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随机、对照试验:一种 5-氟尿嘧啶持续释放剂型治疗失败滤泡的疗效。

Randomized, controlled trial of a sustained delivery formulation of 5-fluorouracil for the treatment of failing blebs.

机构信息

Singapore Eye Research Institute, Singapore.

出版信息

Ophthalmology. 2012 Feb;119(2):314-20. doi: 10.1016/j.ophtha.2011.07.053. Epub 2011 Dec 6.

Abstract

PURPOSE

To determine the efficacy of a subconjunctival injection of hyaluronic acid (HA) with 5-fluorouracil (5FU) formulation as an adjunct in reviving bleb function by needling.

DESIGN

Prospective, randomized, controlled trial.

PARTICIPANTS

Fifty patients with previous trabeculectomy and scheduled by the managing physician for a needling intervention.

METHODS

One eye of each patient was randomized to receive needling with HA-5FU mixture or needling with subconjunctival injection of 5FU solution alone.

MAIN OUTCOME MEASURES

The primary outcome was the percentage of subjects with an intraocular pressure (IOP) <15 mmHg without any medications at 3 months. Secondary outcomes included the need for additional needling procedures and changes in bleb morphology.

RESULTS

Forty-nine subjects (25 in the HA-5FU group and 24 in the 5FU group) completed 3 months of follow-up. At baseline, there was no significant difference between the groups in terms of demographic features, subtype of glaucoma, vertical cup-to-disc ratio, or visual field indices. The mean number of glaucoma medications at baseline was higher in the 5FU group (0.8±1.1 [mean ± standard deviation] vs. 0.2±0.6, P = 0.04). An IOP <15 mmHg without medications was reached in 48.0% of subjects in the HA-5FU group and in 33.3% of subjects in the 5FU group (P = 0.2). At 3 months, both groups demonstrated a significant decrease in IOP from baseline (HA-5FU: decrease of 5.9 mmHg [95% confidence interval, 3.4-8.4]; 5FU: decrease of 6.0 mmHg [95% confidence interval, 3.2-8.2]; P<0.001 for both). Intergroup comparisons for IOP change from baseline was not significant (P = 0.9). However, repeat needling was required more frequently in the 5FU group compared with the HA-5FU group (50.0% vs. 12.0%; P = 0.004). There were no significant differences in the number of reported adverse events, bleb vascularity, or morphology between the 2 groups.

CONCLUSIONS

Subconjunctival injection of HA-5FU to revive bleb function after bleb needling is as effective as 5FU solution. Fewer repeat needlings were required after treatment with HA-5FU, suggesting that the use of a combined formulation of HA-5FU may improve the overall outcomes of bleb needlings.

摘要

目的

通过针刺确定在巩膜下注射透明质酸(HA)与 5-氟尿嘧啶(5FU)制剂联合应用对恢复滤泡功能的疗效。

设计

前瞻性、随机、对照试验。

参与者

五十名曾接受小梁切除术并由主治医生安排进行针刺干预的患者。

方法

每位患者的一只眼随机接受 HA-5FU 混合物的针刺或单独的巩膜下注射 5FU 溶液的针刺。

主要观察指标

主要结局是 3 个月时眼压(IOP)<15mmHg 且无需任何药物的患者比例。次要结局包括需要进行额外的针刺程序以及滤泡形态的变化。

结果

四十九名患者(HA-5FU 组 25 名,5FU 组 24 名)完成了 3 个月的随访。基线时,两组在人口统计学特征、青光眼亚型、垂直杯盘比或视野指数方面无显著差异。5FU 组基线时青光眼药物的平均数量较高(0.8±1.1[均数±标准差] vs. 0.2±0.6,P=0.04)。HA-5FU 组中有 48.0%的患者达到了无药物治疗的 IOP<15mmHg,而 5FU 组中有 33.3%的患者达到了这一水平(P=0.2)。3 个月时,两组的 IOP 均较基线显著下降(HA-5FU 组下降 5.9mmHg[95%置信区间,3.4-8.4];5FU 组下降 6.0mmHg[95%置信区间,3.2-8.2];均 P<0.001)。两组间从基线开始的 IOP 变化的组间比较无显著差异(P=0.9)。然而,与 HA-5FU 组相比,5FU 组更频繁地需要重复针刺(50.0% vs. 12.0%;P=0.004)。两组间报告的不良事件、滤泡血管化或形态均无显著差异。

结论

在滤泡针刺后,通过巩膜下注射 HA-5FU 来恢复滤泡功能与 5FU 溶液一样有效。HA-5FU 治疗后需要重复针刺的次数更少,这表明使用 HA-5FU 的联合制剂可能会改善滤泡针刺的总体效果。

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