Liu John H K, Medeiros Felipe A, Slight J Rigby, Weinreb Robert N
The Hamilton Glaucoma Center and Department of Ophthalmology, University of California, San Diego, La Jolla, California 92093-0946, USA.
Ophthalmology. 2009 Mar;116(3):449-54. doi: 10.1016/j.ophtha.2008.09.054. Epub 2009 Jan 20.
To compare the diurnal and nocturnal effects of brinzolamide and timolol on intraocular pressure (IOP) in patients already receiving monotherapy with latanoprost.
Prospective, open-label, and crossover clinical trial.
Twenty-six patients with glaucoma or ocular hypertension (ages, 44-79 years) who were receiving treatment with 0.005% latanoprost once every evening.
Baseline data of 24-hour IOP were collected in a sleep laboratory while patients were receiving latanoprost monotherapy. Measurements were taken every 2 hours in the sitting and supine positions during the 16-hour diurnal/wake period and in a supine position during the 8-hour nocturnal/sleep period. Patients were randomly assigned to receive an add-on treatment with either 1% brinzolamide 3 times per day or 0.5% timolol gel forming solution once every morning for 8 weeks, and then crossed over to receive the other add-on treatment. At the end of each add-on treatment period, 24-hour IOP data were collected.
Diurnal and nocturnal IOP means were compared among the baseline, the brinzolamide add-on treatment, and the timolol add-on treatment.
During the diurnal period, the mean IOP under brinzolamide or timolol add-on treatment was significantly lower than the baseline IOP in both the sitting and supine positions. There was no statistical difference between the 2 add-on treatments. During the nocturnal period, the supine IOP under brinzolamide add-on treatment was significantly lower than both the baseline and the timolol add-on treatment. There was no difference in nocturnal IOP between the timolol add-on treatment and the baseline.
In patients already receiving the latanoprost monotherapy, adding brinzolamide or timolol significantly reduced IOP during the diurnal period. However, only the brinzolamide add-on treatment had an IOP-lowering efficacy during the nocturnal period.
比较布林佐胺和噻吗洛尔对已接受拉坦前列素单药治疗患者眼压(IOP)的昼夜影响。
前瞻性、开放标签、交叉临床试验。
26例青光眼或高眼压症患者(年龄44 - 79岁),每晚接受0.005%拉坦前列素治疗。
在睡眠实验室收集患者接受拉坦前列素单药治疗时24小时眼压的基线数据。在16小时白天/清醒期,坐位和仰卧位时每2小时测量一次;在8小时夜间/睡眠期,仰卧位时测量。患者随机分配接受为期8周的附加治疗,即每天3次使用1%布林佐胺或每天早晨一次使用0.5%噻吗洛尔凝胶形成溶液,然后交叉接受另一种附加治疗。在每个附加治疗期结束时,收集24小时眼压数据。
比较基线、布林佐胺附加治疗和噻吗洛尔附加治疗期间的昼夜眼压平均值。
在白天期间,布林佐胺或噻吗洛尔附加治疗下的平均眼压在坐位和仰卧位时均显著低于基线眼压。两种附加治疗之间无统计学差异。在夜间期间,布林佐胺附加治疗下的仰卧位眼压显著低于基线和噻吗洛尔附加治疗。噻吗洛尔附加治疗与基线之间的夜间眼压无差异。
在已接受拉坦前列素单药治疗的患者中,添加布林佐胺或噻吗洛尔可显著降低白天眼压。然而,仅布林佐胺附加治疗在夜间具有降低眼压的效果。