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
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
.