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Intravitreal tissue plasminogen activator in the management of central retinal vein occlusion.

机译:玻璃体内组织纤溶酶原激活物在视网膜中央静脉阻塞的管理中。

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PURPOSE: To evaluate the role of intravitreal tissue plasminogen activator (tPA) in the management of central retinal vein occlusion (CRVO) in patients with symptoms for <3 days. METHODS: We evaluated the visual outcome of a consecutive series of patients with CRVO following intravitreal tPA injection. All patients presented with visual acuity worse than 20/50 within 3 days from the onset of symptoms. Main outcome measures included percentage of patients whose final vision improved to 20/50 or better and change in percentage of patients with vision of 20/200 or worse before and after treatment. RESULTS: Twelve patients received intravitreal tPA for CRVO. Nine patients (75%) had best-corrected visual acuity of 20/200 or worse at presentation compared with 4 patients (33%) at the last follow-up after treatment. Five (55%) of these 9 patients had final visual acuity that improved to 20/50 or better. The remaining four patients did not have improvement or their vision continued to worsen. All 4 patients had fluorescein angiographic evidence of >10 disk areas of capillary nonperfusion at presentation. Overall, 8 (67%) of 12 patients had final visual acuity of 20/50 or better. No side effects related to tPA injection were observed. CONCLUSION: Our data suggest that intravitreal tPA injection may have a beneficial role in the management of CRVO when used within a few days of the onset of symptoms in patients with no angiographic evidence of severe capillary nonperfusion even if initial visual acuity is 20/200 or worse.
机译:目的:评估玻璃体内组织纤溶酶原激活物(tPA)在症状<3天的患者中视网膜中央静脉阻塞(CRVO)的管理中的作用。方法:我们评估了玻璃体内tPA注射后连续系列CRVO患者的视觉结果。症状发作后三天内,所有患者的视力均低于20/50。主要结局指标包括最终视力改善至20/50或更高的患者百分比,以及治疗前后视力为20/200或更低的患者百分比的变化。结果:12例患者接受CRVO玻璃体内tPA治疗。治疗后最后一次随访时,有9名患者(75%)的矫正视力达到最佳20/200或更低,而4名患者(33%)的矫正视力更差。这9名患者中有5名(55%)的最终视力提高到20/50或更高。其余四名患者没有改善或他们的视力继续恶化。所有4例患者在就诊时均具有荧光素血管造影证据,显示毛细血管非灌注> 10盘区。总体而言,12例患者中有8例(67%)的最终视力为20/50或更高。没有观察到与tPA注射有关的副作用。结论:我们的数据表明,对于没有血管造影证据表明严重毛细血管非灌注的患者,即使最初的视力为20/200或更差。

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