Safety and Effectiveness of the PRESERFLO® MicroShunt in Primary Open-Angle Glaucoma: Results from a 2-Year Multicenter Study
dc.contributor.author | Beckers, Henny J.M. | |
dc.contributor.author | Aptel, Florent | |
dc.contributor.author | Webers, Carroll A.B. | |
dc.contributor.author | Angeles, Raymund | |
dc.contributor.author | Bluwol, Elisa | |
dc.contributor.author | Martínez De La Casa Fernández-Borrella, José María | |
dc.contributor.author | García Feijoo, Julián | |
dc.contributor.author | Lachkar, Yves | |
dc.contributor.author | Méndez Hernández, Carmen Dora | |
dc.contributor.author | Riss, Isabelle | |
dc.contributor.author | Shao, Hui | |
dc.contributor.author | Pinchuk, Leonard | |
dc.contributor.author | Sadruddin, Omar | |
dc.contributor.author | Shaarawy, Tarek M. | |
dc.date | Received 1 April 2021, Revised 16 July 2021, Accepted 21 July 2021, Available online 28 July 2021, Version of Record 22 March 2022. | |
dc.date.accessioned | 2023-06-16T14:21:29Z | |
dc.date.available | 2023-06-16T14:21:29Z | |
dc.date.issued | 2021-07-27 | |
dc.description.abstract | To assess the safety and effectiveness of the PRESERFLO® MicroShunt (formerly InnFocus MicroShunt) in patients with primary open-angle glaucoma (POAG).The MicroShunt, a controlled ab externo glaucoma filtration surgery device, was investigated in a 2-year, multicenter, single-arm study.Eligible patients were aged 18-85 years with POAG inadequately controlled on maximal tolerated medical therapy with intraocular pressure (IOP) ≥18 and ≤35 mmHg or when glaucoma progression warranted surgery.The MicroShunt was implanted as a stand-alone procedure with adjunctive use of topical mitomycin C (MMC; 0.2-0.4 mg/ml) for 2-3 minutes.The primary effectiveness outcome was IOP reduction and success (not requiring reoperation or pressure failures [IOP > 21 mmHg and < 20% reduction in IOP]) at year 1. Additional end points at year 2 included IOP reduction, success, glaucoma medications, adverse events (AEs), and reoperations. Results are reported in the overall population and subgroups of patients receiving 0.2 or 0.4 mg/ml MMC.In 81 patients, mean (± standard deviation [SD]) IOP decreased from 21.7 ± 3.4 mmHg at baseline to 14.5 ± 4.6 mmHg at year 1 and 14.1 ± 3.2 mmHg at year 2 (P < 0.0001). Overall success (with and without supplemental glaucoma medication use) at year 1 was 74.1%. Mean (± SD) number of medications decreased from 2.1 ± 1.3 at baseline to 0.5 ± 0.9 at year 2 (P < 0.0001), and 73.8% of patients were medication free. Most common nonserious AEs were increased IOP requiring medication or selective laser trabeculoplasty (25.9%) and mild-to-moderate keratitis (11.1%). There were 6 (7.4%) reoperations and 5 (6.2%) needlings by year 2. In an analysis (post hoc) according to MMC concentration, overall success was 78.1% (0.2 mg/ml) and 74.4% (0.4 mg/ml; P = 0.710). In the 0.2 and 0.4 mg/ml MMC groups, 51.9% and 90.3% of patients were medication free, respectively (P = 0.001). There was a trend toward lower IOP and higher medication reduction in the 0.4 mg/ml MMC subgroup.In this study, mean IOP and glaucoma medication reductions were significant and sustained over 2 years postsurgery. No long-term, sight-threatening AEs were reported. Further studies may confirm potential risk/benefits of higher MMC concentration | en |
dc.description.department | Unidad Docente de Inmunología, Oftalmología y ORL | |
dc.description.department | Depto. de Inmunología, Oftalmología y ORL | |
dc.description.faculty | Fac. de Óptica y Optometría | |
dc.description.faculty | Fac. de Medicina | |
dc.description.refereed | TRUE | |
dc.description.status | pub | |
dc.eprint.id | https://eprints.ucm.es/id/eprint/71396 | |
dc.identifier.citation | Beckers, H. J. M., Aptel, F., Webers, C. A. B. et al. «Safety and Effectiveness of the PRESERFLO® MicroShunt in Primary Open-Angle Glaucoma». Ophthalmology Glaucoma, vol. 5, n.o 2, marzo de 2022, pp. 195-209. DOI.org (Crossref), https://doi.org/10.1016/j.ogla.2021.07.008. | |
dc.identifier.doi | 10.1016/j.ogla.2021.07.008 | |
dc.identifier.issn | 2589-4196 | |
dc.identifier.officialurl | https://doi.org/10.1016/j.ogla.2021.07.008 | |
dc.identifier.relatedurl | https://www.sciencedirect.com/science/article/pii/S2589419621001794?via%3Dihub | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/4806 | |
dc.issue.number | 2 | |
dc.journal.title | Ophthalmology Glaucoma | |
dc.language.iso | eng | |
dc.page.final | 209 | |
dc.page.initial | 195 | |
dc.publisher | Elsevier Inc. | |
dc.rights | Atribución 3.0 España | |
dc.rights.accessRights | open access | |
dc.rights.uri | https://creativecommons.org/licenses/by/3.0/es/ | |
dc.subject.cdu | 617.7‑007.681-089 | |
dc.subject.cdu | 615.015.154 | |
dc.subject.cdu | 612.842.6 | |
dc.subject.keyword | Clinical trial | |
dc.subject.keyword | Glaucoma filtration surgery | |
dc.subject.keyword | MIGS | |
dc.subject.keyword | Primary open-angle glaucoma. | |
dc.subject.ucm | Cirugía | |
dc.subject.ucm | Oftalmología | |
dc.subject.ucm | Óptica oftálmica | |
dc.subject.unesco | 3213 Cirugía | |
dc.subject.unesco | 3201.09 Oftalmología | |
dc.title | Safety and Effectiveness of the PRESERFLO® MicroShunt in Primary Open-Angle Glaucoma: Results from a 2-Year Multicenter Study | en |
dc.type | journal article | |
dc.volume.number | 5 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | 273a99c3-2c9f-4dd0-8939-b7ff3593124c | |
relation.isAuthorOfPublication | 558b8023-6d72-4dff-9f99-2e60f6f31843 | |
relation.isAuthorOfPublication | 533dd90f-2b34-4a5f-9cf8-ab8d19454edd | |
relation.isAuthorOfPublication.latestForDiscovery | 558b8023-6d72-4dff-9f99-2e60f6f31843 |