Symptomatic infant characteristics of congenital cytomegalovirus disease in Australia.

BACKGROUND

Human cytomegalovirus (CMV) is the most common cause of viral intrauterine infection. In utero transmission can occur during primary maternal infection, reactivation or reinfection of seropositive mothers.

OBJECTIVE

To describe the aetiology and clinical features of infants diagnosed with congenital CMV and to document maternal factors that were presented.

METHODS

Active national surveillance was initiated in 1999 in collaboration with the Australian Paediatric Surveillance Unit.

RESULTS

Monthly notifications resulted in 70 cases of congenital CMV being identified between 1999 and 2003. Nearly all of the cases were symptomatic with the most common clinical sequelae reported in infected infants being jaundice, thrombocytopaenia, hepatomegaly, petechiae, purpura and splenomegaly. Almost half (43.5%) of the infants had central nervous system (CNS) complications, such as microcephaly, chorioretinitis, sensorineural hearing loss, intracranial calcifications, developmental delay or seizures, with over half presenting two or more CNS abnormalities. Maternal febrile illness was noted in 54.8% of the cases. The majority of mothers were primiparous (46.4%) or secundiparous (39.3%), indicating two different population groups at risk of primary CMV infection.

CONCLUSIONS

This study documents symptomatic congenital CMV cases in Australia.