Cytomegalovirus infection in a single‐centre Australian neonatal cohort. (28th February 2022)

• Record Type: Journal Article
• Authors: Seneviratne, Maheesha; Fernando, Malindu E; Kandasamy, Yogavijayan; White, Andrew; Sabesan, Vanaja; Norton, Robert
• Is Part Of: Journal of paediatrics and child health. Volume 58:Number 7(2022)
• Page Start: 1136
• Page End: 1144
• Publication Date: 2022-02-28
• Subjects: CMV -- development -- sensorineural hearing loss; Children -- Health and hygiene -- Periodicals; Pediatrics -- Periodicals; 618.92
• DOI: 10.1111/jpc.15914
• Languages: English
• ISSNs: 1034-4810

Abstract

Abstract : Aim: Congenital cytomegalovirus (cCMV) is the most common infectious cause of congenital malformation, non‐genetic sensorineural hearing loss and neurodevelopmental sequelae in childhood. The primary aim of this retrospective cohort study was to identify the birth and neurodevelopmental outcomes of neonates diagnosed with symptomatic and asymptomatic cCMV in a large regional tertiary referral hospital. Methods: This was a retrospective cohort study of laboratory‐based cCMV diagnoses in neonates born at a single study centre between January 2005 and January 2020. Audit of medical records was undertaken to evaluate maternal characteristics, symptom patterns, radiological and neurodevelopmental outcomes of neonates meeting the laboratory diagnostic criteria during the first 24 months. Results: There were 45 neonates with proven CMV infection and 27 mothers with proven infection with an associated pregnancy outcome. Nineteen neonates were born at term (>37 weeks). Of these, 32 (71.1%) neonates had a significant intercurrent comorbidity and 22 (48.9%) neonates were reported to have a degree of delay in one or more developmental domains. A large proportion (77.3%) of the symptomatic untreated neonates had an unknown history of maternal infection compared to the asymptomatic (10.0%) and symptomatic treated (53.8%) neonates ( P = 0.001). Conclusion: Up to half of the neonates with cCMV were at risk of developing a degree of developmental delay at our centre. Whether these outcomes are related primarily to CMV infection or are confounded by the co‐existence of prematurity is unclear and needs further evaluation in prospective studies.