POAG, Primary open angle glaucoma

  • 文章类型: Case Reports
    UNASSIGNED:报告一例急性新生血管性青光眼,继发于视网膜中央静脉阻塞,经房角镜辅助的经腔小梁切开术以及近每月一次的抗血管内皮生长因子(VEGF)注射和全视网膜光凝(PRP)治疗。
    未经批准:关贸总协定后9个月,患者在没有用药的情况下实现了眼压控制.然而,她失去了4个月的随访,在此期间没有接受抗VEGF或PRP治疗;她再次表现为急性NVG和完全粘连闭合,并最终进行了房水分流植入。
    未经授权:据我们所知,这是首次报道的ab间角手术尝试通过急性NVG和部分粘连性房角闭合的眼睛通过常规流出途径成功恢复房水流出.我们认为,这可能是在NVG中实现IOP控制的有效方法,至少部分打开角度,只要给予足够的抗新生血管治疗,直到潜在的新生血管驱动达到静止。
    UNASSIGNED: To report a case of acute neovascular glaucoma with partial synechial angle closure secondary to central retinal vein occlusion that underwent gonioscopy-assisted transluminal trabeculotomy as well as near-monthly anti-vascular endothelial growth factor (VEGF) injections and panretinal photocoagulation (PRP) treatments.
    UNASSIGNED: Nine months after GATT, the patient had achieved intraocular pressure control on no medications. However, she was lost to follow up for 4 months and received no anti-VEGF or PRP during that time; she re-presented with acute NVG and complete synechial closure, and ultimately underwent aqueous shunt implantation.
    UNASSIGNED: To our knowledge, this is the first reported attempt of an ab interno angle surgery to successfully restore aqueous outflow through the conventional outflow pathway in an eye with acute NVG and partial synechial angle closure. We posit that this can be an effective approach to achieve IOP control in NVG with at least partially open angles, as long as sufficient anti-neovascular treatments are administered until the underlying neovascular drive achieves quiescence.
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  • 文章类型: Journal Article
    Glaucoma, a progressive optic neuropathy characterized by retinal ganglion cell degeneration and visual field loss, is the leading cause of irreversible blindness worldwide. Intraocular pressure (IOP) is presently the only modifiable risk factor demonstrated to slow or halt disease progression; however, glaucomatous damage persists in almost 50% of patients despite significant IOP reduction. Many studies have investigated the non-IOP-related risk factors that contribute to glaucoma progression as well as interventions that can prevent or delay glaucomatous neurodegeneration and preserve vision throughout life, independently of IOP. A vast number of experimental studies have reported effective neuroprotection in glaucoma, and clinical studies are ongoing attempting to provide strong evidence of effectiveness of these interventions. In this review, we look into the current understanding of the pathophysiology of glaucoma and explore the recent advances in non-IOP related strategies for neuroprotection and neuroregeneration in glaucoma.
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