Schuman J S
New England Eye Center, New England Medical Center Hospitals, Tufts University School of Medicine, Boston, Massachusetts, USA.
Surv Ophthalmol. 1996 Nov;41 Suppl 1:S27-37. doi: 10.1016/s0039-6257(96)82029-7.
The ocular hypotensive efficacy and safety of brimonidine tartrate 0.2%, a highly selective alpha 2-adrenergic agonist, was compared with that of timolol 0.5%, a nonselective beta-blocker in two multicenter, randomized, double-masked studies. Combined data from a 12-month completed study and 6-month interim data from an ongoing study are reported. Efficacy and safety were evaluated at baseline, weeks 1 and 2, and months 1, 2, 3, 6, 9, and 12. Intraocular pressure (IOP) was measured at peak (2 hours after the morning dose) and trough (12 hours after the evening dose). Patients (n = 926) instilled either brimonidine tartrate 0.2% or timolol maleate 0.5% twice daily. At peak, the mean decreases from baseline IOP ranged from 5.9 +/- 3.2 mm Hg to 7.6 +/- 3.6 mm Hg for brimonidine and 6.0 +/- 3.4 mm Hg to 6.6 +/- 3.6 mm Hg for timolol (p < 0.001 within groups compared with baseline). No significant between-group differences were seen at peak except for weeks 1 and 2 and month 3 (p < or = 0.04), when brimonidine had lower mean IOP. At trough the mean decreases from baseline ranged from 3.7 +/- 4.0 mm Hg to 5.0 +/- 3.0 mm Hg for brimonidine and 5.9 +/- 3.4 to 6.6 +/- 3.0 for timolol. A significant between-group difference was seen at trough at all visits (< 0.001), when timolol had a lower mean IOP. Brimonidine and timolol showed sustained efficacy. Both drugs were well-tolerated. The brimonidine group had more ocular allergy, oral dryness and conjunctival follicles. The timolol group had more burning and stinging. In the brimonidine group, 38/513 (7.4%) discontinued treatment due to ocular allergy. The timolol group had significantly lower mean heart rate compared to baseline. The effect on blood pressure was minimal for both drugs. Brimonidine showed efficacy similar to timolol and a relatively low rate of ocular allergy. Brimonidine 0.2% administered twice daily is an effective and safe ocular hypotensive agent that maintains IOP-lowering in chronic use.
在两项多中心、随机、双盲研究中,对高选择性α2肾上腺素能激动剂0.2%酒石酸溴莫尼定与非选择性β受体阻滞剂0.5%噻吗洛尔的降眼压疗效及安全性进行了比较。报告了一项为期12个月的完整研究和一项正在进行的研究的6个月中期数据的合并数据。在基线、第1周和第2周以及第1、2、3、6、9和12个月评估疗效和安全性。在峰值(早晨给药后2小时)和谷值(晚上给药后12小时)测量眼压(IOP)。患者(n = 926)每天滴眼两次,分别使用0.2%酒石酸溴莫尼定或0.5%马来酸噻吗洛尔。在峰值时,酒石酸溴莫尼定组眼压从基线的平均降幅为5.9±3.2 mmHg至7.6±3.6 mmHg,噻吗洛尔组为6.0±3.4 mmHg至6.6±3.6 mmHg(与基线相比,组内p < 0.001)。除第1周、第2周和第3个月外(p≤0.04),峰值时两组间无显著差异,此时酒石酸溴莫尼定的平均眼压较低。在谷值时,酒石酸溴莫尼定组眼压从基线的平均降幅为3.7±4.0 mmHg至5.0±3.0 mmHg,噻吗洛尔组为5.9±3.4至6.6±3.0 mmHg。在所有访视的谷值时,两组间均有显著差异(< 0.001),此时噻吗洛尔的平均眼压较低。酒石酸溴莫尼定和噻吗洛尔均显示出持续疗效。两种药物耐受性良好。酒石酸溴莫尼定组眼部过敏、口干和结膜滤泡较多。噻吗洛尔组烧灼感和刺痛感较多。在酒石酸溴莫尼定组中,38/513(7.4%)因眼部过敏停药。噻吗洛尔组的平均心率与基线相比显著降低。两种药物对血压的影响均最小。酒石酸溴莫尼定显示出与噻吗洛尔相似的疗效,且眼部过敏发生率相对较低。每天滴眼两次的0.2%酒石酸溴莫尼定是一种有效且安全的降眼压药物,长期使用可维持眼压降低。