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A Murine Model of Stent Implantation in the Carotid Artery for the Study of Restenosis
Published on: May 14, 2013
Coronary collateral function long after drug-eluting stent implantation
Pascal Meier1, Rainer Zbinden, Mario Togni
1Department of Cardiology, University Hospital, Bern, Switzerland.
Insights
Drug-eluting stents (DES) impair coronary collateral function compared to bare-metal stents (BMS) long after implantation. This reduced collateral capacity may increase risks during abrupt coronary occlusion.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Biomedical Engineering
Background:
- Drug-eluting stents (DES) may inhibit growth factors crucial for collateral vessel development.
- Coronary collateral circulation is vital for preventing ischemia during occlusive events.
Purpose of the Study:
- To compare coronary collateral function between patients receiving bare-metal stents (BMS) and drug-eluting stents (DES).
Main Methods:
- 120 patients with stable coronary artery disease post-stenting were analyzed.
- Collateral flow index (CFI) was invasively measured 6 months post-implantation.
- Assessment included pressure measurements and intracoronary ECG during balloon occlusion.
Main Results:
- Coronary collateral flow index (CFI) was significantly lower in the DES group compared to the BMS group.
- Patients with DES showed a higher incidence of insufficient collaterals to prevent ischemia during occlusion.
- No significant differences were observed in baseline characteristics or stenosis severity between groups.
Conclusions:
- Drug-eluting stents (DES) are associated with impaired coronary collateral function compared to bare-metal stents (BMS).
- Reduced collateral function following DES implantation could increase the risk of adverse cardiac events during acute coronary occlusion.
Objectives:
This study was designed to compare coronary collateral function in patients after bare-metal stent (BMS) or drug-eluting stent (DES) implantation.
Background:
Drug-eluting stents have an inhibitory effect on the production of cytokines, chemotactic proteins, and growth factors, and may therefore negatively affect coronary collateral growth.
Methods:
A total of 120 patients with long-term stable coronary artery disease (CAD) after stent implantation were included. Both the BMS group and the DES group comprised 60 patients matched for in-stent stenosis severity of the vessel undergoing collateral flow index (CFI) measurement at follow-up and for the duration of follow-up. The primary end point of the investigation was invasively determined coronary collateral function 6 months after stent implantation. Collateral function was assessed by simultaneous aortic, coronary wedge, and central venous pressure measurements (yielding CFI) and by intracoronary electrocardiogram during balloon occlusion.
Results:
There were no differences between the groups regarding age, gender, body mass index, frequency of cardiovascular risk factors, use of cardiovascular drugs, severity of CAD, or site of coronary artery stenoses. Despite equal in-stent stenosis severity (46 +/- 34% and 45 +/- 36%) and equal follow-up duration (6.2 +/- 10 months and 6.5 +/- 5.4 months), CFI was diminished in the DES versus BMS group (0.154 +/- 0.097 vs. 0.224 +/- 0.142; p = 0.0049), and the rate of collaterals insufficient to prevent ischemia during occlusion (intracoronary electrocardiographic ST-segment elevation > or =0.1 mV) was higher with 50 of 60 patients in the DES group and 33 of 60 patients in the BMS group (p = 0.001).
Conclusions:
Collateral function long after coronary stenting is impaired with DES (sirolimus and paclitaxel) when compared with BMS. Considering the protective nature of collateral vessels, this could lead to more serious cardiac events in the presence of an abrupt coronary occlusion.
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