Management of Non-ST-Elevation Myocardial Infarction (NSTEMI)
The management of NSTEMI requires a combination of antiplatelet therapy, anticoagulation, and risk stratification to determine the need for invasive versus conservative strategies, with aspirin as the cornerstone of treatment for all patients. 1, 2
Initial Management
- Administer aspirin 162-325 mg (non-enteric formulation, orally or chewed) as soon as possible after hospital presentation 1
- Admit to a monitored unit with continuous rhythm monitoring for at least 24 hours (or until PCI, whichever comes first) 1, 2
- Administer supplemental oxygen if arterial oxygen saturation is <90% 1, 3
- Consider nitroglycerin for ongoing ischemic symptoms unless contraindicated (systolic BP <90 mmHg, severe bradycardia, tachycardia without heart failure, right ventricular infarction, or recent use of phosphodiesterase inhibitors) 1, 3
- Initiate beta-blockers to reduce myocardial oxygen demand by decreasing heart rate, blood pressure, and myocardial contractility 1, 3
Risk Stratification
- Measure high-sensitivity cardiac troponin (hs-cTn) serially for both diagnosis and prognostic assessment 1, 2
- Perform echocardiography to evaluate regional and global left ventricular function 1, 2
- Assess hemodynamic stability, presence of ongoing ischemia, and risk factors for adverse outcomes 3
- Consider using risk scores such as TIMI Risk Score (age ≥65 years, >3 coronary risk factors, prior angiographic coronary obstruction, ST-segment deviation, >2 angina events within 24h, use of aspirin within 7 days, and elevated cardiac markers) 4
Antiplatelet Therapy
- Continue aspirin 75-162 mg daily long-term for all patients 4
- Administer a loading dose of a P2Y12 inhibitor (clopidogrel, ticagrelor, or prasugrel) if not given before diagnostic angiography 4, 5
- For patients managed with PCI:
Anticoagulation
- Initiate parenteral anticoagulation for all patients in addition to antiplatelet therapy 4, 2
- Options include unfractionated heparin (UFH), enoxaparin, fondaparinux, or bivalirudin 4
- For patients managed conservatively:
- Continue intravenous UFH for at least 48 hours or until discharge 4
- Continue enoxaparin for duration of hospitalization, up to 8 days 4
- Continue fondaparinux for duration of hospitalization, up to 8 days 4
- Either discontinue bivalirudin or continue at a dose of 0.25 mg per kg per hour for up to 72 hours at physician's discretion 4
Management Strategy Selection
- For patients with ongoing ischemia refractory to medical therapy or hemodynamic instability, an early invasive strategy with cardiac catheterization is recommended 1, 3
- For patients managed with PCI:
- For patients managed conservatively:
Long-term Management
- Continue aspirin indefinitely 1, 2
- Continue P2Y12 inhibitor therapy for 12 months unless contraindicated or there is excessive bleeding risk 2, 6
- Initiate beta-blockers for all patients unless contraindicated 1, 2
- Consider ACE inhibitors for patients with heart failure, LV dysfunction (LVEF <0.40), hypertension, or diabetes 1, 2
- Consider ARBs for ACE inhibitor-intolerant patients 1, 2
- Measure LVEF in patients managed conservatively 4
- If LVEF is ≤0.40, consider diagnostic angiography 4
- If LVEF is >0.40, consider a stress test 4
Common Pitfalls and Caveats
- Avoid NSAIDs (except for aspirin) during hospitalization due to increased risks of mortality, reinfarction, hypertension, heart failure, and myocardial rupture 1, 3
- Do not administer immediate-release dihydropyridine calcium channel blockers without adequate beta-blockade 1, 3
- Avoid intravenous ACE inhibitors within the first 24 hours due to increased risk of hypotension 1, 3
- Do not use PDE5 inhibitors (sildenafil within 24 hours, tadalafil within 48 hours) in patients who have received nitrates due to potentially dangerous hypotensive effects 1, 3
- For patients undergoing CABG, manage antiplatelet and anticoagulant therapy as follows: