Outcome of Patients with Venous Thromboembolism and Factor V Leiden or Prothrombin 20210 Carrier Mutations During the Course of Anticoagulation

被引:11
作者
Tzoran, Inna [1 ]
Papadakis, Manolis [2 ]
Brenner, Benjamin [1 ]
Fidalgo, Angeles [3 ]
Rivas, Agustina [4 ]
Wells, Philip S. [5 ]
Gavin, Olga [6 ]
Dolores Adarraga, Maria [7 ]
Moustafa, Fares [8 ]
Monreal, Manuel [9 ]
机构
[1] Rambam Hlth Care Campus, Dept Haematol & Bone Marrow Transplantat, Haifa, Israel
[2] Hosp Papageorgiou, Haematol & Hemostasis Unit, Saloniki, Greece
[3] Hosp Univ Salamanca, Dept Internal Med, Salamanca, Spain
[4] Hosp Univ Araba, Dept Pneumonol, Alava, Spain
[5] Univ Ottawa, Res Inst, Ottawa Hosp, Dept Med, Ottawa, ON, Canada
[6] Hosp Clin Univ Lozano Blesa, Dept Haematol, Zaragoza, Spain
[7] Hosp Montilla, Dept Internal Med, Cordoba, Argentina
[8] Clermont Ferrand Univ Hosp, Dept Emergency, Clermont Ferrand, France
[9] Univ Catolica Murcia, Hosp Univ Germans Trias & Pujol Badalona, Dept Internal Med, Barcelona, Spain
关键词
Anticoagulant therapy; Bleeding; Thrombophilia; Venous thromboembolism; DEEP-VEIN THROMBOSIS; THROMBOPHILIC RISK-FACTORS; SEVERE HEMOPHILIA-A; PULMONARY-EMBOLISM; ANTITHROMBOTIC THERAPY; RECURRENT THROMBOSIS; CLINICAL EXPRESSION; PROSPECTIVE COHORT; PREDICTIVE-VALUE; CARDIAC-SURGERY;
D O I
10.1016/j.amjmed.2016.11.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Individuals with factor V Leiden or prothrombin G20210A mutations are at a higher risk to develop venous thromboembolism. However, the influence of these polymorphisms on patient outcome during anticoagulant therapy has not been consistently explored. METHODS: We used the Registro Informatizado de Enfermedad TromboEmbolica database to compare rates of venous thromboembolism recurrence and bleeding events occurring during the anticoagulation course in factor V Leiden carriers, prothrombin mutation carriers, and noncarriers. RESULTS: Between March 2001 and December 2015, 10,139 patients underwent thrombophilia testing. Of these, 1384 were factor V Leiden carriers, 1115 were prothrombin mutation carriers, and 7640 were noncarriers. During the anticoagulation course, 160 patients developed recurrent deep vein thrombosis and 94 patients developed pulmonary embolism (16 died); 154 patients had major bleeding (10 died), and 291 patients had nonmajor bleeding. On multivariable analysis, factor V Leiden carriers had a similar rate of venous thromboembolism recurrence (adjusted hazard ratio [HR], 1.16; 95% confidence interval [CI], 0.82-1.64), half the rate of major bleeding (adjusted HR, 0.50; 95% CI, 0.25-0.99) and a nonsignificantly lower rate of nonmajor bleeding (adjusted HR, 0.66; 95% CI, 0.43-1.01) than noncarriers. Prothrombin mutation carriers and noncarriers had a comparable rate of venous thromboembolism recurrence (adjusted HR, 1.00; 95% CI, 0.68-1.48), major bleeding (adjusted HR, 0.75; 95% CI, 0.42-1.34), and nonmajor bleeding events (adjusted HR, 1.10; 95% CI, 0.77-1.57). CONCLUSIONS: During the anticoagulation course, factor V Leiden carriers had a similar risk for venous thromboembolism recurrence and half the risk for major bleeding compared with noncarriers. This finding may contribute to decision-making regarding anticoagulation duration in selected factor V Leiden carriers with venous thromboembolism. (C) 2017 Published by Elsevier Inc.
引用
收藏
页码:482.e1 / 482.e9
页数:9
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