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dc.contributor.authorBarrio-Longarela, Sara deles_ES
dc.contributor.authorMartínez Taboada, Víctor Manuel es_ES
dc.contributor.authorBlanco-Olavarri, Pedroes_ES
dc.contributor.authorMerino Fernández, Ana Isabel es_ES
dc.contributor.authorRiancho Zarrabeitia, Leyrees_ES
dc.contributor.authorComins-Boo, Alejandraes_ES
dc.contributor.authorLópez Hoyos, Marcos es_ES
dc.contributor.authorHernández Hernández, José Luis es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-12-02T15:29:03Z
dc.date.available2022-12-02T15:29:03Z
dc.date.issued2022es_ES
dc.identifier.issn1080-0549es_ES
dc.identifier.issn1559-0267es_ES
dc.identifier.urihttps://hdl.handle.net/10902/26808
dc.description.abstractThe adjusted Global Antiphospholipid Syndrome (APS) Score (aGAPSS) is a tool proposed to quantify the risk for antiphospholipid antibody (aPL)-related clinical manifestations. However, aGAPSS has been validated mainly for thrombotic events and studies on APS-related obstetric manifestations are scarce. Furthermore, the majority of them included patients with positive aPL and diferent autoimmune diseases. Here, we assess the utility of aGAPSS to predict the response to treatment in aPL carriers without other autoimmune disorders. One-hundred and thirty-seven women with aPL ever pregnant were included. Sixty-fve meet the APS classifcation criteria, 61 had APS-related obstetric manifestations, and 11 were asymp tomatic carriers. The patients? aGAPSS risk was grouped as low (<6, N=73), medium (6?11, N=40), and high risk (?12, N=24). Since vascular risk factors included in the aGAPSS were infrequent in this population (<10%), the aGAPSS score was mainly determined by the aPL profle. Overall, the live birth rate was 75%, and 37.2% of the patients had at least one adverse pregnancy outcome (APO). When considering patients according to the aGAPSS (high, medium, and low risk), no signifcant diferences were found for pregnancy loss (29.2%, 25%, and 21.9%) or APO (33.3%, 47.5%, and 32.9%). In the present study, including aPL carriers without other autoimmune diseases, aGAPSS is not a valuable tool to identify patients at risk for obstetric complications despite treatment. In these patients with gestational desire, in addition to the aPL profle, other pregnancy-specifc factors, such as age or previous obstetric history, should be consideredes_ES
dc.format.extent14 p.es_ES
dc.language.isoenges_ES
dc.publisherHumana Press Inc.es_ES
dc.rightsAttribution 4.0 International*
dc.rights© The Author(s) 2021*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceClin Rev Allergy Immunol . 2022 Oct;63(2):297-310es_ES
dc.subject.otherPregnancyes_ES
dc.subject.otherAntiphospholipid syndromees_ES
dc.subject.otherAntiphospholipid antibodieses_ES
dc.subject.otherGAPSSes_ES
dc.subject.otherScorees_ES
dc.subject.otherNon-criteria obstetric manifestationses_ES
dc.titleDoes Adjusted Global Antiphospholipid Syndrome Score (aGAPSS) Predict the Obstetric Outcome in Antiphospholipid Antibody Carriers? A Single Center Studyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1007/s12016-021-08915-9es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1007/s12016-021-08915-9es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International