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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorGuevara, Osvaldo
dc.contributor.authorDjavanmardi, Shirin
dc.contributor.authorPiludu, Stefania
dc.contributor.authorOliver-Gutierrez, David
dc.contributor.authorSegura-Duch, Gloria
dc.contributor.authorCastany, Marta
dc.date.accessioned2025-10-22T12:51:29Z
dc.date.available2025-10-22T12:51:29Z
dc.date.issued2025-06
dc.identifier.citationOliver-Gutierrez D, Guevara-Chavarría O, Djavanmardi S, Segura-Duch G, Castany M, Piludu S, et al. Real-Life Effectiveness and Safety of Selective Laser Trabeculoplasty as Primary, Adjunctive, and Substitutive Therapy. Turkish J Ophthalmol. 2025 Jun;55(3):132–40.
dc.identifier.issn2147-2661
dc.identifier.urihttp://hdl.handle.net/11351/13922
dc.descriptionSelective laser trabeculoplasty; Glaucoma; Laser glaucoma therapy
dc.description.abstractObjectives To assess real-world outcomes of selective laser trabeculoplasty (SLT) in naive patients compared to SLT as adjunctive treatment (AT), investigating SLT’s intraocular pressure (IOP) reduction and its potential to decrease topical medication. Materials and Methods Patients undergoing SLT with no prior glaucoma surgery or laser treatment were grouped based on the intended objective: SLT as primary treatment (PT), SLT as AT, and SLT as substitutive treatment (ST). Survival in the PT and AT groups was defined as ≥20% IOP reduction from baseline and IOP ≤21 on two consecutive visits with the same or fewer medications and no additional glaucoma procedure, including repeat SLT. Survival in the ST group was defined as decreasing topical medication while maintaining or reducing IOP. Results The study included 120 eyes of 120 patients with a mean follow-up of 32.7 months. The PT group showed superior IOP reduction than the AT group at 24-36 months (22.1% vs. 14.5%, p=0.039). Non-responders comprised 28.6% of the PT group and 37.0% of the AT group. The PT group demonstrated better survival rates than the AT group at 12, 24, and 36 months (69.0% vs. 47.1%, 38.8% vs. 31.4%, and 31.1% vs. 23.5%, respectively). In the ST group, 34.2% of patients were successful at 12 months, increasing to 38.3% at 24 months. At 24 months, 50.0% of patients had reduced at least one medication. Conclusion SLT showed two-thirds effectiveness, with one-third being non-responders. It was more effective as PT, with higher IOP reduction and success rates. SLT reduced topical medication in half of patients.
dc.language.isoeng
dc.publisherGalenos Publishing House
dc.relation.ispartofseriesTurkish Journal of Ophthalmology;55(3)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectGlaucoma - Cirurgia
dc.subjectPressió intraocular
dc.subjectLàsers en oftalmologia
dc.subjectUlls - Làsers en cirurgia
dc.subjectDrenatge quirúrgic
dc.subject.meshTreatment Outcome
dc.subject.meshTrabeculectomy
dc.subject.meshIntraocular Pressure
dc.subject.meshGlaucoma
dc.subject.mesh/surgery
dc.subject.meshLaser Therapy
dc.titleReal-Life Effectiveness and Safety of Selective Laser Trabeculoplasty as Primary, Adjunctive, and Substitutive Therapy
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.4274/tjo.galenos.2025.75570
dc.subject.decsresultado del tratamiento
dc.subject.decstrabeculectomía
dc.subject.decspresión intraocular
dc.subject.decsglaucoma
dc.subject.decs/cirugía
dc.subject.decstratamiento con láser
dc.relation.publishversionhttps://doi.org/10.4274/tjo.galenos.2025.75570
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Oliver-Gutierrez D, Guevara-Chavarría O, Djavanmardi S, Segura-Duch G, Piludu S] Innova Ocular Verte Barcelona, Barcelona, Spain. [Castany M] Servei d’Oftalmologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid40560133
dc.identifier.wos001529628700001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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