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Intravitreal aflibercept for the treatment of choroidal neovascularization associated with pathologic myopia: a pilot study

机译:玻璃体腔注射阿柏西普治疗与病理性近视相关的脉络膜新生血管

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Purpose: To determine the efficacy of intravitreal aflibercept injections for the treatment of patients with choroidal neovascularization (CNV) associated with pathologic myopia. Methods: In this uncontrolled, prospective cohort study, 31 eyes of 30 consecutive patients affected by CNV associated with pathologic myopia were treated with intravitreal aflibercept (2 mg) as needed following two initial monthly doses and observed over a 12-month follow-up period. The primary endpoint was change in best-corrected visual acuity (BCVA) at month 12, while central retinal thickness (CRT) on optical coherence tomography (OCT), neovascularization activity on fluorescein angiography, the number of aflibercept injections administered, and safety were examined as secondary endpoints. Results: Patients received a mean of 2.6 intravitreal aflibercept injections over the 12-month study period. Compared with baseline, BCVA improved significantly at all time points ( P 20 mmHg during any study visit. Conclusion: The 12-month results of intravitreal aflibercept for myopic CNV using an as-needed regimen were positive, showing benefits in visual and anatomic outcomes and an acceptable tolerability profile.
机译:目的:确定玻璃体腔注射阿柏西普注射液治疗与病理性近视相关的脉络膜新生血管(CNV)患者的疗效。方法:在这项不受控制的前瞻性队列研究中,在连续两个月的初始剂量后,根据需要对连续30例接受病理性近视的CNV影响的30例患者的31眼接受玻璃体腔注射阿柏西普(2 mg)的治疗,并在12个月的随访期内进行观察。主要终点是第12个月时最佳矫正视力(BCVA)的变化,而光学相干断层扫描(OCT)的中央视网膜厚度(CRT),荧光素血管造影的新血管形成活性,所用的abribercept注射次数和安全性进行了检查作为次要端点。结果:在12个月的研究期内,患者平均接受2.6次玻璃体内阿柏西普注射。与基线相比,BCVA在所有时间点均显着改善(在任何研究访视中均P 20 mmHg。)结论:根据需要的方案,玻璃体腔注射阿柏西普用于近视CNV的12个月结果为阳性,显示出视觉和解剖结局以及可接受的公差范围。

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