Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/26996
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dc.contributor.authorÖner, Fatma Alibaz-
dc.contributor.authorKaradeniz, Aslı-
dc.contributor.authorYılmaz, Sema-
dc.contributor.authorBalkarlı, Ayşe-
dc.contributor.authorKimyon, Gezmiş-
dc.contributor.authorYazıcı, Ayten-
dc.contributor.authorÇınar, Muhammet-
dc.contributor.authorYılmaz, Sedat-
dc.contributor.authorYıldız, Fatih-
dc.contributor.authorBilge, Şule Yaşar-
dc.contributor.authorBilgin, Emre-
dc.contributor.authorOmma, Ahmet-
dc.contributor.authorÇetin, Gözde Yıldırım-
dc.contributor.authorÇağatay, Yonca-
dc.contributor.authorKaraaslan, Yaşar-
dc.contributor.authorSayarlıoğlu, Mehmet-
dc.contributor.authorKalyoncu, Umut-
dc.contributor.authorKaradağ, Ömer-
dc.contributor.authorKaşifoğlu, Timuçin-
dc.contributor.authorErken, Eren-
dc.contributor.authorPay, Salih-
dc.contributor.authorÇefle, Ayşe-
dc.contributor.authorKısacık, Bünyamin-
dc.contributor.authorOnat, Ahmet Mesut-
dc.contributor.authorÇobankara, Veli-
dc.contributor.authorDireskeneli, Haner-
dc.date.accessioned2022-06-09T07:19:44Z-
dc.date.available2022-06-09T07:19:44Z-
dc.date.issued2015-02-
dc.identifier.citationÖner, F. A. vd. (2015). "Behçet disease with vascular involvement: Effects of different therapeutic regimens on the incidence of new relapses". Medicine, 94(6).en_US
dc.identifier.issn0025-7974-
dc.identifier.urihttps://doi.org/10.1097/MD.0000000000000494-
dc.identifier.urihttps://journals.lww.com/md-journal/Fulltext/2015/02020/Beh_et_Disease_With_Vascular_Involvement__Effects.10.aspx-
dc.identifier.urihttp://hdl.handle.net/11452/26996-
dc.description.abstractVascular involvement is one of the major causes of mortality and morbidity in Behcet disease (BD). There are no controlled studies for the management of vascular BD (VBD), and according to the EULAR recommendations, only immunosuppressive (IS) agents are recommended. In this study, we aimed to investigate the therapeutic approaches chosen by Turkish physicians during the initial event and relapses of VBD and the association of different treatment options with the relapses retrospectively. Patients with BD (n = 936, female/male: 347/589, mean age: 37.6 +/- 10.8) classified according to ISG criteria from 15 rheumatology centers in Turkey were included. The demographic data, clinical characteristics of the first vascular event and relapses, treatment protocols, and data about complications were acquired. VBD was observed in 27.7% (n = 260) of the patients during follow-up. In 57.3% of the VBD patients, vascular involvement was the presenting sign of the disease. After the first vascular event, ISs were given to 88.8% and AC treatment to 59.8% of the patients. Median duration of AC treatment was 13 months (1-204) and ISs, 22 months (1-204). Minor hemorrhage related to AC treatment was observed in 7 (4.7%) patients. Asecond vascular event developed in 32.9% (n = 86) of the patients. The vascular relapse rate was similar between patients taking only ISs and AC plus IS treatments after the first vascular event (29.1% vs 22.4%, P = 0.28) and was significantly higher in group taking only ACs than taking only ISs (91.6% vs 29.1%, P < 0.001). During follow-up, a third vascular event developed in 17 (n = 6.5%) patients. The relapse rate was also similar between the patients taking only ISs and AC plus IS treatments after second vascular event (25.3% vs 20.8%, P = 0.93). When multivariate analysis was performed, development of vascular relapse negatively correlated with only IS treatments. We did not find any additional positive effect of AC treatment used in combination with ISs in the course of vascular involvement in patients with BD. Severe complications related to AC treatment were also not detected. Our results suggest that short duration of IS treatments and compliance issues of treatment are the major problems in VBD associated with vascular relapses during follow-up.en_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectThrombosisen_US
dc.subjectMortalityen_US
dc.subjectGeneral & internal medicineen_US
dc.subject.meshAdulten_US
dc.subject.meshBehcet Syndromeen_US
dc.subject.meshFemaleen_US
dc.subject.meshFollow-up studiesen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshRecurrenceen_US
dc.subject.meshRetrospective studiesen_US
dc.subject.meshVasculitisen_US
dc.titleBehçet disease with vascular involvement: Effects of different therapeutic regimens on the incidence of new relapsesen_US
dc.typeArticleen_US
dc.identifier.wos000349772200012tr_TR
dc.identifier.scopus2-s2.0-84926480623tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Romatoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0003-0298-4157tr_TR
dc.identifier.volume94tr_TR
dc.identifier.issue6tr_TR
dc.relation.journalMedicineen_US
dc.contributor.buuauthorCoşkun, Belkıs Nihan-
dc.contributor.buuauthorPehlivan, Yavuz-
dc.contributor.researcheridAAG-7155-2021tr_TR
dc.contributor.researcheridAAG-8227-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed25674739tr_TR
dc.subject.wosMedicine, general & internalen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid55646165400tr_TR
dc.contributor.scopusid13205593600tr_TR
dc.subject.scopusBehcet Syndrome; False Aneurysm; Case Reporten_US
dc.subject.emtreeAlpha interferonen_US
dc.subject.emtreeAnticoagulant agenten_US
dc.subject.emtreeAzathioprineen_US
dc.subject.emtreeCorticosteroiden_US
dc.subject.emtreeCyclophosphamideen_US
dc.subject.emtreeImmunosuppressive agenten_US
dc.subject.emtreeInfliximaben_US
dc.subject.emtreeLow molecular weight heparinen_US
dc.subject.emtreeMethotrexateen_US
dc.subject.emtreeWarfarinen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAnticoagulant therapyen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBehcet diseaseen_US
dc.subject.emtreeBleedingen_US
dc.subject.emtreeClinical featureen_US
dc.subject.emtreeDemographyen_US
dc.subject.emtreeEpistaxisen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeGastrointestinal hemorrhageen_US
dc.subject.emtreeHematomaen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeImmunosuppressive treatmenten_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreePhysicianen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeRecurrence risken_US
dc.subject.emtreeRelapseen_US
dc.subject.emtreeRetrospective studyen_US
dc.subject.emtreeTreatment durationen_US
dc.subject.emtreeVascular Behcet diseaseen_US
dc.subject.emtreeVascular diseaseen_US
dc.subject.emtreeBehcet Syndromeen_US
dc.subject.emtreePathologyen_US
dc.subject.emtreeRecurrent diseaseen_US
dc.subject.emtreeVasculitisen_US
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