Department of Ophthalmology, University Medical Center Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Manchester University Hospitals NHS Trust, Manchester Royal Eye Hospital, M13 9WH, Manchester, UK.
BMC Ophthalmol. 2020 Dec 17;20(1):489. doi: 10.1186/s12886-020-01762-w.
Anterior uveitis secondary to topical brimonidine administration is rare and not well-defined. In glaucoma patients using brimonidine, one must consider this phenomenon to avoid mis-diagnosis and over-treatment with topical steroids which in turn may increase intraocular pressure (IOP). This is the largest case series including the longest patient follow-up in the current literature.
Sixteen patients (26 eyes) with consultant diagnosed brimonidine-associated anterior uveitis in a tertiary referral glaucoma clinic presenting between 2015 and 2019 were included in this retrospective case series. Clinical records were taken for descriptive analysis. Main outcome measures were the key clinical features, and disease course (therapy, IOP control, patient outcome).
Key features were conjunctival ciliary injection and mutton fat keratic precipitation in all eyes. The findings were bilateral in 10 patients. Time between initiation of brimonidine treatment and presentation was 1 week to 49 months. Glaucoma sub-types were mostly pseudo-exfoliative and primary open angle glaucoma. Brimonidine treatment was stopped immediately. Additionally, topical corticosteroids were prescribed in 18 eyes and tapered down during the following 4 weeks. Thirteen eyes did not need surgical or laser treatment (median follow-up time 15 months). No patient showed recurrence of inflammation after cessation of brimonidine.
This type of anterior uveitis is an uncommon but important manifestation which should always be considered in glaucoma patients on brimonidine treatment. Although treatable at its root cause, problems may persist, especially with respect to IOP control. The latter may necessitate glaucoma surgery after the resolved episode of the uveitis.
局部使用溴莫尼定引起前葡萄膜炎较为罕见,目前尚未明确其发病机制。在使用溴莫尼定的青光眼患者中,必须考虑到这种现象,以避免误诊和过度使用局部皮质类固醇,否则可能会导致眼内压(IOP)升高。这是目前文献中最大的包含最长患者随访时间的病例系列研究。
本回顾性病例系列研究纳入了 2015 年至 2019 年间在一家三级转诊青光眼诊所就诊的、经会诊诊断为与溴莫尼定相关的前葡萄膜炎的 16 名患者(26 只眼)。记录临床资料并进行描述性分析。主要观察指标为主要临床特征和疾病过程(治疗、IOP 控制、患者结局)。
所有患者均存在结膜睫状充血和角膜云翳,双眼受累 10 例。溴莫尼定治疗开始至就诊的时间为 1 周至 49 个月。青光眼亚型主要为假性剥脱综合征和原发性开角型青光眼。溴莫尼定立即停药,18 只眼局部应用皮质类固醇,在接下来的 4 周内逐渐减量。13 只眼无需手术或激光治疗(中位随访时间 15 个月)。停止溴莫尼定治疗后,无患者出现炎症复发。
这种类型的前葡萄膜炎虽然罕见,但在接受溴莫尼定治疗的青光眼患者中应始终考虑到这种情况。虽然可以针对病因进行治疗,但问题可能仍然存在,尤其是在 IOP 控制方面。在葡萄膜炎缓解后,后者可能需要进行青光眼手术。