HealthCheck Provider Education System

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Overview

Health Supervision

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Health Supervision

Laboratory Tests: Metabolic

DC law requires hospitals and birth centers to screen all newborns (with parental consent) for certain metabolic and hemoglobin disorders. Universal screening and early intervention help prevent life-threatening complications and serious chronic consequences of these diseases, including mental retardation and developmental disabilities.

Remember to consult and follow the DC Medicaid HealthCheck Periodicity Schedule.

 

Universal Newborn

The DC Newborn Metabolic Screening Program screens all District newborns for these disorders:

  • *Sickle cell disease (see next page)
  • G-6-PD deficiency
  • Congenital hypothyroidism
  • Galactosemia
  • Phenylketonuria
  • Maple syrup urine disease
  • Homocystinuria

 

Initial Screening

The DC Department of Health administers the Newborn Screening Program and notifies providers of abnormal test results, provides educational and referral information, monitors results of repeat tests, and tracks those who require treatment.

Perkin Elmer Genetics (1-866-463-6436) contracts with the DC Government to analyze blood samples from all District newborns and to provide test results.

 

Follow-up Screening: The PCP's Role

If the initial blood sample was obtained less than 24 hours after birth or if the sample was unacceptable, the PCP needs to obtain a second blood sample at 1 week of age.

If initial screening results indicate abnormalities, the PCP must:

  • Obtain a repeat blood test.
  • Provide appropriate referrals to pediatric specialists (endocrinology, hematology, genetics).
  • Document all follow-up screening and services in the child's medical record.

 

Resources

DC Newborn Metabolic Screening Program
899 North Capitol St., NE
Washington DC 20002
Phone: (202) 442-9344 or 442-5925

Neo Gen Screening, Inc.
110 Roessler Rd., Suite 200
Pittsburgh, PA 15220
Phone (412) 341-8658; fax (412) 341-8926
E-mail: Registration@neogenscreening.com

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