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首页|期刊导航|中华医学杂志(英文版)|Intravitreal bevacizumab versus triamcinolone acetonide for macular edema due to branch retinal vein occlusion: a matched study

Intravitreal bevacizumab versus triamcinolone acetonide for macular edema due to branch retinal vein occlusion: a matched study

HOU Jing TAO Yong JIANG Yan-rong LI Xiao-xin GAO Lei

中华医学杂志(英文版)2009,Vol.122Issue(22):2695-2699,5.
中华医学杂志(英文版)2009,Vol.122Issue(22):2695-2699,5.DOI:10.3760/cma.j.issn.0366-6999.2009.22.004

Intravitreal bevacizumab versus triamcinolone acetonide for macular edema due to branch retinal vein occlusion: a matched study

Intravitreal bevacizumab versus triamcinolone acetonide for macular edema due to branch retinal vein occlusion: a matched study

HOU Jing 1TAO Yong 1JIANG Yan-rong 1LI Xiao-xin 1GAO Lei2

作者信息

  • 1. Department of Ophthalmology, Peking University People's Hospital, Beijing 100044, China
  • 2. Institute of Pathogen Biology, Chinese Academy of Medical, Sciences & Peking Union Medical College, Beijing 100730, China
  • 折叠

摘要

Abstract

Background Branch retinal vein occlusion (BRVO) is a common retinal vascular disorder of the elderly and both intravitreal triamcinolone acetonide (TA) and intravitreal bevacizumab were reported to be effective. The purpose of this study was to compare intravitreal bevacizumab with intravitreal TA for the treatment of macular edema resulting from BRVO.Methods The retrospectively comparative interventional study included a bevacizumab group of 34 BRVO patients (1.25 mg bevacizumab) and a TA group of 34 BRVO patients (4.0 mg TA), and the two groups were matched by baseline best corrected visual acuity (BCVA). Examinations were designed to be carried out at 1 day, 3 days, 1 month, 2 months, 3 months, 6 months and 1 year after each injection. The mean follow-up was (148.43±130.56) days. Main outcome parameters were BCVA and morphometric measurements of the macula obtained by optical coherence tomography.Results In all follow-ups, the mean changes of BCVA (LogMAR) between two groups were not significantly different (P >0.10). Similarly, the rates of patients who got BCVA improvement >2 lines or lost BCVA >2 lines were not significantly different, either (P >0.10). In both groups, compared with baseline, the mean central macular thickness (CMT) got reduction from 4 weeks to 1 year after initial injection, however, which lost statistical significance at 6-month follow-up in TA group (P=0.25) and lost significance at 3-month and 6-month follow-up in bevacizumab group (P=0.07, 0.21). The mean CMT between two groups differed at 3-month follow-up (P <0.01), while almost kept parallel in other follow-ups (all P >0.40). In TA group, retinal pigment epithelium tear occurred in 1 eye at 8 weeks after initial injection and 12 eyes (35.3%) got intraocular pressure >21 mmHg. In bevacizumab group, no severe complications were observed.Conclusion For BRVO, intravitreal bevacizumab versus intravitreal TA causes a similar increase in visual acuity and reduction of macular edema (except 3-month follow-up) with minor complications during 1 year.

关键词

bevacizumab/branch retinal vein occlusion/triamcinolone acetonide

Key words

bevacizumab/branch retinal vein occlusion/triamcinolone acetonide

引用本文复制引用

HOU Jing,TAO Yong,JIANG Yan-rong,LI Xiao-xin,GAO Lei..Intravitreal bevacizumab versus triamcinolone acetonide for macular edema due to branch retinal vein occlusion: a matched study[J].中华医学杂志(英文版),2009,122(22):2695-2699,5.

基金项目

This study was supported by a grant from the Beijing Natural Science Foundation (No. 7062065). (No. 7062065)

中华医学杂志(英文版)

OACSTPCDMEDLINESCI

0366-6999

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