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Laboratory Tests: Sickle Cell Screening

*Sickle cell disease affects children primarily of African, Mediterranean, or Caribbean heritage, but other ethnic groups can be at risk. Approximately 1 in 400 children of African heritage are affected.

All infants and children at risk for sickle cell disease must be screened, with test results documented in the medical record. If previous test results are not documented, rescreen if the child is at risk. If the child is not at risk (through ethnicity or documented test results), note this in the record.

All newborns in the District of Columbia should be screened for sickle cell disease through DC’s Newborn Screening Program.

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

 

Screening Follow-up

  • Screen all newborns for sickle cell disease as part of DC's Newborn Screening Program.
  • Screen children at risk for sickle cell disease if test results are not documented in child's medical record.
  • Document results of all follow-up hemoglobinopathy screening in the medical record.
  • If child is not at risk (by ethnicity or previous screening), indicate this in medical record.

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