Topical dexamethasone–cyclodextrin nanoparticle eye drops for non‐infectious Uveitic macular oedema and vitritis – a pilot study
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- Shiri Shulman
- Division of Ophthalmology Tel Aviv Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel
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- Gauti Jóhannesson
- Department of Clinical Science, Ophthalmology Umeå University Umeå Sweden
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- Einar Stefánsson
- Department of Ophthalmology National Hospital Reykjavik University of Iceland Reykjavik Iceland
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- Anat Loewenstein
- Division of Ophthalmology Tel Aviv Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel
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- Amir Rosenblatt
- Division of Ophthalmology Tel Aviv Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel
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- Zohar Habot‐Wilner
- Division of Ophthalmology Tel Aviv Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel
書誌事項
- 公開日
- 2015-05-18
- 権利情報
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- http://onlinelibrary.wiley.com/termsAndConditions#vor
- DOI
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- 10.1111/aos.12744
- 公開者
- Wiley
この論文をさがす
説明
<jats:title>Abstract</jats:title><jats:sec><jats:title>Purpose</jats:title><jats:p>To evaluate the safety and efficacy of 1.5% dexamethasone nanoparticle (Dex<jats:styled-content style="fixed-case">NP</jats:styled-content>) drops in eyes with non‐infectious uveitic macular oedema and vitritis.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p><jats:italic>In a</jats:italic> prospective pilot study, Dex<jats:styled-content style="fixed-case">NP</jats:styled-content> drops were administered four times a day for 4 weeks followed by drops tapering over a period of another 4 weeks. Follow‐up time was 12 weeks.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Five eyes with macular oedema and three eyes with vitritis were included in the study. Best corrected visual acuity (BCVA) significantly improved from a median of 0.2 log<jats:styled-content style="fixed-case">MAR</jats:styled-content> to a median of 0.15 log<jats:styled-content style="fixed-case">MAR</jats:styled-content> at 4 weeks' time (p < 0.05). Median <jats:styled-content style="fixed-case">BCVA</jats:styled-content> was 0.175 log<jats:styled-content style="fixed-case">MAR</jats:styled-content> and 0.2 log<jats:styled-content style="fixed-case">MAR</jats:styled-content>, at week 8 and 12, respectively (p > 0.05). Macular oedema significantly improved at all time‐points as compared to baseline (p < 0.05) and resolved in all eyes during follow‐up. One eye had macular oedema relapse at week 12. Vitritis improved in all eyes and resolved completely in two eyes. One eye had intraocular pressure (IOP) elevation which was well controlled with topical antihypertensive treatment, and one eye had cataract progression.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>This short pilot study demonstrates favourable effect of 1.5% Dex<jats:styled-content style="fixed-case">NP</jats:styled-content> eye drops on eyes with non‐infectious uveitic macular oedema and vitritis. Further comparative long‐term studies are warranted to assess this effect.</jats:p></jats:sec>
収録刊行物
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- Acta Ophthalmologica
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Acta Ophthalmologica 93 (5), 411-415, 2015-05-18
Wiley