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STEMI Primer: 101 From Presentation to Cath Lab Michael S. Blanc, FACC, FSCAI Community Heart & Vascular Center San Angelo Community Medical Center San Angelo, TX https://youtu.be/9Wmqq3TfV5w “Vulnerable” Plaque and “Stable” Plaque Libby. Circulation. 1995;91:2844-2850. Most MIs associated with non-flow limiting lesions Severity of Coronary Artery Stenosis before Acute MI 100% 90% 80% 70% 60% % of Patients 50% n = 195 40% 30% 20% 10% 0% <50% 50-70% >70% Circulation Vol 93, No12 June 15, 1996 Ambrose, Giroud, Little, Nobuyoshi, et al Symptoms of Heart Attack Chest discomfort Jaw or arm discomfort Shortness of breath Cold sweat Upset stomach Fatigue Over 25% of patients have no chest discomfort Heart is not heavily innervated and pain is typically not severe Acute Phase Risk Stratification: Pre-infarction characteristics Age > 70 Prior myocardial infarction Female gender Hypertension History of CHF Hyperlipidemia Diabetes Race Clinical Criteria ECG Criteria Chest x-raycardiomegaly Markedly elevated cardiac enzymes Elevated BUN Hemodynamic Criteria Complications VSD/PMD-rupture Myocardial rupture Continuing Medical Implementation …...bridging the care gap Acute Phase Risk Stratification: Physical Examination Clinical assessment of LV dysfunction No history of CHF No CHF with index MI No LBBB, pacemaker or LVH with ST-T’s Absence of Q waves-site of MI or outside index territory 91 % predictive value of EF 40% Killip classification Hemodynamic classification Mechanical complications Continuing Medical Implementation …...bridging the care gap Clinical Signs of LV Dysfunction Hypotension Pulsus alternans Reduced volume carotid LV apical enlargement/displac ement Sustained apex - to S2 Soft S1 Paradoxically split S2 S3 gallop (not S4 = impaired LV compliance) Mitral regurgitation Pulmonary congestion Continuing Medical Implementation …...bridging the care gap rales Acute Phase Risk Stratification: Importance of LV dysfunction % patients Mortality (%) 30-50 5 II Rales, S3, Pulmonary venous hypertension 33 15-20 III Pulmonary edema 15 40 IV Cardiogenic shock 10 80-100 Killip Classification I No CHF Continuing Medical Implementation …...bridging the care gap Figure 6 TIMI Risk Score for STEMI Historical Age 65-74 75 DM/HTN or angina Exam SBP < 100 HR >100 Killip II-IV Weight < 67 kg 2 points 3 points 1 point 3 points 2 points 2 points 1 point Presentation Anterior STE or LBBB Time to rx > 4 hrs 1 point 1 point Risk Score = Total (0 -14) (FRONT) Risk Score 0 1 2 3 4 5 6 7 8 >8 Odds of death by 30D* 0.1 0.3 0.4 0.7 1.2 2.2 3.0 4.8 5.8 8.8 (0.1-0.2) (0.2-0.3) (0.3-0.5) (0.6-0.9) (1.0-1.5) (1.9-2.6) (2.5-3.6) (3.8-6.1) (4.2-7.8) (6.3-12) *referenced to average mortality (95% confidence intervals) (BACK) Complications of Acute Myocardial Infarction • Arrhythmic Complications • Mechanical Complications • Ischemic Complications • Miscellaneous Complications [DVT, PE, Pericarditits, TPA complications, Pneumonia] Mechanical Complications of Acute Myocardial Infarction • Papillary Muscle Rupture – Acute MR • Ventricular Septal Defect • Right Ventricular MI • Free Wall Rupture • Cardiogenic shock • Cardiac Tamponade Acute Mortality Reduction Early Recognition of Symptoms Pre -Hospital Resuscitation of Sudden Death Fast-Track Protocol for Thrombolytic Therapy Code STEMI – Direct PCI protocols Optimal Use of Adjunctive Therapy Monitoring for Complications Evidence Based Risk Stratification Appropriate Revascularization for NSTEMI Continuing Medical Implementation …...bridging the care gap Prognosis Post MI Mortality in the first year post MI averages 10% Subsequently mortality 5% per year 85% of deaths due to CAD 50% of these sudden 50% within first 3 months 33% within the first three weeks Continuing Medical Implementation …...bridging the care gap Early Mortality After AMI Mortality at 25 - 30 Days % Mortality 25 20 15 10 5 0 1967 1970 1979 Pre-CCU CCU b-Block 1986 1990 1993 1997 1999 GISSI-1 ISIS-2 GUSTO GUSTO-3 ASSENT-2 tPA & SK tPA & SK+ASA tPA rPA TNK Continuing Medical Implementation …...bridging the care gap Medications ASA 325 mg po chewed Ticagrelor (Brilinta) 180 mg Alternative-Clopidogrel (Plavix) 600 mg Alternative-Prasugrel (Effient) 60 mg Heparin 5000 unit IV Atorvastatin 80 mg Primary endpoint: CV death, MI or stroke 12 Clopidogrel K-M estimated rate (% per year) 11 11.0 10 9.3 9 Ticagrelor 8 7 6 5 4 3 2 HR: 0.85 (95% CI = 0.74–0.97), p=0.02 1 0 0 1 No. at risk Ticagrelor 4,201 Clopidogrel 4,229 2 3 3,887 3,892 4 5 3,834 3,823 6 7 Months 3,732 3,730 8 9 3,011 3,022 10 11 2,297 2,333 12 1,891 1,868 Beta-Blockers COMMIT: Study design INCLUSION: >45,000 patients with suspected acute MI (ST change or LBBB) within 24 h of symptom onset TREATMENT: Metoprolol 15 mg iv over 15 mins, then 200 mg oral daily vs matching placebo EXCLUSION: Shock, systolic BP <100 mmHg, heart rate <50/min or II/III AV block 1 OUTCOMES: Death & death, re-MI or VF/arrest up to 4 weeks in hospital (or prior discharge) Mean treatment and follow-up: 16 days Effects of Metoprolol COMMIT (N = 45,852) Totality of Evidence (N = 5 Death 13% P=0.0006 30% relative increase in *cardiogenic shock ReMI 22% P=0.0002 VF 15% P=0.002 *Risk factors for cardiogenic shock :heart failure, age > 70 , systolic blood pressure < 120, sinus tachycardia > 110 or heart rate < 60, increased time since onset of STEMI symptoms Lancet. 2005;366:1622. Beta-Blockers Recommendations - Class Ia (B) • ORAL beta-blocker therapy SHOULD BE initiated in the first 24 hours for patients who DO NOT have any of the following: 1) signs of heart failure, 2) evidence of a low output state, 3) increased risk for cardiogenic shock, or 4) relative contraindications to beta blockade 1AVB > 0.24 sec, 2nd- or 3rd-degree heart block reactive airway disease ** There is no study evaluating oral beta blockers alone *Risk factors for cardiogenic shock :heart failure, age > 70 , systolic blood pressure < 120, sinus tachycardia > 110 or heart rate < 60, increased time since onset of STEMI symptoms Beta-Blockers Recommendations - Class IIa (B) • It is reasonable to administer an IV BETA BLOCKER at the time of presentation to STEMI patients who are HYPERTENSIVE and who do not have any of the following: 1) signs of heart failure, 2) evidence of a low output state, 3) increased risk for cardiogenic shock, or 4) relative contraindications to beta blockade 1AVB > 0.24 sec, 2nd- or 3rd-degree heart block reactive airway disease *Risk factors for cardiogenic shock :heart failure, age > 70 , systolic blood pressure < 120, sinus tachycardia > 110 or heart rate < 60, increased time since onset of STEMI symptoms Beta-Blockers Recommendations - Class III (A) • IV beta blockers SHOULD NOT be administered to STEMI patients who have any of the following: 1) signs of heart failure 2) evidence of a low output state 3) increased risk* for cardiogenic shock 4) relative contraindications to beta blockade 1AVB > 0.24 sec, 2nd- or 3rd-degree heart block reactive airway disease *Risk factors for cardiogenic shock :heart failure, age > 70 , systolic blood pressure < 120, sinus tachycardia > 110 or heart rate < 60, increased time since onset of STEMI symptoms Statin Evidence: MIRACL Study Primary Efficacy Measure Placebo Cumulative Incidence (%) 15 17.4% 14.8% Atorvastatin 10 Time to first occurrence of: • Death (any cause) • Nonfatal MI • Resuscitated cardiac arrest • Worsening angina with new objective evidence and urgent rehospitalization 5 Relative risk = 0.84 P = .048 95% CI 0.701-0.999 0 0 4 8 12 Time Since Randomization (weeks) Schwartz GG, et al. JAMA. 2001;285:1711-1718. 16 Reperfusion “Time is Muscle” Brief Review of Thrombolytic Trials GISSI-1: Streptokinase 18% reduction in mortality at 21 d GUSTO-1: tPA. 15% reduction in 30-day mortality compared to Streptokinase GUSTO-3: Reteplase had no benefit over tPA but is easier to use (double bolus) ASSENT: TNKase is similar to tPA but with less non-cerebral bleeding and better mortality with symptoms>4 hrs: Single bolus, fibrin selective, resistance to PAI-1 *Overall risk of ICH is 0.7%; Strokes occurred in 1.4% Anticoagulants •Patients undergoing reperfusion with fibrinolytics should receive anticoagulant therapy for a minimum of 48 hours (unfractionated heparin) or up to 8 days •Anticoagulant regimens with established efficacy include: ♥ UFH (LOE: C) ♥ Enoxaparin (LOE:A) ♥ Fondaparinux (LOE:B) PCI vs Fibrinolysis for STEMI: Frequency (%) Short-Term Clinical Outcomes 35 PCI 30 Fibrinolysis N=7739 P<.0001 25 21 20 15 10 P<.0001 P=.0002 9 13 P=.0003 P<.0001 7 7 7 5 5 2 Death Death, no shock data P=.032 6 P<.0001 1 ReMI 2 Rec. Total Ischemia Stroke 8 7 P=.0004 5 1 Hem. Stroke Major Bleed Death MI CVA Keeley E, et al. Lancet . 2003;361:13-20. Reperfusion Therapy fr Patients with STEMI *Patients with cardiogenic shock or severe heart failure initially seen at a non–PCI-capable hospital should be transferred for cardiac catheterization and revascularization as soon as possible, irrespective of time delay from MI onsetClass I, LOE: B). †Angiography and revascularization should not be performed within the first 2 to 3 hours after administration of fibrinolytic therapy. Reperfusion at a Non–PCI-Capable Hospital Transfer of Patients With STEMI to a PCI-Capable Hospital for Coronary Angiography After Fibrinolytic Therapy Rescue PCI •If evidence of cardiogenic shock, severe heart failure hemodynamically compromising ventricular arrhythmias. •If fibriolysis has failed Evaluate 90 minutes for a <50% ST resolution in lead with greatest elevation SACMC Standards EMS SENDS EKG TO ER MD FROM FIELD Scene time 15 min for STEMI. ER MD MAKES DX and ACTIVATES CATH LAB TEAM One phone call activation ER PRESENTATION-EKG < 5 MIN ER MED BOX DIRECT ADMIT TO CATH LAB SACMC SACMC average DBT 54 min Five years of DBT < 90 min Helicopter Transfer Local EMS should generally be used if available and 30 minute time to destination hospital Whenever possible, helipad adjacent to ED Ground/Air Transfer: Enhance First Responders transportation Early activation of Air Onsite Helipad: Availability of Transport Helicopter capable of transporting patients on 10 minute notice 24/7. When available alternate transport options identified. When Helicopter Not not Available: Identify Plan B: Who is next Immediately activate helicopter transport during initial communication between referring hospital ED and receiving hospital regarding need for reperfusion Referral team activates: Establish a system whereby all patient transfers of any type can be specified as time critical within one hour versus diversion possible