Management of NSTEMI (Non-ST-Elevation Myocardial Infarction)
All NSTEMI patients require immediate dual antiplatelet therapy (aspirin plus ticagrelor preferred), parenteral anticoagulation, high-intensity statin therapy, and risk-stratified invasive coronary angiography within 2-72 hours depending on clinical presentation. 1, 2
Immediate Assessment and Diagnosis
- Obtain 12-lead ECG within 10 minutes of presentation to confirm non-ST-elevation pattern 3
- Measure high-sensitivity troponin at 0 and 1 hour using validated algorithm, or at 0 and 3 hours if 1-hour protocol unavailable 1
- Initiate continuous cardiac monitoring for arrhythmia detection 3
- Perform echocardiography to assess left ventricular function and exclude mechanical complications 1
- Calculate GRACE score for risk stratification to determine timing of invasive strategy 1
Risk-Stratified Timing of Invasive Strategy
Very High-Risk (Immediate angiography <2 hours): 1
- Hemodynamic instability or cardiogenic shock
- Recurrent or ongoing chest pain refractory to medical treatment
- Life-threatening arrhythmias or cardiac arrest
- Mechanical complications of MI
- Acute heart failure with refractory angina or ST-segment deviation
High-Risk (Early angiography <24 hours): 1, 2
- Rise or fall in cardiac troponin compatible with MI
- Dynamic ST- or T-wave changes (symptomatic or silent)
- GRACE score >140
Intermediate-Risk (Invasive strategy <72 hours): 1
- Diabetes mellitus
- Renal insufficiency (eGFR <60 mL/min/1.73 m²)
- LVEF <40% or congestive heart failure
- Early post-infarction angina
- Recent PCI or prior CABG
- GRACE score 109-140
Immediate Antiplatelet Therapy
- Loading dose: 150-325 mg orally immediately
- Maintenance: 75-100 mg daily indefinitely (81 mg daily when combined with ticagrelor) 1
P2Y12 Inhibitor (choose one): 1, 2
- Ticagrelor (preferred for moderate-to-high risk patients): 180 mg loading dose, then 90 mg twice daily for 12 months, regardless of invasive or conservative strategy 1, 2
- Prasugrel: 60 mg loading dose, then 10 mg daily (reduce to 5 mg daily if age ≥75 years or weight <60 kg), only after coronary anatomy is known and PCI planned, contraindicated if prior stroke/TIA 1
- Clopidogrel: 300-600 mg loading dose, then 75 mg daily, reserved for patients who cannot receive ticagrelor or prasugrel, or who require oral anticoagulation 1
The 2014 AHA/ACC guidelines suggest it is reasonable to use ticagrelor in preference to clopidogrel for patients undergoing early invasive or ischemia-guided strategy, while the 2015 ESC guidelines more strongly recommend ticagrelor for all moderate-to-high risk patients with elevated troponin. 1
Parenteral Anticoagulation (Choose One)
For patients managed medically or awaiting angiography: 1, 4, 2
- Fondaparinux (preferred for conservative management): 2.5 mg subcutaneously once daily, best efficacy-safety profile 1, 4
- Enoxaparin: 1 mg/kg subcutaneously every 12 hours (reduce to 1 mg/kg once daily if CrCl <30 mL/min), with optional 30 mg IV loading dose 1, 4, 2
- Unfractionated heparin: 60 IU/kg IV bolus (max 4000 IU), then 12 IU/kg/hour infusion (max 1000 IU/hour), adjusted to aPTT 1.5-2.5 times control 1, 4
For patients proceeding directly to PCI: 1, 2
- Bivalirudin: 0.10 mg/kg loading dose, then 0.25 mg/kg/hour infusion until angiography/PCI, with provisional GP IIb/IIIa inhibitor use only 1
Continue anticoagulation for duration of hospitalization or until PCI performed, up to 48-72 hours for medical management. 1, 4
Glycoprotein IIb/IIIa Inhibitors
Routine upstream GP IIb/IIIa inhibitors are NOT recommended due to increased bleeding without ischemic benefit. 2
Selective use may be considered: 1, 5, 6, 5
- In intermediate-to-high risk patients (positive troponin) during PCI with provisional use only 1
- Eptifibatide: 180 mcg/kg IV bolus, then 2 mcg/kg/min infusion (reduce to 1 mcg/kg/min if CrCl <50 mL/min), with second 180 mcg/kg bolus 10 minutes after first for PCI patients 5
- Tirofiban: Dosing per FDA label, demonstrated 32% risk reduction in composite endpoint of death, MI, or refractory ischemia at 7 days in PRISM-PLUS trial 6
High-Intensity Statin Therapy
Initiate immediately upon admission regardless of baseline cholesterol levels: 1, 2, 3
- Target LDL-C <1.8 mmol/L (<70 mg/dL) 1
- Atorvastatin 80 mg daily is the evidence-based high-intensity regimen 1
- Provides plaque stabilization and anti-inflammatory effects beyond LDL lowering 2
- Continue indefinitely for secondary prevention 1
Additional Acute Medical Management
- Initiate early in patients without contraindications (heart failure, hypotension, bradycardia, heart block) 4
- Particularly important if LVEF ≤40% 1, 3
Nitrates: 4
- For ongoing chest pain, uncontrolled hypertension, or signs of heart failure 4
- Recommended for patients with LVEF ≤40%, heart failure, hypertension, or diabetes 1, 3
- ARBs for ACE inhibitor-intolerant patients 1
Aldosterone blockade (eplerenone): 1
- For post-MI patients already on ACE inhibitor and beta-blocker with LVEF ≤35% and either diabetes or heart failure, without significant renal dysfunction 1
Post-Revascularization and Long-Term Management
Dual antiplatelet therapy: 1, 4, 2, 3
- Continue aspirin plus P2Y12 inhibitor (ticagrelor or clopidogrel) for 12 months after PCI unless excessive bleeding risk 1, 4
- After 12 months, transition to aspirin monotherapy indefinitely 4, 3
If clopidogrel used and CABG planned: 1
- Discontinue clopidogrel 5 days prior to scheduled surgery 1
Special Populations
Renal impairment (CrCl <60 mL/min): 1, 4
- Adjust anticoagulant doses: enoxaparin to 1 mg/kg once daily if CrCl <30 mL/min 1, 4
- Eptifibatide infusion reduced to 1 mcg/kg/min if CrCl <50 mL/min 5
Elderly patients (≥75 years): 4
Patients requiring oral anticoagulation (e.g., atrial fibrillation): 4
- Triple therapy (aspirin + clopidogrel + oral anticoagulant) for acute phase only (up to 1 week) 4
- Transition to dual therapy with oral anticoagulant plus clopidogrel (not ticagrelor or prasugrel) after acute phase, continue for up to 12 months 4, 7
- Then oral anticoagulant monotherapy thereafter 7
Critical Contraindications
Fibrinolytic therapy is contraindicated in NSTEMI and causes harm. 1
Prasugrel should not be administered until coronary anatomy is known. 1