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 mainly1. 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.