Drug-Eluting versus Bare-Metal Stents in Large Coronary Arteries
Patients with coronary artery disease undergoing percutaneous coronary intervention were assigned to receive sirolimus-eluting, everolimus-eluting, or bare-metal stents. At 2 years, there was no significant between-group difference in the rate of death from cardiac causes or nonfatal myocardial infa...
Gespeichert in:
Veröffentlicht in: | The New England journal of medicine 2010-12, Vol.363 (24), p.2310-2319 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Patients with coronary artery disease undergoing percutaneous coronary intervention were assigned to receive sirolimus-eluting, everolimus-eluting, or bare-metal stents. At 2 years, there was no significant between-group difference in the rate of death from cardiac causes or nonfatal myocardial infarction.
First-generation drug-eluting coronary-artery stents (which release sirolimus or paclitaxel) have been shown to reduce the risk of restenosis after percutaneous coronary intervention, as compared with bare-metal stents. However, these drug-eluting stents have also been associated with a risk of late stent thrombosis, which in turn may be associated with death from cardiac causes or nonfatal myocardial infarction.
1
,
2
For patients with stenoses in large coronary arteries, requiring stents of 3.0 mm or more in diameter, the benefits of the use of drug-eluting stents have been considered especially uncertain for two reasons. First, in these patients, the benefit of reducing the . . . |
---|---|
ISSN: | 0028-4793 1533-4406 |
DOI: | 10.1056/NEJMoa1009406 |