Clinically targeted screening for congenital CMV - Potential for integration into the National Hearing Screening Programme

S. Kadambari*, S. Luck, A. Davis, E. J. Williams, J. Berrington, P. D. Griffiths, M. Sharland

*Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    15 Citations (Scopus)

    Abstract

    Screening for a condition should only be undertaken if certain strict criteria are met. Congenital CMV (cCMV) is a leading cause of sensorineuronal hearing loss (SNHL) and meets many of these criteria, but is not currently screened for in the UK. Ganciclovir reduces CMV-induced progressive SNHL if treatment is begun in the first month of life. The Newborn Hearing Screening Programme (NHSP) has been shown to identify SNHL at the earliest possible age. The potential of integrating screening for cCMV into the NHSP is discussed to consolidate the link between screening, early diagnosis and management. Conclusion: The early diagnosis and treatment of cCMV may prevent a small proportion of late SNHL. In the absence of any screening programme, we provide evidence that clinically targeted screening through the NHSP is a potential option in the UK, enhancing the diagnostic pathway and enabling appropriate early treatment to reduce long-term morbidity.

    Original languageEnglish
    Pages (from-to)928-933
    Number of pages6
    JournalActa Paediatrica, International Journal of Paediatrics
    Volume102
    Issue number10
    DOIs
    Publication statusPublished - Oct 2013

    Keywords

    • Congenital CMV
    • Screening
    • Sensorineural hearing loss

    Fingerprint

    Dive into the research topics of 'Clinically targeted screening for congenital CMV - Potential for integration into the National Hearing Screening Programme'. Together they form a unique fingerprint.

    Cite this