Spectrum of hearing disorders and their management in children with CHARGE syndrome.

Abstract

OBJECTIVE:

The CHARGE syndrome is associated with ear anomalies and deafness in addition to other malformations. Deformations of the ossicles or aplasia of the semicircular canals, cochlear hypoplasia, hypoplasia or aplasia of the VIIIth cranial nerve and abnormal routing of the VIIth cranial nerve, sigmoid sinus, and emissaries are typical findings. The aim of this study is to explore the feasibility and procedure of cochlear implantation in patients with CHARGE syndrome and to assess the outcome.

STUDY DESIGN:

Retrospective case review.

SETTING:

Tertiary referral center; cochlear implant program.

PATIENTS:

Ten patients with CHARGE syndrome and 3 patients with CHARGE-like syndrome treated in our center due to hearing impairment. Eleven patients were congenitally deaf, 1 patient had progressive hearing loss, and 1 patient had mixed hearing loss.

INTERVENTION:

Computed tomography of temporal bones and magnetic resonance imaging of the brain; bone-anchored hearing aid surgery, cochlear implantation, rehabilitation results.

MAIN OUTCOME MEASURES:

Surgical suitability and hearing rehabilitation.

RESULTS:

We illustrate the management of preoperative diagnostics, surgical planning, and hearing rehabilitation. One patient with mixed hearing loss underwent bilateral bone-anchored hearing aid surgery. Because 2 patients had bilateral aplasia of the auditory nerves, we recommended an auditory brainstem implant. The unilateral cochlear implantation was performed in 9 patients and bilateral in 1 patient. In selected cases, it was helpful to plan the operation using a simulator for temporal bone surgery. Complex malformations, such as in CHARGE syndrome, with an increased intraoperative risk for complications should be facilitated by using intraoperative digital volume tomography-assisted navigation and intraoperative digital volume tomography control of electrode position. The results after CI surgery vary due to the differing extent of additional disabilities such as developmental delay, intellectual delay, and visual impairment. Nine of our patients showed improved responsiveness with the cochlear implant. Open speech comprehension could not be observed in 8 patients, whereas the follow-up period was less than 1 year in 4 patients. The relatively high age of our patients at implantation might be an important factor.

CONCLUSION:

Careful planning of the treatment of CHARGE syndrome patients with sensorineural hearing loss can, to a limited extent, lead to auditory benefit without increasing surgical complications. Cochlear implantation is therefore indicated after critical assessment.

• Authors: Susan Arndt, Roland Laszig, Rainer Beck, Christian Schild, Wolfgang Maier, Ralf Birkenhäger, Stefanie Kroeger, Thomas Wesarg, Antje Aschendorff
• Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology (Otol Neurotol) Vol. 31 Issue 1 Pg. 67-73 (Jan 2010) ISSN: 1537-4505 [Electronic] United States
• PMID: 19841601 (Publication Type: Journal Article)

Topics

• Abnormalities, Multiple (diagnostic imaging, surgery)
• Adolescent
• Adult
• Audiometry
• Child
• Child, Preschool
• Cochlear Implantation
• Cochlear Implants
• Ear, Inner (diagnostic imaging, surgery)
• Female
• Hearing Disorders (diagnostic imaging, surgery)
• Humans
• Infant
• Magnetic Resonance Imaging
• Male
• Radiography
• Syndrome
• Treatment Outcome