Optic Neuritis
Written 18th July 2020 - Last Update 23rd July 2026
Optic Neuritis
Inflammation of the optic nerve — usually caused by multiple sclerosis (MS), of which it is
often the presenting symptom. See neurology/multiple-sclerosis.md for current disease-
modifying therapy (anti-CD20 agents now first-line for high-efficacy treatment).
Other causes
| Category | Causes |
|---|---|
| Infectious | Viral encephalitis (especially children), sinusitis, meningitis, TB, syphilis, HIV |
| Neoplastic | Metastasis to the optic nerve |
| Drugs/toxins | Lead, methanol, quinine, arsenic, certain antibiotics |
| Rare | Neuromyelitis optica, MOG-IgG disease, diabetes, pernicious anaemia, autoimmune disease, thyroid eye disease (Graves’ ophthalmopathy — see thyroid-eye-disease.md), bee stings, trauma |
Presentation
Demographics: typically age 20–40. Classic triad: vision loss, eye discomfort, reduced colour vision, ± RAPD.
- Vision loss, maximal over 1–2 days, usually a small central or paracentral scotoma; may progress to complete blindness
- Mild eye pain, worse with eye movement
- Only one eye affected
Examination
- Fundoscopy: optic disc may be swollen (papilloedema)
- Reduced visual acuity
- Disturbed colour vision — characteristically out of proportion to the reduction in visual acuity
- Relative afferent pupillary defect (RAPD)
Investigations
Gadolinium-enhanced MRI — to identify demyelinating disease (MS, MOG-IgG, neuromyelitis optica).
Management
- IV methylprednisolone 500–1000 mg, as for an MS flare. This hasn’t been shown to change the long-term visual outcome compared with observation alone, but may speed recovery and delay onset of further MS symptoms — treat if MS is suspected
- Discuss with neurology or ophthalmology
- Most cases resolve spontaneously over 2–3 months