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首页> 外文期刊>Ophthalmology >Posterior sub-Tenon's capsule injection of triamcinolone acetonide prevents panretinal photocoagulation-induced visual dysfunction in patients with severe diabetic retinopathy and good vision.
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Posterior sub-Tenon's capsule injection of triamcinolone acetonide prevents panretinal photocoagulation-induced visual dysfunction in patients with severe diabetic retinopathy and good vision.

机译:Tenon后囊胶囊注射曲安奈德可预防严重糖尿病性视网膜病和良好视力患者的视网膜光凝诱发的视觉功能障碍。

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摘要

PURPOSE: To evaluate prospectively the efficacy of a single sub-Tenon's capsule injection of triamcinolone acetonide (TA) against panretinal photocoagulation (PRP)-induced macular thickening and visual disturbance in patients with severe diabetic retinopathy and good vision. DESIGN: Prospective, comparative, interventional case series. PARTICIPANTS: Twenty eyes of 10 patients with severe nonproliferative diabetic retinopathy or non-high-risk proliferative diabetic retinopathy whose visual acuity was 20/40 or better (<0.3 in logarithm of the minimum angle of resolution [logMAR] acuity) before the PRP, whose retinopathy was bilateral and symmetrical. The averaged parafoveal retinal thickness was more than 300 microm, leading to a worse visual prognosis after PRP. INTERVENTION: Sub-Tenon's capsule injection of 20 mg TA. MAIN OUTCOME MEASURES: Best-corrected visual acuity (BCVA) with logMAR chart and averaged foveal thickness (FT) using the retinal mapping program of optical coherence tomography. METHODS: In all patients, PRP was performed every other week for 4 sessions on both eyes, and 1 week before PRP; 1 eye received the TA injection, and the other eye served as a control. The clinical course of BCVA and FT was monitored for up to 24 weeks after beginning PRP. RESULTS: Before TA injection, BCVA and FT were 0.055+/-0.072 and 235.5+/-37.5 microm in the TA-injected eye and 0.065+/-0.071 and 233.7+/-39.8 microm in the control eye, respectively; there was no significant difference between eyes. After the TA injection, FT in the TA-injected eyes was significantly decreased. During and after the PRP, FT in the control eye increased dramatically and reached 312.0+/-68.2 microm at 24 weeks, which was significantly different from that in the TA-injected eyes (235.3+/-38.6 microm at 24 weeks). Best-corrected visual acuity in the control eye decreased with time to 0.24+/-0.13; in contrast, and BCVA in the TA-injected eye was good (to 0.085+/-0.11) . CONCLUSIONS: As a pretreatment for PRP, a single sub-Tenon's capsuleinjection of TA has beneficial effects for preventing PRP-induced foveal thickening and visual dysfunction in patients with severe diabetic retinopathy and good vision.
机译:目的:前瞻性评估单次特农囊状注射曲安奈德(TA)对严重糖尿病性视网膜病变和良好视力患者的全视网膜光凝(PRP)引起的黄斑增厚和视力障碍的疗效。设计:前瞻性,比较性,介入性病例系列。参与者:在PRP之前,有10例严重非增生性糖尿病性视网膜病或非高危性增生性糖尿病性视网膜病的患者的20眼,其视力为20/40或更高(<最小分辨力[logMAR]视力对数的<0.3),视网膜病变是双侧对称的。平均小凹旁视网膜厚度超过300微米,导致PRP术后视觉预后较差。干预:Sub-Tenon's胶囊注射20 mg TA。主要观察指标:采用光学相干断层扫描的视网膜成像程序,采用logMAR图和平均中央凹厚度(FT)进行最佳矫正视力(BCVA)。方法:在所有患者中,每两周和在PRP前1周,每两周进行一次PRP,共4次。一只眼接受了TA注射,另一只眼作为对照。开始PRP后,长达24周的时间监控BCVA和FT的临床过程。结果:在注射TA之前,注射TA的眼中BCVA和FT分别为0.055 +/- 0.072和235.5 +/- 37.5微米,而在对照眼中,BCVA和FT分别为0.065 +/- 0.071和233.7 +/- 39.8微米。眼睛之间没有显着差异。注射TA后,注射TA的眼睛的FT明显降低。在PRP期间和之后,对照眼的FT显着增加,在24周时达到312.0 +/- 68.2微米,这与注射TA的眼(在24周时为235.3 +/- 38.6微米)有显着差异。对照眼的最佳矫正视力随时间下降至0.24 +/- 0.13;相比之下,注射TA的眼睛中的BCVA很好(至0.085 +/- 0.11)。结论:Tenon亚囊单次注射TA作为PRP的预处理对预防PRP引起的严重糖尿病性视网膜病变和良好视力的中央凹增厚和视觉功能障碍具有有益的作用。

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