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ABSTRACT: Purpose
To report a case and management of persistent hypotony with hypotony-induced maculopathy after CyPass® device implant.Background
The CyPass® was the first supraciliary ab interno device approved by FDA and commercially available. Efficacy studies showed adequate intraocular pressure (IOP)-lowering results in combination with phacoemulsification. Hypotony induced by suprachoroidal minimally invasive glaucoma surgery (MIGS) was reported to be lower than 3% in the population that comprised the COMPASS study.Case description
A 57-year-old female patient with mild open-angle glaucoma with maximum topical medical therapy who underwent sequential bilateral CyPass® implantation developed persistent hypotony. Device obstruction
SUBMITTER: Fernando DV
PROVIDER: S-EPMC7221243 | biostudies-literature | 2019 Sep-Dec
REPOSITORIES: biostudies-literature