Vassileva Petja Ivanova, Hergeldzhieva Tatyana Georgieva
University Eye Hospital "Prof. Pashev", 51 Emanuil Vaskidovich Street, Sofia, 1517, Bulgaria.
Graefes Arch Clin Exp Ophthalmol. 2009 Dec;247(12):1701-6. doi: 10.1007/s00417-009-1170-y. Epub 2009 Aug 13.
Corneal neovascularization is a major risk factor for graft failure after corneal transplantation. The purpose of this study was to investigate the effect of subconjunctival, perilimbal, and/or intrastromal bevacizumab (Avastin) on corneal neovascularization in patients with penetrating keratoplasty (PKP).
Fourteen eyes of 14 patients with high risk corneal transplantation and corneal neovascularization after PKP (nine men and five women with a mean age of 63 years) were included in this non-comparative interventional case series. Indications for PKP were: vascularized leukomas after herpetic keratitis and chemical burn, advanced pseudophakic bullous keratopathy with superficial and deep corneal vascularization, keratoconus, severe infection in hereditary corneal dystrophy, and failed corneal grafts. Subconjunctival, perilimbal, and/or intrastromal bevacizumab of dose of 2.5 mg/ 0.1 ml/ per affected quadrant was injected at the site of neovascularization in each patient at the end of surgery and/or at follow up visits. One or two injections were applied. At each visit a full eye examination with photo documentation was performed. Follow-up period was 2 to 8 months (mean 7.1 months).
Decrease of corneal neovascularization was observed in eleven patients (78.6%). Regression of neovascularization with fading of small vessels was demonstrated. Despite high- risk patient pool, twelve grafts (85.7%) remained transparent for the period of observation, and patients maintained good visual acuity. In two patients with initial graft rejection and vascularization, subconjunctival and perilimbal application of bevacizumab was beneficial in overcoming the corneal inflammation and initial rejection. No adverse reactions have been detected to date in patients with subconjunctival, perilimbal, and/or intrastromal injection of bevacizumab.
Bevacizumab is an efficient and safe additional treatment option for improvement of prognosis in high-risk corneal transplantation with pre- and postoperative corneal neovascularization.
角膜新生血管形成是角膜移植术后移植物失败的主要危险因素。本研究的目的是探讨结膜下、角膜缘和/或基质内注射贝伐单抗(阿瓦斯汀)对穿透性角膜移植术(PKP)患者角膜新生血管形成的影响。
本非对照性介入病例系列纳入了14例PKP术后有角膜新生血管形成的高危角膜移植患者的14只眼(9例男性,5例女性,平均年龄63岁)。PKP的适应证为:疱疹性角膜炎和化学伤后血管化的角膜白斑、伴有浅层和深层角膜血管化的晚期人工晶状体大泡性角膜病变、圆锥角膜、遗传性角膜营养不良的严重感染以及角膜移植失败。在手术结束时和/或随访时,在每位患者新生血管形成部位注射剂量为2.5mg/0.1ml/每个受累象限的结膜下、角膜缘和/或基质内贝伐单抗。进行1或2次注射。每次随访时进行全眼检查并拍照记录。随访期为2至8个月(平均7.1个月)。
11例患者(78.6%)角膜新生血管减少。显示新生血管消退,小血管变淡。尽管患者风险高,但在观察期内12只移植物(85.7%)保持透明,患者视力良好。在2例最初发生移植物排斥和血管化的患者中,结膜下和角膜缘应用贝伐单抗有助于克服角膜炎症和初始排斥反应。迄今为止,结膜下、角膜缘和/或基质内注射贝伐单抗的患者未检测到不良反应。
对于术前和术后有角膜新生血管形成的高危角膜移植患者,贝伐单抗是一种有效且安全的辅助治疗选择,可改善预后。