Intraocular Pressure Changes After Intravitreal Bevacizumab Injection Alone or Combination of Bevacizumab and Triamcinolone Acetonide

N. Barakat, Y. Suleiman, Kahtan Jalloul
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Abstract

Aim: To evaluate intraocular pressure changes after intravitreal injection of Bevacizumab alone or in combination with Triamcinolone Acetonide. Method: Our study included 63 eyes from the ophthalmology department at Tishreen University Hospital who had vascular retinal diseases. The patients were divided into two groups according to the indication of injection. The first group was injected with bevacizumab (B) at a concentration of 2.5mg / 0.1 ml and the second group was injected with the combination treatment of Triamcinolone Acetonide at a concentration of 2mg / 0.05ml with bevacizumab (B+TA) at a concentration of 1.25mg/ 0.05ml. Intraocular pressure was monitored on the Goldman applanation tonometry and values were recorded as follows: before injection, the second injection day, a week after injection, a month after injection and after three months. Results: The mean values of the intraocular pressure mean increased from the second day of injection in the study groups (B) and (B+TA) and the mean of the IOP values before injection (13.34-13.31 mmHg) respectively, and the IOP values showed the maximum in both groups after a week of the injection (17.81-17.31 mmHg) then began to decrease after a month and three months later to (17.34-17.06mmHg) and (17.6-16.75mmHg) mercury respectively, but they remained higher than they were before the injection, and the number of injections had no effect on intraocular pressure. Conclusion: intravitreal injections with both bevacizumab alone or in combination with triamcinolone acetonide resulted in a rise in intraocular pressure, and differences in pressure values were statistically significant within the same group during the studied time periods but were not statistically significant between the two groups, and the number of injections had no effect on intraocular pressure.
贝伐单抗玻璃体内单独注射或贝伐单抗与曲安奈德联合注射后眼压变化
目的:评价贝伐单抗单独或联合曲安奈德玻璃体内注射后眼压的变化。方法:本研究纳入天津大学附属医院眼科血管性视网膜疾病患者63只眼。根据注射指征分为两组。第一组注射浓度为2.5mg / 0.1 ml的贝伐珠单抗(B),第二组注射浓度为2mg / 0.05ml的曲安奈德与浓度为1.25mg/ 0.05ml的贝伐珠单抗(B+TA)联合治疗。在Goldman眼压仪上监测眼压,分别记录注射前、注射第二天、注射后一周、注射后一个月、注射后三个月的眼压。结果:眼压的平均值的意思是增加注入的第二天的学习小组(B)和(B +助教)和眼压值的均值分别注入(13.34 - -13.31毫米汞柱),之前和眼压值显示的最大一个星期后两组注射(17.81 - -17.31毫米汞柱),那么开始减少一个月后,三个月后(17.34 - -17.06毫米汞柱),水星(17.6 - -16.75毫米汞柱),但他们仍高于注射之前,注射次数对眼压无明显影响。结论:玻璃体内注射贝伐单抗或联合曲安奈德均可导致眼压升高,研究时间段内同一组内眼压值差异有统计学意义,两组间差异无统计学意义,注射次数对眼压无影响。
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