Long D A, Johns G E, Mullen R S, Bowe R G, Alexander D, Epstein D L, Weiss M J, Masi R J, Charap A D, Eto C Y
Loma Linda University School of Medicine, CA.
Ophthalmology. 1988 Jun;95(6):735-41. doi: 10.1016/s0161-6420(88)33123-4.
In a double-masked, randomized, controlled clinical trial, the authors evaluated the ocular hypotensive efficacy of twice-daily treatment with levobunolol (0.25 and 0.5%) and betaxolol (0.5%) in 85 patients with open-angle glaucoma or ocular hypertension. During the 3-month study, intraocular pressure (IOP) reductions in the two levobunolol groups were significantly greater than in the betaxolol group. From a mean baseline IOP of approximately 25 mmHg, overall mean reductions were 6.2 and 6.0 mmHg for the 0.25 and 0.5% levobunolol groups, respectively, and 3.7 mmHg for the betaxolol group. No clinically or statistically significant among-group differences were noted in the systemic safety variables evaluated. These data suggest that although all three treatments are effective, levobunolol provides a greater reduction in IOP than betaxolol.
在一项双盲、随机、对照临床试验中,作者评估了每天两次使用左布诺洛尔(0.25%和0.5%)和倍他洛尔(0.5%)治疗85例开角型青光眼或高眼压症患者的降眼压疗效。在为期3个月的研究中,两个左布诺洛尔组的眼压(IOP)降低幅度显著大于倍他洛尔组。从平均基线眼压约25 mmHg开始,0.25%和0.5%左布诺洛尔组的总体平均降低幅度分别为6.2 mmHg和6.0 mmHg,倍他洛尔组为3.7 mmHg。在所评估的全身安全性变量方面,未发现临床或统计学上的组间显著差异。这些数据表明,尽管三种治疗方法均有效,但左布诺洛尔降低眼压的效果优于倍他洛尔。