Optic neuritis

Definition | Aetiology | Pathophysiology | Risk Factors | Signs and Symptoms | Investigations | Management

Definition

Optic neuritis is an inflammatory condition affecting the optic nerve, often associated with demyelinating diseases such as multiple sclerosis, leading to vision loss and eye pain.

Aetiology

  • Demyelinating disease: multiple sclerosis (most common association).
  • Infectious causes: viral infections (e.g., herpes zoster, syphilis, tuberculosis).
  • Autoimmune disorders: neuromyelitis optica, sarcoidosis, systemic lupus erythematosus.
  • Drug-induced: ethambutol, isoniazid, amiodarone.

Pathophysiology

  • Immune-mediated inflammation leads to demyelination of the optic nerve.
  • Axonal injury results in visual impairment and pain due to inflammation.
  • Remyelination may occur, but repeated episodes increase the risk of permanent damage.

Risk Factors

  • Female sex (higher prevalence in multiple sclerosis).
  • Young adults (typically 20-40 years old).
  • Personal or family history of autoimmune diseases.
  • Prior viral infections.

Signs and Symptoms

  • Monocular vision loss: usually sudden and progressive over days.
  • Eye pain: worsened by eye movement.
  • Dyschromatopsia: impaired colour vision, particularly red desaturation.
  • Relative afferent pupillary defect (RAPD): reduced direct pupillary response in the affected eye.
  • Phosphenes: flashes of light with eye movement.

Investigations

  • Clinical assessment: fundoscopy may show optic disc swelling in papillitis; normal in retrobulbar neuritis.
  • MRI brain and orbits: detects white matter lesions suggestive of multiple sclerosis.
  • Blood tests: inflammatory markers, infectious serology if suspected.

Management

These are specialist treatments mainly

1. Acute Treatment:

  • High-dose IV corticosteroids: methylprednisolone for severe cases.
  • Oral corticosteroids: used in some cases but may increase recurrence risk.

2. Disease Modification:

  • Immunomodulatory therapy if associated with multiple sclerosis.

3. Supportive Care:

  • Visual rehabilitation for persistent deficits.
  • Regular ophthalmic and neurological follow up.

4. Referral:

  • Neurology: if multiple sclerosis or neuromyelitis optica is suspected.
  • Ophthalmology: for acute visual symptoms and monitoring.
  • Infectious diseases: if an infectious cause is suspected.