Unstable angina and non-ST-segment myocardial infarction: an evidence-based approach to management
1Department of Emergency Medicine, Box 1149, Mount Sinai School of Medicine, One East 100th Street, New York, NY 10029-6574, USA.
Insights
Unstable angina (UA) and non-ST-segment elevation myocardial infarction (NSTEMI) are acute coronary syndromes. This review covers current evidence-based treatments, including new anti-platelet and anti-thrombotic agents, and invasive strategies for optimal patient management.
Area of Science:
- Cardiology
- Internal Medicine
- Emergency Medicine
Background:
- Unstable angina (UA) and non-ST-segment elevation myocardial infarction (NSTEMI) are critical acute coronary syndromes.
- These conditions carry significant morbidity and mortality risks.
- Accurate diagnosis and risk stratification are essential for timely and appropriate treatment.
Purpose of the Study:
- To review current therapeutic options for UA/NSTEMI.
- To emphasize recent clinical guidelines from the American College of Cardiology and American Heart Association.
- To aid clinicians in incorporating new evidence into practice.
Main Methods:
- Review of evidence supporting current therapeutic options for UA/NSTEMI.
- Emphasis on recent ACC/AHA clinical guidelines.
- Categorization of pharmaceutical agents into anti-ischemic, anti-platelet, and anti-thrombotic therapies.
Main Results:
- Standard therapies include oxygen, aspirin, nitrates, morphine, beta-blockers, and heparin.
- New potent anti-platelet agents (ADP and GPIIb/IIIa inhibitors) are increasingly important.
- Low-molecular-weight heparins offer an effective alternative to unfractionated heparin.
- Advances in percutaneous coronary intervention and drug-eluting stents are significant.
- Ongoing research explores early invasive strategies versus aggressive medical regimens.
Conclusions:
- Effective management of UA/NSTEMI requires integrating history, physical exam, ECG, and biomarkers.
- Tailoring therapy to patient risk profiles is strongly supported by clinical evidence.
- Clinicians face challenges in adopting new treatments and guidelines promptly.
Abstract:
Unstable angina (UA) and non-ST-segment elevation myocardial infarction (NSTEMI) represent two common, closely related acute coronary syndromes with potentially high morbidity and mortality. Integration of information from the history, physical exam, electrocardiogram, and cardiac biomarkers is used to formulate both the diagnosis of UA/NSTEMI and the overall assessment of patient prognosis and risk. Early diagnosis and risk stratification of patients with UA/NSTEMI enable the physician to initiate timely, appropriate treatment. (There is strong clinical evidence supporting the tailoring of specific therapies to the risk profile of the patient.) In recent years, powerful new medical and invasive therapies have been developed. Pharmaceutical agents for UA/NSTEMI may be broadly grouped into one of three categories: anti-ischemic, anti-platelet, and anti-thrombotic agents. Standard therapy for UA/NSTEMI has commonly included oxygen, aspirin, nitrates, morphine, beta-blockers and heparin. Potent new anti-platelet agents, including inhibitors of platelet adenosine diphosphate and glycoprotein IIb/IIIa receptors, play important, expanding roles in the management of these syndromes. Low-molecular-weight heparins have been shown to be an effective alternative to unfractionated heparin in their treatment. Major advances in invasive techniques and devices over the last decade include revascularization with percutaneous coronary intervention and drug-eluting intracoronary stents. Strong interest exists in studying the potential benefits and risks associated with an early invasive therapeutic strategy rather than an aggressive medical regimen for patients with UA/NSTEMI. As new treatments are rapidly added to our growing arsenal of management options, clinicians are constantly challenged with incorporating complex new information and guidelines into their practices in a timely fashion. To assist clinicians with this challenge, this article will review the evidence to support the use of current therapeutic options for UA/NSTEMI, with an emphasis on summarizing the most recent clinical guidelines jointly published by the American College of Cardiology and the American Heart Association.
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