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Effect of prophylactic timolol 0.1% gel on intraocular pressure after an intravitreal injection of ranibizumab: a randomized study

机译:玻璃体腔注射兰尼单抗后预防性噻吗洛尔0.1%凝胶对眼压的影响:一项随机研究

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Purpose: The purpose of this study is to make a prospective evaluation of the effect of timolol 0.1% eye gel on short-term intraocular pressure (IOP) after an intravitreal injection (IVI) of ranibizumab. Participants and methods: One hundred and fifty eyes of 150 IVI-na?ve patients with macular edema caused by various pathological conditions (age-related macular degeneration, central or branch retinal vein occlusion, and diabetic retinopathy) were scheduled to undergo an IVI of ranibizumab (0.5 mg/0.05 cc). The patients were randomly divided into three groups: 50 were not treated with timolol before the IVI (group 1); 50 received an instillation of timolol 0.1% eye gel the evening before the IVI (group 2); and 50 received an instillation of timolol 0.1% eye gel 2 hours before the IVI (group 3). The incidence of clinically significant intraocular hypertensive spikes (>25 mmHg and >40 mmHg) was then assessed. Results: Our findings showed that mean IOP at baseline was significantly higher than at both 5 and 60 minutes after IVI ( P 25 mmHg were recorded at either time in 27 patients (54%) in group 1, 23 patients (44%) in group 2, and 24 patients (48%) in group 3. None of the between-group differences were significant. Spikes of >40 mmHg (which were only detected 5 minutes after IVI) were recorded in nine (18%), eight (16%), and one patient (2%) in groups 1, 2, and 3, respectively. The only significant difference was between the control and group 3 ( P =0.012). Conclusion: An increase in IOP after antivascular endothelial growth factor IVI is a frequent complication. The prophylactic use of timolol 0.1% gel effectively reduced the mean IOP when administered 2 hours before IVI and was also effective in preventing dangerous IOP spikes of >40 mmHg. It is therefore recommended before IVIs as a means of preventing emergency procedures and preserving the health of the optic nerve.
机译:目的:本研究的目的是对玻璃体腔注射兰尼单抗后0.1%噻吗洛尔眼凝胶对短期眼内压(IOP)的影响进行前瞻性评估。参加者和方法:150名因各种病理状况(年龄相关性黄斑变性,视网膜中央或分支视网膜静脉阻塞以及糖尿病性视网膜病变)引起的黄斑水肿幼稚患者中的150只眼计划进行IVI。雷尼单抗(0.5 mg / 0.05 cc)。将患者随机分为三组:50例在IVI之前未接受噻吗洛尔治疗(第1组);第3组为第3组。 50名患者在IVI前一天晚上滴注了0.1%的噻吗洛尔眼药水(第2组); IVI前2小时(第3组)滴注50%的替莫洛尔0.1%眼用凝胶。然后评估临床上明显的眼内高血压尖峰(> 25 mmHg和> 40 mmHg)的发生率。结果:我们的研究结果显示,基线时的平均眼压明显高于IVI后5分钟和60分钟(第1组的27例患者(54%)在任一时间记录P 25 mmHg),第23例的患者(44%) 3组中有2例和24例(48%),组间差异均无统计学意义,其中9例(18%),8例(16例)记录的峰值> 40 mmHg(仅在IVI后5分钟检测到)。 1、2和3组分别为%)和1名患者(2%),唯一的显着差异是对照组和3组之间的差异(P = 0.012)结论:抗血管内皮生长因子IVI后IOP升高预防性使用噻吗洛尔0.1%凝胶可在IVI前2小时有效降低平均IOP,并有效预防> 40 mmHg的危险IOP峰值,因此建议在IVI之前作为预防紧急情况的手段程序并保持视神经健康。

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