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Panretinal photocoagulation and intravitreal triamcinolone acetonide for the management of proliferative diabetic retinopathy with macular edema.

机译:全视网膜光凝和玻璃体内曲安奈德治疗黄斑水肿性增生性糖尿病视网膜病变。

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PURPOSE: To investigate intravitreal triamcinolone acetonide (IVTA) as an adjunctive therapy to panretinal photocoagulation (PRP) in patients with both high-risk proliferative diabetic retinopathy (PDR) and clinically significant macular edema (CSME). METHODS: Thirty-five eyes diagnosed with both high-risk PDR and CSME underwent PRP and a single injection of 4 mg of IVTA (IVTA group). Visual, anatomic, and fluorescein angiographic changes were documented. Any complications resulting from the combined procedure were noted. These data were compared retrospectively to 35 eyes that underwent grid laser treatment to the macula followed 2 weeks later by PRP (laser group). Main outcome measures included change in best-corrected visual acuity, improvement in macular edema (clinical or angiographic), and control of the neovascular disease. RESULTS: Mean follow-up was 9.6 months for the IVTA group and 11.9 months for the laser group. Mean pretreatment best-corrected visual acuity was 20/286 in the IVTA group and20/282 in the laser group (P = 0.80). After 9 months of follow-up, visual acuity was 20/80 in the IVTA group versus 20/156 in the laser group (P = 0.007). Thirty-four percent of eyes in the IVTA group had final vision of 20/40 or better versus 11% in the laser group (P = 0.044). At 9 months follow-up, 84% of IVTA eyes had complete resolution of macular edema versus 46% of laser eyes (P = 0.002). Three eyes in the IVTA group had recurrence of macular edema after 6 months and required reinjection of IVTA. Elevation in intraocular pressure occurred in eight eyes in the IVTA group and responded to topical therapy. Cataract progression was observed in nine eyes in the IVTA group. CONCLUSIONS: The addition of intravitreal triamcinolone acetonide to PRP in the management of patients with both PDR and CSME seems promising. Further study is needed to assess the effect of this combined treatment.
机译:目的:探讨玻璃体内注射曲安奈德(IVTA)作为高危增生性糖尿病视网膜病变(PDR)和临床上显着的黄斑水肿(CSME)患者全视网膜光凝(PRP)的辅助疗法。方法:对35例同时被诊断为高危PDR和CSME的眼睛进行了PRP,单次注射4 mg的IVTA(IVTA组)。视觉,解剖和荧光素血管造影的变化都被记录下来。注意到由联合手术引起的任何并发症。回顾性地将这些数据与35眼接受黄斑栅格激光治疗的眼睛进行比较,然后在2周后进行PRP(激光治疗组)。主要结局指标包括最佳矫正视力的改变,黄斑水肿(临床或血管造影)的改善以及新血管疾病的控制。结果:IVTA组平均随访9.6个月,激光组平均随访11.9个月。 IVTA组的平均预处理最佳矫正视力为20/286,激光组为20/282(P = 0.80)。随访9个月后,IVTA组的视力为20/80,而激光组的视力为20/156(P = 0.007)。 IVTA组中有34%的最终视力为20/40或更好,而激光组中为11%(P = 0.044)。在随访的9个月中,有84%的IVTA眼睛完全解决了黄斑水肿,而有46%的激光眼睛具有完全的黄斑水肿(P = 0.002)。六个月后,IVTA组中的三只眼复发了黄斑水肿,需要再次注射IVTA。 IVTA组中八只眼的眼内压升高,并且对局部治疗有反应。在IVTA组的9只眼中观察到白内障进展。结论:在PRP和CSME患者的管理中,向PRP中加入玻璃体内曲安奈德丙酮酸酯似乎是有希望的。需要进一步的研究来评估这种联合治疗的效果。

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