增殖性糖尿病视网膜病变的治疗。

Comprehensive ophthalmology update Pub Date : 2007-09-01
Kaan Gündüz, Sophie J Bakri
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引用次数: 0

摘要

增殖性糖尿病视网膜病变以糖尿病患者视网膜和/或视盘新生血管为特征。血管内皮生长因子的作用似乎是中心的发病机制增殖性糖尿病视网膜病变。晚期糖基化终产物在增殖性糖尿病视网膜病变玻璃体异常的发展中是重要的。大多数新生血管膜附着于玻璃体后皮层。当后玻璃体施加牵引力时,新生血管复合体边缘被向前拉,导致玻璃体出血。牵引性和/或孔源性视网膜脱离可发生。糖尿病视网膜病变研究表明,对于具有高危特征的眼睛,全视网膜光凝治疗可将严重视力丧失的发生率降低50%,高危特征定义为视盘> 1/3直径的新生血管、视盘出血的新生血管和玻璃体出血的视网膜新生血管。早期治疗糖尿病视网膜病变研究显示,40岁以上伴有严重非增殖性糖尿病视网膜病变(定义为四个象限出血,两个象限静脉珠状,或一个象限视网膜内微血管异常)的II型糖尿病患者也受益于早期全视网膜光凝治疗。糖尿病视网膜病变玻璃体切除术研究显示,仅在1型糖尿病患者中,早期玻璃体切除术(玻璃体出血发生6个月内)与较好的结果相关。玻璃体手术的目的是切除玻璃体,包括后玻璃体,并减轻纤维血管组织的牵引力。分层和分割技术已被用于切除生长在内限制膜上并延伸到玻璃体的纤维血管。全视网膜光凝是增殖性糖尿病视网膜病变玻璃体切除术的重要组成部分。除激光外,抗血管内皮生长因子药物也可作为辅助手段来降低新生血管的风险。玻璃体切除术可能有术中和术后并发症,包括白内障、前玻璃体纤维血管增生、纤维血管向内生长、视网膜脱离和复发性玻璃体出血。视电位取决于术前和术后黄斑的状态,以及视网膜灌注和视神经的健康。随着仪器、技术和药物的进步,玻璃体切除术治疗增殖性糖尿病视网膜病变的效果越来越好。
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Management of proliferative diabetic retinopathy.

Proliferative diabetic retinopathy is characterized by neovascularization originating from the retina and/or optic disk in patients with diabetes mellitus. The role of vascular endothelial growth factor appears to be central in the pathogenesis of proliferative diabetic retinopathy. Advanced glycation end products are important in the development of vitreous abnormalities in proliferative diabetic retinopathy. The majority of the neovascular membranes are adherent to the posterior vitreous cortex. When the posterior hyaloid exerts traction, the edges of the neovascular complex are pulled forward, resulting in vitreous hemorrhage. Tractional and/or rhegmatogenous retinal detachments can occur. The Diabetic Retinopathy Study demonstrated the ability of panretinal photocoagulation to reduce the rate of severe visual loss by 50% for eyes with high-risk characteristics, defined as neovascularization originating from the optic disk > 1/3 disk diameter, any neovascularization originating from the optic disk with hemorrhage, and neovascularization originating from the retina with vitreous hemorrhage. The Early Treatment Diabetic Retinopathy Study showed that patients with type II diabetes mellitus who were older than 40 with severe nonproliferative diabetic retinopathy (defined as hemorrhages in four quadrants, venous beading in two quadrants, or intraretinal microvascular abnormalities in one quadrant) also benefited from early panretinal photocoagulation. The Diabetic Retinopathy Vitrectomy Study showed that early vitrectomy (within 6 months of onset of vitreous hemorrhage) was associated with better results in type I diabetes mellitus patients only. The goals of vitreous surgery are to remove the vitreous, including the posterior hyaloid, and to relieve traction from fibrovascular tissue. Delamination and segmentation techniques have been used in the excision of fibrovascular growth on the internal limiting membrane and extending into the vitreous. Panretinal photocoagulation is an integral component of vitrectomy for proliferative diabetic retinopathy. Anti-vascular endothelial growth factor agents may be used in addition to laser as an adjunct to reduce the risk of neovascularization. Vitrectomy surgery may have intraoperative and postoperative complications, including cataract, anterior hyaloidal fibrovascular proliferation, fibrovascular ingrowth, retinal detachment, and recurrent vitreous hemorrhage. Visual potential depends on the preoperative and postoperative status of the macula, as well as on retinal perfusion and the health of the optic nerve. With the improvement in instruments, techniques, and drugs, the results of vitrectomy in proliferative diabetic retinopathy are improving.

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