High prevalence of sensorineural hearing loss among survivors of neonatal congenital diaphragmatic hernia

Citation
Cmt. Robertson et al., High prevalence of sensorineural hearing loss among survivors of neonatal congenital diaphragmatic hernia, AM J OTOL, 19(6), 1998, pp. 730-736
Citations number
50
Categorie Soggetti
Otolaryngology
Journal title
AMERICAN JOURNAL OF OTOLOGY
ISSN journal
01929763 → ACNP
Volume
19
Issue
6
Year of publication
1998
Pages
730 - 736
Database
ISI
SICI code
0192-9763(199811)19:6<730:HPOSHL>2.0.ZU;2-K
Abstract
Objective: This study aimed to determine the prevalence of sensorineural he aring loss (SNHL) in 2-5-year-old survivors with neonatal respiratory failu re due to congenital diaphragmatic hernia (CDH) with or without the need fo r extracorporeal membrane oxygenation (ECMO). Study Design: The study design was a prospective, multicenter, longitudinal outcome study of consecutively surviving neonates admitted to a single ter tiary intensive care unit. Setting: The study was conducted at four audiologic departments affiliated with tertiary-level intensive care follow-up programs. Patients: Thirty-seven surviving children receiving neonatal intensive care from February 1989 through January 1995 for neonatal respiratory failure d ue to CDH were studied. Excluded were 15 children with early death and 1 ch ild lost to follow-up. Intervention: The initial treatment depended on the severity of neonatal re spiratory failure: ECMO-treated (n = 31,20 survivors) (death before ECMO in itiation, 2) and non-ECMO treated (n = 20, 17 survivors, another survivor l ost to follow-up). Main Outcome Measure: Early childhood audiologic test results were measured . Results: Sensorineural hearing loss was found in almost 60% of subjects: EC MO-treated, 12 (60%) of 20; non-ECMO-treated, 10 (59%) of 17. Of the 22 chi ldren with SNHL, 16 had mild- to-moderate low-frequency sloping to moderate -to-severe high-frequency loss. Of the remaining, six had severe-to-profoun d loss at 500 Hz and above. Seventeen children had normal responses to soun d as newborns or in infancy. Five children were not tested. Documented prog ression was found in nine children. Twenty children currently are using amp lification, and 2 have had cochlear implantation. Conclusions: Or children with CDH in this area presenting early with severe neonatal respiratory failure, SNHL developed in 60% by 2-5 years of lift. Ongoing monitoring of the hearing status of children with CDH is imperative .