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Methotrexate for chronic non-necrotizing anterior scleritis in Chinese patients

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AIM: To evaluate the effectiveness and corticosteroid-sparing capabilities of methotrexate (MTX) in the treatment of chronic non-necrotizing anterior scleritis in Chinese patients. METHODS: A retrospective chart review of all patients with active anterior scleritis between January 2015 and June 2019 was conducted. All patients received 10 to 15 mg/wk MTX orally, and corticosteroids (10 to 40 mg/d prednisolone or equivalent methylprednisolone) with slow tapering. Topical corticosteroid eye drops (1% prednisolone actate, 0.1% dexmathosone or 0.1% fluoromethalone) were applied to control comorbid anterior uveitis at presentation or during follow up. The main outcomes were inflammation control and corticosteroid-sparing success, and secondary outcomes were reduction of immunosuppression load and best-corrected visual acuity (BCVA). RESULTS: Thirty-two eyes (22 patients) were included. The proportion of patients who achieved corticosteroid-sparing success was 50.0% at 3mo and 77.3% at 12mo [8 (36.4%) patients discontinued corticosteroid]. The proportion of eyes that achieved inflammation control was 59.4% at 3mo and 78.1% at 12mo. The immunosuppression load was 5.14±0.87 at presentation and 2.76±2.34 at 12mo (P<0.01). BCVA maintained unchanged or improved in 29 (90.6%) of all affected eyes. One patient discontinued MTX treatment because of an abnormal liver function test, and no other serious adverse effects were observed. CONCLUSION: According to this pilot study, low dose MTX appear to be a well-tolerated and effective treatment for chronic non-necrotizing anterior scleritis patients in the Chinese population.
Title: Methotrexate for chronic non-necrotizing anterior scleritis in Chinese patients
Description:
AIM: To evaluate the effectiveness and corticosteroid-sparing capabilities of methotrexate (MTX) in the treatment of chronic non-necrotizing anterior scleritis in Chinese patients.
METHODS: A retrospective chart review of all patients with active anterior scleritis between January 2015 and June 2019 was conducted.
All patients received 10 to 15 mg/wk MTX orally, and corticosteroids (10 to 40 mg/d prednisolone or equivalent methylprednisolone) with slow tapering.
Topical corticosteroid eye drops (1% prednisolone actate, 0.
1% dexmathosone or 0.
1% fluoromethalone) were applied to control comorbid anterior uveitis at presentation or during follow up.
The main outcomes were inflammation control and corticosteroid-sparing success, and secondary outcomes were reduction of immunosuppression load and best-corrected visual acuity (BCVA).
RESULTS: Thirty-two eyes (22 patients) were included.
The proportion of patients who achieved corticosteroid-sparing success was 50.
0% at 3mo and 77.
3% at 12mo [8 (36.
4%) patients discontinued corticosteroid].
The proportion of eyes that achieved inflammation control was 59.
4% at 3mo and 78.
1% at 12mo.
The immunosuppression load was 5.
14±0.
87 at presentation and 2.
76±2.
34 at 12mo (P<0.
01).
BCVA maintained unchanged or improved in 29 (90.
6%) of all affected eyes.
One patient discontinued MTX treatment because of an abnormal liver function test, and no other serious adverse effects were observed.
CONCLUSION: According to this pilot study, low dose MTX appear to be a well-tolerated and effective treatment for chronic non-necrotizing anterior scleritis patients in the Chinese population.

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