March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Clinical Features and Treatment Outcome of Japanese Patients with Scleritis
Author Affiliations & Notes
  • Kazuhisa Takahashi
    Ophthalmology, Nippon Medical School, Tokyo, Japan
  • Kuniko Wakayama
    Ophthalmology, Nippon Medical School, Tokyo, Japan
  • Hiroshi Takahashi
    Ophthalmology, Nippon Medical School, Tokyo, Japan
  • Junko Hori
    Ophthalmology, Nippon Medical School, Tokyo, Japan
  • Footnotes
    Commercial Relationships  Kazuhisa Takahashi, None; Kuniko Wakayama, None; Hiroshi Takahashi, None; Junko Hori, None
  • Footnotes
    Support  Grants-in-Aid for Scientific Research (C) from Japan Society for the Promotion of Science
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 1255. doi:
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    • Get Citation

      Kazuhisa Takahashi, Kuniko Wakayama, Hiroshi Takahashi, Junko Hori; Clinical Features and Treatment Outcome of Japanese Patients with Scleritis. Invest. Ophthalmol. Vis. Sci. 2012;53(14):1255.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To analyze clinical features, systemic associations, treatment in patients with scleritis.

Methods: : Clinical records of 99 patients with scleritis who presented between April 2004 and September 2011 to the Ophthalmology at Nippon Medical School, Tokyo, were reviewed retrospectively.

Results: : Of the 99 patients, 57.6% had diffuse anterior scleritis, 20% had episcleritis, 16% had nodular anterior scleritis, 4% had necrotizing anterior scleritis, and 2% had posterior scleritis. Mean age at presentation was 53.5±15.2 (range 22-83 years). Secondary ocular complications were observed in 32% of patients, including anterior uveitis in 9%, increased intraocular pressure 31%. Systemic disease association was seen in 20% patients, including rheumatoid arthritis, tuberculosis, relapsing polychondritis, Wegener’s granulomatosis, seronegative arthritis, and so on.100% of episcleritis and 87.7% of diffuse anterior scleritis were treated with only topical application of steroids and/or immunosuppressive drugs. 6.3% of nodular anterior scleritis, 75% of necrotizing anterior scleritis, and 100% of posterior scleritis needed systemic treatments with oral corticosteroids and/or immunosuppressive drugs. 15.2% of scleritis without systemic disease were treated with oral corticosteroids and/or immunosuppressive drugs, biologic agent (anti-TNF agent). On the other hand, 30% of scleritis associated with systemic disease needed systemic medication.

Conclusions: : About 90% of diffuse anterior scleritis and nodular anterior scleritis were treated with only topical application of steroids and/or immunosuppressive drugs. On the other hand, most of necrotizing anterior scleritis and posterior scleritis received oral corticosteroids and/or immunosuppressive drugs, biologic agent. Our report suggested that scleritis associated with a systemic disease needs oral corticosteroids and/or immunosuppressive drugs, biologic agent (anti-TNF) more often than scleritis without systemic disease.

Keywords: autoimmune disease • sclera • clinical (human) or epidemiologic studies: outcomes/complications 
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