首页> 美国卫生研究院文献>Clinical Ophthalmology (Auckland N.Z.) >DEBS – a unification theory for dry eye and blepharitis
【2h】

DEBS – a unification theory for dry eye and blepharitis

机译:DEBS –干眼症和睑缘炎的统一理论

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

For many years, blepharitis and dry eye disease have been thought to be two distinct diseases, and evaporative dry eye distinct from aqueous insufficiency. In this treatise, we propose a new way of looking at dry eye, both evaporative and insufficiency, as the natural sequelae of decades of chronic blepharitis. Dry eye is simply the late form and late manifestation of one disease, blepharitis. We suggest the use of a new term in describing this one chronic disease, namely dry eye blepharitis syndrome (DEBS). Bacteria colonize the lid margin within a structure known as a biofilm. The biofilm allows for population densities that initiate quorum-sensing gene activation. These newly activated gene products consist of inflammatory virulence factors, such as exotoxins, cytolytic toxins, and super-antigens, which are then present for the rest of the patient’s life. The biofilm never goes away; it only thickens with age, producing increasing quantities of bacterial virulence factors, and thus, increasing inflammation. These virulence factors are likely the culprits that first cause follicular inflammation, then meibomian gland dysfunction, aqueous insufficiency, and finally, after many decades, lid destruction. We suggest that there are four stages of DEBS which correlate with the clinical manifestations of folliculitis, meibomitis, lacrimalitis, and finally lid structure damage evidenced by entropion, ectropion, and floppy eyelid syndrome. When one fully understands the structure and location of the glands within the lid, it becomes easy to understand this staged disease process. The longer a gland can resist the relentless encroachment of the invading biofilm, the longer it can maintain normal function. The stages depend purely on anatomy and years of biofilm presence. Dry eye now becomes a very easy disease to understand. We feel that dry eye should be treated and prevented by early and routine biofilm removal through electromechanical lid margin debridement.
机译:多年来,睑缘炎和干眼病被认为是两种截然不同的疾病,而蒸发性干眼与房水不足无关。在本论文中,我们提出了一种新的方法来研究干眼症,包括蒸发性眼功能不足和视力不足,这是数十年来慢性眼睑炎的自然后遗症。干眼症只是一种疾病,睑缘炎的晚期形式和晚期表现。我们建议使用一个新术语来描述这一慢性疾病,即干眼睑缘炎综合征(DEBS)。细菌在称为生物膜的结构内定殖盖缘。生物膜允许启动群体感应基因激活的种群密度。这些新激活的基因产物由炎症毒力因子组成,例如外毒素,细胞溶解毒素和超抗原,这些抗原在患者的余生中都存在。生物膜永远不会消失。它只会随着年龄的增长而增稠,产生越来越多的细菌毒力因子,从而加剧炎症。这些致病因子很可能首先导致卵泡炎症,然后导致睑板腺功能障碍,房水不足,最后在数十年后破坏眼睑。我们建议DEBS有四个阶段,与毛囊炎,睑板炎,泪腺炎的临床表现相关,最后与熵,外翻和眼睑软组织综合征所证明的眼睑结构受损有关。当人们完全了解盖内腺体的结构和位置时,就很容易了解这一阶段性疾病过程。腺体可以抵抗入侵的生物膜的无情侵害的时间越长,它可以维持正常功能的时间就越长。这些阶段完全取决于解剖结构和生物膜存在的年限。现在,干眼症是一种非常容易理解的疾病。我们认为应通过机电盖缘清创术早期和常规清除生物膜来治疗和预防干眼症。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号