首页> 外文期刊>Ophthalmology >Comparison of intravitreal versus posterior sub-Tenon's capsule injection of triamcinolone acetonide for diffuse diabetic macular edema.
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Comparison of intravitreal versus posterior sub-Tenon's capsule injection of triamcinolone acetonide for diffuse diabetic macular edema.

机译:玻璃体腔内注射与特农后囊皮注射曲安奈德治疗弥漫性糖尿病性黄斑水肿的比较。

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PURPOSE: To compare the safety and efficacy of intravitreal versus posterior Sub-Tenon's capsule injection of triamcinolone acetonide for diffuse diabetic macular edema. DESIGN: Prospective, double-masked, randomized controlled trial. PARTICIPANTS: Twelve patients (24 eyes) with bilateral diffuse diabetic macular edema. INTERVENTION: One eye of each patient was randomly assigned to receive a single 4-mg triamcinolone acetonide intravitreal injection and the fellow eye to receive a 40-mg triamcinolone acetonide posterior Sub-Tenon's capsule injection. MAIN OUTCOME MEASURES: Changes in visual acuity and central macular thickness obtained using optical coherence tomography were measured during a 6-month follow-up. Potential treatment complications were monitored, including increases in intraocular pressure (IOP) and cataract progression. RESULTS: Both intravitreal and Sub-Tenon's capsule injections of triamcinolone acetonide resulted in significant but transient improvements in central macular thickness. The mean (+/-standard deviation [SD]) central macular thickness in eyes with intravitreal injection was significantly thinner than in the Sub-Tenon's capsule-injected eyes at 1 month (226.8+/-41.7 microm and 431.5+/-165.8 microm, respectively; P = 0.002) and 3 months (242.3 +/- 93.9 microm and 364.7+/-78.2 microm, respectively; P = 0.005) after triamcinolone acetonide injection. The mean visual acuity (logarithm of the minimum angle of resolution) in the intravitreally injected eyes was significantly better than in the Sub-Tenon's capsule-injected eyes at 3 months post injection (0.832+/-0.293 and 1.107+/-0.339, respectively; P 0.004). Intraocular pressure did not show any significant difference between the 2 forms of triamcinolone acetonide delivery at any follow-up visit, and no eyes had IOPs >25 mmHg. CONCLUSIONS: The findings from our study neither advocate nor support the use of corticosteroids for the treatment of diabetic macular edema, but do imply that both intravitreal and Sub-Tenon's capsule injections of triamcinolone acetonide may be equally tolerated, with short-term performance clearly favoring the intravitreal (4 mg) more than the SBT capsule (40 mg) route for the anatomic and functional aspects of improvement tested in this investigation.
机译:目的:比较玻璃体腔内注射与特农后囊皮注射曲安奈德对弥漫性糖尿病性黄斑水肿的安全性和有效性。设计:前瞻性,双掩蔽,随机对照试验。参与者:12例(24眼)双侧弥漫性糖尿病性黄斑水肿。干预:每位患者的一只眼睛被随机分配接受一次4 mg曲安奈德玻璃体内注射,另一只眼睛接受40毫克曲安奈德丙酮在Sub-Tenon胶囊后注射。主要观察指标:在6个月的随访期间,测量了使用光学相干断层扫描获得的视力和中央黄斑中心厚度的变化。监测潜在的治疗并发症,包括眼内压(IOP)升高和白内障进展。结果:玻璃体腔注射和Sub-Tenon囊内注射曲安奈德均能显着但短暂改善中央黄斑厚度。玻璃体内注射的眼睛在1个月时的平均黄斑中心厚度(+/-标准差[SD])明显小于Sub-Tenon胶囊注射的眼睛(226.8 +/- 41.7微米和431.5 +/- 165.8微米)分别注射曲安奈德后3个月(P = 0.002)和3个月(分别为242.3 +/- 93.9微米和364.7 +/- 78.2微米; P = 0.005)。玻璃体内注射的眼睛在注射后3个月的平均视力(最小分辨角的对数)显着优于Sub-Tenon胶囊注射的眼睛(分别为0.832 +/- 0.293和1.107 +/- 0.339) ; P 0.004)。在任何后续随访中,眼压均未显示两种形式的曲安奈德丙酮酸酯递送之间有任何显着差异,并且没有眼睛的IOP> 25 mmHg。结论:我们的研究结果既不主张也不支持使用糖皮质激素治疗糖尿病性黄斑水肿,但确实暗示玻璃体腔注射和Sub-Tenon胶囊注射曲安奈德均可以耐受,短期表现显然有利玻璃体内注射(4 mg)比SBT胶囊(40 mg)途径在这项研究中测试的解剖学和功能方面有所改善。

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