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Sökning: id:"swepub:oai:gup.ub.gu.se/58649" > Risk of recurrent v...

Risk of recurrent venous thromboembolism or bleeding in relation to thrombophilic risk factors in patients receiving ximelagatran or placebo for long-term secondary prevention of venous thromboembolism

Wahlander, K. (författare)
Eriksson, Henry, 1946 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för akut och kardiovaskulär medicin,Institute of Medicine, Department of Emergeny and Cardiovascular Medicine
Lundstrom, T. (författare)
visa fler...
Billing Clason, S. (författare)
Karolinska Institutet
Wall, U. (författare)
Nystrom, P. (författare)
Wessman, P. (författare)
Schulman, S. (författare)
visa färre...
 (creator_code:org_t)
Wiley, 2006
2006
Engelska.
Ingår i: Br J Haematol. - : Wiley. - 0007-1048 .- 1365-2141. ; 133:1, s. 68-77
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The impact of prothrombotic abnormalities on the risk of recurrent venous thromboembolism (VTE) and bleeding in patients receiving long-term anticoagulation remains unclear. This analysis evaluated the influence of potential prothrombotic risk factors (antithrombin, protein C, protein S, factor V Leiden mutation, prothrombin gene G20210A mutation, cardiolipin antibodies, number of risk factors) on the risk of recurrent VTE or bleeding during treatment with oral ximelagatran (24 mg twice daily) or placebo for 18 months [THRombin Inhibitor in Venous thromboEmbolism (THRIVE) III trial]. Of the 1223 patients in the intention-to-treat population, prothrombotic state was analysed in 559 patients receiving ximelagatran and 540 patients receiving placebo. It is possible that patients at a high risk of recurrent VTE were poorly represented in this analysis because of selection bias. Prothrombotic risk factors were reported in 41% of patients (8% had > or = 2 factors). No significant interactions were found between ximelagatran treatment and potential prothrombotic risk factors for the risk of recurrent VTE or bleeding by Cox proportionate hazard modelling. There was no clear evidence for a higher risk of recurrent VTE or bleeding across subgroups according to the potential prothrombotic factors analysed in this study.

Nyckelord

Antibodies
Anticardiolipin/blood
Anticoagulants/*adverse effects/therapeutic use
Antithrombins/analysis
Azetidines/*adverse effects/therapeutic use
Benzylamines/*adverse effects/therapeutic use
Biological Markers/blood
Blood Coagulation Tests
Ethnic Groups
Europe
Factor V/analysis
Hemorrhage/blood/*chemically induced
Humans
Proportional Hazards Models
Protein S/analysis
Recurrence
Risk
Thromboembolism/blood/*chemically induced/drug therapy
Thrombophilia/ethnology/*genetics
Treatment Outcome

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