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eyeball.jpg (32200 bytes) General features

bulletAffect 15 to 45 years of age, peak 30 to 50 years old
bulletFamale:male ratio 2-3:1
bulletSymptoms progress over hours to days
bulletIn the optic neuritis treatment trial, 92% of the patients had ocular pain.
bulletYoung age and the presence of pain: strongly suggestive of optic neuritis
bulletIn middle aged patients without pain, distinction from ischemic optic neuropathy can be difficult
bullet94% unilateral
bulletUsually improves over 4 weeks
bulletInflammatory demyelination of the Optic nerve
bulletInitial manifestation of MS in 20%
bulletDeveloped during the course of MS in 50%

Description by patient:

bulletBlurred vision
bulletDecreased color perception
bulletImpaired depth perception

Examination

bulletReduced visual acuity
bulletReduced brightness perception
bulletBright color desaturation
bulletAfferent defect not always present
bulletFundoscopic exam frequently normal

Differential Diagnosis

bulletIdiopathic Optic neuritis
bulletMultiple Sclerosis
bulletDevic's Syndrome: with myelitis
bulletPostinfectious: viral, mycoplasma
bulletPost Immunization
bulletSystemic inflammatory disease: SLE, Sarcoidosis
bulletInfections: Lymes, Syphilis
bulletIschemic optic neuropathy: usually painless, older, more acute onset
bulletLeber's Hereditary optic neuropathy: mitochondrial disease
bulletsubacute visual loss
bulletusually becomes bilateral
bulletyoung male, poor recovery
bulletCompressive lesion: more insidious onset

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Testings:

bulletVER: prolonged P100 or reduction in amplititude or both
bulletVisual field: may show diffuse visual field loss
bulletCSF: mild mononuclear pleocytosis,
bulletelevated IgG index or synthesis rate
bulletOligoclonal bands
bulletMRI of head
bulletAbout two thirds of patients with optic neuritis will have enhancing optic nerve lesions.
bulletEnhancement may also be seen in other inflammatory optic neuropathies like sarcoidosis, meningeal processes and radiation optic neuropathy. 

 

Prognosis

bulletMost show improvement in 2 weeks
bulletIncreased risk for developing MS for these patients
bullet   female
bullet   Caucasians
bullet   Family history of MS
bullet   Nonspecific vague neuro symptoms
bullet   CSF abnormalities
bullet   Abnormal MRI
bulletIn ONTT, 51% of patients with three or more white matter lesions that were greater than 3 mm, ovoid, and in periventricular white matter developed multiple sclerosis within five years.
bullet16% of patients with normal MRI scans developed MS in the first five years. 

Treatment

bulletIV Methylprednisone 1 g per day for 3 days,
followed by oral prednisone taper IF
bulletMRI of head suggestive of MS
bulletbilateral Optic neuritis
bulletVisual acuity < 20/60
bulletOral prednisone alone has not been showed to be beneficial
bulletControlled high risk Avonex multiple sclerosis study (CHAMPS)
bulletAge of 18 to 50
bulletHad an acute isolated demyelinating event involving either the optic nerve, spinal cord or brainstem/cerebellum.
bulletHave at least two clinically silent brain MR lesions which were greater or equal to 3 mm in size. One of these lesions needed to be periventricular in location or ovoid in shape.
bulletAll patients received intravenous methylprednisolone, followed by an oral prednisone taper
bulletRandomized by the nature of their clinical events and number of T2 lesions seen on their brain MRI scan. One group were given Avonex while the other group was given placebo.
bulletResult: Avonex may reduce the conversion to multiple sclerosis in high risk patients by approximately 50%.

 

Click here for a full review of Optic Neuritis - by

bulletKen Graham M.D.
Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA .
bulletJoseph Rizzo M.D.
Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA

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