2 Types of Hearing Loss
- Malformations of the outer or middle ear causing permanent conductive hearing loss
- Imperfections in the development of the hearing nerve causing sensorineural hearing loss
This webpage describes issues related to permanent conductive hearing loss only.
Microtia = “small ear” – It comes in different grades in terms of how much the outer ear is underdeveloped. Microtia is usually accompanied by aural atresia or ear canal stenosis (narrowed ear canal, no hearing change).
Atresia – Aural atresia refers to the absence an external ear canal – always results in hearing loss. Often also malformation of the external ear and middle ear, but the inner ear and auditory nerve are frequently normal.
A narrowed ear canal is called a stenotic canal or referred to as ear canal stenosis, which may not affect hearing.
- Congenital microtia/aural atresia is rare with an incidence of 1:10,000 births
- More than 75% of these cases are unilateral, resulting in maximum conductive hearing loss (around 60 dB HL)
- In approximately 25% of cases, the “normal” ear in patients who have one-sided may also have a hearing loss on their normal appearing ear.
Accompanying aural atresia:
- Approximately 12% have a heart deformation
- Approximately 8% have a kidney deformation
- Greater risk to develop cholesteatoma
Atresia and microtia may be associated with syndromes including: Treacher Collins, Crouzon’s, Apert’s, Klippel-Feil, Preiffer
New website for families of children with microtia or atresia: www.earcommunity.com
Improvement via Reconstructive Surgery for Children with Deformed Ears
- Ability to listen binaurally was measured after surgery for unilateral conductive HL – results within the normal range
- No difference in outcomes based on age at time of surgery – 10 yrs to 45 yrs
- Conclusion – no convincing evidence of benefit of early reconstructive surgery for unilateral conductive hearing loss
- Reconstructive surgery for bilateral conductive hearing loss results in worse hearing ability than that achieved from bone-anchored hearing solutions (BAHA)
- BAHA eliminates the conductive hearing loss at most frequencies versus 25-30 dB of conductive hearing loss remaining after reconstructive surgery (this is true only after the BAHA has been implanted).
Permanent conductive hearing loss can also be caused by malformation of or damage to the middle ear structures. Examples would be congenital or early onset of otosclerosis (calcium deposits develop on middle ear bones), middle ear structures damaged due to cholesteatoma, or changes to the eardrum and ossicles due to continuous middle ear disease (chronic ear infections).
Amplification Options for Children with Conductive Hearing Loss
1. Standard hearing aids, especially if the hearing loss is not at the maximum conductive hearing loss level (loss is better than 50+ dB HL)
2. CROS hearing aid (for unilateral issues) has been found to be ineffective or detrimental to listening for school-age children in typical classroom settings
3. Traditional bone conduction hearing aid
4. BAHA with soft band
- The anchoring the device to bone provides an advantage of 10 to 15 dB, especially at the high frequencies of vital importance to proper speech recognition in noise.
- Compared to conventional bone conductors, the BAHA system has better gain at the high frequencies and less distortion.
- Surgical options to open up the ear canal typically does not restore normal hearing (-10 – +15 dB HL) nor does a traditional bone conduction hearing aid whereas a bone anchored device can improve hearing to approximately 15 dB HL
Support for Families:
The Ear Foundation: BAHA Users Support
Ear to Ear Foundation, Inc: http://eartoearfoundation.org/p/about-us.html