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首页> 外文期刊>Acta ophthalmologica Scandinavica >Efficacy and safety of latanoprost versus pilocarpine/timolol maleate fixed combination in patients with primary open-angle glaucoma or ocular hypertension
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Efficacy and safety of latanoprost versus pilocarpine/timolol maleate fixed combination in patients with primary open-angle glaucoma or ocular hypertension

机译:拉坦前列素与匹罗卡品/替莫洛尔马来酸酯固定组合治疗原发性开角型青光眼或高眼压症的疗效和安全性

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摘要

Purpose: This study aimed to compare the safety and effect on intraocular pressure (IOP) of latanoprost given every evening versus pilocarpine/timolol maleate fixed combination (PTFC) given twice daily in patients with primary open-angle glaucoma (POAG) or ocular hypertension (OH).Methods: Following a 6-week, medicine-free period, qualified patients were randomized for Period 1 to either placebo administered every morning and latanoprost every evening or to PTFC administered twice daily. After 8 weeks of treatment, IOP was measured at 08.00, 10.00, 16.00 and 18.00 hours. Patients were then switched to the opposite treatment and underwent a second diurnal evaluation at the end of Period 2. Results: Thirty-two patients completed this study. They demonstrated diurnal baseline IOP of 24.1 +- 2.4 mmHg. Mean diurnal pressure was 16.8 +- 2.1 mmHg on PTFC and 16.9 +- 2.5 mmHg on latanoprost (p = 0.60). No statistical difference between treatments was observed at any individual time-point except at 10.00 hours, when the PTFC group demonstrated an IOP of 15.9 +- 2.3 mmHg and latanoprost 16.8 +- 2.7 mmHg (p = 0.02). There were no statistical differences between groups in unsolicited systemic or ocular adverse events (p > 0.05). However, the PTFC group showed a narrower pupil diameter (2.3 mm) than the latanoprost group (3.7 mm). Additionally, a solicited symptom survey demonstrated mild blurred vision, stinging and ocular pain with PTFC (p < 0.001).Conclusions: Both PTFC and latanoprost are efficacious in reducing diurnal IOP in POAG or OH. However, PTFC may be more effective in the late morning and may have a greater incidence of mild ocular side-effects.
机译:目的:本研究旨在比较初次开角型青光眼(POAG)或高眼压患者每天晚上给予拉坦前列素与每天两次给予毛果芸香碱/噻吗洛尔马来酸酯固定组合(PTFC)的安全性和对眼内压(IOP)的影响(方法:在6周的无药治疗期后,将合格的患者随机分为1期:每天早晨服用安慰剂,每天晚上服用拉坦前列素或每天两次服用PTFC。治疗8周后,在08.00、10.00、16.00和18.00小时测量了IOP。然后将患者转为接受相反的治疗,并在第2期结束时进行了第二次昼夜评估。结果:32位患者完成了本研究。他们的昼夜基线眼压为24.1±2.4 mmHg。在PTFC上,平均日压为16.8±2.1 mmHg,在拉坦前列素上为16.9±2.5 mmHg(p = 0.60)。除PTFC组的IOP为15.9±2.3 mmHg和拉坦前列素16.8±2.7 mmHg(p = 0.02)时,在任何单独的时间点,除10.00小时外,观察到的治疗之间无统计学差异。在未经请求的全身或眼部不良事件中,两组之间无统计学差异(p> 0.05)。但是,PTFC组的瞳孔直径(2.3 mm)比拉坦前列素组(3.7 mm)窄。此外,一项征集症状调查显示,使用PTFC可以减轻轻度视力模糊,刺痛和眼痛(p <0.001)。结论:PTFC和拉坦前列素均能有效降低POAG或OH的昼夜IOP。但是,PTFC在清晨可能更有效,并且轻度眼部副作用的发生率可能更高。

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