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综合眼科医生眼中的前葡萄膜炎。

Anterior uveitis for the comprehensive ophthalmologist.

作者信息

Xie Jim S, Ocampo Vanessa, Kaplan Alexander J

机构信息

Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada.

Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, ON, Canada; Scarborough Health Network, Rheumatology Department, Scarborough, ON, Canada.

出版信息

Can J Ophthalmol. 2025 Apr;60(2):69-78. doi: 10.1016/j.jcjo.2024.07.013. Epub 2024 Aug 8.

Abstract

Anterior uveitis presents a diagnostic challenge due to its wide array of etiologies and clinical manifestations. This narrative review aims to equip general ophthalmologists with a comprehensive understanding of anterior uveitis epidemiology, diagnosis, and treatment. Particular emphasis is placed on developing a tailored and stepwise strategy, rather than a one-size-fits-all approach, for the workup and treatment of anterior uveitis. Chest radiography and serologic testing for syphilis, human leukocyte antigen B27, and angiotensin-converting enzyme are appropriate routine investigations in cases of severe, bilateral, recurrent, or chronic anterior uveitis. Additional testing should be guided by clinical findings and regional epidemiology, especially when considering expensive and invasive modalities. Investigations that are obtained in the absence of clinical and epidemiologic orientation are of limited utility and incur significant costs to patients and health care systems. Most cases of anatomically isolated anterior uveitis resolve with topical corticosteroids, but some patients require escalation to systemic immunomodulatory therapy (IMT). IMT should be considered in patients who respond poorly to corticosteroids, develop side effects related to corticosteroids that limit their use, require high doses to maintain disease remission, or have concomitant systemic inflammatory disease. Comprehensive ophthalmologists should feel comfortable comanaging patients that require conventional disease-modifying antirheumatic drugs/antimetabolite therapy (i.e., methotrexate, azathioprine, and mycophenolate mofetil) with rheumatologists and providing guidance on ocular dosing. When uveitis quiescence cannot be achieved despite maximally tolerated antimetabolite therapy, patients should be referred to a uveitis specialist for consultation and consideration of IMT escalation. The timing of uveitis referral may depend on local factors specific to health care jurisdictions.

摘要

前葡萄膜炎因其病因和临床表现种类繁多,给诊断带来了挑战。本叙述性综述旨在使普通眼科医生全面了解前葡萄膜炎的流行病学、诊断和治疗。特别强调制定一种量身定制的、循序渐进的策略,而非一刀切的方法,用于前葡萄膜炎的检查和治疗。对于严重、双侧、复发性或慢性前葡萄膜炎病例,胸部X线摄影以及梅毒、人类白细胞抗原B27和血管紧张素转换酶的血清学检测是合适的常规检查。额外的检测应根据临床发现和地区流行病学来指导,尤其是在考虑昂贵和侵入性检查方法时。在缺乏临床和流行病学指导的情况下进行的检查效用有限,会给患者和医疗保健系统带来巨大成本。大多数解剖学上孤立的前葡萄膜炎病例通过局部使用皮质类固醇可得到缓解,但一些患者需要升级为全身免疫调节治疗(IMT)。对于对皮质类固醇反应不佳、出现与皮质类固醇相关的副作用而限制其使用、需要高剂量以维持疾病缓解或患有全身性炎症性疾病的患者,应考虑进行IMT。综合眼科医生应放心地与风湿病学家共同管理需要常规改善病情抗风湿药物/抗代谢物治疗(即甲氨蝶呤、硫唑嘌呤和霉酚酸酯)的患者,并就眼部用药提供指导。当尽管使用了最大耐受剂量的抗代谢物治疗仍无法实现葡萄膜炎静止时,应将患者转诊至葡萄膜炎专科医生处进行咨询并考虑升级IMT。葡萄膜炎转诊的时机可能取决于医疗保健辖区特有的当地因素。

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