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dc.contributor.authorMartínez Taboada, Víctor Manuel es_ES
dc.contributor.authorMicieces Gómez, Anaes_ES
dc.contributor.authorDel Barrio Longarela, Saraes_ES
dc.contributor.authorMerino Fernández, Ana Isabel es_ES
dc.contributor.authorComíns Boo, Alejandraes_ES
dc.contributor.authorLópez Hoyos, Marcos es_ES
dc.contributor.authorRiancho Zarrabeitia, Leyrees_ES
dc.contributor.authorGálvez, Rafaeles_ES
dc.contributor.authorHernández Hernández, José Luis es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-01-31T11:45:23Z
dc.date.available2025-01-31T11:45:23Z
dc.date.issued2024es_ES
dc.identifier.issn2075-4418es_ES
dc.identifier.urihttps://hdl.handle.net/10902/35283
dc.description.abstractBackground/Objectives: ACR/EULAR has recently developed new classification criteria for antiphospholipid syndrome (APS). The present study aims to analyze the impact of these new 2023 ACR/EULAR classification criteria in a cohort of pregnant women with primary APS. Methods: Retrospective cohort study of 93 consecutive pregnant women attending the Autoimmune Diseases Pregnancy Clinic, a multidisciplinary unit of a tertiary care teaching hospital, between 2005 and 2023. All of them fulfilled the Sydney classification criteria for APS. Women diagnosed with rheumatic autoimmune diseases other than APS were excluded. Results: Twenty-four out of ninety-three patients (25.8%) met the 2023 ACR/EULAR criteria for APS. Patients who met the new classification criteria were very similar to those who did not, except for being younger (p < 0.001), and had a lower number of clinical pregnancies (p = 0.004). The obstetric domain was clearly underrepresented in women who fulfilled the 2023 ACR/EULAR criteria (p < 0.001). Patients meeting the new classification criteria were primarily characterized by preterm births before 34 weeks due to severe placentation disorders (p = 0.004). Women with early and late fetal loss were significantly underrepresented (p < 0.0001 and 0.03, respectively). Nearly half of these patients had thrombocytopenia (p < 0.001). Serologically, these patients showed a higher frequency of persistent lupus anticoagulant (p = 0.02) and a lower frequency of IgM isotype antiphospholipid antibodies (p = 0.05). Conclusions: Almost three-quarters of the patients included in the study did not meet the 2023 ACR/EULAR criteria. Most patients who could not be classified according to these new classification criteria were those with early and/or late fetal deaths, as well as patients carrying only IgM aCL/AB2GPI antibodies. The high specificity of the 2023 ACR/EULAR criteria, restricted to severe placentation disorders, may leave the majority of patients with obstetric APS out of the new classification criteria.es_ES
dc.format.extent14 p.es_ES
dc.language.isoenges_ES
dc.rights© 2024 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 (https:// creativecommons.org/licenses/by/ 4.0/).*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceDiagnostics (Basel), 2024, 14(19), 2162es_ES
dc.subject.otherPregnancy
dc.subject.otherObstetric morbidity
dc.subject.otherFetal loss
dc.subject.otherAntiphospholipid syndrome
dc.subject.otherAntiphospholipid
dc.subject.otherAntibodies
dc.subject.otherClassification criteria
dc.titleImpact of the 2023 ACR/EULAR Classification Criteria in Women with Primary Antiphospholipid Syndrome during Pregnancyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/diagnostics14192162es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/diagnostics14192162es_ES
dc.type.versionpublishedVersiones_ES


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© 2024 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 (https://
creativecommons.org/licenses/by/
4.0/).Excepto si se señala otra cosa, la licencia del ítem se describe como © 2024 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 (https:// creativecommons.org/licenses/by/ 4.0/).