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首页> 外文期刊>Advances in Therapy >Ocular hypotensive efficacy of brimonidine 0.15% as adjunctive therapy with latanoprost 0.005% in patients with open-angle glaucoma or ocular hypertension
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Ocular hypotensive efficacy of brimonidine 0.15% as adjunctive therapy with latanoprost 0.005% in patients with open-angle glaucoma or ocular hypertension

机译:溴莫尼定0.15%作为开角型青光眼或高眼压症患者的辅助治疗与拉坦前列素0.005%的辅助治疗

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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 ≥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-Transmission and reproduction of this material in whole or part without prior written approval are prohibited. 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.
机译:进行这项研究是为了评估溴莫尼定Purite®的降压功效。对于开角型青光眼或高眼压症患者,给予0.15%(Alphagan?P 0.15%; Allergan,Inc.,加利福尼亚州尔湾市)辅助治疗,并加用拉坦前列素0.005%(Xalatan ?;辉瑞公司,纽约,纽约)。在这项多中心,开放标签的前瞻性评估中,至少接受6周拉坦前列素单药治疗的43名患者的眼内压(IOP)≥18 mm Hg。主要结局指标为药物作用达到峰值时的眼压(上午10时,或溴莫尼定早上剂量0.15%后约2小时)。还测量了在谷药效应时的IOP(上午8时,或溴莫尼定的夜间剂量后约12小时)。基线IOP为21.9(±2.3)mm Hg。治疗1个月后,在达到峰值药物作用(P <.001)时,与拉坦前列素治疗的基线值相比,平均IOP降低了5.8 mm Hg(26%),在谷底时(P <.001)降低了3.3 mm Hg(15%)。 。在第2个月就诊时,在达到峰值药物作用(P <.001)时,从拉坦前列素治疗的基线值开始,平均IOP降低了5.1 mm Hg(23%),在谷底时(P = .002)降低了2.0 mm Hg(9%) 。禁止使用0.15%的溴莫尼定Purite,从统计学上讲,拉坦前列素可进一步降低IOP。未经事先书面许可,严禁全部或部分传播和繁殖该材料。处理后的基线值。这些发现表明,对于需要进一步降低IOP的拉坦前列素患者,溴莫尼定Purite 0.15%是一种有效的辅助治疗方法。

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