
Late adverse events after drug-eluting stent implantation.
Stents that elute antiproliferative drugs prevent restenosis after percutaneous coronary artery revascularization, reducing the need for repeat procedures. Randomized trials in low-risk patients supported initial regulatory approval for drug-eluting stents (DES). In 2006, meta-analyses of long-term outcomes from these trials associated DES use with adverse events, believed to be attributable to late stent thrombosis, occurring more than 9 months after the initial procedure. This article appraises these late adverse effects and illustrates the power and shortcomings of large national registries, focused, well-conducted clinical trials, and meta-analyses of clinical trial data. This timely, robust evidence base reflects an alignment of academic, industry, and public health priorities.
Duke Scholars
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- United States
- Time Factors
- Risk Factors
- Registries
- Meta-Analysis as Topic
- Humans
- Drug-Eluting Stents
- Coronary Thrombosis
- Coronary Restenosis
- Clinical Trials as Topic
Citation

Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- United States
- Time Factors
- Risk Factors
- Registries
- Meta-Analysis as Topic
- Humans
- Drug-Eluting Stents
- Coronary Thrombosis
- Coronary Restenosis
- Clinical Trials as Topic