Optic Neuritis

Optic neuritis is inflammation of the optic nerve, the cable that carries visual information from the eye to the brain. It typically causes rapid vision loss, pain with eye movement, and color vision changes. While it often improves on its own, optic neuritis can be a first sign of multiple sclerosis.

What Optic Neuritis Feels Like

Typical symptoms include:

• Vision loss developing over hours to days
• Usually affects one eye at a time
• Vision may be blurry, dim, or have a "film" over it
• Pain with eye movement—characteristic symptom
• Pain may precede vision loss by a few days
• Color vision changes—red appears washed out
• Vision worse with heat or exercise (Uhthoff phenomenon)
• Flashing lights with eye movement (phosphenes)

What Causes Optic Neuritis

Demyelinating Disease (Most Common)

Multiple Sclerosis (MS)

• Optic neuritis is first symptom in ~20% of MS patients
• 50% of people with optic neuritis develop MS within 15 years
• MRI findings help predict MS risk

Neuromyelitis Optica (NMO/Devic's disease)

• Autoimmune attack on optic nerve and spinal cord
• Often more severe than MS-related optic neuritis
• AQP4 antibody positive
• Higher risk of poor recovery

MOG Antibody Disease (MOGAD)

• Autoimmune condition with MOG antibodies
• Can cause severe but often recoverable optic neuritis
• May be bilateral
• Different treatment approach than MS

Other Causes

• Infections (viral, Lyme disease, syphilis, cat-scratch disease)
• Inflammatory conditions (sarcoidosis, lupus)
• Vaccination-related (rare)
• Idiopathic (no cause found)

When to Seek Care

How Optic Neuritis Is Diagnosed

Clinical Examination

• Visual acuity—usually reduced
• Color vision—red desaturation characteristic
• Pupil exam—relative afferent pupillary defect (RAPD) present
• Visual field—various patterns of loss
• Fundus exam—optic disc may look normal or swollen

Key Tests

• MRI brain and orbits with contrast

  • Shows optic nerve inflammation
  • Brain lesions predict MS risk
  • Essential for diagnosis and prognosis

• Optical coherence tomography (OCT)

  • Measures nerve fiber layer thickness
  • May show swelling acutely
  • Thinning develops over months

• Visual evoked potentials (VEP)

  • Shows delayed signal conduction
  • Can remain abnormal even after visual recovery

• Blood tests

  • NMO-IgG (AQP4 antibodies)
  • MOG antibodies
  • Other tests based on suspected causes

• Lumbar puncture—sometimes needed

Treatment Options

Observation

For typical optic neuritis:

• Vision often improves on its own over 2-12 weeks
• Most people recover good vision
• Treatment may not change final outcome but speeds recovery

IV Methylprednisolone

When used:

• Severe vision loss
• Pain significantly affecting quality of life
• Need faster recovery (work, bilateral involvement)

Protocol:

• Typically 1 gram IV daily for 3-5 days
• May be followed by oral steroids (taper)
• Speeds recovery but may not change final outcome

Important: Oral steroids alone (without IV) may increase recurrence risk

For NMO/MOGAD

More aggressive treatment needed:

• High-dose IV steroids
• Plasmapheresis if severe or not responding
• Long-term immunosuppression to prevent relapses

Prognosis and Recovery

Visual Recovery

• Most patients recover good vision (85-90% recover to 20/40 or better)
• Recovery usually begins within 2-4 weeks
• Continues for several months
• Some color or contrast vision deficit may persist
• Vision may temporarily worsen with heat/exercise (Uhthoff phenomenon)

Risk of Multiple Sclerosis

For detailed information about the connection between optic neuritis and MS, including what MRI findings mean for your risk and treatment decisions, see our guide: Optic Neuritis and MS Risk - Understanding Your Diagnosis.

MRI brain findings predict MS risk:

MRI Finding	15-Year MS Risk
Normal MRI (no lesions)	~25%
1 or more brain lesions	~72%

Other factors affecting risk:

• Female sex
• Younger age
• Presence of oligoclonal bands in spinal fluid

Recurrence

• About 35% have another episode of optic neuritis within 10 years
• May affect same or opposite eye
• Consider disease-modifying treatment if MS or NMO diagnosed

Living with Optic Neuritis

During Acute Phase

• Rest your eyes when fatigued
• Use good lighting
• Avoid excessive heat (hot showers, saunas)
• Pain medication as needed
• Plan for reduced activities temporarily

After Recovery

• Regular neuro-ophthalmology and/or neurology follow-up
• MRI surveillance if MS risk factors present
• Monitor for new symptoms
• Consider disease-modifying therapy if indicated

Frequently Asked Questions

Will I go blind from optic neuritis?

Complete permanent blindness from optic neuritis is rare. Most people recover functional vision. However, some degree of vision loss or color vision changes may persist.

Does optic neuritis mean I have MS?

Not necessarily. About half of people with optic neuritis develop MS over 15 years. MRI findings help predict individual risk. Many people never develop MS.

Why does my vision get worse when I'm hot?

This is called Uhthoff phenomenon. Demyelinated nerves conduct signals more slowly when warm. It's temporary—vision returns to baseline when you cool down. It doesn't mean optic neuritis is recurring.

Can optic neuritis come back?

Yes, recurrence is possible in about 35% of cases within 10 years. It may affect the same eye or the other eye. Recurrent optic neuritis increases suspicion for MS, NMO, or MOGAD.

Should I start MS treatment?

This decision depends on MRI findings, presence of oligoclonal bands, and individual risk factors. If MS risk is high, early treatment may reduce future attacks. Discuss with your neurologist.

Can I drive with optic neuritis?

During acute vision loss, likely not. After recovery, it depends on your visual acuity and field. Discuss driving restrictions with your doctor.

References