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Conductive hearing loss

From Wikipedia, the free encyclopedia
Conductive hearing loss
Anatomy of the human ear.
SpecialtyENT surgery

Conductive hearing loss (CHL) is a type of hearing impairment that occurs when sound waves are unable to efficiently travel through the outer ear, tympanic membrane (eardrum), or middle ear structures such as the ossicles. [1] This blockage or dysfunction prevents sound from being effectively conducted to the inner ear, resulting in reduced hearing ability. CHL can either impact one ear, called unilateral conductive hearing loss, or both ears, called bilateral conductive hearing loss.[2] Common causes include ear infections, fluid in the middle ear, earwax buildup, damage to the eardrum, or abnormalities in the ossicles.

CHL can occur alone or alongside sensorineural hearing loss, in which case it is classified as mixed hearing loss. Depending on the underlying cause, CHL is often treatable and sometimes reversible through medical interventions, such as medication, surgery, or assistive devices like hearing aids. However, chronic or permanent cases may require long-term management to improve hearing and communication abilities.[3]

Signs and symptoms

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CHL makes all sounds seem faint or muffled. The hearing loss is usually worse in lower frequencies. Congenital conductive hearing loss is identified through newborn hearing screening or may be identified because the baby has microtia or other facial abnormalities. CHL developing during childhood is usually due to otitis media with effusion and may present with speech and language delay or difficulty hearing. A later onset of CHL may have an obvious cause, such as an ear infection, trauma, or upper respiratory tract infection, or may have an insidious onset related to chronic middle ear disease, otosclerosis, or a tumour of the nasopharynx. Earwax is a very common cause of CHL, which may present suddenly when the wax blocks sound from getting through the external ear canal to the middle and inner ear.[4]

Causes

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Common causes of CHL include:[5]

External ear

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  • Cerumen (earwax) or foreign body in the external auditory canal
  • Otitis externa, infection or irritation of the outer ear
  • Exostoses, abnormal growth of bone within the ear canal
  • Tumor of the ear canal
  • Congenital stenosis or atresia of the external auditory canal (narrow or blocked ear canal).
    • Ear canal stenosis & atresia can exist independently or may result from congenital malformations of the auricle such as microtia or anotia.[6]
  • Acquired stenosis (narrowing) of the external auditory canal following surgery or radiotherapy

Middle ear

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Fluid accumulation is the most common cause of CHL in the middle ear, especially in children.[7] Major causes are ear infections or conditions that block the eustachian tube, such as allergies or tumors.[7] Blocking of the eustachian tube leads to decreased pressure in the middle ear relative to the external ear, and this causes decreased motion of both the ossicles and the tympanic membrane.[8]

Inner ear

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The third window effect is caused by:

Diagnosis

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Diagnosis requires a detailed history, local examination of the ear, nose, throat, and neck, and detailed hearing tests. In children, a more detailed examination may be required if the hearing loss is congenital.

Otoscopy

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Examination of the external ear canal and eardrum is important and helps identify problems located in the outer ear up to the tympanic membrane.

Differential testing

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For basic screening, CHL can be identified using the Rinne test with a 256 Hz tuning fork. The Rinne test, in which a patient is asked to say whether a vibrating tuning fork is heard more loudly adjacent to the ear canal (air conduction) or touching the bone behind the ear (bone conduction), is negative, indicating that bone conduction is more effective than air conduction. A normal, or positive, result is when air conduction is more effective than bone conduction.

With a one-sided conductive component, the combined use of both the Weber and Rinne tests is useful. If the Weber test is used, in which a vibrating tuning fork is touched to the midline of the forehead, the person will hear the sound more loudly in the affected ear because background noise does not mask the hearing on this side.

The following table compares sensorineural hearing loss to conductive:

Criterion Sensorineural hearing loss Conductive hearing loss
Anatomical site Inner ear, cranial nerve VIII, or central processing centers Middle ear (ossicular chain), tympanic membrane, or external ear
Weber test Sound localizes to the normal ear Sound localizes to the affected ear (ear with conductive loss)
Rinne test Positive Rinne; air conduction - bone conduction (both air and bone conduction are decreased equally, but the difference between them is unchanged). Negative Rinne; bone conduction - air conduction (bone/air gap)

Tympanometry

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Tympanometry, or acoustic impedance testing, is a simple objective test of the ability of the middle ear to transmit sound waves from the outer ear to the middle ear and to the inner ear. This test is usually abnormal with conductive hearing loss. A type B tympanogram reveals a flat response, due to fluid in the middle ear (otitis media) or an eardrum perforation.[9] A type C tympanogram indicates negative middle ear pressure, which is commonly seen in eustachian tube dysfunction.[9] A type A tympanogram indicates a shallow compliance of the middle ear, which is commonly seen in otosclerosis.[9]

Audiometry

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Pure tone audiometry, a standardized hearing test over a set of frequencies from 250 Hz to 8000 Hz, may be conducted by a medical doctor, audiologist or audiometrist, with the result plotted separately for each ear on an audiogram. The shape of the plot reveals the degree and nature of hearing loss, distinguishing conductive hearing loss from other forms. A conductive hearing loss is characterized by a difference of at least 15 decibels between the air conduction threshold and bone conduction threshold at the same frequency. On an audiogram, the "x" represents responses in the left ear at each frequency, while the "o" represents responses in the right ear at each frequency.

CT scan

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Most causes of CHL can be identified by physical examination, but if it is important to image the bones of the middle ear or inner ear, then a CT scan is required. A CT scan is useful in cases of congenital conductive hearing loss, chronic suppurative otitis media or cholesteatoma, ossicular damage or discontinuity, otosclerosis, and third window dehiscence. Specific MRI scans can be used to identify cholesteatoma.

Management

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Management falls into three modalities: surgical treatment, pharmaceutical treatment, and supportive, depending on the nature and location of the specific cause.[3]

In cases of infection, antibiotics or antifungal medications are an option. Some conditions are amenable to surgical intervention, such as middle ear fluid, cholesteatoma, and otosclerosis. If conductive hearing loss is due to head trauma, surgical repair is an option.[10] If absence or deformation of ear structures cannot be corrected, or if the patient declines surgery, hearing aids which amplify sounds are a possible treatment option.[7] Bone conduction hearing aids are useful as they deliver sound directly, through bone, to the cochlea or organ of hearing, bypassing the pathology. These can be on a soft or hard headband or can be inserted surgically, a bone-anchored hearing aid, of which there are several types. Conventional air conduction hearing aids can also be used.

See also

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References

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  1. Sooriyamoorthy, T.; De Jesus, O. (August 23, 2023). Conductive Hearing Loss. Treasure Island (FL): StatPearls Publishing. PMID 33085414. NBK563267.
  2. "Conductive Hearing Loss: Treatment Can Help, But Get It Early". Cleveland Clinic. Archived from the original on 2026-03-08. Retrieved 2026-06-18.
  3. 1 2 Hill-Feltham, Penny R.; Johansson, Martin L.; Hodgetts, William E.; Ostevik, Amberley V.; McKinnon, Brian J.; Monksfield, Peter; Sockalingam, Ravi; Wright, Tracy; Tysome, James R. (2021-04-01). "Hearing outcome measures for conductive and mixed hearing loss treatment in adults: a scoping review". International Journal of Audiology. 60 (4): 239–245. doi:10.1080/14992027.2020.1820087. ISSN 1499-2027. PMID 32985284. S2CID 222161183.
  4. Nieto, Hannah; Dearden, James; Dale, Stacey; Doshi, Jayesh (2017-03-09). "Paediatric hearing loss". BMJ: j803. doi:10.1136/bmj.j803. ISSN 0959-8138.
  5. "Hearing Loss". HealthCentral. Retrieved 8 June 2013.
  6. Kempfle, Judith S.; Remenschneider, Aaron K. (March 2024). "Management of congenital conductive hearing loss". Operative Techniques in Otolaryngology-Head and Neck Surgery. 35 (1): 26–36. doi:10.1016/j.otot.2024.01.004. ISSN 1043-1810.
  7. 1 2 3 Ruben, Robert J. (April 2007). "Hearing Loss and Deafness". The Merck Manual. Retrieved 8 June 2013.
  8. 1 2 Page 152 in:Rex S. Haberman (2004). Middle Ear and Mastoid Surgery. New York: Thieme Medical Pub. ISBN 1-58890-173-4.
  9. 1 2 3 Onusko, Edward M. (2004-11-01). "Tympanometry". American Family Physician. 70 (9): 1713–1720. ISSN 0002-838X. PMID 15554489.
  10. "Types, Causes and Treatment". Hearing Loss Association of America. Retrieved 8 June 2013.
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