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dc.contributor.authorGálvez-Sánchez, Rafael
dc.contributor.authorSalmón González, Zaida
dc.contributor.authorFernández-García, Magdalena
dc.contributor.authorCerveró Varona, Andrea
dc.contributor.authorGonzález-Mesones, Belén
dc.contributor.authorLópez Hoyos, Marcos 
dc.contributor.authorMartínez Taboada, Víctor Manuel 
dc.contributor.authorHernández Hernández, José Luis 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-07-29T08:33:55Z
dc.date.available2025-07-29T08:33:55Z
dc.date.issued2025
dc.identifier.issn2077-0383
dc.identifier.urihttps://hdl.handle.net/10902/36840
dc.description.abstractBackground/Objectives: Retinal vein occlusion (RVO) represents a common ophthalmological disorder that, if untreated, often leads to severely impaired vision. The classic vascular risk factors, aging and glaucoma, represent the core pathogenic factors for RVO. However, antiphospholipid syndrome (APS) has been involved in a non-negligible number of patients with RVO. The main objective of the present study was to assess the performance of the new 2023 ACR/EULAR classification criteria for APS in a cohort of patients with RVO fulfilling the Sydney classification criteria. Methods: A prospective study of consecutive patients with RVO diagnosed with APS in a third-level university hospital. The new 2023 ACR/EULAR classification criteria for APS were applied to all patients. Vascular risk factors, the antiphospholipid antibody (aPL) profile, clinical management, and clinical outcomes were assessed and compared between those fulfilling the Sydney and the 2023 ACR/EULAR criteria. Results: Sixty-nine RVO-APS patients were included in the study. After applying the new classification criteria, 18 patients (26.1%) did not fulfill the new criteria for APS. Specifically, 17 (24.6%) were excluded due to the new Domain 8 (p < 0.001) as they presented only aPL IgM serology, and 1 patient (1.4%) was excluded due to having high venous thromboembolic risk (VTE) with a clinical domain score < 3. Interestingly enough, the presence of high arterial risk (45.1% vs. 50%; p = 0.72) was greater than the presence of high VTE (3.9% vs. 5.6%; p = 0.99); in both cases, the 51 RVO-APS patients were classified with the 2023 ACR/EULAR criteria, and the 18 cases were excluded according to the new classification criteria. Except for the expected differences in serological domains (Domain 7, p < 0.001, and Domain 8, p < 0.001), we did not find other significant differences in terms of prognosis or risk of recurrence between both groups of patients. Conclusions: The implementation of the new ACR/EULAR 2023 classification criteria for APS resulted in the exclusion of about one out of four previously diagnosed RVO-APS patients. The higher prevalence of manifestations of high arterial risk compared with high VTE among both newly classified and excluded APS patients highlights the importance of monitoring cardiovascular risk factors for both the prevention and the management of potential retinal and cardiovascular events.es_ES
dc.format.extent13 p.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rights© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceJournal of Clinical Medicine, 2025, 14, 2826es_ES
dc.subject.otherAntiphospholipid antibodieses_ES
dc.subject.otherAntiphospholipid syndromees_ES
dc.subject.otherRetinal vein occlusiones_ES
dc.subject.otherVascular risk factorses_ES
dc.subject.otherClassification criteriaes_ES
dc.titleImpact of the 2023 ACR/EULAR antiphospholipid syndrome criteria on retinal vein occlusion patientses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/jcm14082826es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/jcm14082826
dc.type.versionpublishedVersiones_ES


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© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) licenseExcepto si se señala otra cosa, la licencia del ítem se describe como © 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license