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首页> 外文期刊>Clinical ophthalmology >The clinical effectiveness of tafluprost on Japanese normal-tension glaucoma patients
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The clinical effectiveness of tafluprost on Japanese normal-tension glaucoma patients

机译:他氟前列素对日本正常血压青光眼患者的临床疗效

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Purpose: This study evaluates the effect of tafluprost on visual field progression in normal-tension glaucoma (NTG) in a Japanese population under daily clinical practice settings. Patients and methods: This is a post-marketing, multicenter, non-interventional, observational study. Patients with NTG who initiated tafluprost treatment were registered and prospectively observed for 2–3 years to investigate its effectiveness on visual field progression and intraocular pressure (IOP) and safety in Japan. Visual field progression was evaluated using mean deviation (MD) slopes in a visual field analysis set that comprised patients with reliable Humphrey visual fields taken at 5 or more time points throughout the 2–3 years. Results: Of the 1,454 patients registered from 160 medical institutions, 1,353 were set for safety analysis and 416 were set for visual field analysis. Due to insufficient effectiveness or safety reasons 194 patients discontinued tafluprost, and 388 patients discontinued tafluprost due to being lost to follow-up or another reason. The MD slopes were ?0.09±0.85 dB/year in the entire visual field analysis set, -0.02±0.80 dB/year in na?ve monotherapy patients, ?0.07±0.68 dB/year in switching monotherapy patients, and ?0.32±1.04 dB/year in concomitant therapy patients. In na?ve monotherapy, a significant difference in MD slopes was observed between patients with an IOP reduction of 10% or higher (0.11±0.73 dB/year) vs patients with an IOP reduction of <10% (?0.22±0.87 dB/year). Significant differences were also observed in the subset analyses when the patients were divided by both MD and IOP at baseline, and presence of vitreoretinal concomitant disease. The adverse reactions were observed in 9.53% patients without any serious adverse reactions. Conclusion: An at least 10% IOP reduction with tafluprost monotherapy in 56.7% of the treatment-na?ve NTG eyes was sufficient to significantly reduce the MD rate of progression.
机译:目的:本研究评估了在日常临床实践中,塔氟前列素对日本人群正常血压青光眼(NTG)视野进展的影响。患者和方法:这是一项售后,多中心,非干预的观察性研究。登记了开始使用他氟前列素治疗的NTG患者,并对其进行了2至3年的前瞻性观察,以研究其在日本对视野发展,眼压(IOP)和安全性的有效性。使用视野分析集中的平均偏差(MD)斜率评估视野进展,该分析集中了在2-3年中于5个或更多个时间点拍摄的具有可靠汉弗莱视野的患者。结果:在160家医疗机构登记的1,454例患者中,有1,353例进行了安全性分析,有416例进行了视野分析。由于有效性或安全性原因不足,有194例患者停用了塔夫普罗斯特,而388例患者由于失去随访或其他原因而中止了他氟普罗斯特。在整个视野分析集中,MD斜率分别为?0.09±0.85 dB /年,初次单药治疗患者为-0.02±0.80 dB /年,切换为单药治疗患者为?0.07±0.68 dB /年和?0.32±1.04伴随治疗患者的dB /年。在单纯的单药治疗中,观察到IOP降低10%或更高(0.11±0.73 dB /年)的患者与IOP降低<10%(?0.22±0.87 dB /年)的患者之间MD斜率存在显着差异。年)。当在基线时用MD和IOP将患者除以玻璃体视网膜合并症时,在子集分析中也观察到了显着差异。在9.53%的患者中观察到了不良反应,没有任何严重的不良反应。结论:使用tafluprost单药治疗的未治疗NTG眼中IOP降低至少10%,足以显着降低MD进展。

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