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Expert Consensus on the Use of the PRESERFLO™ MicroShunt Device in the Treatment of Glaucoma: A Modified Delphi Panel

dc.contributor.authorKhawaja, Anthony P.
dc.contributor.authorStalmans, Ingeborg
dc.contributor.authorAptel, Florent
dc.contributor.authorBarton, Keith
dc.contributor.authorBeckers, Henny J. M.
dc.contributor.authorKlink, Thomas
dc.contributor.authorMarchini, Giorgio
dc.contributor.authorMartínez De La Casa Fernández-Borrella, José María
dc.contributor.authorSimonsen, Jan H.
dc.contributor.authorToteberg Harms, Marc
dc.contributor.authorVass, Clemens
dc.contributor.authorAbegão Pinto, Luís
dc.date.accessioned2023-06-22T12:55:21Z
dc.date.available2023-06-22T12:55:21Z
dc.date.issued2022-07-07
dc.description.abstractIntroduction: The implantation of the PRESERFLO™ MicroShunt (PMS) device has been shown to significantly lower increased intraocular pressure (IOP) in patients with primary open-angle glaucoma (POAG). However, guidelines on best practice for patient selection and pre-/peri-/postoperative care management are lacking. The aim of this modified Delphi panel was to achieve expert consensus on the role of the PMS to treat patients with glaucoma in Europe. Methods: Twelve European glaucoma surgeons experienced with the PMS procedure participated in a three-round modified Delphi panel. A targeted literature review and expert steering committee guided round 1 questionnaire development. Consensus was set at a pre-defined threshold of at least 70% of panellists selecting ‘Strongly disagree’/‘Disagree’ or ‘Strongly agree’/‘Agree’ for six–point Likert scale questions, or at least 70% selecting the same option for multiple-choice questions. Questions not reaching consensus were restated/revised for the next round, following guidance from free-text responses/scoping questions. Results: Consensus was achieved for 60.3% (n = 38/63), 60.0% (n = 18/30), and 100.0% (n = 11/11) of Likert/multiple-choice questions in rounds 1, 2, and 3, respectively. There was agreement that the PMS procedure is effective at reducing IOP in patients with high-tension POAG (greater than 21 mmHg). Although surgical techniques may vary slightly, consensus was reached on several points, including the importance of posterior application of mitomycin C (MMC). Panellists agreed that the PMS postoperative follow-up appointment schedule is reasonably predictable and mostly characterised by fewer visits than with trabeculectomy, particularly in the early phase. Although panellists agreed that combined cataract/PMS surgery and the use of non-MMC wound-healing modulators/antifibrotics during the procedure are possible, further data are needed to determine efficacy. Conclusion: The expert consensus reached in this panel will help inform best practice guidelines in the treatment of patients with glaucoma in Europe. Panellists also highlighted key areas for future research to improve understanding of the PMS in the treatment algorithm of glaucoma.en
dc.description.departmentUnidad Docente de Inmunología, Oftalmología y ORL
dc.description.facultyFac. de Óptica y Optometría
dc.description.refereedTRUE
dc.description.sponsorshipSanten SA
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/77780
dc.identifier.citationKhawaja, A. P., Stalmans, I., Aptel, F. et al. «Expert Consensus on the Use of the PRESERFLOTM MicroShunt Device in the Treatment of Glaucoma: A Modified Delphi Panel». Ophthalmology and Therapy, vol. 11, n.o 5, octubre de 2022, pp. 1743-66. DOI.org (Crossref), https://doi.org/10.1007/s40123-022-00529-4.
dc.identifier.doi10.1007/s40123-022-00529-4
dc.identifier.issn2193-6528 Print ISSN 2193-8245
dc.identifier.officialurlhttps://doi.org/10.1007/s40123-022-00529-4
dc.identifier.relatedurlhttps://link.springer.com/article/10.1007/s40123-022-00529-4
dc.identifier.urihttps://hdl.handle.net/20.500.14352/73329
dc.issue.number5
dc.journal.titleOphthalmology and Therapy
dc.language.isoeng
dc.page.final1766
dc.page.initial1743
dc.publisherSpringer
dc.relation.projectID(MR/T040912/1)
dc.rightsAtribución-NoComercial 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/es/
dc.subject.cdu617.7-007.681
dc.subject.cdu617.7-089
dc.subject.keywordConsensus
dc.subject.keywordDelphi method
dc.subject.keywordEurope
dc.subject.keywordGlaucoma
dc.subject.keywordMicroShunt
dc.subject.keywordOpen-angle glaucoma
dc.subject.keywordPRESERFLO™
dc.subject.ucmCirugía
dc.subject.ucmOftalmología
dc.subject.unesco3213 Cirugía
dc.subject.unesco3201.09 Oftalmología
dc.titleExpert Consensus on the Use of the PRESERFLO™ MicroShunt Device in the Treatment of Glaucoma: A Modified Delphi Panelen
dc.typejournal article
dc.volume.number11
dspace.entity.typePublication
relation.isAuthorOfPublication273a99c3-2c9f-4dd0-8939-b7ff3593124c
relation.isAuthorOfPublication.latestForDiscovery273a99c3-2c9f-4dd0-8939-b7ff3593124c

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