Treatment of Non-ST-Elevation Myocardial Infarction (NSTEMI)
The cornerstone of NSTEMI treatment includes dual antiplatelet therapy with aspirin plus a P2Y12 inhibitor (preferably ticagrelor), anticoagulation, and an early invasive approach for high-risk patients, along with adjunctive medical therapy including statins, beta-blockers, and ACE inhibitors. 1
Initial Management
Antiplatelet Therapy
Aspirin:
P2Y12 Inhibitor (choose one):
Anticoagulation (choose one)
- Unfractionated heparin (UFH): IV bolus and infusion for at least 48 hours or until PCI 2
- Enoxaparin: 1 mg/kg SC every 12 hours (maximum 10,000 IU twice daily) for duration of hospitalization up to 8 days 2
- Fondaparinux: 2.5 mg SC daily (preferred in patients with high bleeding risk) 1
- Bivalirudin: Alternative to heparin, especially in patients with heparin-induced thrombocytopenia 1
Anti-ischemic Therapy
- Nitroglycerin: IV for ongoing chest pain 2
- Contraindications: SBP <90 mmHg, severe bradycardia (<50 bpm), tachycardia (>100 bpm) without heart failure, right ventricular infarction 2
- Beta-blockers: Begin within a few days if not initiated acutely 2
- Avoid IV beta-blockers in patients with signs of heart failure, low cardiac output, or risk for cardiogenic shock 2
Risk Stratification and Invasive Strategy
Risk Assessment Tools
- GRACE Risk Score: Predicts in-hospital and long-term outcomes 1
- TIMI Risk Score: Predicts in-hospital and long-term outcomes 1
Timing of Invasive Strategy
Immediate invasive strategy (<2 hours):
- Hemodynamic instability or cardiogenic shock
- Refractory angina despite medical treatment
- Life-threatening arrhythmias or cardiac arrest
- Mechanical complications of MI
- Acute heart failure with refractory angina 1
Early invasive strategy (<24 hours):
- Elevated cardiac troponin
- Dynamic ECG changes
- GRACE score >140 1
Invasive strategy within 72 hours:
- Diabetes mellitus
- Renal insufficiency (eGFR <60 mL/min/1.73 m²)
- LVEF <40% or heart failure
- Recent PCI or prior CABG
- GRACE score >109 and <140 1
Revascularization Options
Percutaneous Coronary Intervention (PCI): Preferred for most patients 2
- Continue aspirin
- Continue P2Y12 inhibitor
- Discontinue anticoagulant therapy after uncomplicated PCI 2
Coronary Artery Bypass Grafting (CABG): Consider for patients with:
- Left main disease
- Three-vessel disease
- Complex coronary anatomy
- Note: Discontinue P2Y12 inhibitors prior to CABG (clopidogrel: 5 days, ticagrelor: 5 days, prasugrel: 7 days) 1
Secondary Prevention
Pharmacological Therapy
- High-intensity statin therapy: All patients without contraindications 1
- Beta-blockers: Continue indefinitely 2
- ACE inhibitors/ARBs: Especially for patients with LVEF ≤40%, hypertension, diabetes, or chronic kidney disease 1
- Avoid IV ACE inhibitors within first 24 hours due to hypotension risk 1
- Aldosterone antagonists: For patients with LVEF ≤40% and either heart failure or diabetes 2
Duration of Dual Antiplatelet Therapy (DAPT)
- Medical management (no stent): Aspirin indefinitely plus P2Y12 inhibitor for up to 12 months 2
- PCI with stent: Aspirin indefinitely plus P2Y12 inhibitor for at least 12 months for DES and up to 12 months for BMS 2
Special Considerations
High Bleeding Risk
- Consider shorter duration of DAPT
- Consider fondaparinux as anticoagulant
- Consider proton pump inhibitor for GI protection 1
Diabetes
- More aggressive antiplatelet therapy
- Early invasive strategy preferred 1
Elderly
- Adjust medication doses
- Monitor renal function
- Higher risk of bleeding complications 2
Common Pitfalls to Avoid
- Delaying antiplatelet therapy: Initiate immediately upon diagnosis
- Administering NSAIDs: Avoid all NSAIDs except aspirin due to increased risks of mortality and complications 1
- Administering nitrates to patients with:
- SBP <90 mmHg
- Severe bradycardia (<50 bpm)
- Recent phosphodiesterase inhibitor use (sildenafil within 24h, tadalafil within 48h) 2
- Using immediate-release calcium channel blockers without beta-blockers 2
- Missing high-risk NSTEMI patients who may benefit from very early intervention (those with total coronary occlusion represent ~30% of NSTEMI cases) 4
By following this comprehensive approach to NSTEMI management, focusing on rapid diagnosis, risk stratification, and appropriate interventions, patient outcomes can be significantly improved with reductions in mortality and recurrent events.