1 / 89

STEMI Primer: 101 From Presentation to Cath Lab

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.

jeremyr
Download Presentation

STEMI Primer: 101 From Presentation to Cath Lab

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. STEMI Primer: 101From Presentation to Cath Lab Michael S. Blanc, FACC, FSCAI Community Heart & Vascular Center San Angelo Community Medical Center San Angelo, TX

  2. https://youtu.be/9Wmqq3TfV5w

  3. “Vulnerable” Plaque and “Stable” Plaque Libby. Circulation. 1995;91:2844-2850.

  4. Severity of Coronary Artery Stenosis before Acute MI Most MIs associated with non-flow limiting lesions Circulation Vol 93, No12 June 15, 1996 Ambrose, Giroud, Little, Nobuyoshi, et al

  5. 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

  6. Age > 70 Prior myocardial infarction Female gender Hypertension History of CHF Hyperlipidemia Diabetes Race Clinical Criteria ECG Criteria Chest x-ray-cardiomegaly Markedly elevated cardiac enzymes Elevated BUN Hemodynamic Criteria Complications VSD/PMD-rupture Myocardial rupture Acute Phase Risk Stratification: Pre-infarction characteristics Continuing Medical Implementation …...bridging the care gap

  7. 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

  8. Hypotension Pulsus alternans Reduced volume carotid LV apical enlargement/displacement Sustained apex - to S2 Soft S1 Paradoxically split S2 S3 gallop (not S4 = impaired LV compliance) Mitral regurgitation Pulmonary congestion rales Clinical Signs of LV Dysfunction Continuing Medical Implementation …...bridging the care gap

  9. Acute Phase Risk Stratification:Importance of LV dysfunction Continuing Medical Implementation …...bridging the care gap

  10. Complications of Acute Myocardial Infarction • Arrhythmic Complications • Mechanical Complications • Ischemic Complications • Miscellaneous Complications • [DVT, PE, Pericarditits, TPA complications, Pneumonia]

  11. Mechanical Complications of Acute Myocardial Infarction • Papillary Muscle Rupture – Acute MR • Ventricular Septal Defect • Right Ventricular MI • Free Wall Rupture • Cardiogenic shock • Cardiac Tamponade

  12. 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

  13. 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

  14. b-Block ASSENT-2 CCU GUSTO GUSTO-3 GISSI-1 Pre-CCU ISIS-2 Early Mortality After AMI Mortality at 25 - 30 Days SK SK+ASA tPA tPA & rPA tPA & TNK Continuing Medical Implementation …...bridging the care gap

  15. 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

  16. Primary endpoint: CV death, MI or stroke 12 11 10 9 8 7 6 5 4 3 2 1 0 Clopidogrel 11.0 9.3 Ticagrelor K-M estimated rate (% per year) HR: 0.85 (95% CI = 0.74–0.97), p=0.02 0 1 2 3 4 5 6 7 8 9 10 11 12 Months No. at risk Ticagrelor 4,201 3,887 3,834 3,732 3,011 2,297 1,891 Clopidogrel 4,229 3,892 3,823 3,730 3,022 2,333 1,868

  17. Beta-Blockers

  18. COMMIT: Study design INCLUSION: >45,000 patients with suspected acute MI (ST change orLBBB) 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

  19. Effects of Metoprolol COMMIT (N = 45,852) Totality of Evidence (N = 52,411) Death13%P=0.0006 ReMI22%P=0.0002 30% relative increase in *cardiogenic shock VF15%P=0.002 Lancet. 2005;366:1622. *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

  20. 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: • signs of heart failure, • evidence of a low output state, • increased risk for cardiogenic shock, or • 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

  21. 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: • signs of heart failure, • evidence of a low output state, • increased risk for cardiogenic shock, or • 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

  22. Beta-Blockers • Recommendations - Class III (A) • IV beta blockers SHOULD NOT be administered to STEMI patients who have any of the following: • signs of heart failure • evidence of a low output state • increased risk* for cardiogenic shock • 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

  23. Statin Evidence: MIRACL Study Primary Efficacy Measure Placebo 17.4% 15 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 Cumulative Incidence (%) 5 Relative risk = 0.84P = .048 95% CI 0.701-0.999 0 0 4 8 12 16 Time Since Randomization (weeks) Schwartz GG, et al. JAMA. 2001;285:1711-1718.

  24. Reperfusion

  25. “Time is Muscle”

  26. 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%

  27. 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)

More Related