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首页> 外文期刊>Oman Journal of Ophthalmology >Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis
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Ranibizumab in patients with dense cataract and proliferative diabetic retinopathy with rubeosis

机译:雷尼单抗治疗重度白内障和糖尿病性视网膜增生伴红斑病

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Background:To evaluate the safety of ranibizumab as a surgical adjunct during cataract surgery in patients with proliferative diabetic retinopathy (PDR) with rubeosis, and to evaluate the efficacy and adverse effects of ranibizumab in treating PDR with rubeosis.Materials and Methods:Three intravitreal injections of 0.5 mg ranibizumab were administered on day-1, months-1 and -2 with cataract surgery 6-16 days after first injection. Retreatments with ranibizumab injections and pan-retinal photocoagulation (PRP) were given if recurrence or persistence of PDR was noted between months-3 and -11. Safety observation visits occurred at months-12, -18 and -24. Primary end points were incidence and severity of adverse events (AEs) that were related to both cataract surgery and treatment of PDR with rubeosis through month -12.Results:Of six patients screened, four (mean age 61.3 years) were enrolled. No AEs were noted with either cataract surgery or treatment of PDR. Neovascularization of iris (NVI) promptly regressed by 4 days after first ranibizumab injection, prior to cataract surgery in three of four patients (one had significantly regressed NVI by post-injection day-3 visit); NVI was not noted in any patient at 2 weeks after first ranibizumab injection. Recurrence of rubeosis or NVA after 3 monthly injections was not observed in any. At month-12, PDR was not present when assessed clinically and by fluorescein angiogram (FA). Only one patient developed neovascularization of disc and neovascularization elsewhere and required retreatments at months-5 and -9.Conclusions:Multiple intravitreal injections of ranibizumab may be a safe, effective treatment adjunct for PDR and diabetes-related rubeosis.
机译:背景:评价兰尼单抗在白内障手术中对患有糖尿病的增生性糖尿病视网膜病变(PDR)患者的安全性,并评估兰尼单抗在红宝石病治疗PDR中的疗效和不良作用。材料与方法:3次玻璃体内注射在第1天,第1个月和第2天,首次注射后6-16天进行白内障手术,分别给予0.5 mg雷珠单抗。如果在第3个月至-11个月之间发现PDR复发或持续存在,则使用兰尼单抗注射液和全视网膜光凝(PRP)进行再治疗。安全观察拜访发生在第12,-18和-24个月。主要终点是与白内障手术和PDR伴红斑病治疗相关的不良事件的发生率和严重程度,直至-12个月。结果:筛查的6例患者中,有4例(平均年龄61.3岁)入组。白内障手术或PDR治疗均未发现不良事件。首次兰尼单抗注射后4天,虹膜新血管形成迅速消退,四名患者中的三名在白内障手术前(在注射后第3天就使NVI显着消退);首次接受兰尼单抗注射后2周,未在任何患者中发现NVI。每月注射3次后,未观察到红疹或NVA的复发。在临床第12个月时,通过荧光素血管造影(FA)进行评估时不存在PDR。只有一名患者出现椎间盘新血管形成和其他地方发生新血管形成,需要在第5和-9个月再次治疗。结论:兰尼单抗多次玻璃体内注射可能是PDR和糖尿病相关性红斑病的一种安全,有效的治疗辅助手段。

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