hero image

Long Term Follow-up

Long Term Follow-up

Why Ongoing Follow-Up Is Important Typical Follow-Up Schedule
Early detection of changes in hearing, vision, or development allows children with cCMV to receive the interventions they need to reach their full potential. A collaborative care approach—including pediatricians, specialists, and early intervention providers—plays a critical role in supporting healthy growth and development.
  • First Year of Life: Frequent visits for hearing checks, developmental assessments, and medical evaluations.

  • Toddler and Preschool Years: Continued hearing tests every 6–12 months and developmental screenings at regular intervals.

  • School Age: Ongoing hearing monitoring, as well as academic and behavioral evaluations to support learning and social development.

    Check out the American Academy of Audiology guidelines for follow-up of hearing and balance in children with congenital CMV. 

Congenital cytomegalovirus (cCMV) infection can have a wide range of outcomes, from no apparent symptoms at birth to significant long-term health challenges. Even infants who appear healthy at birth may develop complications months or years later. For this reason, long-term monitoring and follow-up care are essential.

  • Late-Onset Hearing Loss: Children with cCMV are at risk for hearing loss that can develop or progress after the newborn period. Regular hearing assessments are recommended through early childhood.

  • Vision and Neurological Development: Some children may experience vision problems, motor delays, or cognitive differences that are not apparent at birth. Early identification allows for timely intervention services.

  • Speech and Language Development: Because cCMV can affect hearing and brain development, speech and language delays are common. Monitoring ensures early access to speech therapy if needed.

  • Growth and Overall Health: Ongoing evaluation by pediatric specialists, such as audiologists, ophthalmologists, and developmental pediatricians, helps detect and manage complications as they arise.

The doctors knew Cameron's problem was viral, but they couldn't pinpoint the virus. Finally, after about 2 days, my placenta lab test came back and it was infected with CMV. I was so relieved that Cameron was going to survive, but I was not ready for the next bombshell. The NICU doctor told us that as a result of is brain damage, Cameron would not be able to “walk, talk or learn."
— Julie, Mother