Time course of conjunctival hyperemia induced by omidenepag isopropyl ophthalmic solution 0.002%: a pilot, comparative study versus ripasudil 0.4%

BMJ Open Ophthalmology 5 巻 e000538- 頁 2020-08-02 発行
アクセス数 : 241
ダウンロード数 : 81

今月のアクセス数 : 2
今月のダウンロード数 : 1
ファイル情報(添付)
BMJOpOphthalm_5_e000538.pdf 883 KB 種類 : 全文
タイトル ( eng )
Time course of conjunctival hyperemia induced by omidenepag isopropyl ophthalmic solution 0.002%: a pilot, comparative study versus ripasudil 0.4%
作成者
Terao Etsuko
Nakakura Shunsuke
Fujisawa Yasuko
Nagata Yuki
Ueda Kanae
Kobayashi Yui
Oogi Satomi
Dote Saki
Shiraishi Miku
Yoneda Tsuyoshi
Fukushima Atsuki
Asaoka Ryo
収録物名
BMJ Open Ophthalmology
5
開始ページ e000538
抄録
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.
内容記述
The article has been presented at the 30th Annual Meeting of the Japanese Glaucoma Society on 7 September 2019.
言語
英語
資源タイプ 学術雑誌論文
出版者
BMJ
発行日 2020-08-02
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.
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/.
出版タイプ Version of Record(出版社版。早期公開を含む)
アクセス権 オープンアクセス
収録物識別子
[ISSN] 2397-3269
[DOI] 10.1136/ bmjophth-2020-000538
[DOI] https://doi.org/10.1136/ bmjophth-2020-000538