The Journal of Pediatrics
Volume 143, Issue 1 , Pages 16-25, July 2003

Effect of ganciclovir therapy on hearing in symptomatic congenital cytomegalovirus disease involving the central nervous system: a randomized, controlled trial

From the Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama; the Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, the Department of Pediatrics, Baylor College of Medicine, Houston, Cook Children's Medical Center, Fort Worth, Texas; the Department of Pediatrics, University of California at San Diego, San Diego, California; the Department of Pediatrics, University of Arkansas, Little Rock, Arkansas; and the Department of Pediatrics, University of Alberta, Edmonton, Canada

Received 16 April 2002; received in revised form 28 October 2002 and 28 January 2003; accepted 25 March 2003.

See editorial, p. 4.

Abstract 

Objective To evaluate the efficacy and safety of ganciclovir therapy in neonates with congenital cytomegalovirus (CMV) disease.

Study design Neonates with symptomatic CMV disease involving the central nervous system were randomly assigned to receive 6 weeks of intravenous ganciclovir versus no treatment. The primary end point was improved brainstem-evoked response (BSER) between baseline and 6-month follow-up (or, for patients with normal baseline hearing, normal BSER at both time points).

Results From 1991 to 1999, 100 patients were enrolled. Of these, 42 patients had both a baseline and 6-month follow-up BSER audiometric examination and thus were evaluable for the primary end point. Twenty-one (84%) of 25 ganciclovir recipients had improved hearing or maintained normal hearing between baseline and 6 months versus 10 (59%) of 17 control patients (P=.06). None (0%) of 25 ganciclovir recipients had worsening in hearing between baseline and 6 months versus 7 (41%) of 17 control patients (P<.01). A total of 43 patients had a BSER at both baseline and at 1 year or beyond. Five (21%) of 24 ganciclovir recipients had worsening of hearing between baseline and ≥1 year versus 13 (68%) of 19 control patients (P<.01). A total of 89 patients had absolute neutrophil counts determined during the course of the study; 29 (63%) of 46 ganciclovir-treated patients had grade 3 or 4 neutropenia during treatment versus 9 (21%) of 43 control patients (P<.01).

Conclusions Ganciclovir therapy begun in the neonatal period in symptomatically infected infants with CMV infection involving the central nervous system prevents hearing deterioration at 6 months and may prevent hearing deterioration at ≥1 year. Almost two thirds of treated infants have significant neutropenia during therapy.

Abbreviations:  ANC, Absolute neutrophil count, CSF, Cerebrospinal fluid, ALT, Alanine aminotransferase, CASG, Collaborative Antiviral Study Group, BSER, Brainstem-evoked response, CMV, Cytomegalovirus, CNS, Central nervous system

 
  •  Committee membership of the National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group is listed at http://www.casg.uab.edu.

 Supported under contract with the Virology Branch, Division of Microbiology and Infectious Diseases of the National Institute of Allergy and Infectious Diseases (NIAID), NO1-AI-15113 and NO1-AI-62554, and by grants from the General Clinical Research Center Program (RR-032) and the State of Alabama.Presented at the 40th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC), Toronto, Ontario, Canada; 2000; Abstract 1942. Recipient of the ICAAC Program Committee Award in the area of Therapy of Microbial Diseases.

PII: S0022-3476(03)00192-6

doi:10.1016/S0022-3476(03)00192-6

The Journal of Pediatrics
Volume 143, Issue 1 , Pages 16-25, July 2003