Feghali J G, Kaufman P L
Am J Ophthalmol. 1985 Dec 15;100(6):777-82. doi: 10.1016/s0002-9394(14)73366-5.
In a double-masked randomized prospective study, 19 adult white subjects with primary open-angle glaucoma or ocular hypertension were treated twice daily with drops of 0.25% betaxolol (a relatively selective beta 1-adenoceptor antagonist) or placebo for six weeks. The nine betaxolol-treated subjects demonstrated a statistically significant average decrease in intraocular pressure of 3.8 +/- 5 mm Hg, evident after one week and persisting throughout the entire six-week treatment period. The ten placebo-treated subjects exhibited a statistically nonsignificant increase in intraocular pressure of 0.4 +/- 2.4 mm Hg. Mean systemic arterial blood pressure, pulse rate, corneal sensitivity, pupil diameter, and basal tear secretion remained unchanged in both groups. Transient stinging upon instillation of the eyedrops was the only side effect in the betaxolol-treated subjects but in no case did it necessitate cessation of therapy.
在一项双盲随机前瞻性研究中,19名患有原发性开角型青光眼或高眼压症的成年白人受试者,每天两次滴用0.25%倍他洛尔(一种相对选择性的β1 - 肾上腺素能受体拮抗剂)或安慰剂,为期六周。接受倍他洛尔治疗的9名受试者眼压平均下降3.8±5毫米汞柱,具有统计学意义,在一周后即可显现,并在整个六周治疗期持续存在。接受安慰剂治疗的10名受试者眼压平均升高0.4±2.4毫米汞柱,无统计学意义。两组受试者的平均体循环动脉血压、脉搏率、角膜敏感性、瞳孔直径和基础泪液分泌均保持不变。滴眼药水时的短暂刺痛是倍他洛尔治疗组受试者唯一的副作用,但在任何情况下都无需停止治疗。