Bivalirudin versus Unfractionated Heparin during Percutaneous Coronary Intervention

Bivalirudin is a new direct thrombin inhibitor. In patients undergoing PCI for stable coronary disease, bivalirudin and unfractionated heparin resulted in similar overall outcomes, but there was less major bleeding with bivalirudin. Bivalirudin is a new direct thrombin inhibitor. In patients undergo...

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Veröffentlicht in:The New England journal of medicine 2008-08, Vol.359 (7), p.688-696
Hauptverfasser: Kastrati, Adnan, Neumann, Franz-Josef, Mehilli, Julinda, Byrne, Robert A, Iijima, Raisuke, Büttner, Heinz Joachim, Khattab, Ahmed A, Schulz, Stefanie, Blankenship, James C, Pache, Jürgen, Minners, Jan, Seyfarth, Melchior, Graf, Isolde, Skelding, Kimberly A, Dirschinger, Josef, Richardt, Gert, Berger, Peter B, Schömig, Albert
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Sprache:eng
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Zusammenfassung:Bivalirudin is a new direct thrombin inhibitor. In patients undergoing PCI for stable coronary disease, bivalirudin and unfractionated heparin resulted in similar overall outcomes, but there was less major bleeding with bivalirudin. Bivalirudin is a new direct thrombin inhibitor. In patients undergoing PCI for stable coronary disease, bivalirudin and unfractionated heparin resulted in similar overall outcomes, but there was less major bleeding with bivalirudin. Percutaneous coronary intervention (PCI) is commonly used to treat patients with coronary artery disease. To minimize the risk of thrombotic complications during and shortly after the procedure, many different antithrombotic regimens have been investigated and are currently in use. Increasing evidence of the adverse consequences of periprocedural bleeding suggests that protection from thrombotic complications should not be the sole measure by which antithrombotic therapies are evaluated. 1 Aspirin, clopidogrel, and heparin are established antithrombotic drugs that are widely recommended according to current guidelines on PCI. 2 Pretreatment with 300 to 600 mg of clopidogrel increasingly is used before PCI because of mounting . . .
ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa0802944