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Published on: February 3, 2021
Adjunctive pharmacotherapy before percutaneous coronary intervention in non-ST-elevation acute coronary syndromes:
1The Lindner Center for Research and Education, 2123 Auburn Avenue, Suite 424, Cincinnati, Ohio 45219, USA. lindner@fuse.net
Insights
Vascular inflammation drives acute coronary syndromes (ACS) and recovery after percutaneous coronary intervention (PCI). Anti-inflammatory effects of common ACS medications may explain their long-term clinical benefits.
Area of Science:
- Cardiovascular Medicine
- Inflammation Biology
Background:
- Vascular inflammation is a key factor in acute coronary syndromes (ACS) and post-percutaneous coronary intervention (PCI) vascular injury.
- The severity of vascular inflammation correlates with adverse long-term clinical outcomes, including death, myocardial infarction, and restenosis.
Purpose of the Study:
- To review the anti-inflammatory properties of pharmacologic therapies used in ACS treatment.
- To hypothesize that modulating vascular inflammation contributes to the long-term benefits of these therapies.
- To propose a therapeutic algorithm for non-ST-elevation ACS management.
Main Methods:
- Review of anti-inflammatory effects of aspirin, clopidogrel, low-molecular-weight heparin (LMWH), platelet glycoprotein (GP) IIb/IIIa inhibitors, statins, and angiotensin-converting enzyme (ACE) inhibitors.
- Clinical risk stratification and coronary revascularization strategy integration.
- Application of current American College of Cardiology (ACC)/American Heart Association (AHA) guidelines.
Main Results:
- Multiple ACS pharmacotherapies possess distinct anti-inflammatory actions.
- These anti-inflammatory effects are hypothesized to be a common mechanism for long-term clinical benefit.
- A treatment algorithm for non-ST-elevation ACS is presented.
Conclusions:
- The anti-inflammatory actions of ACS medications may underlie their long-term efficacy.
- Targeting vascular inflammation could be a unifying therapeutic strategy.
- Clinical guidelines and risk stratification are essential for optimal ACS management.
Abstract:
Vascular inflammation is central to the pathogenesis of acute coronary syndromes (ACS) and the response to vascular injury after percutaneous coronary intervention (PCI). For both ACS and PCI, the magnitude of vascular inflammation is linked to adverse late clinical outcomes (e.g., death, recurrent myocardial infarction [MI] or ischemia, and restenosis). Many pharmacologic therapies with demonstrated efficacy for the treatment of ACS have anti-inflammatory properties, which are distinct from their perceived primary mechanism of action. The anti-inflammatory effects of aspirin, clopidogrel, low-molecular-weight heparin (LMWH), platelet glycoprotein (GP) IIb/IIIa receptor inhibitors, statins, and angiotensin converting enzyme (ACE) inhibitors are reviewed, and the hypothesis is generated that modulation of vascular inflammation at least in part contributes a common basis for the long-term clinical benefit ascribed to these medications. A therapeutic algorithm based on clinical risk stratification and coronary revascularization strategy is proposed for incorporating the current American College of Cardiology (ACC)/American Heart Association (AHA) guideline recommendations for treatment of patients who present with non-ST-elevation ACS.
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