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新加坡亚洲人群玻璃体内注射的安全性与并发症

Safety and complications of intravitreal injections performed in an Asian population in Singapore.

作者信息

Xu Yanping, Tan Colin S

机构信息

Department of Ophthalmology, National Healthcare Group Eye Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, 308433, Singapore.

Fundus Image Reading Center, National Healthcare Group Eye Institute, Singapore, Singapore.

出版信息

Int Ophthalmol. 2017 Apr;37(2):325-332. doi: 10.1007/s10792-016-0241-4. Epub 2016 May 28.

DOI:10.1007/s10792-016-0241-4
PMID:27236451
Abstract

There has been a rapid rise in the use of intravitreal injections, such as anti-vascular endothelial growth factor (anti-VEGF) agents, performed over the past few years for the treatment of ocular neovascular diseases. This study aims to review the systemic and ocular adverse events among patients treated at a tertiary eye center over a period of 8 years. A retrospective review of all intravitreal injections of anti-VEGF performed over an 8-year period at a tertiary eye care center in Singapore was done. We report the frequency of systemic and ocular adverse events and compared it among the various anti-VEGF agents. A total of 14 001 intravitreal injections were performed on 2225 patients from January 1, 2007 to December 31, 2014, and this included 9992 bevacizumab (71.4 %), 3306 ranibizumab (23.6 %) and 703 aflibercept (5.0 %) injections. Systemic complications related to treatment were 26 (1.17 %) deaths (from any cause), of which 11 (0.49 %) were from fatal thromboembolic events, 7 (0.31 %) non-fatal thromboembolic events and two (0.09 %) serious non-ocular hemorrhage. Ocular complications included one (0.007 %) endophthalmitis, three (0.021 %) traumatic cataracts, and one (0.007 %) retinal detachment. Rates of death and thromboembolic events were similar among ranibizumab (lucentis), bevacizumab (avastin) and aflibercept (Eylea). The systemic and ocular complications associated with intravitreal injections among Asian patients at a tertiary eye center are relatively low and reflect the safety of the treatments.

摘要

在过去几年中,玻璃体内注射(如抗血管内皮生长因子(anti-VEGF)药物)在治疗眼部新生血管疾病方面的使用迅速增加。本研究旨在回顾一家三级眼科中心8年期间接受治疗的患者的全身和眼部不良事件。对新加坡一家三级眼科护理中心8年期间进行的所有抗VEGF玻璃体内注射进行了回顾性研究。我们报告了全身和眼部不良事件的发生率,并在各种抗VEGF药物之间进行了比较。2007年1月1日至2014年12月31日,共对2225例患者进行了14001次玻璃体内注射,其中包括9992次贝伐单抗(71.4%)、3306次雷珠单抗(23.6%)和703次阿柏西普(5.0%)注射。与治疗相关的全身并发症包括26例(1.17%)死亡(各种原因),其中11例(0.49%)死于致命性血栓栓塞事件,7例(0.31%)非致命性血栓栓塞事件,2例(0.09%)严重非眼部出血。眼部并发症包括1例(0.007%)眼内炎、3例(0.021%)外伤性白内障和1例(0.007%)视网膜脱离。雷珠单抗(Lucentis)、贝伐单抗(Avastin)和阿柏西普(Eylea)之间的死亡率和血栓栓塞事件发生率相似。在一家三级眼科中心,亚洲患者玻璃体内注射相关全身和眼部并发症相对较低,反映了治疗的安全性。

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