Department of Ophthalmology, Hospital C.T.O. of Naples, Naples, Italy.
Graefes Arch Clin Exp Ophthalmol. 2010 Jun;248(6):785-91. doi: 10.1007/s00417-010-1303-3. Epub 2010 Feb 5.
The purpose of this study is to evaluate the role, the safety and the effectiveness of intravitreal bevacizumab (IVB) injections as an adjunct to vitrectomy in the management of severe proliferative diabetic retinopathy (PDR).
Case-Control Study
Randomized controlled trial performed on 72 eyes of 68 patients affected by vitreous haemorrhage (VH) and tractional retinal detachment (TRD), which occurred as a consequence of active proliferative diabetic retinopathy (PDR). We randomly assigned eligible patients in a 1: 1: 1 ratio to receive a sham injection or an intravitreal injection of 1.25 mg of bevacizumab, either 7 or 20 days before the vitrectomy. In order to obtain three homogeneous groups of surgical complexity, we assigned to the following preoperative parameters a score from 0 to 3: a) vitreous haemorrhage, b) prior retinal laser-photocoagulation, c) morphological types of retinal detachment such as focal, hammock, central diffuse, table-top. Complete ophthalmic examinations and color fundus photography were performed at baseline and 1, 6, 12, and 24 weeks after the surgery.
Intraoperative management, safety, efficacy of IVB at different time injection as an adjunct to vitrectomy in the management of severe PDR RESULTS: Group A (sham injection): intraoperative bleeding occurred in 19 cases (79.1%), the use of endodiathermy was necessary in 13 patients (54.1%), relaxing retinotomy was performed on one patient (4.1%), and in four cases (16.6%) iatrogenic retinal breaks occurred. The surgical mean time was 84 minutes (SD 12 minutes). Group B (bevacizumab administered 7 days before vitrectomy): intraoperative bleeding occurred in two cases (8.3%) and the use of endodiathermy was necessary in two patients (8.3%). No iatrogenic breaks occurred during the surgery. The surgical mean time was 65 minutes (SD 18 minutes). Group C (bevacizumab administered 20 days before vitrectomy): intraoperative bleeding occurred in three cases (12.5%), the use of endodiathermy was necessary in three patients (1.5%), and an iatrogenic break occurred in one patient (4.1%) while the delamination of fibrovascular tissue was being performed. The surgical mean time was 69 minutes (SD 21 minutes). The average difference in the surgical time was statistically significant between group A and group B (p = 0.025), and between group A and group C (p = 0.031). At the end of the surgery, the retina was completely attached in all eyes. At the 6-month follow-up, we observed the development of tractional retinal detachment (TRD) in one out of 24 patients from group C (4%).
A preoperative intravitreal injection of bevacizumab may represent a new strategy for the surgical treatment of severe PDR by reducing retinal and iris neovascularization: this would make surgery much easier and safer, thus improving the anatomical and functional prognosis. According to our study, the best surgical results are achieved performing the IVB 7 days preoperatively.
本研究旨在评估玻璃体内注射贝伐单抗(IVB)作为玻璃体切割术辅助治疗严重增殖性糖尿病视网膜病变(PDR)的作用、安全性和有效性。
病例对照研究
对 68 例 72 只眼进行了随机对照试验,这些眼均因增殖性糖尿病视网膜病变(PDR)而发生玻璃体积血(VH)和牵引性视网膜脱离(TRD)。我们将符合条件的患者随机分配到 1:1:1 的比例,分别接受假注射或玻璃体内注射 1.25mg 贝伐单抗,注射时间分别为玻璃体切割术前 7 天和 20 天。为了获得三种手术复杂度均相同的组,我们将以下术前参数分配为 0 至 3 分:a)玻璃体积血,b)先前的视网膜激光光凝,c)视网膜脱离的形态类型,如局灶性、吊床型、中央弥漫性、桌面型。在基线和手术 1、6、12 和 24 周后进行全面眼科检查和彩色眼底照相。
术中管理、安全性、IVB 在不同时间注射作为严重 PDR 玻璃体切割术辅助治疗的疗效。
A 组(假注射):术中出血 19 例(79.1%),13 例(54.1%)需要使用内电凝,1 例(4.1%)行松解性视网膜切开术,4 例(16.6%)发生医源性视网膜裂孔。手术平均时间为 84 分钟(SD 12 分钟)。B 组(玻璃体切割术前 7 天给予贝伐单抗):术中出血 2 例(8.3%),2 例(8.3%)需要使用内电凝。手术过程中未发生医源性裂孔。手术平均时间为 65 分钟(SD 18 分钟)。C 组(玻璃体切割术前 20 天给予贝伐单抗):术中出血 3 例(12.5%),3 例(1.5%)需要使用内电凝,1 例(4.1%)在分离纤维血管组织时发生医源性裂孔。手术平均时间为 69 分钟(SD 21 分钟)。A 组与 B 组(p=0.025)和 A 组与 C 组(p=0.031)之间手术时间的平均差异具有统计学意义。手术结束时,所有眼的视网膜均完全贴附。在 6 个月的随访中,我们观察到 C 组 1 例(4%)患者出现牵引性视网膜脱离(TRD)。
术前玻璃体内注射贝伐单抗可能通过减少视网膜和虹膜新生血管化,为严重 PDR 的手术治疗提供一种新策略:这将使手术更容易、更安全,从而改善解剖和功能预后。根据我们的研究,在术前 7 天进行 IVB 效果最佳。