Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/7921
DC FieldValueLanguage
dc.contributor.authorMirjana Kovačen_US
dc.contributor.authorŽeljko Mikovićen_US
dc.contributor.authorGorana Mitićen_US
dc.contributor.authorValentina Đorđevićen_US
dc.contributor.authorVesna Mandićen_US
dc.contributor.authorLjiljana Rakičevićen_US
dc.contributor.authorDragica Radojkovićen_US
dc.date.accessioned2019-09-30T09:05:20Z-
dc.date.available2019-09-30T09:05:20Z-
dc.date.issued2014-01-01-
dc.identifier.issn10760296en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/7921-
dc.description.abstractThe study was conducted to evaluate the effect of anticoagulant therapy in women with thrombophilia and to detect the possible differences among carriers of mutations (factor V [FV] Leiden and FIIG20210) and those with natural anticoagulant deficiency. The 4-year prospective investigation included 85 pregnant women, with a history of recurrent fetal loss (RFL). They were treated with prophylactic doses of low-molecular-weight heparin (nadroparin) starting from 6 to 8 weeks of gestation. Pregnancy outcomes were evaluated based on the thrombophilia type. Carriers of thrombophilic mutations had a live birth rate of 93%, compared to 41.6% for women with natural anticoagulant deficiencies. Significant differences between the groups were also observed for intrauterine fetal death, intrauterine growth restriction, and postpartum thrombosis. The optimal therapy for women with natural anticoagulant deficiency and RFL remains unclear and future prospective study with a large number of patients is required to determine the best treatment for these severe thrombophilic conditions. © The Author(s) 2013.en_US
dc.language.isoenen_US
dc.relation.ispartofClinical and Applied Thrombosis/Hemostasisen_US
dc.subjectinherited thrombophiliaen_US
dc.subjectlow-molecular-weight heparinen_US
dc.subjectpregnancy outcomeen_US
dc.titleDoes anticoagulant therapy improve pregnancy outcome equally, regardless of specific thrombophilia type?en_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1177/1076029612468940-
dc.identifier.pmid20-
dc.identifier.scopus2-s2.0-84893439242-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84893439242-
dc.description.versionPublisheden_US
dc.relation.lastpage189en_US
dc.relation.firstpage184en_US
dc.relation.issue2en_US
dc.relation.volume20en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptMedicinski fakultet, Katedra za patološku fiziologiju i laboratorijsku medicinu-
crisitem.author.parentorgMedicinski fakultet-
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