Format

Send to

Choose Destination
See comment in PubMed Commons below
Arch Dis Child Fetal Neonatal Ed. 2006 Jul;91(4):F257-62. Epub 2006 Mar 10.

Low prevalence of hearing impairment among very low birthweight infants as detected by universal neonatal hearing screening.

Author information

1
Speech and Hearing Center, The Chaim Sheba Medical Center, Tel Hashomer, Israel 52621. rothd@post.tau.ac.il

Abstract

OBJECTIVES:

To (a) study the prevalence of hearing impairment in a cohort of very low birthweight (VLBW) infants and (b) evaluate the effectiveness of transient evoked otoacoustic emissions (TEOAE) as a first stage in-hospital hearing screening tool in this population.

STUDY DESIGN:

The study group was a cohort of 346 VLBW infants born in 1998-2000 at The Sheba Medical Center. The prevalence of hearing impairment in the study group was compared with that of all other newborn infants participating in a universal newborn hearing screening programme during the same period. To evaluate the effectiveness of TEOAE, a control group of 1205 healthy newborns who had no known risk factors for hearing impairment was selected. The results and follow up of hearing screening for these infants were examined retrospectively.

RESULTS:

Only one VLBW infant (0.3%) was diagnosed with bilateral sensory-neural hearing loss. In addition, nine infants (2.7%) were diagnosed with conductive hearing loss. Bronchopulmonary dysplasia and low Apgar score were the most significant factors for predicting the occurrence of conductive hearing loss. The percentage of VLBW infants who successfully passed the in-hospital TEOAE screening was 87.2, compared with 92.2% in the full term control group. No false negative cases were detected on follow up.

CONCLUSIONS:

The study shows a low incidence of sensory-neural hearing loss in a cohort of VLBW infants and a relatively high incidence of conductive hearing loss. TEOAE screening was found to be an effective first stage in-hospital hearing screening tool in this population.

PMID:
16531449
PMCID:
PMC2672719
DOI:
10.1136/adc.2005.074476
[Indexed for MEDLINE]
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire Icon for PubMed Central
    Loading ...
    Support Center