首页> 外文期刊>BMC Ophthalmology >Efficacy and tolerability of fixed-combination bimatoprost/timolol versus fixed-combination dorzolamide/brimonidine/timolol in patients with primary open-angle glaucoma or ocular hypertension: a multicenter, prospective, crossover study
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Efficacy and tolerability of fixed-combination bimatoprost/timolol versus fixed-combination dorzolamide/brimonidine/timolol in patients with primary open-angle glaucoma or ocular hypertension: a multicenter, prospective, crossover study

机译:固定组合比马前列素/替莫洛与固定组合多佐胺/溴莫尼定/替莫洛在原发性开角型青光眼或高眼压症患者中的疗效和耐受性:一项多中心,前瞻性,交叉研究

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Background Fixed-combination ocular hypotensives have multiple advantages, but triple-therapy dorzolamide/brimonidine/timolol (dorz/brim/tim) is only available in Latin and South America, and information on its relative efficacy is limited. This study compares the efficacy and tolerability of fixed-combination bimatoprost/timolol (bim/tim) and dorz/brim/tim in Mexican patients with primary open-angle glaucoma or ocular hypertension. Methods In this investigator-masked, crossover study, patients with unmet target intraocular pressure (IOP) on once-daily bim/tim or twice-daily dorz/brim/tim received the opposite medication for 3?months before returning to their pre-baseline medication for 3?months. IOP was evaluated before and after morning instillation at months 2, 3, 5 and 6. Primary endpoints were mean IOP change and Ocular Surface Disease Index? (OSDI) score at each visit. The intent-to-treat population was the a priori analysis population, but due to the number of discontinuations, the per-protocol and intent-to-treat populations were used for the primary efficacy and sensitivity analyses, respectively. Results Seventy-eight and 56 patients were included in the intent-to-treat and per-protocol populations, respectively. At month 3, statistically significant IOP reductions from baseline were observed in the bim/tim (P?
机译:背景技术固定组合式降压药具有多重优势,但是多佐胺/溴莫尼定/替莫洛尔(dorz / brim / tim)三联疗法仅在拉丁美洲和南美可用,有关其相对疗效的信息有限。这项研究比较了固定组合比马前列素/替莫洛尔(bim / tim)和dorz / brim / tim在墨西哥原发性开角型青光眼或高眼压患者中的疗效和耐受性。方法在这项由研究者掩盖的交叉研究中,每日一次bim / tim或每天两次dorz / brim / tim的目标眼压(IOP)未达到目标的患者在返回基线之前接受相反的药物治疗3个月。用药3个月。在第2、3、5和6个月早晨滴注前后评估IOP。主要终点是平均IOP变化和眼表疾病指数? (OSDI)得分。意向性治疗人群是先验分析人群,但由于停药的数量,按方案和意向性治疗人群分别用于主要疗效和敏感性分析。结果意向性治疗人群和按方案治疗人群分别为78例和56例。在第3个月,无论评估时间如何,在bim / tim(P 0.01)和dorz / brim / tim(P 0.0001)组中,从基线观察到IOP降低均具有统计学意义。在第6个月,回到bim / tim的患者的IOP没有显着增加(无论评估时间如何),但是在灌输研究前进行评估时,回到dorz / brim / tim的患者的IOP出现了统计学上的显着增长(P≤0.001)。治疗。意向治疗和按方案分析人群的结果相似。在按方案分析中,在第3个月采用bim / tim的患者中有70%的IOP <14?mm Hg,在第6个月(即在3个月后)下降至58%(P?= 0.0061)。 dorz / brim / tim治疗)。在第3个月接受dorz / brim / tim的患者中,有38%的IOP <14?mm Hg,回到bim / tim后仍具有可比性。两组的OSDI评分和不良事件发生率相似。结论在对dorz / brim / tim和bim / tim的疗效进行的第一个直接比较中,从dorz / brim / tim转换为bim / tim的患者表现出IOP改善/降低。当返回dorz / brim / tim时,IOP升高至研究开始时所见的水平,这表明每天一次的bim / tim可能具有更大的降低IOP的功效。 bim / tim和dorz / brim / tim的耐受性都很好,眼表损伤最小。试用注册ClinicalTrials.gov:NCT01737853(2012年10月9日注册)

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