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What is sensorineural hearing loss?

02/03/2025

Understanding sensorineural hearing loss

Sensorineural hearing loss (SNHL) is the most common form of permanent hearing impairment. It occurs when the delicate hair cells in the inner ear, or the nerve pathways that transmit sound to the brain, become damaged.

Unlike conductive hearing loss—which is due to problems in the outer or middle ear—sensorineural loss is generally permanent. This condition can result from a range of factors, including age-related degeneration, exposure to loud noises, head injuries, or other health-related issues. Early diagnosis and intervention are key in managing its impact on communication and quality of life.

Symptoms of sensorineural hearing loss

Sensorineural hearing loss can be caused by a variety of conditions, but it is most commonly caused by the natural ageing process, which accounts for around 90% of this type of hearing loss. It affects 1 in 7 over the age of 65. Changes in your hearing as you get older are normal, but if you’re concerned about your hearing, help and support from your local Amplifon clinic is never too far away. We offer a variety of different hearing aid solutions that can help make hearing the things around you just a bit clearer.

Causes of sensorineural hearing loss

Sensorineural hearing loss typically arises from damage to the inner ear’s hair cells or the neural pathways that convey sound. The principal causes include:

Ageing

Often referred to as presbycusis, age-related hearing loss occurs as the sensory cells gradually deteriorate, especially affecting the perception of high-frequency sounds.

Exposure to loud noises

Both sudden exposure to extremely loud sounds and prolonged exposure to high decibel levels (such as in industrial environments or at concerts) can cause irreversible damage.

Head injury

Trauma to the head may impact the cochlea and auditory nerves, leading to sensorineural impairment.

Viral infections

Infections, or other viruses that target the inner ear can cause inflammation and permanent damage.

Ototoxic medications

Certain drugs, including some antibiotics and chemotherapy agents, can have toxic effects on the inner ear.

Genetic factors

A family history of hearing loss can increase an individual’s risk.

Ménière's disease

This inner ear disorder, which also causes vertigo and tinnitus, can contribute to sensorineural hearing loss.

In some cases, the condition may affect only one ear—known as unilateral sensorineural hearing loss—often due to specific events or conditions such as acoustic neuroma or idiopathic sudden loss.

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Bilateral and unilateral sensorineural hearing loss

Sensorineural hearing loss can affect both ears (bilateral) or just one ear (unilateral):

What is bilateral sensorineural hearing

This form impacts both ears and is most commonly associated with the ageing process, chronic noise exposure, or systemic conditions. Bilateral loss often results in difficulties with sound localisation and understanding speech, especially in noisy environments.

Causes of unilateral hearing loss

Affecting only one ear, unilateral loss can still pose significant challenges. It may lead to issues with sound directionality and can impair communication in complex auditory settings. Causes of unilateral loss include acoustic neuroma, sudden idiopathic events, or localised trauma.

Sudden sensorineural hearing loss

Sudden sensorineural hearing loss (SSNHL) is an unexpected, rapid loss of hearing that typically occurs in one ear over the span of hours or even minutes. Although relatively rare, it is considered a medical emergency. Treatment usually involves prompt administration of corticosteroids and other interventions aimed at restoring hearing.

The exact cause often remains unclear, although viral infections, vascular incidents, or autoimmune responses are possible contributors. Immediate medical attention is crucial to maximise the chance of recovery.

Acute sensorineural hearing loss

Acute sensorineural hearing loss refers to a rapid decline in hearing ability that develops over several days or weeks. While not as instantaneous as SSNHL, this form of hearing loss still demands swift action to prevent further deterioration. As with sudden sensorineural hearing loss, early diagnosis and treatment—often involving medication and rehabilitative measures—are essential. Determining the underlying cause, whether it be infection, trauma, or an adverse drug reaction, is key to effective management.

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Sensorineural hearing loss audiogram

An audiogram is a fundamental diagnostic tool that graphically represents an individual’s hearing ability across various frequencies and intensities. In sensorineural hearing loss, the audiogram generally shows:

  • High-frequency loss: damage to the cochlear hair cells typically results in reduced sensitivity to higher frequency sounds.
  • Flat or sloping curve: a consistent degree of hearing loss may be observed across multiple frequencies, often in a flat or gradually sloping pattern.
  • No air-bone gap: unlike conductive hearing loss, sensorineural hearing loss does not display a significant difference between air conduction and bone conduction thresholds.

Conductive vs sensorineural hearing loss

Understanding the difference between conductive and sensorineural hearing loss is crucial for accurate diagnosis and treatment planning:

Conductive hearing loss

This type occurs when sound is impeded in the outer or middle ear due to factors such as ear infections, fluid accumulation, or structural abnormalities. Treatments may include medication or surgery, and in many cases, hearing can be fully restored.

Sensorineural hearing loss

By contrast, sensorineural hearing loss stems from damage to the inner ear or auditory nerve. This form is typically permanent, though its effects can be mitigated through hearing aids, cochlear implants, and other interventions.

FAQs

What are 3 causes of sensorineural hearing loss?

The three most common causes of sensorineural hearing loss (SNHL) are:

  • Ageing (Presbycusis): over time, the inner ear’s hair cells naturally deteriorate, leading to gradual hearing loss.
  • Noise exposure: prolonged or sudden exposure to loud noises can permanently damage the hair cells in the cochlea.
  • Genetic factors: some people inherit a predisposition to sensorineural hearing loss, which may develop early or later in life.

Other causes include head trauma, infections, ototoxic medications, and inner ear diseases.

Can hearing aids help sensorineural hearing loss?

Yes, hearing aids are one of the most effective treatments for sensorineural hearing loss. They amplify sound to compensate for the loss of hearing sensitivity.

There's no a best type of hearing aid for sensorineural hearing loss, because it depends on the severity of the condition. For mild to moderate SNHL, behind-the-ear (BTE) and receiver-in-canal (RIC) hearing aids are popular choices. For severe cases, power hearing aids or cochlear implants may be recommended.

Do cochlear implants work for sensorineural hearing loss?

Yes, cochlear implants can be an effective solution for severe or profound sensorineural hearing loss when hearing aids are no longer sufficient. Unlike hearing aids, which amplify sound, cochlear implants bypass damaged hair cells and directly stimulate the auditory nerve. They are especially beneficial for individuals with little to no natural hearing ability.

Can sensorineural hearing loss be cured?

Currently, there is no cure for sensorineural hearing loss, as the damage to inner ear hair cells is usually permanent. However, treatment options such as hearing aids, cochlear implants, and auditory rehabilitation can significantly improve communication and quality of life. Research into regenerative medicine and gene therapy offers hope for future treatments.

Can sensorineural hearing loss get worse?

Yes, sensorineural hearing loss can worsen over time, particularly if caused by ageing, progressive conditions, or continued exposure to loud noises. Regular hearing check-ups and protective measures—such as avoiding excessive noise exposure and monitoring medication side effects—can help slow further deterioration.

Can otosclerosis cause sensorineural hearing loss?

Yes, while otosclerosis primarily causes conductive hearing loss due to abnormal bone growth in the middle ear, in some cases, it can also lead to sensorineural hearing loss if the condition affects the inner ear. This is known as cochlear otosclerosis, where the abnormal bone growth damages the cochlea and impacts nerve function.

Does Ménière’s disease cause sensorineural hearing loss?

Yes, Ménière’s disease can cause fluctuating sensorineural hearing loss, often accompanied by vertigo, tinnitus, and a feeling of ear fullness. Over time, the hearing loss may become progressive and permanent, primarily affecting low-frequency sounds in the early stages.

How to tell if hearing loss is sensorineural or conductive?

A hearing test (audiometry) performed by an audiologist is the best way to determine whether hearing loss is sensorineural or conductive. Key differences include:

  • Sensorineural hearing loss affects high-pitched sounds, making speech unclear even at louder volumes. It is typically permanent and affects the inner ear or auditory nerve.
  • Conductive hearing loss results from blockages or damage in the outer/middle ear, making sounds seem muffled but not distorted. It may be temporary and can often be treated with medication or surgery.

An audiogram and bone conduction test can accurately diagnose the type of hearing loss.

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