首页> 外文期刊>Investigative ophthalmology & visual science >Associated Treatment With Intravitreal Bevacizumab And Macular Photocoagulation For Macular Edema Secondary To Central Retinal Vein Occlusion (CRVO)
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Associated Treatment With Intravitreal Bevacizumab And Macular Photocoagulation For Macular Edema Secondary To Central Retinal Vein Occlusion (CRVO)

机译:玻璃体内贝伐单抗联合黄斑光凝治疗中央视网膜静脉阻塞(CRVO)继发的黄斑水肿

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Purpose: : The primary objective is to evaluate the safety of the intravitreal bevacizumabe (IVB) associated to macular photocoagulation in the treatment of macular edema secondary to CRVO. The secondary objective is to evaluate the number of injections needed. Methods: : phase I, non-comparative, consecutive, single-arm study of patients with macular edema secondary to CRVO. All patients were submitted to a complete ophthalmological examination, including best-corrected ETDRS visual acuity (BCVA), slit-lamp biomicroscopy, intraocular pressure (IOP) and fundus examination. Fluorescein angiography (FA) and OCT central macular thickness (CMT) measurements were also performed. Patients were seen at baseline, one and seven days after the injections, and every 4 weeks thereafter. FA and OCT were performed at baseline, D30, D60, D90, D120, D150 and D180. A minimum of three consecutive injection four weeks apart up to a maximum of six injections were given until OCT CMT reaches 250 ?μm or less. Laser photocoagulation was performed 4 weeks after CMT goal. Main inclusion criteria: eyes with macular edema; BCVA a?¤ 20/40 and a?¥ 20/800 in the study eye and a?¥ 20/40 in the fellow eye; age a?¥ 50 years old and OCT a?¥ 250 ?μm. Main exclusion criteria: intraocular pressure a?¥ 24 mmHg, iris, angle or fundus neovascularization; CRVO 12 months, use of any intravitreous drug in the past 3 months. Results: : eight eyes of eight patients (3 women and 5 men) were enrolled. Baseline results: mean BCVA was 0.81 logMar (range, 0.4 - 1.0) and CMT was 499 ?μm (range, 278 - 885 ?μm). Mean age was 63.75 years-old (range, 50-82). Seven were Caucasians and 1 was black. Mean number of injections was 3.6 (range, 3-6). At baseline FA showed a non isquemic type in 6 patients and in 2 patients the ischemic form. Last follow-up results: mean BCVA was 0.6 logMar (range, 0.4 - 0.8) and CMT was 210 ?μm (range, 139 -250 ?μm). IOP was within the normal limits throughout the follow-up period. FA didna??t show development of retinal ischemia. After the laser treatment no patient needed a new injection. Neither ocular nor systemic adverse effects were recorded during the study period. Conclusions: : the use of intravitreal bevacizumab associated with macular photocoagulation showed no ocular or systemic adverse effects. VA has improved and CMT measured by OCT has decreased and combined treatment may decrease the need for additional injections. Clinical Trial: : www.irtc.ir, IRTC201011295270N1.
机译:目的::主要目的是评估与黄斑光凝相关的玻璃体内贝伐单抗(IVB)在治疗CRVO继发的黄斑水肿中的安全性。次要目标是评估所需的注射次数。方法::I期,非对照,连续,单臂研究CRVO继发的黄斑水肿患者。所有患者均接受了全面的眼科检查,包括最佳矫正的ETDRS视力(BCVA),裂隙灯生物显微镜检查,眼内压(IOP)和眼底检查。还进行了荧光素血管造影(FA)和OCT黄斑中心厚度(CMT)测量。在基线,注射后第1天和第7天以及此后每4周观察患者。 FA和OCT在基线,D30,D60,D90,D120,D150和D180进行。至少要间隔四个星期连续进行三次连续注射,最多可以进行六次注射,直到OCT CMT达到250 µμm或更小。 CMT目标后4周进行激光光凝。主要纳入标准:黄斑水肿眼; BCVA在研究眼中为20/40,在视眼中为20/800,在同眼为20/40。年龄50岁,华侨城250元。主要排除标准:眼内压≥24 mmHg,虹膜,角或眼底新血管形成; CRVO 12个月,过去3个月内使用任何玻璃体内药物。结果:纳入八名患者(三名女性和五名男性)的八只眼。基线结果:平均BCVA为0.81 logMar(范围0.4-1.0),CMT为499μm(范围278-885μm)。平均年龄为63.75岁(范围为50-82岁)。高加索人七人,黑人一人。平均注射次数为3.6(范围3-6)。在基线时,FA在6例患者中显示为非缺血性类型,在2例患者中为缺血性形式。最近的随访结果:平均BCVA为0.6 logMar(范围0.4-0.8),CMT为210μm(范围139 -250μm)。在整个随访期间,眼压均在正常范围内。 FA未显示出视网膜缺血的发展。激光治疗后,没有患者需要重新注射。在研究期间,没有记录到眼部和全身的不良反应。结论:玻璃体腔注射贝伐单抗联合黄斑光凝治疗无眼部或全身不良反应。 VA改善,OCT测得的CMT降低,联合治疗可能会减少对其他注射剂的需求。临床试验:: www.irtc.ir,IRTC201011295270N1。

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