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使用每日一次的比马前列素、噻吗洛尔凝胶剂或拉坦前列素进行24小时眼压控制:一项为期1个月的随机对照临床试验。

24-Hour IOP control with once-daily bimatoprost, timolol gel-forming solution, or latanoprost: a 1-month, randomized, comparative clinical trial.

作者信息

Walters Thomas R, DuBiner Harvey B, Carpenter Susan P, Khan Bashir, VanDenburgh Amanda M

机构信息

Keystone Research, Austin, Texas, USA.

出版信息

Surv Ophthalmol. 2004 Mar;49 Suppl 1:S26-35. doi: 10.1016/j.survophthal.2003.12.017.

Abstract

PURPOSE

To compare the efficacy and safety of once-daily (QD) bimatoprost, latanoprost, and timolol gel-forming solution in providing 24-hour intraocular pressure (IOP) control.

DESIGN

This was a randomized, multicenter, investigator-masked, prospective, parallel-group, clinical trial.

PARTICIPANTS

Patients with open-angle glaucoma or ocular hypertension.

INTERVENTION

After washout of any previous ocular hypotensive medications, patients were randomly assigned to treatment with bimatoprost 0.03% ophthalmic solution QD (n=38) or latanoprost 0.005% ophthalmic solution QD (n=38) between 7 and 9 pm, or timolol maleate 0.5% gel-forming ophthalmic solution QD (n=39) between 7 and 9 am for 1 month.

MAIN OUTCOME MEASURES

The primary outcome measure, circadian IOP, was measured at eight time points over the course of 24 hours beginning at 8 am on day 28 and with the last measurement at 8 am on day 29. IOP was also measured at 8 am and 10 am at baseline and at 8 am on day 14. Safety measures included adverse events, biomicroscopy, visual acuity, heart rate, and blood pressure.

RESULTS

At 10 am (peak drug effect) on day 28, the mean IOP reduction from baseline was significantly greater with bimatoprost (9.3 mm Hg, 40.3%) than with timolol gel (7.1 mm Hg, 31.1%; P=.024, Wilcoxon rank sum test) or latanoprost (7.4 mm Hg, 33.3%). In the overall analysis of IOP measured over the course of 24 hours, mean IOP was significantly lower with bimatoprost or latanoprost than with timolol gel (P<.001; analysis of repeated measures). The analysis of repeated measures also showed a significant difference between bimatoprost and latanoprost (P=.003). In the area-under-the-curve analysis, bimatoprost and latanoprost were superior to timolol gel (P< or =.018) but comparable to each other (P> or =.223). All treatment regimens were well tolerated, with few discontinuations due to adverse events. There were no significant effects on systemic safety parameters.

CONCLUSION

Once-daily bimatoprost or latanoprost provided significantly better 24-hour IOP control than timolol gel in patients with glaucoma or ocular hypertension. Some measurements suggested a trend for greater efficacy of bimatoprost over latanoprost. All three treatments were well tolerated.

摘要

目的

比较每日一次(QD)使用比马前列素、拉坦前列素和噻吗洛尔凝胶剂控制24小时眼压(IOP)的疗效和安全性。

设计

这是一项随机、多中心、研究者设盲、前瞻性、平行组临床试验。

参与者

开角型青光眼或高眼压症患者。

干预措施

在停用任何先前的降眼压药物后,患者于晚上7点至9点被随机分配接受0.03%比马前列素滴眼液QD治疗(n = 38)或0.005%拉坦前列素滴眼液QD治疗(n = 38),或于上午7点至9点接受0.5%马来酸噻吗洛尔凝胶剂QD治疗(n = 39),为期1个月。

主要观察指标

主要观察指标昼夜眼压在第28天上午8点开始的24小时内的八个时间点进行测量,最后一次测量在第29天上午8点。眼压在基线时上午8点和10点以及第14天上午8点也进行测量。安全指标包括不良事件、生物显微镜检查、视力、心率和血压。

结果

在第28天上午10点(药物作用高峰),比马前列素使眼压从基线平均降低幅度(9.3 mmHg,40.3%)显著大于噻吗洛尔凝胶(7.1 mmHg,31.1%;P = 0.024,Wilcoxon秩和检验)或拉坦前列素(7.4 mmHg,33.3%)。在对24小时内测量的眼压进行的总体分析中,比马前列素或拉坦前列素治疗组的平均眼压显著低于噻吗洛尔凝胶组(P < 0.001;重复测量分析)。重复测量分析还显示比马前列素和拉坦前列素之间存在显著差异(P = 0.003)。在曲线下面积分析中,比马前列素和拉坦前列素优于噻吗洛尔凝胶(P ≤ 0.018),但彼此相当(P ≥ 0.223)。所有治疗方案耐受性良好,因不良事件停药的情况很少。对全身安全参数无显著影响。

结论

对于青光眼或高眼压症患者,每日一次使用比马前列素或拉坦前列素在控制24小时眼压方面显著优于噻吗洛尔凝胶。一些测量结果表明比马前列素的疗效有高于拉坦前列素的趋势。所有三种治疗耐受性良好。

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