2019
DOI: 10.1097/ijg.0000000000001371
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Tube Shunt Revision With Excision of Fibrotic Capsule Using Mitomycin C With and Without Ologen—a Collagen Matrix Implant: A 3-Year Follow-up Study

Abstract: Precis: Tube revision with capsule excision in failed glaucoma drainage devices (GDDs) has good medium-term success effectively reducing the intraocular pressure (IOP) and medication burden. Implantation of Ologen may limit the complications, particularly erosion. Purpose: To evaluate the 36-month outcomes of tube shunt revision with capsule excision using Mitomycin C (MMC) versus MMC with Ologen—a collagen matrix implant. … Show more

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Cited by 10 publications
(4 citation statements)
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“…Removal of the fibrous capsule improves short-term IOP control, but does not typically yield long-term results due to frequent re-encapsulation. Unfortunately, Ologen does not seem to improve these results in cases of adult glaucoma [25]. Anecdotally, we have also seen minimal benefit of Ologen in revision of AGVs in pediatric glaucomas.…”
Section: Discussionmentioning
confidence: 82%
“…Removal of the fibrous capsule improves short-term IOP control, but does not typically yield long-term results due to frequent re-encapsulation. Unfortunately, Ologen does not seem to improve these results in cases of adult glaucoma [25]. Anecdotally, we have also seen minimal benefit of Ologen in revision of AGVs in pediatric glaucomas.…”
Section: Discussionmentioning
confidence: 82%
“…For statistical analyses, BCVA scores were converted to the logarithm of the minimum angle of resolution (logMAR). IOP spike was defined as an increase in IOP of > 50% or > 10 mmHg, relative to the preoperative IOP [ 56 , 57 ]. To limit the bias from postoperative conditions and to ensure that the postoperative outcomes of eyes can be associated with CE-TMS, postoperative data of eyes that underwent additional glaucoma surgeries were censored in the analysis of subsequent follow-up time points.…”
Section: Methodsmentioning
confidence: 99%
“…Demographic, baseline and postoperative clinical data were extracted from patients' charts. Efficacy measures included changes in IOP (measured using the Goldman applanation tonometry) and anti-glaucoma medications (scored according to the number of active pharmacologic classes) [30,31]. Safety comprised intra-or postoperative adverse events, best-corrected visual acuity (BCVA), cup-to-disc ratio (CDR), visual field mean deviation (VF-MD), increase in the number of glaucoma medications or secondary glaucoma interventions for uncontrolled IOP.…”
Section: Outcome Measures and Data Analysismentioning
confidence: 99%