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联合青光眼治疗的眼部舒适度:0.2%溴莫尼定/0.5%噻吗洛尔与2%多佐胺/0.5%噻吗洛尔的比较

Ocular comfort of combination glaucoma therapies: brimonidine 0.2%/timolol 0.5% compared with dorzolamide 2%/timolol 0.5%.

作者信息

Chan Kenny, Testa Madalena, McCluskey Peter

机构信息

Department of Ophthalmology, Liverpool Hospital, Liverpool, New South Wales, Australia.

出版信息

J Ocul Pharmacol Ther. 2007 Aug;23(4):372-6. doi: 10.1089/jop.2006.0131.

DOI:10.1089/jop.2006.0131
PMID:17803436
Abstract

PURPOSE

Successful management of glaucoma and ocular hypertension requires patient compliance with the therapeutic regimen. Because ocular discomfort affects compliance, we compared the comfort of brimonidine 0.2%/timolol 0.5% and dorzolamide 2%/timolol 0.5%.

METHODS

In this single-centre, randomized, double-masked, internally controlled/paired-eye study, 30 subjects without a significant ocular surface disease received brimonidine 0.2%/timolol 0.5% in 1 eye and dorzolamide 2%/timolol 0.5% in the fellow eye. They evaluated discomfort at 30-40 s and 5 min postinstillation.

RESULTS

At 30-40 s, brimonidine 0.2%/timolol 0.5% provided significantly lower mean ocular discomfort scores than dorzolamide 2%/timolol 0.5% (P < 0.0001). This pattern persisted at 5 min but was not statistically significant. Significant differences were seen in the subjects' determination of the more comfortable treatment (P < 0.0001): brimonidine 0.2%/timolol 0.5% was rated as more comfortable than dorzolamide 2%/timolol 0.5% by 80% of subjects at 30-40 s and by 27% at 5 min. Only 10% of subjects at each time point rated dorzolamide 2%/timolol 0.5% as more comfortable. The remaining subjects reported no preference at either time point. No adverse events were reported.

CONCLUSIONS

Brimonidine 0.2%/timolol 0.5% was significantly more comfortable than dorzolamide 2%/timolol 0.5% upon instillation. Patients with ocular hypertension or glaucoma may be more compliant with brimonidine 0.2%/timolol 0.5% treatment.

摘要

目的

成功管理青光眼和高眼压症需要患者遵守治疗方案。由于眼部不适会影响依从性,我们比较了0.2%溴莫尼定/0.5%噻吗洛尔和2%多佐胺/0.5%噻吗洛尔的舒适度。

方法

在这项单中心、随机、双盲、内部对照/双眼配对研究中,30名无明显眼表疾病的受试者一只眼使用0.2%溴莫尼定/0.5%噻吗洛尔,另一只眼使用2%多佐胺/0.5%噻吗洛尔。他们在滴药后30 - 40秒和5分钟评估不适感。

结果

在30 - 40秒时,0.2%溴莫尼定/0.5%噻吗洛尔的平均眼部不适评分显著低于2%多佐胺/0.5%噻吗洛尔(P < 0.0001)。这种模式在5分钟时持续存在,但无统计学意义。在受试者对更舒适治疗的判定上存在显著差异(P < 0.0001):在30 - 40秒时,80%的受试者认为0.2%溴莫尼定/0.5%噻吗洛尔比2%多佐胺/0.5%噻吗洛尔更舒适,在5分钟时这一比例为27%。在每个时间点,只有10%的受试者认为2%多佐胺/0.5%噻吗洛尔更舒适。其余受试者在两个时间点均表示无偏好。未报告不良事件。

结论

滴药时,0.2%溴莫尼定/0.5%噻吗洛尔比2%多佐胺/0.5%噻吗洛尔明显更舒适。高眼压症或青光眼患者可能对0.2%溴莫尼定/0.5%噻吗洛尔治疗的依从性更高。

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