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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.
Objective:
To report results of audiometric evaluations in high-risk congenital diaphragmatic hernia survivors and their exposure to audiological risk factors (mechanical ventilation, high frequency oscillation, aminoglycoside therapy and neuromuscular blocking agents).
Design:
All newborns with high-risk congenital diaphragmatic hernia born between January 2003 and June 2009 were treated consecutively at the Neonatal Intensive Care Unit, Pediatric Hospital, University of Padova. Thirty-two survived and 26 of them underwent formal audiological evaluation (tonal and speech audiometry, otoacoustic emission, and immitance measurements) and follow up.
Results:
Twenty-one children had normal hearing; 4 had conductive hearing loss, which was successfully treated; and 1 had severe sensorineural hearing loss and suffers from Turner syndrome.
Conclusions:
Our series revealed a lower prevalence of sensorineural hearing loss in high-risk congenital diaphragmatic hernia survivors than in other studies, suggesting that the association between hearing loss and congenital diaphragmatic hernia has yet to be accurately defined and fully elucidated.
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