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A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma

PURPOSE: To evaluate 3-year safety and intraocular pressure (IOP) following two trabecular microbypass stents in phakic and pseudophakic subjects with open-angle glaucoma (OAG) not controlled on preoperative medication. PATIENTS AND METHODS: In this prospective pilot study, phakic or pseudophakic su...

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Autores principales: Donnenfeld, Eric D, Solomon, Kerry D, Voskanyan, Lilit, Chang, David F, Samuelson, Thomas W, Ahmed, Iqbal Ike K, Katz, L Jay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639560/
https://www.ncbi.nlm.nih.gov/pubmed/26604675
http://dx.doi.org/10.2147/OPTH.S91732
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author Donnenfeld, Eric D
Solomon, Kerry D
Voskanyan, Lilit
Chang, David F
Samuelson, Thomas W
Ahmed, Iqbal Ike K
Katz, L Jay
author_facet Donnenfeld, Eric D
Solomon, Kerry D
Voskanyan, Lilit
Chang, David F
Samuelson, Thomas W
Ahmed, Iqbal Ike K
Katz, L Jay
author_sort Donnenfeld, Eric D
collection PubMed
description PURPOSE: To evaluate 3-year safety and intraocular pressure (IOP) following two trabecular microbypass stents in phakic and pseudophakic subjects with open-angle glaucoma (OAG) not controlled on preoperative medication. PATIENTS AND METHODS: In this prospective pilot study, phakic or pseudophakic subjects with OAG and IOP between 18 mmHg and 30 mmHg on one preoperative topical ocular hypotensive medication underwent medication washout. Thirty-nine qualified subjects with preoperative unmedicated IOP ≥22 mmHg and ≤38 mmHg received two stents. Postoperative examinations were scheduled at Day 1, Week 1, Months 1, 3, 6, and 12, and semiannually through Month 60. Ocular hypotensive medication was considered if postoperative IOP exceeded 21 mmHg. IOP, medication use, and safety were assessed at each visit. Subject follow-up through Month 36 was completed. RESULTS: Thirty-six eyes (92.3%; 95% confidence interval [CI] 79.1%, 98.4%) achieved the primary efficacy end point of Month 12 reduction in IOP ≥20% from baseline (unmedicated IOP) without ocular hypotensive medication. Four subjects required medication during the Month 36 follow-up period. Mean IOP at 36 months for subjects not taking medication was 15.2 mmHg. At 36 months, subjects sustained mean IOP decrease of 9.1±2.7 mmHg (95% CI 8.0 mmHg, 10.14 mmHg), or 37% IOP reduction, from unmedicated baseline IOP. Compared to preoperative medicated IOP, subjects had mean reduction at Month 36 of 5.5±2.7 mmHg (95% CI 4.5 mmHg, 6.6 mmHg), or 26% reduction. Both measures of IOP reduction were highly significant (P<0.001). Other than one case of early postoperative hyphema that resolved at 1 week, no postoperative adverse events were attributed to stent implantation. CONCLUSION: In a pilot study, two trabecular microbypass stents to treat OAG subjects on one preoperative medication provided statistically significant, sustained, and safe reduction of IOP to ≤15 mmHg without medication through 36 months.
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spelling pubmed-46395602015-11-24 A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma Donnenfeld, Eric D Solomon, Kerry D Voskanyan, Lilit Chang, David F Samuelson, Thomas W Ahmed, Iqbal Ike K Katz, L Jay Clin Ophthalmol Original Research PURPOSE: To evaluate 3-year safety and intraocular pressure (IOP) following two trabecular microbypass stents in phakic and pseudophakic subjects with open-angle glaucoma (OAG) not controlled on preoperative medication. PATIENTS AND METHODS: In this prospective pilot study, phakic or pseudophakic subjects with OAG and IOP between 18 mmHg and 30 mmHg on one preoperative topical ocular hypotensive medication underwent medication washout. Thirty-nine qualified subjects with preoperative unmedicated IOP ≥22 mmHg and ≤38 mmHg received two stents. Postoperative examinations were scheduled at Day 1, Week 1, Months 1, 3, 6, and 12, and semiannually through Month 60. Ocular hypotensive medication was considered if postoperative IOP exceeded 21 mmHg. IOP, medication use, and safety were assessed at each visit. Subject follow-up through Month 36 was completed. RESULTS: Thirty-six eyes (92.3%; 95% confidence interval [CI] 79.1%, 98.4%) achieved the primary efficacy end point of Month 12 reduction in IOP ≥20% from baseline (unmedicated IOP) without ocular hypotensive medication. Four subjects required medication during the Month 36 follow-up period. Mean IOP at 36 months for subjects not taking medication was 15.2 mmHg. At 36 months, subjects sustained mean IOP decrease of 9.1±2.7 mmHg (95% CI 8.0 mmHg, 10.14 mmHg), or 37% IOP reduction, from unmedicated baseline IOP. Compared to preoperative medicated IOP, subjects had mean reduction at Month 36 of 5.5±2.7 mmHg (95% CI 4.5 mmHg, 6.6 mmHg), or 26% reduction. Both measures of IOP reduction were highly significant (P<0.001). Other than one case of early postoperative hyphema that resolved at 1 week, no postoperative adverse events were attributed to stent implantation. CONCLUSION: In a pilot study, two trabecular microbypass stents to treat OAG subjects on one preoperative medication provided statistically significant, sustained, and safe reduction of IOP to ≤15 mmHg without medication through 36 months. Dove Medical Press 2015-11-03 /pmc/articles/PMC4639560/ /pubmed/26604675 http://dx.doi.org/10.2147/OPTH.S91732 Text en © 2015 Donnenfeld et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Donnenfeld, Eric D
Solomon, Kerry D
Voskanyan, Lilit
Chang, David F
Samuelson, Thomas W
Ahmed, Iqbal Ike K
Katz, L Jay
A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma
title A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma
title_full A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma
title_fullStr A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma
title_full_unstemmed A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma
title_short A prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma
title_sort prospective 3-year follow-up trial of implantation of two trabecular microbypass stents in open-angle glaucoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639560/
https://www.ncbi.nlm.nih.gov/pubmed/26604675
http://dx.doi.org/10.2147/OPTH.S91732
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