Tan Annelie N, Cornelissen Michiel F, Webers Carroll A B, Erckens Roel J, Berendschot Tos T J M, Beckers Henny J M
Maastricht University Medical Centre, University Eye Clinic, Maastricht, The Netherlands.
Department of Ophthalmology, Leiden University Medical Centre, Leiden, The Netherlands.
Acta Ophthalmol. 2018 Feb;96(1):24-30. doi: 10.1111/aos.13489. Epub 2017 Sep 18.
To evaluate long-term outcomes on efficacy and safety of severe uveitic glaucoma treated with a Baerveldt glaucoma implant (BGI).
A retrospective study of 47 eyes of 47 patients with uveitic glaucoma treated by a BGI between September 2002 and September 2015. Main outcome measures were intraocular pressure (IOP), number of glaucoma medications, course of the uveitis, visual acuity (VA) and complications.
Mean IOP dropped from 30.6 ± 8.1 mmHg with 3.6 ± 1.1 glaucoma medications at baseline to 10.6 ± 4.3 mmHg with 1.0 ± 1.3 glaucoma medications after a mean follow-up of 63.6 ± 43.1 months. In the majority of cases, IOP remained stable during follow-up. However, especially in several patients with viral uveitis, episodes with IOP peaks were observed during a flare-up despite a functioning implant. These peaks remained below preoperative levels. During follow-up, 16 patients (34%) experienced a clinically significant VA loss, mainly because of late-stage glaucoma or hypotony maculopathy. Early postoperative complications were transient choroidal effusion (n = 5), shallow/flat anterior chamber (n = 4), hyphaema (n = 2) and suprachoroidal haemorrhage (n = 1). The most important late postoperative complication was hypotony maculopathy (n = 5), three of these in juvenile idiopathic arthritis (JIA) patients.
The BGI is an effective and safe treatment for patients with refractive secondary glaucoma due to uveitis. In a majority of patients, VA remains stable and a low and stable IOP is maintained over time with an acceptable number of complications. In particular, patients with viral uveitis and glaucoma should be closely monitored for IOP peaks that may occur during episodes of a flare-up of uveitis, whereas at the other end of the spectrum, patients with JIA seem much more prone to hypotony maculopathy.
评估使用Baerveldt青光眼植入物(BGI)治疗严重葡萄膜炎性青光眼的长期疗效和安全性。
对2002年9月至2015年9月期间接受BGI治疗的47例葡萄膜炎性青光眼患者的47只眼进行回顾性研究。主要观察指标为眼压(IOP)、青光眼药物使用数量、葡萄膜炎病程、视力(VA)及并发症。
平均随访63.6±43.1个月后,眼压从基线时的30.6±8.1mmHg伴3.6±1.1种青光眼药物,降至10.6±4.3mmHg伴1.0±1.3种青光眼药物。在大多数病例中,随访期间眼压保持稳定。然而,尤其是在一些病毒性葡萄膜炎患者中,尽管植入物功能正常,但在葡萄膜炎发作期间仍观察到眼压峰值。这些峰值仍低于术前水平。随访期间,16例患者(34%)出现了具有临床意义的视力丧失,主要原因是晚期青光眼或低眼压性黄斑病变。术后早期并发症为短暂性脉络膜脱离(n=5)、浅/扁平前房(n=4)、前房积血(n=2)和脉络膜上腔出血(n=1)。最重要的术后晚期并发症是低眼压性黄斑病变(n=5),其中3例发生在幼年特发性关节炎(JIA)患者中。
BGI是治疗葡萄膜炎所致屈光性继发性青光眼患者的一种有效且安全的方法。在大多数患者中,视力保持稳定,随着时间的推移眼压维持在低水平且稳定,并发症数量可接受。特别是,对于病毒性葡萄膜炎和青光眼患者,应密切监测葡萄膜炎发作期间可能出现的眼压峰值,而在另一个极端,JIA患者似乎更容易发生低眼压性黄斑病变。