不稳定型心绞痛和非st段抬高心梗的治疗课件.ppt
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1、Acute Coronary Syndromes:Management of UA/NSTEMIOverview of 2003 Updates to the ACC/AHA Guideline for UA/NSTEMI Assess likelihood of CAD Risk stratification Target therapy:more aggressive treatment in higher-risk patients Anti-ischemic,antithrombotic therapy Invasive vs conservative strategy Dischar
2、ge planning(risk factor modification and long-term medical therapy)ACC/AHA,American College of Cardiology/American Heart Association;UA,unstable angina;NSTEMI,nonST-segment elevation myocardial infarction.Braunwald E,et al.J Am Col.Cardiol.2000;36:970-1062.Acute Management of UA/NSTEMIAnti-Ischemic
3、TherapyOxygen,bed rest,ECG monitoringNitroglycerin-BlockersACE inhibitorsUA,unstable angina;NSTEMI,non-ST-segment elevation myocardial infarction;ECG,electrocardiogram;ACE,angiotensin-converting enzyme.Braunwald E,et al.J Am Coll Cardiol.2000;36:970-1062.Antithrombotic TherapyAntiplatelet therapyAnt
4、icoagulant therapyPossible ACSAspirinAspirin+IV Heparin+IV Platelet GP IIb/IIIa AntagonistDefinite ACS With Invasive Strategy(Catheterization/PCI)or High Risk(IIa)*ClopidogrelAspirin+SQ LMWH*orIV HeparinLikely/Definite ACSClopidogrel*Class IIa:enoxaparin preferred over UFH unless CABG planned within
5、 24 hours.ACC,American College of Cardiology;AHA,American Heart association;ACS,acute coronary syndrome;PCI,percutaneous coronary intervention;SQLMWH,subcutaneous low molecular-weight heparin;IV,intravenous.Braunwald E,et al.J Am Coll Cardiol.2000;36:970-1062.ACC/AHA Class I Recommendations for Anti
6、thrombotic Therapy*17.16.5*PlaceboASA05101520Patients(%)Unstable Angina 25.011.0*ASA01020303.31.9*ASA0123411.89.4*ASA051015Acute MIAspirin in Acute Coronary Syndromes*P.0001Death or MI*P=.003Reocclusion*P=.012MI*P.001DeathN=3973995134198587860085878600MI,myocardial infarction;ASA,acetylsalicylic aci
7、d;RISC,Research on InStability in Coronary artery disease.RISC Group.Lancet.1990;336:827-830.Roux S,et al.J Am Coll Cardiol.1992;19:671-677.ISIS-2.Lancet.1988;2:349-360.PlaceboPlaceboPlaceboAspirin in Acute Coronary Syndromes12.93.9*ASA05101511.93.3*ASA05101512.96.2*ASA0510152.21.3*ASA00.511.522.5UA
8、/NSTEMIPrimary PreventionStable Angina*P.0001MI*P=.0003MI*P=.008Death or MI*P=.012Death or MIN=1103411037155178279276118121MI,myocardial infarction;ASA,acetylsalicylic acid;RISC,Research on InStability in Coronary artery disease;ISIS-2,Second International Study of Infarct Survival.PHS.N Engl J Med.
9、1989;321:129-35.Ridker PM,et al.AJC.1991;114:835-839.Cairns JA,et al.N Engl J Med.1985;313:1369-1375.Theroux P,et al.N Engl J Med.1988;319:1105-1111.PlaceboPlaceboPlaceboPlaceboPatients(%)Indirect Comparisons of ASA Doses on Vascular Events in High-Risk Patients*Odds reduction.Treatment effect P.000
10、1.ASA,acetylsalicylic acid.Adapted with permission from BMJ Publishing Group.Antithrombotic Trialists Collaboration.BMJ.2002;324:71-86.0.51.01.52.0500-1500 mg34 19160-325 mg19 2675-150 mg12 32162 mg/d(n=2179)Primary end point16.418.6Death,MI,stroke6.26.1Death2.81.7MI2.02.1Stroke2.12.8Urgent hospital
11、 care9.510.6Urgent resuscitation7.310.0Internal bleeding2.43.3Any bleeding11.115.4Transfusion1.02.0Clopidogrel+ASA(N=6259)Placebo+ASA*(N=6303)CURE:Major Bleeding at 1 year by ASA Dose 200 mg(N=4110)3.7%4.9%P value for trend.0001.0009*P=.0001.P=.0009.Adapted from Peters RJG,et al.Circulation.2003;108
12、:1682-1687.ASA DoseRR:Death/MIASA Alone 68/655=10.4%Heparin+ASA 55/698=7.9%BBBBBBB0.1110Summary Relative Risk0.67(0.44-0.1.02)TherouxRISCCohen 1990ATACSHoldrightGurfinkelComparison of Heparin+ASA vs ASA AloneASA,acetylsalicylic acid;RISC,Research on InStability in Coronary artery disease;ATACS,Antit
13、hrombotic Therapy in Acute Company Syndromes;RR,relative risk;MI,myocardial infarction.Oler A,et al.JAMA.1996;276:811-815.(with permission)TIMI,Thrombosis in Myocardial Infarction;ESSENCE,Efficacy and Safety of Subcutaneous Enozapam in NonQ-Wave Coronary Events;UHF,unfractionated heparin;ENOX,enoxap
14、arin;MI,myocardial infarction;OR,odds ratio.Antman EM,et al.Circulation.1999;100:1602-1608.(with permission)TIMI IIB/ESSENCE Metanalysis:Enoxaparin vs Unfractionated Heparin8.6 7.1 0.82(0.69-0.97)18 .026.5 5.2 0.79(0.65-0.96)21 .025.3 4.1 0.77(0.62-0.95)23 .021.81.4 0.80(0.55-1.16)20 .24 0.512Day281
15、443UFH(%)ENOX(%)OR(95 CI)Favors ENOXFavors UFHPORDeath or MI%0123456789081624324048566472Patients(%)Hours from Randomization7.3%5.5%RRR 24%P=.026UFH(n=1957)ENOX(n=1953)UHF,unfractionated heparin;ENOX,enoxaparin;RRR,relative risk ratio.Antman EM.Circulation.1999;100:1593-1601.(with permission)TIMI II
16、B:Early Phase Death/MI/Urgent Revasc0123456789081624324048566472Patients(%)Hours from Randomization7.3%5.5%RRR 24%P=.026UFH(n=1957)ENOX(n=1953)4.6%1.8%0%2%4%6%UFHEnoxaparinP=.03Major Bleeds96 HoursINTERACT:Enoxaparin vs Unfractionated Heparin With GP IIb/IIIa InhibitorsGoodman SG,et al.Circulation.2
17、003;107:238-244.9%5%0%2%4%6%8%10%Death/MI30 DaysP=.031UFHEnoxaparinPercentA-Phase Study DesignUA/NSTEMIFinal A visit 30 days Randomize-24 hours Chest pain Min 0 hourMax 120 hourTirofiban+ASA Hour 0Aggressive or conservativecare per local practice20261961ENOX1mg/kg q12 hrUFHWeight-adjustedZZ Treat&Ev
18、aluate for Z-Phase2018195239871 endpoint 7 daysBlazing M.presented at ACC 2003.0102030024681012UFHEnoxaparinUFHENOXDays From RandomizationEvent Rates(%)Day 78.4%(169 events)9.4%(184 events)Blazing M.presented ACC 2003.Enox Test vs OutcomesMoliterno DJ,et al.JACC.2003;42:1132-1139.(with permission)De
19、ath/MI/Urg TVRBleeding302520151050200 250 300 350 400 450 500 550 600200 250 300 350 400 450 500 550 600Probability of MACE(%)Probability of Any Bleeding(%)302520151050ENOX Time(sec)ENOX Time(sec)Direct Thrombin Inhibitor Trialists CollaborationDirect Thrombin Inhibitor Trialists Collaborative Group
20、.Lancet.2002;359:294-302.(with permission)11 RCTS36,000 PtsACS,PCI Death orMyocardialInfarctionDirect ThrombinInhibitorHeparin(N=18,736)(N=17,184)OR(95%Cl)End of treatment7 days30 daysEnd of treatment7 days3 daysDeathMyocardialInfarctionEnd of treatment7 days30 daysEnd of treatment7 days30 daysStrok
21、eMajor bleedingduring treatmentIntracranial bleeding during treatment815(4.3%)883(5.1%)947(5.0%)990(5.8%)1399(7.4%)1409(8.2%)355(1.9%)346(2.0%)422(2.2%)395(2.3%)685(3.6%)642(3.7%)522(2.8%)596(3.5%)601(3.2%)672(3.9%)876(4.7%)917(5.3%)62(0.33%)60(0.35%)72(0.38%)70(0.41%)120(0.64%)110(0.64%)360(1.90%)4
22、03(2.30%)21(0.11%)28(0.16%)0.01.02.0Direct ThrombinInhibitorHeparin Better0.85(0.77-0.94%)0.88(0.80-0.96%)0.91(0.84-0.99%)0.97(0.83-1.13%)1.00(0.87-1.16%)1.01(0.90-1.12%)0.80(0.71-0.90%)0.81(0.72-0.91%)0.87(0.79-0.95%)0.95(0.66-1.35%)0.94(0.68-1.31%)1.01(0.78-1.31%)0.75(0.65-0.87%)0.72(0.42-1.23%)Ea
23、rly invasive strategy+/-GP IIb/IIIa Catheterization within 8 hours of last subcutaneous doseUA/NSTEMIIdentified,LMWH-GP IIb/IIIa+GP IIb/IIIa Catheterization between 8-12 hours of last subcutaneous doseNo additionalUFH or LMWHAdditionalEnoxaparin0.3 mg/kg IV bolusSupplementwith UFH 50U/kg,aim forACT
24、200-250Supplementwith UFH 0.1 g/LCAPTUREPRISM14.810.27.59.105101520TnI 0.1 g/LP0.1P.0014.919.65.25.80510152025HeparinTirofibanHeparinAbciximab+HeparinDeath or MI at 30 days(%)GP IIb/IIIa Inhibition in TnI+Patients by Revascularization:PRISM StudyTnI,troponin I;PRISM,Platelet Receptor Inhibition for
25、Ischemic Syndrome Management study;MI,myocardial infarction.Heeschen C,et al.Lancet.1999;354:1757-1762.(with permission)Death/MI at 30 Days0.37(0.15-0.93)P=.020.30(0.10-0.84)P=.0041612840051015202530Event rate(%)Follow-up(days)No revascularizationRevascularizationHeparinHeparinTirofiban TirofibanGP
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