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Published on: June 8, 2017
Integration of congenital cytomegalovirus screening within a newborn hearing screening programme
Rachael Beswick1, Michael David2, Hideki Higashi3
1Child and Youth Community Health, Children's Health Queensland Hospital and Health Service, Brisbane, Queensland, Australia.
Insights
Targeted salivary cytomegalovirus (CMV) screening for newborns referred from hearing tests is feasible and cost-effective. This approach can identify congenital CMV (cCMV) early to improve hearing outcomes.
Area of Science:
- Neonatal screening
- Infectious disease diagnostics
- Public health interventions
Background:
- Congenital cytomegalovirus (cCMV) is a leading cause of non-genetic sensorineural hearing loss in infants.
- Early identification and intervention for cCMV can mitigate hearing impairment.
- Current screening methods for cCMV are limited in widespread application.
Purpose of the Study:
- To evaluate the feasibility and cost-effectiveness of implementing targeted salivary cytomegalovirus (CMV) polymerase chain reaction (PCR) testing within a newborn hearing screening program.
- To assess the practical and financial viability of integrating cCMV screening into existing audiology referral pathways.
Main Methods:
- A prospective study was conducted across three tertiary maternity hospitals in Queensland, Australia.
- Infants referred from newborn hearing screening were offered salivary swabs for CMV PCR testing.
- Positive CMV PCR results triggered medical assessment and potential treatment with oral valganciclovir.
Main Results:
- Parental consent for salivary cCMV screening was high at 83.0%.
- The prevalence of cCMV in infants with confirmed hearing loss was 3.64%.
- Implementation costs for cCMV screening were found to be negligible compared to non-screening management.
Conclusions:
- Integrating salivary cCMV testing into universal newborn hearing screening is a realistic and achievable strategy.
- The program demonstrated practical feasibility and financial viability in the Australian context.
- This targeted screening approach holds promise for improving hearing outcomes in infants with cCMV.
Aim:
Targeted screening by a salivary cytomegalovirus (CMV) polymerase chain reaction (PCR) of infants who 'refer' on their newborn hearing screen has been suggested as an easy, reliable and cost-effective approach to identify and treat babies with congenital CMV (cCMV) to improve hearing outcomes. This study aimed to investigate the feasibility and cost-effectiveness of introducing targeted salivary cCMV testing into a newborn hearing screening programme.
Methods:
The study included three tertiary maternity hospitals in Queensland, Australia between August 2014 and April 2016. Infants who 'referred' on the newborn hearing screen were offered a salivary swab for CMV PCR at the point of referral to audiology. Swabs were routinely processed and tested for CMV DNA by real-time quantitative PCR. Parents of babies with a positive CMV PCR were notified, and the babies were medically assessed and, where appropriate, were offered treatment (oral valganciclovir).
Results:
Of eligible infants, the parents of 83.0% (234/283) consented to the cCMV screen. Of these, 96.6% returned a negative result (226/234), and 3.4% (8/234) returned a positive result (three true positive; five false positive). The prevalence of cCMV for infants with confirmed hearing loss was 3.64% (P = 2/55; confidence interval = 0.44-12.53%). The cost comparison suggests the cost implementation of cCMV screening (and subsequent potential treatment benefits and management over time), compared to non-screening (and subsequent management), to be negligible.
Conclusion:
Incorporating cCMV testing into Universal Newborn Hearing Screening within Queensland is realistic and achievable, both practically and financially.
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