Volume 165, Number 12, 885-890, DOI: 10.1007/s00431-006-0192-2

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Selecting neonates with congenital cytomegalovirus infection for ganciclovir therapy

Koenraad Smets, Kris De Coen, Ingeborg Dhooge, Lieve Standaert, Sabrina Laroche, Ludo Mahieu, Noël Logghe, Veerle Cossey and An Boudewyns

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Abstract

Objective  

The objective of this study is to look for evidence based or scientific guidelines for selection of newborns with congenital cytomegalovirus (CMV) infection that might benefit from treatment with ganciclovir.

Materials and methods  

A literature search was conducted involving the MEDLINE database and the Cochrane Collaboration Library. Abstracts were reviewed to select pertinent articles dealing with ganciclovir therapy in neonates. References from selected articles as well as from reviews were screened for additional relevant articles. In total, 13 case reports (16 patients in all), three descriptive uncontrolled studies (20 patients in all), two randomized dose-comparative studies (54 patients in all) and one randomized controlled study (42 patients) were identified.

Observations  

All reported patients presented with central nervous system manifestation of CMV infection. Only the randomized controlled study showed a reduction of hearing deterioration in the treated group. Published predictors of hearing loss in congenitally CMV infected children allow identification of candidates that might benefit from treatment. Studies so far are promising but of insufficient number to make evidence based recommendations about indications for treatment of congenital CMV. As such, studies are very difficult to conduct and treatment of infants at high risk of hearing loss may appear justified. There is scientific data to help clinicians in selecting a subgroup of infants that is at higher risk of hearing deterioration and therefore might benefit the most from ganciclovir therapy.

Keywords  Ganciclovir - Congenital cytomegalovirus infection - Treatment - Sensorineural hearing loss

Prepared for the Flemish Society of Pediatrics’ Neonatology and Perinatal Epidemiology Working Group: Aerssens Peter, MD, department of Pediatrics, Virga Jesse Hospital, Hasselt, Belgium; Casaer Alexandra, MD, Neonatal Intensive Care Unit, St Jan Hospital, Bruges, Belgium; Cools Filip, MD, Neonatal Intensive Care Unit, Free University of Brussels, Brussels Belgium; Deloof Els, MD, department of Pediatrics, Heilig-Hart Hospital, Leuven, Belgium; Jeannin Philippe, MD, department of Pediatrics, Jan Palfijn Hospital, Gent, Belgium; Naulaers Gunnar, MD, PhD, Neonatal Intensive Care Unit, University Hospital Leuven, Leuven, Belgium; Peirens Geertrui, MD, Child & Family, Hasselt, Belgium; Schatteman Isabelle, MD, department of Otorhinolaryngology, St Augustinus Hospital, Wilrijk, Belgium; Van Laer Paul, MD, Namen, Belgium; Van Mol Christine, MD, Neonatal Intensive Care Unit, St Augustinus Hospital, Wilrijk, Belgium

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