Hearing assessment in high-risk congenital diaphragmatic hernia survivors

Carla Morando1, Paola Midrio, Piergiorgio Gamba

  • 1Neonatal Intensive Care Unit, Department of Pediatrics, University of Padova, Via Giustiniani 3, 35128 Padova, Italy. carla.morando@unipd.it

Insights

Congenital diaphragmatic hernia survivors show a lower rate of sensorineural hearing loss than previously reported. Further research is needed to fully understand the relationship between hearing impairment and congenital diaphragmatic hernia.

Area of Science:

  • Pediatric Otolaryngology
  • Neonatal Intensive Care
  • Audiology

Background:

  • Congenital diaphragmatic hernia (CDH) is a serious condition requiring intensive neonatal care.
  • Survivors of high-risk CDH are potentially exposed to audiological risk factors.
  • Hearing loss is a known complication in some high-risk infant populations.

Purpose of the Study:

  • To evaluate audiometric outcomes in survivors of high-risk congenital diaphragmatic hernia.
  • To assess the impact of specific audiological risk factors on hearing in these survivors.

Main Methods:

  • Retrospective analysis of 32 high-risk CDH survivors (born 2003-2009).
  • Formal audiological evaluations including tonal/speech audiometry, otoacoustic emissions, and immitance measurements were performed on 26 survivors.
  • Follow-up assessments were conducted.

Main Results:

  • Twenty-one children (80.8%) had normal hearing.
  • Four children (15.4%) presented with conductive hearing loss, which was successfully treated.
  • One child (3.8%) had severe sensorineural hearing loss and Turner syndrome.

Conclusions:

  • The prevalence of sensorineural hearing loss in this cohort of high-risk CDH survivors appears lower than reported in other studies.
  • The precise association between congenital diaphragmatic hernia and hearing loss requires further investigation.
  • Audiological monitoring is crucial for high-risk CDH survivors.
Abstract

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