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首页> 外文期刊>Journal of Ophthalmology >Effect of a Topical Combination of Latanoprost and Pranoprofen on Intraocular Pressure and the Ocular Surface in Open-Angle Glaucoma Patients
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Effect of a Topical Combination of Latanoprost and Pranoprofen on Intraocular Pressure and the Ocular Surface in Open-Angle Glaucoma Patients

机译:拉坦前列素和普萘洛芬的局部联合用药对开角型青光眼患者眼压和眼表的影响

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Objective. A prospective study was performed to observe the effects of nonsteroidal anti-inflammatory drug (NSAID) eyedrops on intraocular pressure (IOP) and the ocular surface in primary open-angle glaucoma (POAG) patients treated with 0.005% latanoprost eyedrops. Methods. Forty-eight subjects were randomized into two study groups (NSAID and control). Latanoprost was continued for 10 weeks in all subjects. At the end of week 4, pranoprofen was added in the NSAID group, and treatment lasted for 4 weeks, whereas patients in the control group were treated with latanoprost alone. IOP was measured in both groups every 2 weeks, and the changes in the ocular surface in the NSAID group were evaluated once a month. Results. Pranoprofen addition resulted in a decrease in IOP in the NSAID group compared to the control group (). After pranoprofen was discontinued, IOP significantly increased in the NSAID group (), remaining approximately at the same IOP as when they were being treated with latanoprost alone. During the same examination, no significant variations in IOP were found in the control group. Patients who were treated with latanoprost alone showed gradual improvements in ocular surface symptom scores and conjunctival hyperemia scores during the first four weeks of treatment (). When pranoprofen eyedrops were added, ocular surface symptom scores decreased (), but conjunctival hyperemia scores did not change significantly. Conclusions. For POAG patients treated with latanoprost, the combination of pranoprofen can not only significantly enhance the latanoprost-induced IOP-lowering effect but also relieve the uncomfortable ocular symptoms caused by latanoprost.
机译:目的。进行了一项前瞻性研究,以观察非甾体抗炎药(NSAID)滴眼液对接受0.005%拉坦前列素滴眼液治疗的原发性开角型青光眼(POAG)患者眼内压(IOP)和眼表的影响。方法。 48位受试者被随机分为两个研究组(NSAID和对照组)。所有受试者均接受拉坦前列素治疗10周。在第4周结束时,在NSAID组中添加了pranoprofen,治疗持续了4周,而对照组中的患者仅接受了拉坦前列素治疗。两组均每2周测量一次IOP,并每月评估一次NSAID组的眼表变化。结果。与对照组相比,普拉诺洛芬的添加导致NSAID组的IOP降低()。停用pranoprofen后,NSAID组()的IOP显着增加,与单独接受拉坦前列素治疗时的IOP保持大致相同。在相同的检查过程中,对照组的IOP没有明显变化。单独接受拉坦前列素治疗的患者在治疗的前四周内,其眼表症状评分和结膜充血评分逐渐改善()。当添加pranoprofen滴眼液时,眼表症状评分降低(),但结膜充血评分没有明显变化。结论。对于接受拉坦前列素治疗的POAG患者,普罗洛芬的组合不仅可以显着增强拉坦前列素引起的IOP降低效果,而且还可以缓解拉坦前列素引起的不适的眼部症状。

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