Item type |
デフォルトアイテムタイプ_(フル)(1) |
公開日 |
2023-03-18 |
タイトル |
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タイトル |
Time course of conjunctival hyperemia induced by omidenepag isopropyl ophthalmic solution 0.002%: a pilot, comparative study versus ripasudil 0.4% |
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言語 |
en |
作成者 |
Terao, Etsuko
Nakakura, Shunsuke
Fujisawa, Yasuko
Nagata, Yuki
Ueda, Kanae
Kobayashi, Yui
Oogi, Satomi
Dote, Saki
Shiraishi, Miku
Tabuchi, Hitoshi
Yoneda, Tsuyoshi
Fukushima, Atsuki
Asaoka, Ryo
Kiuchi, Yoshiaki
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アクセス権 |
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アクセス権 |
open access |
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アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
権利情報 |
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権利情報 |
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. |
権利情報 |
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権利情報 |
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
内容記述 |
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内容記述 |
Objective We investigated the detailed time course of conjunctival hyperemia induced by omidenepag isopropyl ophthalmic solution 0.002% (omidenepag), a selective prostaglandin E2 receptor 2 agonist. Methods and analysis We recruited 34 healthy subjects and administered omidenepag in the right eye and ripasudil 0.4% in the left eye. We evaluated conjunctival hyperemia using slit-lamp photography at baseline and after 15, 30, 60, 120, 180 and 360 min. The conjunctival hyperemia score was graded by three independent observers using a scale from 0 (none) to 3 (severe). We also evaluated conjunctival hyperemia by the pixel coverage of conjunctival blood vessels (per cent coverage) determined using a conjunctival hyperemia-analysing software. Results In omidenepag, the conjunctival hyperemia score and per cent coverage peaked at both 30 min (mean score±SD: 1.57±0.67 and 11.90%±3.66%, respectively) and then gradually decreased at 60 min (10.79%±3.32%) and 120 min (1.10±0.52) when they reached a level that was not significantly different from the baseline values. For ripasudil 0.4%, the peak time of the conjunctival hyperemia score and per cent coverage were both at 15 min (score: 2.42±0.54 and 15.26%±3.38%). The degree of conjunctival hyperemia was significantly higher for ripasudil 0.4% than that for omidenepag from 15 to 30 min in both the conjunctival hyperemia score and per cent coverage (p<0.007 by Bonferroni correction). Conclusion Conjunctival hyperemia induced by omidenepag gradually peaks to moderate severity, though weaker compared with that induced by ripasudil 0.4%, and subsides relatively quickly. |
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言語 |
en |
内容記述 |
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内容記述タイプ |
Other |
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内容記述 |
The article has been presented at the 30th Annual Meeting of the Japanese Glaucoma Society on 7 September 2019. |
出版者 |
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出版者 |
BMJ |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
出版タイプ |
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出版タイプ |
VoR |
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出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
関連情報 |
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識別子タイプ |
DOI |
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関連識別子 |
10.1136/ bmjophth-2020-000538 |
関連情報 |
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識別子タイプ |
DOI |
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関連識別子 |
https://doi.org/10.1136/ bmjophth-2020-000538 |
収録物識別子 |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
2397-3269 |
開始ページ |
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開始ページ |
e000538 |
書誌情報 |
BMJ Open Ophthalmology
BMJ Open Ophthalmology
巻 5,
p. e000538,
発行日 2020-08-02
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旧ID |
51558 |