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Comparing clinical outcomes of vitamin K antagonists vs non-vitamin K antagonists in anticoagulant therapy for mesenteric venous thrombosis

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dc.contributor.authorKim, Young-Hye-
dc.contributor.authorKim, Hyeon Ju-
dc.contributor.authorPark, Suehyun-
dc.contributor.authorHwang, Deokbi-
dc.contributor.authorKim, Hyung-Kee-
dc.contributor.authorHuh, Seung-
dc.contributor.authorYun, Woo-Sung-
dc.date.accessioned2024-06-20T07:00:28Z-
dc.date.available2024-06-20T07:00:28Z-
dc.date.issued2024-09-
dc.identifier.issn2213-333X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/70848-
dc.description.abstractObjective: Non-vitamin K antagonist oral anticoagulants have shown similar efficacy and lower bleeding rates than vitamin K antagonists for venous thromboembolism. However, this has not been proven in mesenteric vein thrombosis. This study aimed to compare the clinical outcomes of vitamin K antagonists and non-vitamin K antagonist oral anticoagulants. Methods: Between January 2014 and July 2022, mesenteric vein thrombosis was diagnosed on computed tomography in 225 patients in a tertiary hospital. Among them, a total of 44 patients who underwent long-term anticoagulation therapy over 3 months were enrolled in this study. Patients were divided into two groups based on the anticoagulant used: vitamin K antagonists (Group 1, n = 21) and non-vitamin K antagonist oral anticoagulants (Group 2, n = 23). The efficacy outcomes were symptom recurrence and thrombus resolution on follow-up computed tomography, and the safety outcome was bleeding complications. Results: The median age of the patients was 56 years (range, 46-68 years), and 52% were men. The most common risk factors were unprovoked intra-abdominal infections (30%). The median duration of anticoagulation therapy was 13 months (20 months in Group 1 vs 6 months in Group 2; P = .076). Of the 44 patients, 17 (39%) received the standard treatment. The median follow-up period was longer in Group 1 than in Group 2 (57 vs 28 months; P = .048). No recurrence of mesenteric vein thrombosis-related symptoms were observed in either group. The median duration of follow-up computed tomography was 31 months (42 months in Group 1 vs 18 months in Group 2; P = .064). Computed tomography revealed complete thrombus resolution, partial resolution, and no changes in 71%, 19%, and 10%, respectively (P = .075). Regarding bleeding complications, varix bleeding and melena developed in two patients in Group 2, and anticoagulation treatment thereafter ceased. Conclusions: Despite the short follow-up duration in the non-vitamin K antagonist oral anticoagulants group, there was no clinically significant difference in the thrombus resolution rate or bleeding complications when compared with the vitamin K antagonists group. Although research on the long-term effects of non-vitamin K antagonist oral anticoagulants in patients is limited, non-vitamin K antagonist oral anticoagulants can be considered an alternative to conventional treatments. © 2024 The Author(s)-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier Inc.-
dc.titleComparing clinical outcomes of vitamin K antagonists vs non-vitamin K antagonists in anticoagulant therapy for mesenteric venous thrombosis-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.jvsv.2024.101903-
dc.identifier.scopusid2-s2.0-85195490636-
dc.identifier.wosid001297430000001-
dc.identifier.bibliographicCitationJournal of Vascular Surgery: Venous and Lymphatic Disorders, v.12, no.5-
dc.citation.titleJournal of Vascular Surgery: Venous and Lymphatic Disorders-
dc.citation.volume12-
dc.citation.number5-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaSurgery-
dc.relation.journalResearchAreaCardiovascular System & Cardiology-
dc.relation.journalWebOfScienceCategorySurgery-
dc.relation.journalWebOfScienceCategoryPeripheral Vascular Disease-
dc.subject.keywordPlusSPLANCHNIC VEIN-THROMBOSIS-
dc.subject.keywordPlusORAL ANTICOAGULANTS-
dc.subject.keywordPlusPROGNOSTIC-FACTORS-
dc.subject.keywordPlusRIVAROXABAN-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordAuthorAnticoagulation-
dc.subject.keywordAuthorMesenteric venous thrombosis-
dc.subject.keywordAuthorNon-Vitamin K antagonists-
dc.subject.keywordAuthorVitamin K antagonists-
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