Optic neuritis treatment trial. One-year follow-up results
R. W. Beck and P. A. Cleary
Department of Ophthalmology, University of South Florida College of Medicine, Tampa 33612.
OBJECTIVE--To determine the efficacy of corticosteroids as treatment for
acute demyelinative optic neuritis after completion of 1 year of patient
follow-up in the Optic Neuritis Treatment Trial. DESIGN--Randomized placebo
controlled multicenter clinical trial. SETTING--Fifteen university or
hospital-based centers throughout the United States. PATIENTS--Four hundred
fifty-seven patients with acute demyelinative optic neuritis between 18 and
46 years of age. INTERVENTION--Either intravenous methylprednisolone sodium
succinate (250 mg every 6 hours) for 3 days followed by oral prednisone (1
mg/kg per day) for 11 days, oral prednisone (1 mg/kg per day) for 14 days,
or oral placebo for 14 days. The first two regimens were followed by a
short taper of corticosteroid therapy. MAIN OUTCOME MEASURES--Visual
acuity, visual field, contrast sensitivity, and color vision.
RESULTS--Visual acuity at 1 year was 20/40 or better in 95% of the placebo
group, 94% of the intravenous group, and 91% of the oral prednisone group.
Comparing each corticosteroid group with the placebo group, there were no
statistically significant differences in the distributions of any of the
four measures of visual function. Patients in the oral prednisone group
suffered a higher rate of new attacks of optic neuritis than patients in
either of the other two groups. CONCLUSIONS--The visual benefit from
treating acute optic neuritis with intravenous followed by oral
corticosteroids is short term, limited to an accelerated rate of recovery.
The decision whether to prescribe this regimen for optic neuritis, or to
prescribe no treatment, must be made for each patient on an individual
basis. Oral prednisone alone, in the dose range used in the Optic Neuritis
Treatment Trial, should not be prescribed.
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