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Intravitreal triamcinolone acetonide for radiation maculopathy after plaque radiotherapy for choroidal melanoma.

机译:玻璃体内曲安奈德用于脉络膜黑色素瘤斑块放疗后的放射性黄斑病变。

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OBJECTIVE:: To evaluate the effect of intravitreal triamcinolone acetonide on patients with visually symptomatic radiation-induced maculopathy after plaque radiotherapy for choroidal melanoma. DESIGN:: In this prospective, nonrandomized, single-center case series of 31 patients with visually symptomatic radiation-induced maculopathy after plaque radiotherapy for choroidal melanoma at the Ocular Oncology Service at Wills Eye Hospital of Thomas Jefferson University, triamcinolone acetonide (4 mg/1 mL) was injected through the pars plana into the vitreous cavity using sterile technique. Status of radiation maculopathy and final visual acuity were the main outcome measures. RESULTS:: At the time of diagnosis of choroidal melanoma, visual acuity was 20/20 to 20/50 in 90% (n = 28), 20/60 to 20/200 in 10% (n = 3), and 20/400 or worse in none of the patients. The mean radiation dose to the foveola was 5,122 cGy (median, 3,280 cGy; range, 1,000-16,100 cGy). Radiation maculopathy developed at a mean of 22 months(median, 16 months; range, 6-96 months) after plaque radiotherapy. In all cases, the choroidal melanoma was regressed, and there was no retinal detachment or neovascularization of the retina, optic disk, or iris. At the time of diagnosis of radiation maculopathy, visual acuity was 20/20 to 20/50 in 19% (6/31), 20/60 to 20/200 in 58% (18/31), and 20/400 or worse in 23% (7/31) of patients. After intravitreal injection of triamcinolone acetonide, visual acuity was stable or improved in 91% (20/22) of patients by 1 month and 45% (14/31) by 6 months. Mean foveal thickness by optical coherence tomography was 417 mum at injection and 207 mum at 1 month and 292 mum at 6 months after injection. CONCLUSIONS:: Intravitreal triamcinolone acetonide can stabilize or improve visual acuity in some patients with radiation-induced maculopathy, but its effect might not be lasting.
机译:目的:评价玻璃体内曲安奈德对脉络膜黑色素瘤斑块放疗后视觉症状性辐射诱发的黄斑病变的疗效。设计:在托马斯·杰斐逊大学威尔斯眼医院眼肿瘤科对斑状脉络膜黑色素瘤进行斑块放疗后的31例视觉症状性辐射诱发性黄斑病的前瞻性,非随机,单中心病例系列中,曲安奈德(4 mg /使用无菌技术将1 mL)穿过睑板注入玻璃体腔。放射黄斑病变的状态和最终视力是主要的结局指标。结果:在诊断脉络膜黑色素瘤时,视力90%(n = 28)为20/20至20 / 50,10%(n = 3)为20/60至20/200,而20 /所有患者均不超过400。中心凹的平均辐射剂量为5,122 cGy(中位数为3,280 cGy;范围为1,000-16,100 cGy)。斑块放疗后平均22个月(中位16个月;范围6-96个月)发生放射性黄斑病变。在所有情况下,脉络膜黑色素瘤均消退,并且视网膜,视盘或虹膜无视网膜脱离或新生血管形成。诊断为放射性黄斑病时,视力为19%(6/31)为20/20至20/50,58%(18/31)为20/60至20/200,且为20/400或更差在23%(7/31)的患者中。玻璃体腔注射丙酮酸曲安奈德后,视力稳定或改善的患者有91%(20/22)的患者在1个月时达到视力稳定或改善了视力,在6个月的患者中达到了45%(14/31)。光学相干断层扫描的平均中央凹厚度在注射后为417 mm,注射后1个月为207 mm,注射后6个月为292 mm。结论:玻璃体腔注射曲安奈德可以稳定或改善某些放射性黄斑病变患者的视力,但其作用可能不会持久。

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