (Sickle Cell) screen results”
        • Note: Results can only be released to the legal adult patient, or to a parent/guardian when the patient is a minor.
      • Individuals may submit required forms and identification by mail or in person.
        • Mailing/In-Person Address:
          DPH Public Health Laboratory – Attn: QA Office
          Hayne Building
          8231 Parklane Road
          Columbia, SC 29223
      • Processing time: By law, the PHL may take up to 30 days to complete a request. Typical processing time is 5–10 business days after receiving all required information.

Patients Born Outside South Carolina

  • If the individual was not born in South Carolina, please contact the newborn screening program in the state of birth.
  • DPH cannot provide results for individuals born in another state.
  • If newborn results cannot be located, consider:
    • Testing through the individual’s healthcare provider.
    • Testing services offered by a local sickle cell foundation.

Sickle Cell Foundations in South Carolina

These organizations may provide testing, counseling, or support services:

  • James R. Clark Memorial Sickle Cell Foundation
    1420 Gregg St., Columbia, SC 
    (800) 506-1273
  • L.D. Barksdale Sickle Cell Anemia Foundation
    645 South Church St., Spartanburg, SC 
    (864) 582-9420
  • Orangeburg Area Sickle Cell Foundation
    825 Summers Ave., Orangeburg, SC 
    (803) 534-1716
  • COBRA Human Services Agency – Sickle Cell Program
    3962 Rivers Ave., Charleston, SC
    (800) 354-4704

Need Help?

If you have questions about requesting Hemoglobin (Sickle Cell) screening results, please contact the Public Health Laboratory Monday–Friday, 8:30 a.m.–4:30 p.m.

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Result Reporting and Interpretation

Abnormal results are reviewed by the DPH laboratory follow-up team and sent directly to providers for clinical follow-up. 

  • In the case of a critical test result, the primary healthcare provider listed on the newborn screening card will be directly contacted by the Newborn Screening Program. 
  • The healthcare provider will need to contact the family to arrange for an additional screening or confirmatory testing.

DPH Newborn Screening eReports Portal

Normal results are not called and are available to providers through the secure DPH Newborn Screening eReports Portal, accessible 24/7.

SC Cystic Fibrosis NBS Testing Algorithms

Infants under 30 days oldInfants over 30 days old
Cystic fibrosis testing algorithm imageCystic fibrosis testing algorithm image

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Religious Refusals and Exemptions

Neonatal Screening for Inborn Metabolic Errors and Hemoglobinopathies, Sections 44-37-30 and 44-37-35 of the South Carolina Code of Laws requires: 

  • Every child born in South Carolina is required to have a newborn screen.
  • Parents may only exempt testing based on religious grounds.
  • Parents must sign a religious exemption/refusal form if they decline the newborn screen. 
  • The hospital must keep a copy of the refusal form and send the original to the DPH NBS Program via one of the following methods:
    • Mail the original to:
      Newborn Screening
      SC DPH Public Health Laboratory
      8231 Parklane Road
      Columbia, SC, 29223
    • Fax a scanned copy to: (803) 898-0337
    • Send a copy via encrypted email to: NBS@dph.sc.gov
      • Please include "DPH PHI" in the subject line. To send the email securely, follow your facility’s email encryption process.
  • One copy can be given to the parent or guardian. One copy is filed under consents at the health department/facility where the form was signed. 
  • The form will be retained according to DPH medical records retention schedule 18810 “Newborn Screening Follow-Up Documentation Records”, records group number: 169.
  • The form will be retained by the PHL Newborn Screening Follow-Up Office for a period of 9 years.
  • After this time period is met, the information will be stored at the State Records Center for 10 years and then destroyed.

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Unsatisfactory Specimens

If a newborn screening specimen is received and determined to be unacceptable for any reason, it is classified as unsatisfactory. In such cases, our follow-up team will notify the infant’s healthcare provider by mail to request collection of a repeat specimen.

Training Flyers

Training Videos

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Supply Requests

If you are a healthcare professional in need of more DPH 1327 NBS Dried Blood Spot Collection Cards or manilla envelopes, please contact the Public Health Laboratory Supply Department: phl-supply@dph.sc.gov, (803) 896-0913.

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Newborn Screening Bloodspot Training

The DPH State Public Health Laboratory can provide interactive hands-on newborn screening (NBS) training utilizing infant heel simulators, practice newborn screening cards, and other materials. Trainings are offered at no cost to all South Carolina providers. 

Training topics covered:

  • Overview of newborn screening
  • SC conditions tested
  • Specimen collection 
  • Identifying improper specimens 
  • Packaging & shipping 
  • Abnormal results

All levels of newborn experience are welcome. Trainees will receive a DPH Newborn Screening training certificate at the completion of the training.

Sign up for training by sending an email to nbsqi@dph.sc.gov or calling (803) 896-1140.

Training flyers:

Comments from past trainings: 

  • “Learned so much, staff made it comfortable, felt like a discussion with round table input and improvements.”
  • “Awesome training! We loved hearing our site location stats and ways we can improve our collections!”
  • “It was an excellent presentation with interactive education for staff. It was the right length and excellent material presented.”

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Educational Resources for Providers

The South Carolina Newborn Screening Program offers free educational materials and resources to all healthcare professionals upon request.

For Providers

Newborn Screening Training Flyers

External Resources

  • Newborn Screening ACT Sheets and Algorithms: Provides downloadable guidance sheets and diagnostic algorithms to assist healthcare providers in managing various genetic conditions.
  • Baby’s First Test: The most comprehensive source for information about newborn screening in the U.S. Includes condition details, state-specific screening info, and family stories.
  • CDC - Newborn Screening: Public health guidance and education from the Centers for Disease Control and Prevention. Great for understanding the science behind screening.
  • HRSA - Heritable Disorders: Learn about national policies and the Recommended Uniform Screening Panel (RUSP) from the Health Resources and Services Administration.
  • HRSA - About Newborn Screening: This Health Resources & Services Administration page explains the essentials of Newborn Screening (NBS) in the U.S.
  • Expecting Health: Works collectively with organizations, healthcare professionals, people, and communities to provide the right information at the right time - from planning a pregnancy to early infant care.
  • NewSTEPs - NBS Disorders: Summarizes the disorders included in or under consideration for newborn screening and provides an interactive table of those conditions for program use. 

Videos

For Parents

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Becoming a New Submitter

Healthcare practices and facilities that wish to become a new submitter for newborn screening must complete the steps below to establish access and communication with DPH.

How to Apply

  • Step 1: Email Required Information
    • Send an email to NBSQI@dph.sc.gov with the following details:
      • Clinic full name
      • Complete clinic mailing address
      • Clinic phone number
      • Clinic fax number
      • Clinic email address
    • This information allows DPH to create your facility profile in the newborn screening system.
  • Step 2: eReports Access
  • Step 3: Await Confirmation
    • Once your submission is received and processed, the DPH Laboratory will provide your account credentials and instructions for submitting newborn screening specimens.

Need Help?

Need Supplies?

If you need to order supplies, such as DPH 1327 NBS Collection Cards or manilla envelopes, please contact the Public Health Laboratory Supply Department: phl-supply@dph.sc.gov, (803) 896-0913

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Correcting a Newborn Screening Lab Report

If a newborn screening laboratory report contains incorrect patient or specimen demographic information, a request can be submitted to correct the report.

Steps to Submit a Correction

  1. Download the Correction Form 
    Obtain the DPH- 4493 - Correction Request for Submitted Newborn Screening Specimen Form (pdf).
  2. Complete the Form
    Fill out all required fields accurately. Incomplete or unsigned forms may delay processing.
  3. Submit the Form 
    • Send the completed form along with:
      • A copy of the original Newborn Screening Report to be corrected.
      • Your site's official fax cover sheet.
    • Submission Options:
      • Fax: (803) 896-3862
      • Encrypted email: NBSLAB@dph.sc.gov
        • Please include "DPH PHI" in the subject line. To send the email securely, follow your facility’s email encryption process.

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Documents and Forms

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Meetings and Recorded Sessions

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References and Resources

  1. South Carolina Newborn Screening Manual: Detailed procedural manual (specimen collection, follow-up, provider responsibilities, appendices).
  2. South Carolina Newborn Screening Collaborative: A hospital–public health quality improvement initiative to improve specimen transport time and timeliness.
  3. South Carolina Neonatal Screening Regulations (60–80): State regulatory requirements for newborn metabolic and hemoglobinopathy testing.
  4. South Carolina Code §44-37-30 (Neonatal testing/blood sample storage/confidentiality statute): This state law discusses mandates, exemptions, confidentiality, and storage of newborn screening specimens.
  5. South Carolina Rare Disease Advisory Council: A resource hub for rare diseases in SC, linking to newborn screening information.
  6. CDC - Newborn Screening: Public health guidance and education from the Centers for Disease Control and Prevention. Great for understanding the science behind screening.
  7. Baby’s First Test - South Carolina: A family- and provider-focused site that shows how newborn screening works in SC (conditions, educational materials, and more).
  8. ACMG - American College of Medical Genetics and Genomics: Professional guidance and medical information on genetic testing and newborn screening practices from the American College of Medical Genetics and Genomics.
  9. HRSA - Heritable Disorders: Learn about national policies and the Recommended Uniform Screening Panel (RUSP) from the Health Resources and Services Administration.
  10. Expecting Health: Works collectively with organizations, healthcare professionals, people, and communities to provide the right information at the right time - from planning a pregnancy to early infant care.
  11. HRSA- Newborn Screening Results and Follow-Up: Detailed information on the interpretation of newborn screening results and recommended follow-up procedures. It outlines result categories for blood spot, hearing, and critical congenital heart disease (CCHD) screenings. 

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Contact Information

Contact the Newborn Screening Program
Division Director
Beth Bair, MS, PhD
Program Director
bairea@dph.sc.gov 
(803) 896-0991

Administrative Support and NBS General Inquiries
Toshiro Washington
NBS Lab Administrative Assistant
washints@dph.sc.gov 
(803) 896-0795

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FAQ

Yes. Since 1962, newborn screening has been mandated by South Carolina Code of Laws, Care of the Newly Born, Sections 44-37-30 and 44-37-35 and South Carolina (SC) Code of Regulations 60-80 Neonatal Screening for Inborn Metabolic Errors and Hemoglobinopathies.

There is no DPH consent form for newborn screening. All infants born in SC are required by law to be screened. 

View the South Carolina Newborn Screening Manual, which includes laws, regulations, and official departmental instructions, for more information. 

Parents may refuse the tests only on religious objections. To obtain a Parental Statement of Religious Objection form, download the appropriate pdf below:

Blood for the dried blood spot (DBS) specimen is collected by performing a heel stick on the newborn, ideally between 24 and 48 hours after birth. A few drops of blood are gently expressed from the baby's heel onto an approved filter paper card (Form DPH-1327). One large drop of blood should be applied to each pre-printed circle on the card. There are seven pre-printed circles on the card. If one large drop of blood is applied per circle, the blood should fully saturate the circles without layering or oversaturating. The specimen is then allowed to air-dry completely for at least 3 hours before packaging for transport. 

Unacceptable methods for collecting a newborn screen: 

  • From umbilical cord blood. 
  • From the arch of the infant’s foot. 
  • From a newborn’s fingers. 
  • From a newborn’s earlobes. 
  • From an area that is swollen or was previously punctured. 
  • From an uncleared intravenous (IV) line.

Waiting at least 24 hours after birth before collecting a newborn screening specimen is critical for accurate detection of many conditions. A specimen collected before 24 hours of life could give false positive or false negative test results. The 24-hour period allows time for the baby’s metabolism to stabilize and for abnormal levels of certain markers (e.g., amino acids, hormones, enzymes) to become detectable. Blood specimens should be collected from newborns between 24 and 48 hours of life.

Exceptions to the 24-hour rule: 

  • A newborn screen should always be collected prior to transfusion or discharge. 
  • Facilities responsible for transferring an infant are encouraged to collect a newborn screen prior to the transfer.

An unsatisfactory specimen is one that cannot be accurately tested by the laboratory due to poor quality. The most common reasons include (but are not limited to):

  • Quantity insufficient: not enough blood in the circles or the blood didn’t soak through to the back of the card
  • Clotted or layered: oversaturation or multiple drops layered in one circle
  • Contaminated: if the blood on the card comes into contact with a foreign substance such as alcohol, powder, lotion, or other substance
  • Partial unsatisfactory specimen: some spots are acceptable, but not enough are usable for the lab to complete all required tests

If a specimen is deemed unsatisfactory, a repeat collection is required as soon as possible to avoid delays in screening.

For more information on unsatisfactory specimens, please see the Educational Resources for providers section

For Birthing Hospitals (Courier Pickup)

  • A statewide overnight courier service picks up specimens Sunday night through Friday night. 
  • The courier does not operate on Saturday nights because the newborn screening laboratory is closed on Sundays. 
    • Specimens collected on Saturday evenings should be held in a secure, dry place and shipped with the next scheduled pickup.

For All Other Submitters (e.g., pediatric clinics, home birth providers)

Submitters who are not served by the hospital courier have two options:

  • Option 1: Use Overnight Shipping
    • Use a reliable overnight shipping service, (e.g., UPS, FedEX), to send specimens directly to the lab. When using a shipping service, keep a record with the name of the patient and the tracking number to ensure the specimen arrives at the public health laboratory. 
    • Shipping address:
      South Carolina Public Health Laboratory
      Attn: Newborn Screening  
      8231 Parklane Road, Columbia, SC, 29223
  • Option 2: Drop Off at a Local Health Department
    • Submitters may drop off specimens at their nearest SC public health department
    • These locations have regular courier pickups that route specimens to the state lab. 
    • Contact your local public health office for drop-off hours and instructions.

If the adoption is finalized or a legal guardian is in place, you may enter the adoptive parent or legal guardian’s information in the mother’s information section. Be sure to include their contact information to ensure proper communication of results.

If the adoption is not yet finalized, you may enter the name of the law firm in the mother’s information section. Be sure to include their contact information to ensure proper communication of results.

Always enter the physician’s demographics and the newborn’s medical record number (MRN); this assists the NBS program if there is an abnormal result. 

The newborn screen should be collected before a transfusion if possible. 

If a blood transfusion is expected, the first specimen should be collected on admission. Additionally, a specimen should be collected between 24–48 hours of age, regardless of TPN (total parenteral nutrition) status.Collecting before transfusion helps ensure accurate screening results, as transfusions can affect certain test outcomes.

  • If this is not possible, collect the initial specimen and indicate the date of the most recent transfusion. Infants who receive transfusions after collecting the initial newborn screen should have a repeat hemoglobin, biotinidase deficiency, and galactosemia screening 120 days after the date of the last transfusion.
  • If the date of the last transfusion is unknown, put the date of hospital discharge as the date of the most recent transfusion.

For more information, please see pages 7 and 8 of the South Carolina Newborn Screening Manual or contact our Follow-Up team at nbsfollowup@dph.sc.gov

In premature, low birth weight, NICU, and/or sick infants, screening results may be invalid due to immaturity and/or the stress of prematurity/illness. To ensure the best specimen:

  • If the infant is receiving only IV fluids or total parenteral nutrition/ hyperalimentation, the specimen may be collected if the infant is at least 24 hours of age, and the lab slip is clearly marked “TPN or NPO.”
  • All premature, low birth weight, NICU, and/or sick infants shall receive their initial screening by 2 days of age, regardless of their health status.

For more information, please see pages 7 and 8 of the South Carolina Newborn Screening Manual or contact our Follow-Up team at nbsfollowup@dph.sc.gov

No, it is not acceptable to use umbilical cord blood for newborn screening. 

  • Cord blood may contain maternal cells, which can interfere with accurate testing. 
  • It may not reflect the infant’s true metabolic or hematologic status.
  • Using cord blood can lead to false-positive or false-negative results.

If you're having difficulty collecting blood for a newborn screening:

  • Warm the infant’s heel with a warm pack or wrap for 3–5 minutes to increase blood flow.
  • Ensure the baby is well-hydrated and consider feeding just before the procedure.
  • Position the foot below the heart and gently massage the heel from ankle to toe to stimulate blood flow.
  • Use the correct lancet size and puncture the recommended area (the outer sides of the heel).
  • Avoid excessive squeezing, which can dilute the specimen with tissue fluid.
  • Allow drops to fall freely onto the card — don’t scrape or press the heel to the filter paper.

Yes. Newborn screening may be performed on all infants under a year old. After babies reach six months of age, any specimens collected from them are tested using a modified testing panel. Some tests are not performed after six months of age. 

Yes. Newborn screening is required by South Carolina state law for babies born in the state, regardless of where they are born — including at home or in a birth center. The process for collecting the newborn screening specimen is the same as in a hospital setting: 

  • A qualified midwife, nurse, or provider collects a heel stick blood specimen between 24–48 hours after birth using an approved filter paper card (Form DPH-1327). 
  • The card is air-dried for at least 3 hours before it is packaged for shipment. 
  • The dried specimen is then sent to the SC Public Health Laboratory via priority overnight shipping or dropped off at a local SC public health department.  

Re-testing may be necessary for several reasons to ensure accurate and reliable newborn screening results. Some of the most common reasons include:

  • Poor specimen quality: the blood spots may have been insufficient, contaminated, improperly dried, etc. affecting test accuracy.
  • Abnormal results: if the first screen shows an out-of-range result, a repeat newborn screening specimen will be needed to retest. 
  • Interfering factors: blood transfusions, TPN (total parenteral nutrition), or certain medications can interfere with results.
  • Premature infants, low birth weight, NICU, and/or sick infants: Infants < 34 weeks gestation and/or < 2500 g at birth typically require repeat screening at 28 days of age or at discharge, regardless of initial results (per DPH NICU protocol). For more information, please see pages 7 and 8 of the South Carolina Newborn Screening Manual or contact our Follow-Up team at nbsfollowup@dph.sc.gov.

In all situations listed above, a repeat specimen will be requested by the newborn screening follow up team.

If a newborn relocates to South Carolina from another state, healthcare providers should:

  • Verify that a newborn screen was completed in the original state and obtain a copy of the results.
  • Repeat the newborn screen in South Carolina if:
    • The infant is under 6 months of age and there is no documented screen.
    • The previous screen was incomplete or did not meet SC standards (e.g., collected too early, poor quality, etc.).
    • There is clinical concern or a family history of a screened condition.

Document the screening status in the child’s medical record and notify the South Carolina Newborn Screening Follow-up Program at nbsfollowup@dph.sc.gov for additional guidance.

To order newborn screening collection forms and mailing envelopes, please contact PHL-supply@dph.sc.gov with the following information:  

  • Provider Name 
  • Provider Full Address 
  • Contact Name/Phone Number 
  • Type and number of supplies being requested

eReports is South Carolina’s secure electronic results portal that allows authorized healthcare providers and facilities to view and download reports. Click Here to access the portal. 

New providers and their staff can be granted access to eReports for patients under 1 year old.

  1. Fill out: User Access Agreement (DPH 3268) (one for each user)
  2. Submit the completed forms:
    1. Email to: nbslab@dph.sc.gov
    2. For help, call: (803) 896-9530
  3. Any results greater than 1 year:
    1. Submit a request to:
    2. Email to: nbslab@dph.sc.gov
    3. For help, call: (803) 896-9530

If you are having trouble accessing eReports with your login, please contact our Laboratory Information Management System (LIMS) department for assistance: 

Yes. Each user must fill out and sign a User Access Agreement (DPH 3268)

After signing and completing the Agreement, return it via mail, fax or electronic scan to: 

  • SC DPH PHL 
    LIMS Administrator  
    8231 Parklane Rd, Columbia, SC 29223 
  • Fax: (803) 896-3862  
  • Email: NBSLab@dph.sc.gov 

If a newborn screening report is missing from the eReports portal:

  • Check the search criteria — verify the baby's name and date of birth are entered correctly.
  • If you are still having trouble locating results, please contact our LIMS department for assistance:

If you are experiencing technical difficulties with the South Carolina Newborn Screening eReports portal, or if the portal is unavailable, please contact the South Carolina Public Health Laboratory for assistance:

 

You can request a manual for using eReports by contacting our LIMS department for assistance:

eReports is a system that contains Protected Health Information (PHI) and uses security measures to protect patient data. These measures are aligned with HIPAA compliance standards to ensure the confidentiality, integrity, and security of all patient results.

  1. Fill out: Correction Form (DPH 4493) (one for each corrected report needed)
  2. Submit the completed forms:
    1. Email forms to: nbslab@dph.sc.gov
    2. For help, call: (803) 896-9530

All newborns are screened for Sickle Cell as part of the newborn screen. It is listed as Hemoglobinopathies on the Newborn Screening Report.  

For Pediatric Clinics:

  1. Fill out an Authorization to Release Information to Newborn Screening for Inborn Metabolic Errors and Hemoglobinopathies (DPH 1878). The form will need to be filled out by the patient if over the age of 18 years and the a parent/legal guardian if the patient is under the age of 18 years.
  2. Submit the completed form:
    1. Email form to: nbslab@dph.sc.gov
    2. For help, call: (803) 896-9530

Patient or Parent:

  1. Fill out an Authorization to Release Health Information (DPH 1623). The form will need to be filled out by the patient if over the age of 18 years and a parent/legal guardian if under the age of 18 years.
  2. Submit the completed form. The person signing the form must also submit a copy of their driver’s license for identity verification. Mail to: 
    Public Health Laboratory
    Attn: QA Office
    8231 Parklane Road
    Columbia, SC 29223

For help, call (803) 896-0899 or (803) 896-3897

  1. Fill out an Authorization to Release Health Information (DPH 1623). The form will need to be filled out by the patient if over the age of 18 years and a parent/legal guardian if under the age of 18 years.
  2. Submit the completed form. The person signing the form must also submit a copy of their driver’s license for identity verification. Mail to: 
    Public Health Laboratory
    Attn: QA Office
    8231 Parklane Road
    Columbia, SC 29223

For help, call (803) 896-0899 or (803) 896-3897

Healthcare practices and facilities that wish to become a new submitter for newborn screening must complete the steps below to establish access and communication with DPH.

Step 1: Email Required Information

  • Send an email to NBSQI@dph.sc.gov with the following details: 
    • Clinic full name 
    • Complete clinic mailing address 
    • Clinic phone number 
    • Clinic fax number 
    • Clinic email address 
  • This information allows DPH to create your facility profile in the newborn screening system.

Step 2: eReports Access 

DPH no longer mails printed newborn screening reports. All results must be accessed electronically and securely through the DPH Newborn Screening eReports Portal. 

  • To request access to the portal, complete an Authorized User and Confidentiality Agreement (DPH 3268) 
    • Each staff member needing access must complete a form. 
  • Submit completed forms as instructed on the document. 
  • This ensures compliance with privacy and data security requirements.

Step 3: Await Confirmation

Once your submission is received and processed, the DPH Laboratory will provide your account credentials and instructions for submitting newborn screening specimens. 

Need Help?

For questions or assistance with becoming a new submitter, please contact NBSlab@dph.sc.gov or call (803) 896-4777.

Interested in NBS Training?

The DPH State Public Health Laboratory can provide interactive hands-on newborn screening (NBS) training utilizing infant heel simulators, practice newborn screening cards, and other materials. Trainings are offered at no cost to all South Carolina providers.  

Training topics covered:  

  • Overview of newborn screening  
  • SC Conditions Tested  
  • Specimen Collection  
  • Identifying Improper Specimens  
  • Packaging & Shipping  
  • Abnormal Results  

Sign up for training by sending an email to nbsqi@dph.sc.gov or call (803) 896-1140.

If results of testing are abnormal, the newborn screening program may recommend additional testing and, in addition to the notification requirements established in Section 44-37-30(B)(1), notify one or more of the following to ensure timely provision of follow-up services: 

  • the physician or healthcare provider attending the child's birth or his/her designee; 
  • the physician or healthcare provider responsible for newborn care in the hospital; or 
  • the physician or healthcare provider identified for follow-up care after the newborn's discharge from the hospital.

Depending upon the severity of abnormal screening results, the physician will receive either phone and/or fax notification from the department, soon after laboratory results are known.   

  • If results of testing are abnormal, time-sensitive, and/or time-critical, the department may, in addition to notification requirements established in Section 44-37-30(B)(1) and (2), notify and provide information about the abnormal, time-sensitive, or time-critical screening results to a qualified pediatric specialist.

The attending physician (healthcare provider of record) is responsible for informing the parents or legal guardian of normal and abnormal newborn screening lab results, according to the newborn screening law. 

Depending upon the severity of abnormal screening results, the physician will receive either phone and/or fax notification from the newborn screening program soon after the laboratory results are known.

Newborn screening staff provide technical assistance and recommendations to physicians when reporting critical abnormal results. The attending physician will initiate appropriate medical follow-up and diagnosis when any abnormal test results occur.

The baby’s primary care provider will receive the newborn screening results if they are listed as the attending physician on the newborn screening collection form. If the attending physician listed on the collection form will not be providing follow up care for the infant, he or she must notify the newborn screening program with the name of the provider who will be providing follow-up care. 

It is vital that notifications regarding changes in provider are made in a timely manner to ensure that results are communicated to the correct provider.

The baby’s provider should alert the Newborn Screening Follow-Up team at nbsfollowup@dph.sc.gov that a baby is no longer in their care.

If an attending physician is unable to locate an infant who needs further testing or treatment, the physician shall notify the SC Newborn Screening Program. 

If the infant is at high risk of morbidity/mortality, the SC Newborn Screening Program will contact the appropriate DPH area staff, law enforcement, and/or emergency personnel, to make a home visit. 

In low-risk instances, DPH may contact the parents by phone or mail to inform them of the need for additional testing. 

  • Each public health area has additional Maternal and Child Health (MCH) and Epidemiology staff designated to facilitate follow-up services in emergency situations. Department staff will make all reasonable efforts to locate any infant at high risk of morbidity/mortality for further services.

Yes. The American College of Medical Genetics and Genomics (ACMG) provides ACT Sheets and Algorithms for healthcare providers looking for information on genetic conditions (identified through newborn screening and beyond) to help inform clinical decision making. Due to the rarity of many genetic conditions, ACT Sheets and Algorithms are excellent refreshers on the conditions, diagnoses, and next steps for patients. Learn more at the ACMG website.

Appropriate genetic counseling should be offered to all families of children with abnormal test results as outlined in the Official Departmental Instructions.

Most genetic counseling and testing services require a medical referral from a doctor. You can also contact providers directly to inquire about their services and whether a referral is needed. Note, this list is not inclusive of all prospective providers.

Families may also benefit from other programs, particularly if a disorder is confirmed:

If you have a question about a specific test result, you should contact the Newborn Screening Follow-Up team at:

A ‘Within Acceptable Limits’ result does not exclude the possibility that a newborn has one or more of the disorders on the panel.  If clinical suspicion exists for any of the disorders, diagnostic testing is recommended.

All specimens will be stored at minus 20° Centigrade for 12 months. This period allows for any necessary repeat testing, quality assurance, or program evaluation. After that time, they are destroyed in a scientifically acceptable manner. 

Specimens from infants diagnosed with a condition identified through screening may be stored for a longer period.

Newborn screening test results are finalized in a report format which are generally available within 4 - 5 business days of when the laboratory receives the specimen. Secondary testing takes longer to complete; in these instances, the reporting timeframe may be extended.

When a newborn screening specimen is deemed unsatisfactory, it must be recollected. Submit a new specimen as soon as possible.

The Newborn Screening Laboratory operates on Saturdays and some state holidays

The methods outlined below are only to be used in extraordinary circumstances when a heel stick cannot be performed. Heel stick is the preferred method for optimal laboratory results for the newborn screen. 

Important note: These methods often result in a specimen that is clotted, layered, scratched or contaminated and have an increased risk of being deemed unsatisfactory to test, which would require a recollect. This could result in critical delays in testing, disorder identification and in the health of the infant. Please consider these potential problems before opting to collect the newborn screen by one of the following methods.

Capillary Tube Collection

Blood collection using capillary tubes is discouraged because it increases the risk of a clotted, layered specimen or a torn or chafed card. If capillary tube collection becomes necessary due to clinical circumstances:

  • For each circle to be filled, use a sterile, plain tube. Anti-coagulants such as EDTA, citrate, and heparin will interfere with analysis. 
  • Touch the tip of the capillary tube to the blood drop from the heel and allow the blood to flow into the tube. (The tube may fill better by holding it in a near horizontal position as it touches the drop of blood).
  • Immediately after filling the capillary tube, apply the contents to the center of the first circle on the newborn screening card, allowing the blood to flow out and fill one circle. 
  • Waiting too long may allow the blood and plasma to separate and interfere with test analysis. 
  • Do not touch the tube to the filter paper. 
  • Do not dab the blood on or “color in” the circle. 
  • Apply blood to only one side of the filter paper. 
  • Do not apply multiple capillary specimens to the same circle.   
  • Continue the steps above for each circle on the filter paper.

Venous Blood Collection

Although discouraged, if circumstances warrant venous blood collection:

  • Avoid drawing from an extremity where an IV is in place. 
  • Using appropriate pediatric blood drawing techniques, obtain the sample through a butterfly (winged) blood collection set. 
  • Remove or shorten catheter length so the blood can flow freely onto all the filter paper circles. 
  • Syringe collection of the blood is discouraged because the lack of anticoagulant and time delays can cause clot formation and separation of the specimen.

Umbilical Catheter Collection

  • To avoid contamination from substances previously infused through the line, draw 2 - 2.5 cc’s before collecting the newborn screening specimen. 
  • Collect the blood in a syringe and apply it to the circles immediately to avoid blood clots that would make the specimen unsatisfactory. 
  • Fill all circles with one large drop of blood and let the blood soak through to the other side of the card. Allow the blood to completely dry for 3 – 4 hours before sending the newborn screening specimens to the Public Health Laboratory.

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