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首页> 外文期刊>Journal of ocular pharmacology and therapeutics: The official journal of the Association for Ocular Pharmacology and Therapeutics >Efficacy and Safety of Dexamethasone Intravitreal Implant for Treatment of Refractory Macular Edema Secondary to Retinal Vein Occlusion in Taiwan
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Efficacy and Safety of Dexamethasone Intravitreal Implant for Treatment of Refractory Macular Edema Secondary to Retinal Vein Occlusion in Taiwan

机译:地塞米松玻璃体内植入物治疗台湾继发性视网膜静脉阻塞难治性黄斑水肿的疗效和安全性

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摘要

Purpose: To evaluate the long-term efficacy and safety of slow-release dexamethasone intravitreal implant (DEX implant) in patients with refractory macular edema (ME) secondary to retinal vein occlusion (RVO) in Taiwan. Methods: We conducted a retrospective chart review of patients with a diagnosis of ME secondary to RVO who received the DEX implant at Kaohsiung Veterans General Hospital from October 2010 to February 2014. Results: A total of 28 patients with an average age of 60.711.1 years were examined. Of these patients, 17 were diagnosed with branch RVO (BRVO) and 11 were diagnosed with central RVO (CRVO). The mean maximal change in vision from the baseline after the final injection was an improvement of 1.7 +/- 2.8 lines (equivalent to 8.5 ETDRS letters; p<0.0001). The response to the first injection was similar across both BRVO and CRVO groups, but patients with BRVO showed a more favorable response than those with CRVO after the second injection. The response in patients who had refractory ME after at least 3 previous interventions was similar to the whole group. Three patients (10.7%) had elevated intraocular pressure (IOP) that was well controlled by IOP-lowering medications. None of these patients required laser or glaucoma surgery. Five patients (17.9%) exhibited cataract progression during the observation period. Conclusion: The DEX implant is an effective and safe treatment for ME, secondary to RVO, including refractory ME.
机译:目的:评价缓释地塞米松玻璃体内植入物(DEX植入物)对台湾继发于视网膜静脉阻塞(RVO)的难治性黄斑水肿(ME)患者的长期疗效和安全性。方法:我们对2010年10月至2014年2月在高雄荣民总医院接受DEX植入的诊断为RVO继发性ME的患者进行了回顾性图表回顾。结果:总共28例患者的平均年龄为60.711.1岁年审查。在这些患者中,有17名被诊断患有分支RVO(BRVO),而11名被诊断患有中枢RVO(CRVO)。最后一次注射后,与基线相比,平均视力的最大变化是改善了1.7 +/- 2.8线(相当于8.5个ETDRS字母; p <0.0001)。 BRVO和CRVO组对第一次注射的反应相似,但BRVO患者显示出比第二次注射后CRVO更好的反应。至少经过3次干预后患有难治性ME的患者的反应与整个组相似。 3例(10.7%)的眼压升高(IOP)受降眼压药物良好控制。这些患者均不需要激光或青光眼手术。五名患者(17.9%)在观察期内表现出白内障进展。结论:DEX植入物是继RVO继发于RVO(包括难治性ME)后的一种安全有效的ME治疗方法。

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