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PCI  after  MI,  When ? Ahmed Magdy, MD, FACC, FSCAI National Heart Institute, Cairo
Optimizing  Reperfusion  for STEMI ,[object Object],[object Object],[object Object]
Assessing Reperfusion Options for Patients with STEMI 1 ,[object Object],[object Object],* If presentation is <3 hours from onset and no delay to an invasive strategy, there is no preference  for either strategy JACC 44: 671, 2004 Fibrinolysis preferred if: Invasive strategy preferred if: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Patients Transported by EMS After Calling 9-1-1 Onset of  STEMI  Symptoms Call 911 Call Fast 9-1-1  EMS  Dispatch ,[object Object],[object Object],[object Object],EMS  Triage Plan Not PCI Capable Hospital PCI Capable Hospital Interhospital Transfer Hospital Fibrinolysis: Door-to-needle  within<30 min EMS transport:EMS to Balloon within 90  min Patient self-transport: Hospital Door-to-Balloon within 90 min EMS transport EMS on scene   Within 8 min Dispatch 1 min Patient 5 min after Symptom   onset Goals Total ischemic time: Within 120 min * * Golden hour = First 60 min Adapted from Panel A Figure 1 Antman et al. JACC 2004;44:676 .
 
Gersh, B. J. et al. JAMA 2005;293:979-986. 1)Time is myocardium  2)Infarct size is outcome   Relationship Between Duration of Symptoms of MI Before Reperfusion Therapy, Mortality Reduction, and Extent of Myocardial Salvage Modified by collaterals,ischemic preconditioning,myocardial oxygen uptake, other vessels
Gersh, B. J. et al. JAMA 2005;293:979-986. 1)Time is myocardium  2)Infarct size is outcome   Relationship Between Duration of Symptoms of MI Before Reperfusion Therapy, Mortality Reduction, and Extent of Myocardial Salvage Modified by collaterals,ischemic preconditioning,myocardial oxygen uptake, other vessels  Symptom onset to hosp Arrival  2 hr Thrombolysis given, 2 ½ hr Symptom onset to balloon 3 ½ hr Thrombolysis  induced reperfusion  3 ½ hr
Importance of Rapid Time to  Treatment With  Fibrinolysis  in STEMI Time from onset of symptoms to treatment (hours) Absolute % difference  in mortality at 35 days 3.5%   2.5%     1.8%     1.6%     0.5%     0.0 1.0 3.0 2.0 4.0 0 – 1 2 – 3 4 – 6 7 – 12 12 – 24 The Fibrinolytics Therapy Trialists’ collaborative group.  Lancet . 1994; 343:311.
PCI  In-hospital Mortality  vs Door to Balloon Time Door to Balloon Time (hours) In-hosp Death Rate 0-1.4 1.5-1.9 2.0-2.9 >3.0 N= 2,322 Brodie BR, JACC 47, 2006 N=384 N=493 N=750 N=673
 
 
 
Recent Influences of Practice Salvage is Time Dependant  ,[object Object],[object Object],[object Object]
Mortality rates with  primary PCI  as a function of PCI-related   time delay Circle   sizes  = sample size of the  individual study. Solid line = weighted meta-regression .  62 min Benefit Favors PCI Harm Favors Lysis For Every 10 min delay to PCI: 1% reduction in mortality difference towards lytics P = 0.006 0 20 40 60 80 100 PCI-Related  Time Delay  (door-to-balloon -  door to needle) Absolute Risk Difference in Death  (%) -5 0 5 10 15 Nallamothu BK, Bates ER.  Am J Cardiol.  2003;92:824-6
Causes of Time Waste ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Thrombolytics are Frequently  Used During Off Hours
PCI post thrombolysis in STEMI ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
PCI post thrombolysis in STEMI: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],CAPTIM RESCUE, REACT PACT PRAGUE GRACIA 2 ASSENT-4 FINESSE   SIAM III GRACIA 1 CAPITAL AMI WEST CARESS « Open artery hypothesis » OAT SWISSI II
[object Object],PCI post thrombolysis in STEMI: ,[object Object],[object Object]
PCI post  thrombolysis in STEMI: RATIONALE  ,[object Object],[object Object],[object Object]
 
Rescue PCI
 
Impact of TIMI Flow  Pre-PCI on Infarct Size
Facilitated Angioplasty
 
 
 
 
 
 
Primary, secondary and bleeding end points in FINESSE End points Primary PCI (%)  Abciximab +PCI%)  (abcixima/ reteplase) -facilitated PCI (%)  p, combined+ PCI vs primary PCI  p, combin +PCIvs abciximab-facilitate  Primary end point*  10.7 10.5 9.8 NS NS All-cause mortality  4.5 5.5 5.2 NS NS Complications of MI  8.9 7.5 7.4 NS NS Death  4.5 5.5 5.2 NS NS TIMI major bleeding  2.6 4.1 4.8 0.025 NS TIMI minor bleeding  4.3 6.0 9.7 <0.001 0.006
 
 
(Earlier ) Delayed PCI
OAT Occluded Artery Trial
OAT Occluded Artery Trial
Disadvantages of OAT
 
 
 
 
 
 
 
 
 
 
Comments on CARESS ,[object Object],[object Object],[object Object]
Post-Lysis PCI studies GRACIA-1 SIAM III CAPITAL MI CARESS P=0.001 P=0.0008 P=0.04 P=0.001 N=1436
 
T rial of  R outine  AN gioplasty and  S tenting after  F ibrinolysis to  E nhance  R eperfusion in  A cute  M yocardial  I nfarction The TRANSFER-AMI trial   Warren J. Cantor, David Fitchett, Bjug Borgundvaag, Michael Heffernan, Eric A. Cohen, Laurie J. Morrison, John Ducas, Anatoly Langer, Shamir Mehta, Charles Lazzam, Brian Schwartz, Vladimir Dzavik, Amparo Casanova, Paramjit Singh, Shaun G. Goodman on behalf of the TRANSFER-AMI Investigators
Background ,[object Object],[object Object],[object Object]
Objective ,[object Object],[object Object],[object Object],[object Object]
PCI Centre Cath Lab Community Hospital Emergency Department   Cath / PCI within 6 hrs regardless of reperfusion status Cath and Rescue PCI    GP IIb/IIIa Inhibitor TNK + ASA + Heparin / Enoxaparin + Clopidogrel “ Pharmacoinvasive Strategy” Urgent  Transfer to PCI Centre Assess chest pain, ST   resolution at 60-90 minutes after randomization ‘ High Risk’ ST Elevation MI within 12 hours of symptom onset Failed Reperfusion* Successful Reperfusion Elective Cath     PCI > 24 hrs later “ Standard Treatment” * ST segment resolution < 50% & persistent chest pain, or hemodynamic instability Repatriation of stable patients within 24 hrs of PCI Randomization stratified by age (≤75 vs. > 75) and by enrolling site
Procedures Cardiac Cath performed (%) Time- TNK to Cath (hrs) PCI performed (%) Stent used (% of PCI cases) Time- TNK to PCI (hrs) PCI within 6 hrs of TNK (%) PCI within 12 hrs of TNK (%) GP IIb/IIIa inhibitor use (%) Time- TNK to GP IIb/IIIa inhib. (hrs)  IABP use (%) CABG performed (%) Standard  Treatment (n=508) 82 27 (4, 69) 62 98 18 (4, 73) 38 47 53 11 (4, 63) 6 8 Pharmacoinvasive Strategy (n=522) 97 3 (2, 4) 84 98 4 (3, 5) 89 97 73 4 (3, 5) 7 6 PRELIMINARY
Selected Medications Used ASA 1 st  6 hrs Clopidogrel 1 st  6 hrs * Heparin Enoxaparin Beta Blocker 1 st  6 hrs ASA at discharge Clopidogrel at discharge Beta Blocker at discharge ACE Inhibitor at discharge Lipid Lowering at discharge Standard  Treatment (n=508) 97 69 57 55 61 85 73 79 74 80 Pharmacoinvasive Strategy (n=522) 98 87 57 51 55 85 79 81 73 81 * p< 0.05 PRELIMINARY
0 2 4 6 8 10 12 14 16 18 0 5 10 15 20 25 30 10.6 16.6 Days from Randomization % of Patients n=496 n=508 422 468 415 466 415 463 414 461 414 460 412 457 Primary Endpoint: 30-Day Death, re-MI, CHF, Severe Recurrent Ischemia, Shock  PRELIMINARY OR=0.537 (0.368, 0.783); p=0.0013   Standard PCI > 24 hrs (n=496) Invasive < 6 hrs (n=508)
Components of Primary Endpoint Death Reinfarction Recurrent Ischemia Death/MI/Ischemia New / worsening CHF Cardiogenic Shock Standard  Treatment (n=498) 3.6 6.0 2.2 11.7 5.2 2.6 Pharmacoinvasive Strategy (n=512) 3.7 3.3 0.2 6.5 2.9 4.5 P-Value 0.94 0.044 0.019 0.004 0.069 0.11 PRELIMINARY
Safety Endpoints - Bleeding Intracranial hemorrhage TIMI scale Major Major (non-CABG-related) GUSTO scale Moderate Severe Severe (non-CABG-related) Transfusions Standard  Treatment (n=498) 1.2 4.6 3.2 2.2 1.4 1.2 5.5 Pharmacoinvasive Strategy (n=512) 0.2 4.3 2.2 3.5 0.6 0.6 7.1 P-Value 0.066 0.88 0.33 0.26 0.22 0.34 0.31 PRELIMINARY
Summary ,[object Object]
Summary  ,[object Object],[object Object],[object Object]
Conclusions ,[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],TRANSFER-MI Trial Design: TRANSFER-MI was a randomized study comparing pharmacoinvasive strategy  (transfer to PCI center for routine early PCI within 6 hrs)  with standard treatment (early transfer only for failed reperfusion) for  high-risk  STEMI patients receiving thrombolysis at  non-PCI centers (N=1,060).  The primary endpoint was 30-day composite of death, reinfarction, recurrent Ischemia, CHF, shock. Standard Pharmacoinvasive 30 Day Composite (death, reinfarction, recurrent ischemia, CHF, shock)  OR = 0.537 p =0.0013 Kastrani, K et al. Presented at ACC, 2008  @2008, American Heart Association. All rights reserved. % of pts
Interpretation ,[object Object],[object Object]
PCI for AMI Strategies
In summary: European GL
Egypt COMBATMI 2010  March 24-26, Cairo Sheraton Hotel
2010 4 th .  Acute  Cardiac Care Course   EGYPT COMBAT MI 2010 Cairo Sheraton, March 24-26, 2010

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PCI after MI - When is the optimal time for PCI after a myocardial infarction

  • 1. PCI after MI, When ? Ahmed Magdy, MD, FACC, FSCAI National Heart Institute, Cairo
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  • 6. Gersh, B. J. et al. JAMA 2005;293:979-986. 1)Time is myocardium 2)Infarct size is outcome Relationship Between Duration of Symptoms of MI Before Reperfusion Therapy, Mortality Reduction, and Extent of Myocardial Salvage Modified by collaterals,ischemic preconditioning,myocardial oxygen uptake, other vessels
  • 7. Gersh, B. J. et al. JAMA 2005;293:979-986. 1)Time is myocardium 2)Infarct size is outcome Relationship Between Duration of Symptoms of MI Before Reperfusion Therapy, Mortality Reduction, and Extent of Myocardial Salvage Modified by collaterals,ischemic preconditioning,myocardial oxygen uptake, other vessels Symptom onset to hosp Arrival 2 hr Thrombolysis given, 2 ½ hr Symptom onset to balloon 3 ½ hr Thrombolysis induced reperfusion 3 ½ hr
  • 8. Importance of Rapid Time to Treatment With Fibrinolysis in STEMI Time from onset of symptoms to treatment (hours) Absolute % difference in mortality at 35 days 3.5%  2.5%  1.8%   1.6%  0.5%  0.0 1.0 3.0 2.0 4.0 0 – 1 2 – 3 4 – 6 7 – 12 12 – 24 The Fibrinolytics Therapy Trialists’ collaborative group. Lancet . 1994; 343:311.
  • 9. PCI In-hospital Mortality vs Door to Balloon Time Door to Balloon Time (hours) In-hosp Death Rate 0-1.4 1.5-1.9 2.0-2.9 >3.0 N= 2,322 Brodie BR, JACC 47, 2006 N=384 N=493 N=750 N=673
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  • 14. Mortality rates with primary PCI as a function of PCI-related time delay Circle sizes = sample size of the individual study. Solid line = weighted meta-regression . 62 min Benefit Favors PCI Harm Favors Lysis For Every 10 min delay to PCI: 1% reduction in mortality difference towards lytics P = 0.006 0 20 40 60 80 100 PCI-Related Time Delay (door-to-balloon - door to needle) Absolute Risk Difference in Death (%) -5 0 5 10 15 Nallamothu BK, Bates ER. Am J Cardiol. 2003;92:824-6
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  • 17. Thrombolytics are Frequently Used During Off Hours
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  • 25. Impact of TIMI Flow Pre-PCI on Infarct Size
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  • 33. Primary, secondary and bleeding end points in FINESSE End points Primary PCI (%) Abciximab +PCI%) (abcixima/ reteplase) -facilitated PCI (%) p, combined+ PCI vs primary PCI p, combin +PCIvs abciximab-facilitate Primary end point* 10.7 10.5 9.8 NS NS All-cause mortality 4.5 5.5 5.2 NS NS Complications of MI 8.9 7.5 7.4 NS NS Death 4.5 5.5 5.2 NS NS TIMI major bleeding 2.6 4.1 4.8 0.025 NS TIMI minor bleeding 4.3 6.0 9.7 <0.001 0.006
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  • 51. Post-Lysis PCI studies GRACIA-1 SIAM III CAPITAL MI CARESS P=0.001 P=0.0008 P=0.04 P=0.001 N=1436
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  • 53. T rial of R outine AN gioplasty and S tenting after F ibrinolysis to E nhance R eperfusion in A cute M yocardial I nfarction The TRANSFER-AMI trial Warren J. Cantor, David Fitchett, Bjug Borgundvaag, Michael Heffernan, Eric A. Cohen, Laurie J. Morrison, John Ducas, Anatoly Langer, Shamir Mehta, Charles Lazzam, Brian Schwartz, Vladimir Dzavik, Amparo Casanova, Paramjit Singh, Shaun G. Goodman on behalf of the TRANSFER-AMI Investigators
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  • 56. PCI Centre Cath Lab Community Hospital Emergency Department Cath / PCI within 6 hrs regardless of reperfusion status Cath and Rescue PCI  GP IIb/IIIa Inhibitor TNK + ASA + Heparin / Enoxaparin + Clopidogrel “ Pharmacoinvasive Strategy” Urgent Transfer to PCI Centre Assess chest pain, ST  resolution at 60-90 minutes after randomization ‘ High Risk’ ST Elevation MI within 12 hours of symptom onset Failed Reperfusion* Successful Reperfusion Elective Cath  PCI > 24 hrs later “ Standard Treatment” * ST segment resolution < 50% & persistent chest pain, or hemodynamic instability Repatriation of stable patients within 24 hrs of PCI Randomization stratified by age (≤75 vs. > 75) and by enrolling site
  • 57. Procedures Cardiac Cath performed (%) Time- TNK to Cath (hrs) PCI performed (%) Stent used (% of PCI cases) Time- TNK to PCI (hrs) PCI within 6 hrs of TNK (%) PCI within 12 hrs of TNK (%) GP IIb/IIIa inhibitor use (%) Time- TNK to GP IIb/IIIa inhib. (hrs) IABP use (%) CABG performed (%) Standard Treatment (n=508) 82 27 (4, 69) 62 98 18 (4, 73) 38 47 53 11 (4, 63) 6 8 Pharmacoinvasive Strategy (n=522) 97 3 (2, 4) 84 98 4 (3, 5) 89 97 73 4 (3, 5) 7 6 PRELIMINARY
  • 58. Selected Medications Used ASA 1 st 6 hrs Clopidogrel 1 st 6 hrs * Heparin Enoxaparin Beta Blocker 1 st 6 hrs ASA at discharge Clopidogrel at discharge Beta Blocker at discharge ACE Inhibitor at discharge Lipid Lowering at discharge Standard Treatment (n=508) 97 69 57 55 61 85 73 79 74 80 Pharmacoinvasive Strategy (n=522) 98 87 57 51 55 85 79 81 73 81 * p< 0.05 PRELIMINARY
  • 59. 0 2 4 6 8 10 12 14 16 18 0 5 10 15 20 25 30 10.6 16.6 Days from Randomization % of Patients n=496 n=508 422 468 415 466 415 463 414 461 414 460 412 457 Primary Endpoint: 30-Day Death, re-MI, CHF, Severe Recurrent Ischemia, Shock PRELIMINARY OR=0.537 (0.368, 0.783); p=0.0013 Standard PCI > 24 hrs (n=496) Invasive < 6 hrs (n=508)
  • 60. Components of Primary Endpoint Death Reinfarction Recurrent Ischemia Death/MI/Ischemia New / worsening CHF Cardiogenic Shock Standard Treatment (n=498) 3.6 6.0 2.2 11.7 5.2 2.6 Pharmacoinvasive Strategy (n=512) 3.7 3.3 0.2 6.5 2.9 4.5 P-Value 0.94 0.044 0.019 0.004 0.069 0.11 PRELIMINARY
  • 61. Safety Endpoints - Bleeding Intracranial hemorrhage TIMI scale Major Major (non-CABG-related) GUSTO scale Moderate Severe Severe (non-CABG-related) Transfusions Standard Treatment (n=498) 1.2 4.6 3.2 2.2 1.4 1.2 5.5 Pharmacoinvasive Strategy (n=512) 0.2 4.3 2.2 3.5 0.6 0.6 7.1 P-Value 0.066 0.88 0.33 0.26 0.22 0.34 0.31 PRELIMINARY
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  • 67. PCI for AMI Strategies
  • 69. Egypt COMBATMI 2010 March 24-26, Cairo Sheraton Hotel
  • 70. 2010 4 th . Acute Cardiac Care Course EGYPT COMBAT MI 2010 Cairo Sheraton, March 24-26, 2010

Notas do Editor

  1. Review recent influences/randomized clinical trials (RCTs) in reperfusion that have impacted the guidelines and that this will be reviewed in-depth during this session: Superiority of PPCI over fibrinolysis if Door-to-Balloon completed in a timely fashion (Keeley &amp; Grines, European STEMI Guidelines 2003 heralded PPCI as the preferred method of reperfusion) Plain old balloon angioplasty (POBA) has become almost extinct in the states. The most commonly used PPCI in the US- Stents + GP IIb-IIIa Inhibitor Drug eluting stents (DES) in STEMI is on the horizon Finally, acknowledgement that Time Matters in PPCI. Zwolle group, CADDILAC data, Nallamathou and Bates (graph on Door- to- Balloon minus Door-to- Needle), etc. Recommendations for time to reperfusion for PPCI (time from first medical contact-to-balloon; door-to-balloon) have been lowered to within 90 minutes Phase III studies on GP IIb-IIIa + ½ dose TNK-tPA, ½ dose rPA as well as Enoxaparin + full dose TNK-tPA have been published and reviewed. Studies with other antithrombins (including, ASSENT-3 ASSENT-3+, HERO-2). Awaiting EXTRACT (ENOX vs UFH with any lytic). To date, nothing Phase III scheduled with Bivalrudin and newer fibrinolytics. Recent predominantly European STEMI trials influence the guidelines Prehospital received a Phase IIa rating-explored in TIMI 19, CAPTIM, ASSENT-3 + European Transfer Trials (PRAGUE experience, DANAMI-2) and their transferability to the US system is in question; Guidelines emphasize ‘Prehospital Destination Protocols’.
  2. “ The mortality benefit associated with primary percutaneous coronary intervention in ST-segment elevation myocardial infarction may be lost if door-to-balloon time is delayed by &gt; 1 hour as compared with fibrinolytic therapy door-to-needle time. Interventional cardiology laboratories endeavoring to achieve the benefits of primary percutaneous coronary intervention seen in randomized clinical trials should aim to match their short door-to-balloon times”. (pg. 824) Legend key (pg.825) Absolute risk reduction in 4- to 6-week mortality rates with primary PCI as a function of PCI-related time delay. Circle sizes reflect the sample size of the individual study. Values &gt; 0 represent benefit and values &lt; 0 represent harm. Solid line , weighted meta-regression .   Nallamothu BK, Bates ER. Am J Cardiol. 2003;92:824-6