The 24-hour intraocular pressure control by tafluprost/timolol fixed combination after switching from the concomitant use of tafluprost and timolol gel-forming solution, in patients with primary open-angle glaucoma

被引:4
作者
Nakamoto, Kenji [1 ]
Takeshi, Masahiko [2 ]
Hiraoka, Toshihiko [2 ,3 ]
Eguchi, Mayuko [2 ,4 ]
Nakano, Yuichiro [1 ,2 ]
Otsuka, Naomi [5 ]
Hizaki, Hiroko [5 ]
Akai, Hiromi [5 ]
Hashimoto, Masayo [5 ]
机构
[1] Nippon Med Sch, Dept Ophthalmol, Tokyo, Japan
[2] Shinanozaka Clin, Tokyo, Japan
[3] Hiraoka Eye Clin, Saitama, Japan
[4] Musashiurawa Eye Clin, Saitama, Japan
[5] Santen Pharmaceut Co Ltd, Global R&D, Japan Med Affairs, Osaka, Japan
关键词
intraocular pressure; tafluprost; circadian IOP; 24-hour IOP; timolol gel;
D O I
10.2147/OPTH.S152507
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective: The aim of this study was to evaluate the 24-hour intraocular pressure (IOP)-control effect of the tafluprost/timolol fixed combination (TAF/TIM-FC) in patients with primary open-angle glaucoma after they switched from the concomitant use of tafluprost and timolol gel-forming solution. Patients and methods: Twenty patients with primary open-angle glaucoma (12 male and 8 female; mean +/- SD age, 57.0 +/- 7.1 years) were included in this study. The patients were treated for 8 weeks with the concomitant administration of tafluprost and timolol gel-forming solution (evening dosing). At the end of this period, the patients underwent 24-hour IOP monitoring (measured at 21:00, 01:00, 05:00, 09:00, 13:00 and 17:00). IOP was measured with Goldmann applanation tonometer (GAT) and Icare PRO at sitting position at all timepoints and additionally, at supine position with Icare PRO tonometer at 01:00 and 05:00. The patients were then all switched to TAF/TIM-FC treatment (evening dosing). After 8 weeks, the 24-hour IOP monitoring was repeated. Results: Nineteen patients completed the study. The mean 24-hour IOPs in the concomitant and TAF/TIM-FC phases were 13.8 +/- 2.7 vs 13.3 +/- 2.8 mmHg (P=0.0033) with the GAT in the sitting position and 13.96 +/- 2.56 vs 13.48 +/- 2.56 mmHg (P=0.0120) with the Icare PRO in habitual positions. In comparison with the concomitant phase, significantly lower IOP was observed for the TAF/TIM-FC phase at 21:00 and 01:00 with the GAT and at 01:00 with the Icare PRO. In addition, the maximum IOP and fluctuations in IOP in habitual positions were lower for the TAF/TIM-FC phase than for the concomitant phase. Conclusion: TAF/TIM-FC showed a stable 24-hour IOP-lowering effect and was equally or more effective than the concomitant use of tafluprost and timolol gel, both when sitting and when in habitual positions.
引用
收藏
页码:359 / 367
页数:9
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