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804<br />
70th AIOC Proceedings, Cochin 2012<br />
with PTO. Out of 200 patients selected 141 patients were treated with part time<br />
occlusion of 6hrs/day. 14 patients received medical therapy, combination of<br />
Levodopa (250mg) and Carbidopa (25 mg), dose titrated according to age, for<br />
a period of 3 months. 25 patients received CDP choline 500-1000mg (7-28mg/<br />
kg/day) daily orally for a period of 14 days. 20 patients were given 20mg<br />
Fluoxetine for 4 months in addition to part time occlusion of 6 hrs/day. All<br />
patients were followed up monthly for 6 months.<br />
Patients with any degree of visual improvement considered “Responders”.<br />
Number of patient responding and degree of response of therapy compared<br />
among groups.<br />
RESULTS<br />
Out of 200 patients’ records studied for this study 141 received part time<br />
occlusion with good compliance. Of these 141 patients 99 patients showed<br />
visual improvement with the therapy with average 4 line of improvement in<br />
LogMAR scale. This constitute 70% of patients in part time occlusion group to<br />
be responders.<br />
Of the 14 cases in this study who underwent medical therapy with Levodopa+<br />
Carbidopa only 2 cases showed improvement in their visual acuity while<br />
11 cases showed no improvement in visual acuity even after 3 months of<br />
initiation of therapy. After which medical therapy was terminated and patients<br />
were advised other treatment modality or cosmetic surgical correction for<br />
strabismus. Of these 2 (14%) responders average improvement in visual acuity<br />
was 2 LogMAR lines. 10 patients out of 25 receiving CDP Choline showed<br />
visual improvement. Improvement started at two weeks with maximum<br />
patients improving by 4 weeks. These 40% responders showed 1.4 LogMAR<br />
lines of visual improvement. In 20 patients, where Fluoxetine was added to<br />
part time occlusion, 16 patients showed improvement in visual acuity with<br />
4.53 LogMAR lines of visual improvement. None of the patients recieveing<br />
medical therapy (Levodopa or CDP choline) reported any adverse effect of the<br />
drug.<br />
DISCUSSION<br />
Our retrospective analysis of data in patients treated with medical therapy<br />
alone met with very marginal success in terms of both, number of patients<br />
responding to therapy and number of lines of visual improvement. Responders<br />
in various treatment groups noted were 70%, 14%, 40% and 80% respectively.<br />
In responders the mean LogMAR line of improvement noted was 4 lines in<br />
PTO group, 1.4 lines in Citicholine group, 2 lines in Levodopa group and 4.53<br />
in Fluoxetine with PTO group. This clearly showed better results in occlusion<br />
group and in patients where occlusion was supplemented with medical