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Published on: August 25, 2014
Congenital cytomegalovirus screening in neonates born after 35 weeks gestation-is targeted screening beneficial?
Mary Liza Aldon1, Gayatiri Raveentheran1, Zubair Amin1,2
1Department of Neonatology, Khoo Teck Puat-National University Children Medical Institute, National University Healthcare System, Singapore, Singapore.
Insights
Targeted screening for congenital Cytomegalovirus (cCMV) is feasible and cost-effective in Singapore. Early detection through this method can prevent hearing loss in newborns.
Area of Science:
- Neonatal screening
- Infectious diseases
- Public health
Background:
- Congenital Cytomegalovirus (cCMV) is the leading non-genetic cause of sensorineural hearing loss in children.
- Early treatment within the first months of life is crucial for preventing hearing loss.
- Evaluating targeted screening strategies is important for resource allocation in healthcare.
Purpose of the Study:
- To assess the utility, feasibility, and cost-effectiveness of targeted cCMV screening in a Singaporean tertiary hospital.
- To compare the costs of targeted screening versus universal or no screening.
- To identify neonates at risk for cCMV for early intervention.
Main Methods:
- A retrospective analysis of 5,277 neonates born at ≥35 weeks gestation between February 2022 and January 2023.
- Screening criteria included failed hearing screening, low birth weight (<2.5kg), small for gestational age (SGA), or clinical suspicion.
- Urine samples were tested for CMV using polymerase chain reaction (PCR); clinical and audiological data were collected.
Main Results:
- 6% (305/5,277) of neonates met screening criteria; 0.06% (3/5,277) were diagnosed with cCMV.
- The targeted screening model's cost was S$146,656.30, significantly lower than universal screening (S$853,890.16).
- Three cCMV-positive neonates received timely treatment with Valganciclovir, with one initially failing but later passing hearing tests.
Conclusions:
- Targeted cCMV screening is feasible and complements universal newborn hearing screening.
- This strategy enables cost-effective early detection and intervention for cCMV in neonates.
- Implementing targeted screening can improve outcomes for infants at risk of cCMV-related complications.
Introduction:
Congenital Cytomegalovirus (cCMV) is the most common congenital viral infection and leading cause of non-genetic sensorineural hearing loss in children. Timely treatment within the first months of life can prevent hearing loss. We evaluated utility, feasibility, and short-term cost implications of targeted cCMV screening in a tertiary public healthcare institution in Singapore.
Methods:
We analyzed data from neonates born at ≥35 weeks gestation from 1st February 2022 to 31st January 2023, at the National University Hospital, Singapore. Screening criteria for CMV testing were neonates who failed hearing screening at birth, had a birth weight <2.5 kg, small for gestational age (SGA), or had clinical suspicion for cCMV. Urine samples were obtained within two weeks of birth for CMV polymerase chain reaction (PCR) testing. We collected clinical, ophthalmological, neuroimaging, laboratory, and audiological data. A limited, short-term cost analysis was performed to compare costs of three cCMV screening strategies (universal, targeted, and no screening) two years after implementation.
Results:
Out of 5,277 neonates, 305 (6%) met the screening criteria. Among those screened, 70.5% (215/305) were SGA or had a birth weight <2.5 kg, and 23.3% (71/305) failed the hearing screen. The overall diagnostic yield was 0.06% (3/5,277). There was one false positive result (0.3%; 1/305). Three neonates (0.98%; 3/305) were diagnosed with cCMV by urine PCR. One was SGA without intracranial abnormality, and two had low birth weight with intracranial calcifications. None had cytopenia or transaminitis, and all ophthalmology screenings were normal. All infected neonates were started on Valganciclovir. One neonate failed the hearing test at one month of age but passed repeat assessments by three months. Two neonates exhibited upper motor neuron signs in the lower limbs and are on long-term follow-up. The total estimated direct treatment-related cost without cCMV screening was S$104,445.79. In the targeted screening model, the total cost was S$146,656.30, compared to S$853,890.16 in the universal screening model.
Conclusion:
We demonstrated the feasibility of targeted cCMV screening, which complements universal newborn hearing screening in a tertiary neonatal center in Singapore. Targeted cCMV screening can be implemented cost-effectively during the neonatal period, enabling early detection and intervention.
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