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视网膜分支静脉阻塞继发黄斑水肿时玻璃体内注射药物与标准治疗的比较。

Comparison of injection of intravitreal drugs with standard care in macular edema secondary to branch retinal vein occlusion.

作者信息

Lee Kyungmin, Jung Heeyoung, Sohn Joonhong

机构信息

HanGil Eye Hospital, Incheon, Korea.

出版信息

Korean J Ophthalmol. 2014 Feb;28(1):19-25. doi: 10.3341/kjo.2014.28.1.19. Epub 2014 Jan 21.

Abstract

PURPOSE

To compare the long-term efficacy and safety of intravitreal triamcinolon with or without rescue laser therapy (intravitreal triamcinolone injection [IVTA] group), bevacizumab with or without rescue laser treatment (intravitreal bevacizumab injection [IVB] group), or a combination of both with or without rescue laser therapy (IVTA + IVB group), with standard care for patients with macular edema secondary to branch retinal vein occlusion (BRVO).

METHODS

We reviewed the medical records of 151 patients treated with intravitreal injection with or without rescue laser for treatment of macular edema caused by BRVO, and who were followed up at 1, 3, 6, 12, and 24 months. During the observation period, rescue grid laser or repeated intravitreal injection with initial drug was performed if recurrence of macular edema was confirmed. Visual acuity, change in visual acuity, and intraocular pressure were compared in each phase.

RESULTS

Totals of 16%, 5.6%, and 0% of participants in the three groups showed significant visual loss of more than three lines of the Snellen chart at last follow-up. The IVTA group was the least effective treatment modality, with statistical significance. The development rates of elevated intraocular pressure were similar among the groups.

CONCLUSIONS

Although IVTA yielded effects similar to those of standard grid photocoagulation based on the Standard Care vs Corticosteroid for Retinal Vein Occlusion study, IVB or IVTA + IVB with or without rescue laser treatment resulted in improvement in visual acuity at 24 months after the start of treatment and was associated with few serious adverse side effects. Thus, these approaches could be useful for treating macular edema arising secondary to BRVO.

摘要

目的

比较单纯玻璃体腔注射曲安奈德(玻璃体腔注射曲安奈德组)、单纯玻璃体腔注射贝伐单抗(玻璃体腔注射贝伐单抗组)、两者联合应用(玻璃体腔注射曲安奈德+玻璃体腔注射贝伐单抗组),在联合或不联合补救性激光治疗时,与视网膜分支静脉阻塞(BRVO)继发黄斑水肿患者的标准治疗相比的长期疗效和安全性。

方法

我们回顾了151例接受玻璃体腔注射(联合或不联合补救性激光)治疗BRVO所致黄斑水肿患者的病历,并在1、3、6、12和24个月进行随访。在观察期内,若确认黄斑水肿复发,则进行补救性格栅激光治疗或重复初始药物的玻璃体腔注射。比较各阶段的视力、视力变化和眼压。

结果

三组参与者中,分别有16%、5.6%和0%在末次随访时视力下降超过Snellen视力表3行。玻璃体腔注射曲安奈德组是疗效最差的治疗方式,具有统计学意义。各组眼压升高的发生率相似。

结论

虽然基于视网膜静脉阻塞的标准治疗与皮质类固醇研究,玻璃体腔注射曲安奈德产生的效果与标准格栅光凝相似,但玻璃体腔注射贝伐单抗或玻璃体腔注射曲安奈德+玻璃体腔注射贝伐单抗联合或不联合补救性激光治疗,在治疗开始24个月后可提高视力,且严重不良副作用较少。因此,这些方法可能有助于治疗BRVO继发的黄斑水肿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2d8/3913978/ae5b449fb385/kjo-28-19-g001.jpg

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