Department of Ophthalmology, APHP, South Paris University, Le Kremlin-Bicêtre, France
Center for Immunology of Viral infections and Autoimmune diseases (IMVA), IDMIT Infrastructure CEA, Université Paris Sud, Fontenay-aux-Roses Cedex, France.
Br J Ophthalmol. 2019 Oct;103(10):1475-1480. doi: 10.1136/bjophthalmol-2018-312581. Epub 2019 Jan 12.
BACKGROUND/AIMS: Dry eye disease (DED) is categorised by pathophysiology as aqueous deficient dry eye (ADDE), evaporative dry eye (EDE) or mixed. Treatment should be tailored to DED pathophysiology, but this is challenging to determine. This Delphi consultation aimed to categorise and weight signs and symptoms to help identify the evaporative or aqueous deficient DED origin.
A panel of French DED experts created an initial list of 77 DED signs and symptoms. In a Delphi consultation, experts categorised items by DED pathophysiology. Likert scoring was used to indicate whether items were strongly or moderately indicative of ADDE or EDE. Items could also be judged non-applicable to DED, with the opportunity to suggest alternative diagnoses.
Experts attributed 19 items (of which 11 were strongly indicative) to a pathophysiology of EDE and 12 items (of which four were strongly indicative) to ADDE. Items scored strongly indicative with agreement >90% for EDE were previous chalazia, rosacea/rhinophyma, telangiectasias of eyelid margin and thick non-expressible meibomian gland secretions, and for ADDE were Sjögren syndrome or associated disease, and Schirmer <5 mm after 5 min (without anaesthesia). Seventeen items indicated neither pathophysiology and 18 items were found to be suggestive of alternative diagnoses.
This Delphi consultation categorised signs and symptoms, using an innovative weighting system to identify DED pathophysiology. An algorithm integrating the weighting of each sign and symptom of an individual patient would be valuable to help general ophthalmologists to classify the DED subtype and tailor treatment to DED underlying mechanism.
背景/目的:干眼疾病(DED)根据病理生理学分为水样液缺乏性干眼症(ADDE)、蒸发过强型干眼症(EDE)或混合型。治疗应根据 DED 的病理生理学进行调整,但这一点很难确定。本德尔菲咨询旨在对体征和症状进行分类和加权,以帮助确定蒸发过强型或水样液缺乏型 DED 的病因。
一组法国 DED 专家创建了一份最初的 77 项 DED 体征和症状清单。在德尔菲咨询中,专家根据 DED 的病理生理学对项目进行分类。李克特评分用于表示项目是否强烈或中度提示 ADDE 或 EDE。也可以判断项目是否不适用于 DED,并提供替代诊断的机会。
专家将 19 项(其中 11 项强烈提示)归因于 EDE 的病理生理学,12 项(其中 4 项强烈提示)归因于 ADDE。EDE 具有>90%一致性的强烈提示项目包括先前的霰粒肿、酒渣鼻/鼻赘、睑缘毛细血管扩张和浓稠不可表达的睑板腺分泌物,ADDE 强烈提示项目包括干燥综合征或相关疾病以及 Schirmer 测试<5mm(无麻醉)。17 项指标既不提示 EDE 也不提示 ADDE,18 项指标提示其他诊断。
本德尔菲咨询使用创新的加权系统对体征和症状进行分类,以确定 DED 的病理生理学。整合个体患者每项体征和症状权重的算法将有助于普通眼科医生对 DED 亚型进行分类,并根据 DED 的潜在机制进行治疗。