4.4 Article

Outcomes of severe uveitic glaucoma treated with Baerveldt implant: can blindness be prevented?

Journal

ACTA OPHTHALMOLOGICA
Volume 96, Issue 1, Pages 24-30

Publisher

WILEY
DOI: 10.1111/aos.13489

Keywords

Baerveldt glaucoma implant; glaucoma; intraocular pressure; uveitic glaucoma

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PurposeTo evaluate long-term outcomes on efficacy and safety of severe uveitic glaucoma treated with a Baerveldt glaucoma implant (BGI). MethodsA 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. ResultsMean IOP dropped from 30.68.1mmHg with 3.6 +/- 1.1 glaucoma medications at baseline to 10.6 +/- 4.3mmHg with 1.0 +/- 1.3 glaucoma medications after a mean follow-up of 63.6 +/- 43.1months. 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. ConclusionThe 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.

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