What is the management of Non-ST-Elevation Myocardial Infarction (NSTEMI)?

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Last updated: October 9, 2025View editorial policy

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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:
    • Continue dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 inhibitor 4, 6
    • Consider an intravenous GP IIb/IIIa inhibitor (abciximab, eptifibatide, or tirofiban) for troponin-positive and other high-risk patients 4

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:
    • Continue aspirin 4
    • Administer a loading dose of a P2Y12 inhibitor if not started before diagnostic angiography 4
    • Consider an IV GP IIb/IIIa inhibitor for high-risk patients 4
    • Discontinue anticoagulant therapy after PCI for uncomplicated cases 4
  • For patients managed conservatively:
    • Continue aspirin 4
    • Administer a loading dose of a P2Y12 inhibitor if not given before diagnostic angiography 4
    • Discontinue IV GP IIb/IIIa inhibitor if started previously 4
    • Continue anticoagulant therapy as outlined above 4

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:
    • Continue aspirin 4
    • Discontinue clopidogrel/prasugrel 5-7 days before CABG 4
    • Discontinue IV GP IIb/IIIa inhibitor 4 hours before CABG 4
    • Continue UFH, but discontinue enoxaparin 12-24 hours before CABG, fondaparinux 24 hours before CABG, and bivalirudin 3 hours before CABG 4

References

Guideline

Management of NSTEMI in Patients with a History of Subdural Hemorrhage

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of NSTEMI with Resolved Symptoms

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Demand Ischemia NSTEMI

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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