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Audition: Disorders

The World Health Organisation (WHO), in its factsheet on deafness and hearing impairment, refers to hearing impairment as “the complete or partial loss of the ability to hear from one or both ears. The level of impairment can be mild, moderate, severe or profound.”

The classifications are based on hearing thresholds (see Table 1, next page), most commonly measured using a standard procedure known as pure tone audiometry. In this approach, a measure of the quietest sound an individual can perceive is recorded at a number of different frequencies of sound. Plotting these values creates the audiogram.

WHO estimates from 2001 suggest that if an audiogram were to be recorded for every individual on the planet, approximately 600 million people worldwide would have a hearing loss affecting both ears, and 250 million of these would be of moderate-to-profound severity.

The actual level of disability resulting from a hearing loss is influenced by many factors beyond hearing thresholds. These factors include the amount of distortion in audible sounds, difficulties in processing and filtering auditory information, and the complexity of listening environment exposed to in a hearing impaired person's daily life. In general, a hearing loss of moderate or worse severity in both ears is deemed of particular clinical significance because, to be audible, a significant proportion of speech sounds must be raised beyond normal conversational levels. This has important consequences for the development of speech and language in children, which may be limited unless measures are taken to overcome the loss.

Additional to the level of hearing loss, the affected site or sites along the auditory pathway are used when labeling hearing impairments. Divisions are usually made into conductive (affecting the outer or middle ear), cochlear, retrocochlear (affecting the nerve of hearing), and central (affecting the cognitive processing of sound information).

This entry describes different types of hearing loss as well as some information on the relevant management options available.

Conductive Disorders

A conductive hearing loss occurs when the passage of sound between the outer ear and the cochlea is disrupted.

Obstruction of the Outer Ear Canal

Perhaps the most obvious cause of a conductive hearing loss is the inability of airborne sound waves to reach the tympanic membrane, as a result of occlusion of the ear canal. This may be caused by swelling or discharge resulting from infection (otitis externa), foreign bodies, or cerumen (ear-wax). Abnormalities during fetal development can result in a complete absence or a progressive narrowing of the ear canal, known as atresia or stenosis, respectively. The latter may occur later in life as a result of exostoses, bony growths commonly associated with extended exposure to cold water, such as repeated sea swimming.

Perforations

A hole, or perforation, in the tympanic membrane reduces the amount of sound energy passed from the ear canal into the middle ear bones. A perforation can be caused by a shock wave traveling down the ear canal from an explosion or an impact across the surface of the ear. Alternatively, the tympanic membrane may rupture during acute middle ear infections, alleviating the intense pain associated with a “bulging” eardrum. On rare occasions, middle ear infections may progress to the air-filled spaces situated in the mastoid area behind the ear, the surgical treatment of which may result in a cavity that links the mastoid to the ear canal, often with an accompanying conductive hearing loss.

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