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Intravitreal bevacizumab (avastin) in central retinal vein occlusion.

机译:视网膜中央静脉阻塞的玻璃体内贝伐单抗(avastin)。

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PURPOSE: To describe the effects of intravitreal bevacizumab in eyes with macular edema resulting from central retinal vein occlusions (CRVO). METHODS: Retrospective consecutive case series of patients diagnosed with macular edema from CRVO who received intravitreal bevacizumab. RESULTS: Thirty eyes of 29 patients with an average age of 72 years (range, 54-87 years) had intravitreal bevacizumab injections. Mean follow-up was 18.1 weeks. Initial mean visual acuity was 20/394. At the 1- and 2-month follow-up, mean visual acuity improved to 20/237 (n = 26, P = 0.04) and 20/187 (n = 21, P = 0.008), respectively. At the 3- and 4-month follow-up, visual acuity improved from 20/228 to 20/157 (n = 15, P = 0.05) and from 20/313 to 20/213 (n = 11, P = 0.03), respectively. No significant changes in visual acuity were found after 4 months though the number of patients in this group was small. Duration of treatment effect following an injection appears to be limited to 2 months for most patients. No ocular or systemic adverse reactions were noted. CONCLUSIONS: The visual benefits of intravitreal bevacizumab for macular edema due to CRVO are apparent early but are not sustained without repeated injections. Larger clinical studies with long-term follow-up will be necessary to better elicit the best regimen for this therapy.
机译:目的:描述玻璃体内贝伐单抗在视网膜中央静脉阻塞(CRVO)引起的黄斑水肿眼中的作用。方法:回顾性连续病例系列患者接受玻璃体内贝伐单抗诊断为CRVO的黄斑水肿。结果:29例患者的30眼平均年龄为72岁(范围54-87岁)接受了玻璃体内贝伐单抗注射。平均随访18.1周。最初的平均视力为20/394。在1个月和2个月的随访中,平均视力分别提高到20/237(n = 26,P = 0.04)和20/187(n = 21,P = 0.008)。在3个月和4个月的随访中,视力从20/228提高到20/157(n = 15,P = 0.05),从20/313提高到20/213(n = 11,P = 0.03) , 分别。尽管该组的患者人数很少,但在4个月后未发现视敏度有明显变化。对于大多数患者,注射后的治疗效果持续时间似乎仅限于2个月。未观察到眼部或全身不良反应。结论:玻璃体内贝伐单抗对CRVO引起的黄斑水肿的视觉益处在早期很明显,但如果不反复注射就不能持续。长期随访的更大临床研究对于更好地得出该疗法的最佳治疗方案是必要的。

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