Topical dexamethasone–cyclodextrin nanoparticle eye drops for non‐infectious Uveitic macular oedema and vitritis – a pilot study

  • Shiri Shulman
    Division of Ophthalmology Tel Aviv Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel
  • Gauti Jóhannesson
    Department of Clinical Science, Ophthalmology Umeå University Umeå Sweden
  • Einar Stefánsson
    Department of Ophthalmology National Hospital Reykjavik University of Iceland Reykjavik Iceland
  • Anat Loewenstein
    Division of Ophthalmology Tel Aviv Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel
  • Amir Rosenblatt
    Division of Ophthalmology Tel Aviv Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel
  • 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
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 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>

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