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Progressive, Long-Term Hearing Loss in Congenital CMV Disease After Ganciclovir Therapy
Author(s) -
Tatiana M. Lanzieri,
A. Chantal Caviness,
Peggy Blum,
Gail J. DemmlerHarrison,
Shahzad Ahmed,
Hanna Baer,
Amit Bhatt,
Frank R. Brown,
Francis I. Catlin,
David K. Coats,
Jane C Edmonds,
Marily Flores,
Daniel Franklin,
Cindy Gandaria,
Jewel M. Greer,
Carol Griesser,
Mohamed A. Hussein,
Isabella Iovino,
A S Istas,
Haoxing D. Jin,
Mary K Kelinske,
Joseph T. Klingen,
Antone Laurente,
Thomas Littman,
Mary Murphy,
Jerry A. Miller,
Christopher T. Nelson,
Daniel E. Noyola,
Evelyn A. Paysse,
Alan K. Percy,
Sara Reis,
Ann Reynolds,
Judith C Rozelle,
O’Brien Smith,
Paul G. Steinkuller,
Marie Turcich,
Sherry Vinson,
Robert G. Voigt,
Bethann F. Walmus,
Jill Williams,
Daniel Williamson,
Kimberly G. Yen,
Martha D. Yow
Publication year - 2021
Publication title -
journal of the pediatric infectious diseases society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.269
H-Index - 31
eISSN - 2048-7207
pISSN - 2048-7193
DOI - 10.1093/jpids/piab095
Subject(s) - medicine , ganciclovir , sensorineural hearing loss , pediatrics , hearing loss , cytomegalovirus , surgery , human cytomegalovirus , herpesviridae , viral disease , audiology , immunology , virus
Background Long-term hearing outcomes among children with symptomatic congenital cytomegalovirus (CMV) disease who received 6-week ganciclovir therapy early in life are unknown. Methods Longitudinal study of 76 children with symptomatic congenital CMV disease, born 1983-2005, who were categorized into three groups: group A treated with ganciclovir; group B untreated who had microcephaly, chorioretinitis, or sensorineural hearing loss (SNHL; ≥25 dB) diagnosed in the first month of life (congenital); and group C untreated who did not meet criteria for group B. Results Patients in groups A (n = 17), B (n = 27), and C (n = 32) were followed to median age of 13, 11, and 13 years, respectively. In group A, patients received ganciclovir for median of 40 (range, 11-63) days; 7 (41%) had grade 3 or 4 neutropenia. Congenital SNHL was diagnosed in 11 (65%) patients in group A, 15 (56%) in group B, and none in group C. Early-onset SNHL was diagnosed between ages ≥1-12 months in an additional 4 (24%), 6 (22%), and 8 (25%) patients in groups A, B, and C, respectively. By the end of follow-up, 12 (71%), 16 (59%), and 7 (22%) of patients in groups A, B, and C, respectively, had severe (>70 dB) SNHL in the better-hearing ear. Conclusions In this study, most patients with symptomatic congenital CMV disease and congenital or early-onset SNHL eventually developed hearing loss severe enough to have been potential candidates for cochlear implantation, with or without 6-week ganciclovir therapy. Understanding long-term hearing outcomes of patients treated with 6-month oral valganciclovir (current standard of care) is needed.

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