Temporal spectrum of ischemic complications with percutaneous coronary intervention: the ESPRIT experience
Warren J Cantor1, James E Tcheng, James C Blankenship
1St. Michael's Hospital, Division of Cardiology, 30 Bond Street, Toronto, Ontario, Canada, M44-1W8. cantorw@smh.toronto.on.ca
Insights
Most ischemic complications after percutaneous coronary intervention occur within 24 hours, peaking at 12-18 hours. Glycoprotein IIb/IIIa inhibitors effectively reduce these early risks.
Area of Science:
- Cardiology
- Interventional Cardiology
Background:
- Percutaneous coronary intervention (PCI) is a common procedure for coronary artery disease.
- Ischemic complications following PCI can lead to significant morbidity and mortality.
- Understanding the timing and risk factors for these complications is crucial for patient management.
Purpose of the Study:
- To determine the timing of ischemic complications within 30 days after PCI.
- To analyze the risk of complications in relation to time post-randomization.
- To evaluate the role of glycoprotein IIb/IIIa inhibitors in mitigating early ischemic events.
Main Methods:
- Analysis of data from the Enhanced Suppression of the Platelet IIb/IIIa Receptor with Integrilin Therapy (ESPRIT) trial.
- Inclusion of patients undergoing PCI.
- Assessment of ischemic complications (death, myocardial infarction, target vessel revascularization) within 30 days.
Main Results:
- 8.6% of patients (178/2064) experienced ischemic complications within 30 days.
- Over 85% of complications occurred within 24 hours post-randomization, with the highest risk between 12-18 hours.
- 31% of patients with myocardial infarction (MI) within 24 hours had normal CK-MB at 6 hours.
- No rebound increase in events after eptifibatide cessation; treatment benefit persisted to 30 days.
Conclusions:
- Ischemic complications after PCI are concentrated in the early post-procedural period, particularly within the first 24 hours.
- Myocardial infarction may not be immediately evident by standard biomarker measurements (CK-MB) at 6 hours.
- Glycoprotein IIb/IIIa inhibitors represent a key modifiable factor in reducing the risk of early ischemic complications following PCI.
Abstract:
We determined the timing of ischemic complications within 30 days after percutaneous coronary intervention (PCI) in patients enrolled in the Enhanced Suppression of the Platelet IIb/IIIa Receptor with Integrilin Therapy (ESPRIT) trial. Complications (death, myocardial infarction [MI], target vessel revascularization) occurred in 178 of 2064 patients (8.6%) within 30 days. More than 85% of complications occurred within the 24 hours following randomization, with the greatest risk hazard at 12-18 hours. Unexpectedly, 31% of patients who ultimately met criteria for an endpoint MI within 24 hours of PCI had completely normal CK-MB concentrations at the first 6-hour measurement. There was no rebound increase in events after cessation of eptifibatide. Treatment benefit persisted to 30 days. Post-procedural MI is often not detected until greater than or equal to 12 hours after PCI. Treatment with a glycoprotein IIb/IIIa inhibitor is the only modifiable parameter that reduces the risk for early ischemic complications.
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