Purpose: To describe the outcome of a series of Acanthamoeba keratitis treated with a similar regimen. Methods: All cases diagnosed with Acanthamoeba keratitis in a referral centre from June 1994 through June 1997 were included. Diagnosis of Acanthamoeba keratitis was based in clinical presentation and laboratory results. Positive laboratory identification of Acanthamoeba from corneal scraping or contact lens was required, unless the patient had very characteristic symptoms (severe pain) and signs of the infection, including perineural infiltrates. Initial intensive treatment included topical polyhexamethylene biguanide (PHMB) 0.02%, propamidine isothionate 0.1% and broad-spectrum antibiotics. The treatment was gradually tapered. After documented response to anti-acanthamoeba therapy, topical steroids were introduced; they were discontinued before cessation of the anti-Acanthamoeba regimen. Results: Six males and four females, with a mean age of 30.0 +/- 7.4 years were included in this study. All cases weared contact lenses. On presentation ail cases had severe pain, and epitheliopathy was associated with stromal infiltrate in most (seven of ten) cases. Four patients had anterior uveitis. Perineural infiltrates were present in three cases and ring infiltrate in one patient. Anti-amoebic treatment was started 12.7 +/- 7.2 days after beginning of symptoms. The clinical response to therapy was very satisfactory in all patients. Within two to three weeks all patients had remarkable lessening of pain and photophobia, and improvement of clinical signs. At two to three months, visual acuity had improved in all patients. Two patients required penetrating keratoplasty for visual rehabilitation. Conclusion: The use of PHMB and propamidine cured all cases of Acanthamoeba keratitis. Cautious introduction of steroids was associated with expedited resolution of inflammation and provided symptomatic relief.
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Univ Calif San Francisco, FI Proctor Fdn, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Oldenburg, Catherine E.
Acharya, Nisha R.
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Univ Calif San Francisco, FI Proctor Fdn, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Acharya, Nisha R.
Tu, Elmer Y.
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Univ Illinois, Dept Ophthalmol & Visual Sci, Chicago, IL USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Tu, Elmer Y.
Zegans, Michael E.
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Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Surg, Hanover, NH 03756 USA
Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Microbiol & Immunol, Hanover, NH 03756 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Zegans, Michael E.
Mannis, Mark J.
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Univ Calif Davis, Dept Ophthalmol & Vis Sci, Sacramento, CA 95817 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Mannis, Mark J.
Gaynor, Bruce D.
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Univ Calif San Francisco, FI Proctor Fdn, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Gaynor, Bruce D.
Whitcher, John P.
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Univ Calif San Francisco, FI Proctor Fdn, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Whitcher, John P.
Lietman, Thomas M.
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Univ Calif San Francisco, FI Proctor Fdn, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Lietman, Thomas M.
Keenan, Jeremy D.
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Univ Calif San Francisco, FI Proctor Fdn, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA