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Hearing Loss - Causes - Sensorineural Hearing Loss unitron.com | Sudden Sensorineural Hearing Loss otohns.net | Sensorineural hearing loss - Dr.G.K.HEBBAR'S MICRO EAR SURGERY & ENT entcentre.com | COOL: Sensorineural Hearing Loss Evaluation entdoctors.org |
Sensorineural hearing loss is a type of hearing loss in which the root cause lies in the vestibulocochlear nerve (Cranial nerve VIII), the inner ear, or central processing centers of the brain. The Weber test, in which a tuning fork is touched to the midline of the forehead, localizes to the normal ear in people with this condition. The Rinne test, which tests air conduction vs. bone conduction is positive (normal), though both bone and air conduction are reduced equally. Sensorineural hearing loss can be mild, moderate, or severe, including total deafness. The great majority of human sensorineural hearing loss is caused by abnormalities in the hair cells of the organ of Corti in the cochlea. There are also very unusual sensorineural hearing impairments that involve the VIIIth cranial nerve (the Vestibulocochlear nerve) or the auditory portions of the brain. In the rarest of these sorts of hearing loss, only the auditory centers of the brain are affected. In this situation, central hearing loss, sounds may be heard at normal thresholds, but the quality of the sound perceived is so poor that speech can not be understood. Most sensory hearing loss is due to poor hair cell function. The hair cells may be abnormal at birth, or damaged during the lifetime of an individual. There are both external causes of damage, like noise trauma and infection, and intrinsic abnormalities, like deafness genes. Sensory hearing loss (also called sensorineural hearing loss) may also result from abnormalities of the VIII cranial nerve. Sensory hearing loss that results from abnormalities of the central auditory system in the brain is called Central Hearing Impairment. Since the auditory pathways cross back and forth on both sides of the brain, deafness from a central cause is unusual. This type of hearing loss can also be caused by prolonged exposure to very loud noise. For example, wearing headphones on full blast for a few hours.
[edit] Differential diagnosisTable 1. A table comparing sensorineural to conductive hearing loss
Sensorineural hearing loss may be congenital or acquired. [edit] Congenital
[edit] Acquired
[edit] Long term exposure to environmental noisePopulations of people living near airports or freeways are exposed to levels of noise typically in the 65 to 75 dbA range. If lifestyles include significant outdoor or open window conditions, these exposures over time can degrade hearing. The U.S. EPA and various states have set noise standards to protect people from these adverse health risks. The EPA has identified the level of 70 db(A) for 24 hour exposure as the level necessary to protect the public from hearing loss (EPA, 1974).
[edit] GeneticHearing loss can be inherited. Both dominant and recessive genes exist which can cause mild to profound impairment. If a family has a dominant gene for deafness it will persist across generations because it will manifest itself in the offspring even if it is inherited from only one parent. If a family had genetic hearing impairment caused by a recessive gene it will not always be apparent as it will have to be passed onto offspring from both parents Dominant and recessive hearing impairment can be syndromic or nonsyndromic. Recent gene mapping has identified dozens of nonsyndromic dominant (DFNA#) and recessive (DFNB#) forms of deafness.
[edit] Disease or illness
[edit] Medications
Some medications cause irreversible damage to the ear, and are limited in their use for this reason. The most important group is the aminoglycosides (main member gentamicin). Various other medications may reversibly affect hearing. This includes some diuretics, viagra and NSAIDs, and macrolide antibiotics. Extremely heavy Vicodin abuse is known to cause hearing impairment. There has been speculation that radio talk show host Rush Limbaugh's hearing loss was at least in part caused by his admitted addiction to narcotic pain killers, in particular Vicodin and OxyContin. [edit] Physical trauma
[edit] TreatmentPreviously, sensorineural hearing loss has been treated with hearing aids, which amplify sounds at pre-set frequencies to overcome a sensorineural hearing loss in that range; or cochlear implants, which stimulate the cochlear nerve directly. Some research suggests that idebenone alone or combined with Vitamin E may delay the onset of hearing loss or perhaps reverse it[citation needed]. Use of these agents for this purpose is considered experimental at this time. Some audiologists and ENTs have reported that if severe noise-induced hearing loss (exposures exceeding 140dB) is treated immediately (within 24 hours) with a course of steroids, that it can often be almost completely reversed. This, however, is anecdotal only; at the current time no known research has been made to either support or deny these claims. [edit] References
[edit] External links
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