Newborn Dried Blood-Spot Screening
Newborn Screening is a public health activity used for early identification of infants affected by certain genetic, metabolic, hormonal and/or functional conditions. This course covers screening for 29 heritable disorders and genetic diseases performed through dried blood-spot testing.
Complimentary thanks to support from the Virginia Department of Health.
Upon completion of this course, you should be able to:
- Identify common conditions that are found through the Newborn Screening Program
- Identify short-and long-term consequences of these conditions in neonates
- Discuss the hospital and nurse role in the newborn screening process
- Describe care of the neonate with a positive screen result
- Describe the process of collecting a dried blood-spot specimen and transporting it to the lab for analysis
Learning Method and Medium:
Learners participate in the interactive learning modules by correctly answering multiple choice questions dispersed throughout. Learners will be prompted to try again if a question is answered incorrectly. The course will open in a new tab – to exit the course, simply close that tab.
This publication and website is supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) as part of an award totaling $12,287,553. The contents are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by HRSA, HHS, or the U.S. Government. For more information, please visit HRSA.gov.
Purchase grants one learner one year’s access to lessons and quizzes (access expires 365 days from date of course activation.)
Estimated time to complete: 1 hour
Credit/contact hours: 1 hour
Expiration Date: May 31, 2020
Certificate of Completion