We conducted a study to analyse the presentation, risk factors, ocular mani
festations and ophthalmic management results of Stevens-Johnson syndrome (S
JS) in Indian patients. A total of 20 patients with SJS with ocular involve
ment were studied. Female predominance (70%) was observed. The age ranged f
rom 10 to 30 years (mean +/- SD: 16.85 +/- 5.96), The commonest precipitati
ng risk factor was oral drug intake (80%), sulphonamide (30%; sulphamethoxa
zole-trimethoprim) being the commonest. One patient had reaction to ciprofl
oxacin which has not been reported previously. Four patients (20%) had spon
taneous onset with no identifiable risk factor. None of the patients had sp
ecific infection per se as a risk factor, Conjunctival involvement and its
sequelae were the major ocular manifestations. At presentation, the majorit
y of the eyes (68%) had visual acuity less than 3/60, Despite appropriate m
edical treatment and surgical interventions (11 eyes; 28%) vision continued
to deteriorate, In 1 eye, the vision improved after stem cell transplantat
ion. Therapeutic penetrating keratoplasty could preserve ocular integrity i
n 1 patient,
Copyright (C) 2000 S. Karger AG, Basel.