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0.15%溴莫尼定作为0.005%拉坦前列素辅助治疗开角型青光眼或高眼压症患者的降眼压疗效。

Ocular hypotensive efficacy of brimonidine 0.15% as adjunctive therapy with latanoprost 0.005% in patients with open-angle glaucoma or ocular hypertension.

作者信息

Mundorf Thomas, Noecker Robert J, Earl Melissa

机构信息

Private Practice, Charlotte, NC, USA.

出版信息

Adv Ther. 2007 Mar-Apr;24(2):302-9. doi: 10.1007/BF02849898.

DOI:10.1007/BF02849898
PMID:17565920
Abstract

This study was undertaken to evaluate the ocular hypotensive efficacy of brimonidine Purite 0.15% (Alphagan P 0.15%; Allergan, Inc., Irvine, Calif) given as adjunctive therapy with latanoprost 0.005% (Xalatan; Pfizer Inc., New York, NY( to patients with open-angle glaucoma or ocular hypertension. In this multicenter, open-label, prospective evaluation, the intraocular pressure (IOP) of the 43 enrolled patients was > or =18 mm Hg after at least 6 wk of latanoprost monotherapy. The primary outcome measure was IOP at peak drug effect )10 AM, or approximately 2 h after the morning dose of brimonidine 0.15%(. IOP at trough drug effect (8 AM, or approximately 12 h after the evening dose of brimonidine) was also measured. Baseline IOP was 21.9 (+/-2.3) mm Hg. After 1 mo of treatment, additional mean IOP reductions from latanoprost-treated baseline values were 5.8 mm Hg (26%) at peak drug effect (P<.001) and 3.3 mm Hg (15%) at trough (P<.001). At the month 2 visit, additional mean IOP reductions from latanoprost-treated baseline values were 5.1 mm Hg (23%) at peak drug effect (P<.001) and 2.0 mm Hg (9%) at trough (P=.002). Brimonidine Purite 0.15% provided statistically significant additional reductions in IOP from latanoprost-treated baseline values. These findings suggest that brimonidine Purite 0.15% is an efficacious adjunctive therapy in patients given latanoprost who require additional lowering of IOP.

摘要

本研究旨在评估0.15%的酒石酸溴莫尼定(阿法根0.15%;艾尔建公司,加利福尼亚州欧文市)作为0.005%拉坦前列素(适利达;辉瑞公司,纽约州纽约市)辅助治疗药物,用于开角型青光眼或高眼压症患者时的降眼压疗效。在这项多中心、开放标签的前瞻性评估中,43名入组患者在接受至少6周的拉坦前列素单药治疗后,眼压(IOP)≥18 mmHg。主要观察指标为药物效应峰值时(上午10点,即0.15%酒石酸溴莫尼定晨服后约2小时)的眼压。还测量了药物效应谷值时(上午8点,即酒石酸溴莫尼定晚服后约12小时)的眼压。基线眼压为21.9(±2.3)mmHg。治疗1个月后,与拉坦前列素治疗的基线值相比,药物效应峰值时平均眼压进一步降低5.8 mmHg(26%)(P<0.001),药物效应谷值时降低3.3 mmHg(15%)(P<0.001)。在第2个月就诊时,与拉坦前列素治疗的基线值相比,药物效应峰值时平均眼压进一步降低5.1 mmHg(23%)(P<0.001),药物效应谷值时降低2.0 mmHg(9%)(P = 0.002)。0.15%的酒石酸溴莫尼定与拉坦前列素治疗的基线值相比,能使眼压在统计学上显著进一步降低。这些研究结果表明,对于需要进一步降低眼压的拉坦前列素治疗患者,0.15%的酒石酸溴莫尼定是一种有效的辅助治疗药物。

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引用本文的文献

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Efficacy and Safety of Switching from Prostaglandin Analog Therapy to Prostaglandin / Timolol Fixed Combination or Prostaglandin / Brimonidine Therapy.从前列腺素类似物疗法转换为前列腺素/噻吗洛尔固定复方制剂或前列腺素/溴莫尼定疗法的疗效与安全性。
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Intraocular pressure-lowering combination therapies with prostaglandin analogues.
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Drugs. 2012 Jul 9;72(10):1355-71. doi: 10.2165/11634460-000000000-00000.