Purpose: To compare the long-term efficacy of different systemic thera
peutic regimens for patients with noninfectious anterior scleritis to
establish guidelines for institution of therapy. Methods: Therapeutic
failure of systemic nonsteroidal anti-inflammatory drugs (NSAIDs), sys
temic steroidal anti-inflammatory drugs, and systemic nonsteroidal imm
unosuppressive drugs was evaluated in 132 patients with noninfectious
anterior scleritis (diffuse, nodular, or necrotizing types). Results:
In patients with diffuse scleritis, therapeutic failure for initial re
gimens occurred in 7% of patients treated with NSAIDs, in 16% of patie
nts treated with steroids, and in 27% of patients treated with immunos
uppressive drugs. In patients with nodular scleritis, therapeutic fail
ure for initial regimens occurred in 9% of patients treated with NSAID
s, in 28% of patients treated with steroids, and in 25% of patients tr
eated with immunosuppressive drugs. Addition or substitution of steroi
ds or immunosuppressive drugs as second- or third-line therapies helpe
d control the scleritis. In patients with necrotizing scleritis, thera
peutic failure for initial regimens occurred in 1 00% of patients trea
ted with NSAIDs, in 91% of patients treated with steroids, and in 26%
of patients treated with immunosuppressive drugs. Conclusions: In pati
ents with diffuse and nodular scleritis, NSAIDs should be the initial
choice; in case of therapeutic failure, steroids should be added or su
bstituted as second-line therapy, tapering and discontinuing them as s
oon as possible while maintaining remission with continued NSAIDs; in
case of therapeutic failure, immunosuppressive drugs should be added o
r substituted as third-line therapy. In patients with necrotizing scle
ritis, immunosuppressive drugs should be the initial choice.