Risk stratification in the patient with ST elevation MI
Percutaneous coronary intervention Microchapters |
PCI Complications |
---|
PCI in Specific Patients |
PCI in Specific Lesion Types |
Risk stratification in the patient with ST elevation MI On the Web |
American Roentgen Ray Society Images of Risk stratification in the patient with ST elevation MI |
FDA on Risk stratification in the patient with ST elevation MI |
CDC on Risk stratification in the patient with ST elevation MI |
Risk stratification in the patient with ST elevation MI in the news |
Blogs on Risk stratification in the patient with ST elevation MI |
Directions to Hospitals Treating Percutaneous coronary intervention |
Risk calculators and risk factors for Risk stratification in the patient with ST elevation MI |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Definition
- Chest pain or classic symptoms for more than 30 minutes.
- ST-segment elevation of at least 1 mV in 2 contiguous leads, or new left bundle branch block.
- Increase of cardiac enzyme levels.
Risk stratification in patient presenting with STEMI
- The Thrombolysis in Myocardial Infarction (TIMI) risk score for STEMI:
- The TIMI risk score for STEMI was created from simple arithmetic sum of independent predictors of mortality weighted according to the adjusted odds ratios from logistic regression analysis.
- The patient pool (n=14114) came from the Intravenous nPA for Treatment of Infarcting Myocardium Early II trial (TIME II).
- The TIMI risk score was subsequently validated in an unselected heterogeneous community population through the National Registry of Myocardial Infarction (NRMI) 3 & 4.
- The Global Registry of Acute Coronary Events (GRACE) risk score for ACS:
- The GRACE risk score was created from a multivariable logistic regression model using ACS patients enrolled in the GRACE registry (N=11389).
- The GRACE risk score was validated using subsequent cohort of patients enrolled in GRACE (n=3972) and the Global Use of Strategies to Open Occluded Coronary Arteries IIb (GUSTO-IIb) trial (n=12142).
Primary percutaneous coronary intervention versus thrombolysis therapy
- Several randomized multi-center clinical trials have demonstrated superiority of primary PCI in comparison to thrombolysis. A review of 23 clinical trials found PCI was better than thrombolysis in reducing short term mortality (7% vs 9%; P=0.0002), death excluding the SHOCK trial data (5% vs 7%; p=0.0003), non-fatal reinfarction (3% vs 7%; p<0.0001), stroke (1% vs 2%; p=0.0004) and the combined end point of death, non-fatal reinfarction and stroke (8% vs 14%; p<0.0001) (Primary angioplasty versus intravenous thrombolytic therapy for acute myocardial infarction: a quantitative review of 23 randomised trials. Keeley EC et al; Lancet 2003 Jan 04;361(9351):13-20).
- ACC/AHA guideline on management of STEMI gave the following recommendation regarding to PCI:
- Class I indication:
- Expected door to balloon time goal of 90 minutes or less.
- Duration of symptom is less than 3 hours and the expected door to balloon time minus the expected door to needle time for thrombolysis is less than 1 hour. Otherwise, thrombolysis is generally preferred.
- Duration of symptom is greater than 3 hours.
- Patient is in cardiogenic shock and has severe congestive heart failure and/or Killip class III.
- Class IIa indication:
- Patient 75 years or above who developes cardiogenic shock within 36 hours of MI onset who can be revascularized within 18 hours of sock.
- Duration of symptom within 12-24 hours with severe CHF and/or Killip class III, hemodynamic or electric instability, or persistent ischemia.
- Class I indication: