Garweg Justus G
Berner Augenklinik am Lindenhofspital, Affiliation: Klinik und Poliklinik für Augenheilkunde, Inselspital, Universität Bern, Bremgartenstr 119, 3012, Bern, Schweiz.
Swiss Eye Institute, Rotkreuz, Schweiz.
Ophthalmologe. 2019 Oct;116(10):942-950. doi: 10.1007/s00347-019-0870-x.
Modern treatment of uveitis aims at a complete control of inflammatory activity, preservation of visual function and the prevention of secondary organ damage as a consequence of the underlying inflammatory disease and its treatment.
This article gives an update about the strategies of pharmacological and surgical options for uveitis.
The outcomes reported here are based on a PubMed search using the terms <"uveitis" AND "therapy"> and <"uveitis" AND "surgery" OR "surgical treatment">. All prospective studies and case series with more than 20 cases as well as review articles from the last 5 years along with cited cross-references were evaluated.
Local and systemic corticosteroids form the foundation of treatment after exclusion of an infectious etiology. If uveitis activity is not controlled within 6 weeks or if the daily corticosteroid dosage is unacceptably high, a treatment escalation using immunomodulatory drugs is required. If a complete control of inflammatory activity is not achieved, in a third phase treatment is supplemented by antibody-based treatment or cytokines, so-called biologics, with the aim of complete long-term freedom from disease without local or systemic steroid treatment. This target is achieved in 65-80% and guarantees long-term functional stability and anatomical integrity. Early treatment escalation in cases of persisting or recurrent activity as a rule prevents new secondary organ damage. Surgical options are utilized for diagnostic purposes, the administration of intravitreal drugs and for treatment of secondary complications.
Just like the majority of immunological diseases, uveitis is a chronic disease requiring long-term and possibly lifelong treatment and remission (absence of inflammation without treatment) is achieved in only <20%. Surgical interventions can be performed with a good prognosis, if the optic nerve head and macula are not involved. They have a substantially lower complication rate when freedom from symptoms exists preoperatively for at least 3 months.
葡萄膜炎的现代治疗旨在完全控制炎症活动、保留视觉功能,并预防潜在炎症性疾病及其治疗导致的继发性器官损害。
本文介绍葡萄膜炎的药物治疗和手术治疗策略的最新情况。
本文报告的结果基于在PubMed上使用检索词<“葡萄膜炎”和“治疗”>以及<“葡萄膜炎”和“手术”或“手术治疗”>进行的搜索。对所有前瞻性研究、病例数超过20例的病例系列以及过去5年的综述文章及其引用的交叉参考文献进行了评估。
在排除感染性病因后,局部和全身使用皮质类固醇是治疗的基础。如果葡萄膜炎活动在6周内未得到控制,或者每日皮质类固醇剂量高得难以接受,则需要使用免疫调节药物升级治疗。如果未实现对炎症活动的完全控制,在第三阶段,治疗需辅以基于抗体的治疗或细胞因子(即所谓的生物制剂),目标是在不进行局部或全身类固醇治疗的情况下实现长期完全无病。这一目标在65%至80%的患者中得以实现,并保证了长期功能稳定性和解剖完整性。对于持续或复发活动的病例,尽早升级治疗通常可预防新的继发性器官损害。手术可用于诊断目的、玻璃体内药物给药以及继发性并发症的治疗。
与大多数免疫性疾病一样,葡萄膜炎是一种慢性疾病,需要长期甚至可能终身治疗,仅不到20%的患者可实现缓解(未经治疗时无炎症)。如果视神经乳头和黄斑未受累,手术干预的预后良好。如果术前至少3个月无症状,手术并发症发生率会大幅降低。