首页> 外文期刊>Ophthalmology >Efficacy of latanoprost or fixed-combination latanoprost-timolol in patients switched from a combination of timolol and a nonprostaglandin medication.
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Efficacy of latanoprost or fixed-combination latanoprost-timolol in patients switched from a combination of timolol and a nonprostaglandin medication.

机译:拉坦前列素或固定组合拉坦前列素-替莫洛尔在患者中的功效从替莫洛尔和非前列腺素类药物的组合转换而来。

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PURPOSE: To compare latanoprost with the fixed-combination latanoprost-timolol in glaucoma or ocular hypertension patients switched from a combination glaucoma therapy with timolol and another nonprostaglandin medication. DESIGN: Prospective randomized clinical trial. METHODS: Glaucoma or ocular hypertension patients receiving a combined treatment of timolol 0.5% and another nonprostaglandin medication (pilocarpine 4%, alpha-agonist, or a topical carbonic anhydrase inhibitor) underwent a 30-day washout of their medications. A masked observer then measured their intraocular pressure (IOP). The subjects were randomized to either latanoprost or fixed-combination latanoprost-timolol eyedrops to use once daily at 7 am. The IOP was measured again 30 days after the patients started using one of the study drugs by the same examiner at the same time. MAIN OUTCOME MEASURE: Comparison of the study medications' hypotensive effect. RESULTS: Fifty-three eyes (28 in the latanoprost group and 25 in the latanoprost-timolol group) from 28 patients were included in the study. The IOP reduction was greater in both study groups compared with the previous combination therapy with timolol and another nonprostaglandin medication in millimeters of mercury (7.7+/-2.3 vs. 5.5+/-2.3, P<0.001, for the latanoprost group; 8.5+/-3.5 vs. 6.3+/-2.7, P<0.001, for the latanoprost-timolol group) and percentage (35.8+/-8.2% vs. 25.6+/-8.9%, P<0.001, for the latanoprost group; 38.6+/-8.7% vs. 28.6+/-9.0%, P<0.001, for the latanoprost-timolol group). There was no statistical difference between latanoprost and fixed-combination latanoprost-timolol in reducing IOP, in either millimeters of mercury (P = 0.3) or percentage (P = 0.2). CONCLUSIONS: Both latanoprost and fixed-combination latanoprost-timolol may be viable substitutes for timolol and another nonprostaglandin medication in glaucoma or ocular hypertension patients.
机译:目的:在青光眼或高眼压患者中,将拉坦前列素与拉坦前列素-替莫洛尔的固定组合进行比较,将青光眼与替莫洛尔和另一种非前列腺素类药物联合治疗。设计:前瞻性随机临床试验。方法:接受0.5%噻吗洛尔和另一种非前列腺素药物(毛果芸香碱4%,α-激动剂或局部碳酸酐酶抑制剂)联合治疗的青光眼或高眼压患者,需要对其药物进行30天冲洗。然后,戴面具的观察者测量了他们的眼内压(IOP)。将受试者随机分为拉坦前列素或固定组合拉坦前列素-噻吗洛尔滴眼液,每天早上7点使用一次。患者在同一时间同时由同一名检查员开始使用一种研究药物后30天再次测量IOP。主要观察指标:比较研究药物的降压作用。结果:来自28名患者的53只眼(拉坦前列素组为28只,拉坦前列素-替莫洛尔组为25只)。与先前的联合使用噻吗洛尔和另一种非前列腺素药物的毫米汞柱治疗相比,两个研究组的IOP降低幅度更大(拉坦前列素组7.7 +/- 2.3与5.5 +/- 2.3,P <0.001,P <0.001; 8.5+ /-3.5 vs. 6.3 +/- 2.7,对于拉坦前列素-替莫洛尔组,P <0.001)和百分比(35.8 +/- 8.2%vs.25.6 +/- 8.9%,对于拉坦前列素组; P <0.001; 38.6 +/- 8.7%,而拉坦前列素-噻吗洛尔组为28.6 +/- 9.0%,P <0.001)。拉坦前列素和固定组合拉坦前列素-噻吗洛尔在降低眼压方面没有统计学差异,无论是汞的毫米数(P = 0.3)还是百分比(P = 0.2)。结论:在青光眼或高眼压症患者中,拉坦前列素和固定组合拉坦前列素-替莫洛尔均可作为替莫洛尔和另一种非前列腺素药物的可行替代品。

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