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ACUTE CORONARY SYNDROME

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pseudo aneurysm. Arrhythmia: *Tachyarrhythmia's. supraventricular. ventricular *Brady arrhythmias ... Lv aneurysm. Lv thrombosis Arterial embolism. ADMIRAL ... – PowerPoint PPT presentation

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Title: ACUTE CORONARY SYNDROME


1
ACUTE CORONARY SYNDROME
  • ACUTE CORONARY SYNDROME (ACS), including those
    associated with or without ST- segment elevation,
    share in common pathophysiology mediated by
    activated platelets and thrombin superimposed on
    a culprit plaque

2
ACS
  • No ST elevation
  • Unstable angina
  • NSTEMI
  • NQMI
  • QMI
  • ST elevation
  • QMI
  • NQMI

3
B. Primary
A. Secondary
C. Postinfarction (lt 2 weeks)
Classification
Braunwald classification of unstable angina Braunwald classification of unstable angina Braunwald classification of unstable angina Braunwald classification of unstable angina Braunwald classification of unstable angina


I New onset, severe or accelerated angina IA IB IC
II Subacute rest angina (gt 48 hours ago) IIA IIB IIC
III Acute rest angina (within 48 hours) IIIA IIIB IIIC
4
MI ST elevationNew bundle branch blockECG changes of posterior MIEvolution of Q waves 2  upper limit of CK-MB, CK Troponins T gt 0.2 ng/dlTroponin I gt 1.0-1.5 ng/dl

       Minimal injury Aborted ST elevation MITransient ST elevationST depressionT inversionMinor non-specific ECG changes lt 2  elevation CK-MB, CK Troponins T 0.01-0.2 ng/dl Troponin I 0.1 or 0.4 ng/dl to 1.0-1.5 ng/dl

       UA Transient ST elevationST depressionT inversionMinor non-specific ECG changesNormal ECG CK-MB, CK below upper limit Troponins T lt 0.01 ng/dl Troponin I lt 0.1 or 0.4 ng/dl
5
Prior risk
  -   older age (gt 65 years)
  -   prior myocardial infarction or heart failure
  -   co morbidity diabetes, hypertension
  -   impaired renal function
6
Acute ischemic risk
  -   refractory or recurrent ischemic pain
  -   ECG ST segment depression or transient ST elevation during pain
  -   ECG T wave inversion (lower risk than ST segment depression or transient ST elevation)
  -   impaired left ventricular function with ischemia
  -   release of cardiac enzymes CK, CK-MB, troponin T or troponin I
  -   raised C reactive protein (high sensitivity assay)
7
Management of AMI
  • ASA or other anti platelets
  • O2
  • Analgesics
  • Anticoagulants
  • GP IIb/IIIa inhibitors
  • Nitrate
  • B blocker
  • ACEi
  • Thrombolytic
  • Mechanical reperfusion

8
PCI in AMI
  • Primary
  • Rescue
  • Early lt 4 days
  • Deferred gt 4 days

9
Complication of AMI
  • Mechanical
  • Pump failuregtgtshock
  • Free wall rupture
  • Interventricular rupture
  • Papillary muscle rupturegtgtMR
  • pseudo aneurysm
  • Arrhythmia
  • Tachyarrhythmia's
  • supraventricular
  • ventricular
  • Brady arrhythmias
  • Bundle branch block

10
Other complications of AMI
  • Recurrent chest pain
  • Recurrent MI
  • Pericarditis
  • Deep vein thrombosisgtgtPulmonary emboli
  • Lv aneurysm
  • Lv thrombosisgtgtArterial embolism

11
ADMIRAL abciximab before direct angioplasty and
stenting in myocardial infarction regarding acute
and long-term follow300 pt, GP IIb/IIIa inhibitor
  • Composite end point at 30 days 6 abciximab and
    14.6 in the placebo
  • Mortality at 30-day 3.4 abciximab group and
    6.6 in the placebo
  • Urgent revascularization 1.3 abciximab and
    6.6 in placebo
  • Mortality at 6 months 3.4 abciximab group and
    7.3 in the placebo
  • Composite end point at 6 months 7.4 abciximab
    and 15.9 in the placebo


  • NEJM 2001344

12
CADILLAC controlled abciximab and device
investigation to lower late angioplasty
complications2081 pt effect of IIb/IIIa
inhibitor
  • Primary out come at 6 m MI, death, TVR, CVA
  • Hospital mortality 1-1.6
  • Strokes 0.4
  • Re-infarction 0.6 PTCA
  • 0 PCTA abciximab
  • 0.8 stent
  • 0.2 stent abciximab
  • TVR 2.3 PTCA
  • 0.2 PCTA abciximab
  • 0.8 stent
  • 0.2 stent abciximab


  • AHA 1999

13
CADILLAC controlled abciximab and device
investigation to lower late angioplasty
complications
  • Recurrent ischemia
  • 4.9 PTCA
  • 1.4 PTCA
    abciximab
  • 3.9 stent
  • 1.2
    stent abciximab


  • AHA 1999

14
GUSTO V global use of strategies to open
occluded coronary arteries16588 pt
fibrinolytic/- GP IIb/IIIa inhibitor
  • Mortality at 24-h 2.3 with reteplase and 2.2
    in reteplase abciximab
  • Mortality at 7-d 4,5 with reteplase and 4.3 in
    reteplase abciximab
  • Mortality at 30-d 5.9 in reteplase and 5.6 in
    the reteplase abciximab
  • Stroke 0.3 in reteplase and 0.2 in the
    reteplase abciximab
  • Re-infarction 3.5 in reteplase and 2.3 in the
    reteplase abciximab
  • MACE at 7-d 20.6 in reteplase and 16.2 in
    reteplase abciximab
  • More non-intracranial bleeding complications in
    the combination group
  • The rates of intracranial hemorrhage and
    non-fatal disabling stroke were similar in
    patientslt 75 years


  • Lancet 2001

15
STENT-PAMI primary angioplasty in myocardial
infarctionPCI/- stent in ACS 900 pt
  • angina at 6 months occurred in 11.3 patients in
    the stent and 16.9 in angioplasty
  • TVR 7.7 vs. 17.0 in stent and angioplasty
  • The primary end point 12.6 and 20.1
  • 6-month mortality 4.2 and 2.7



NEJM 1999
16
STENT-PAMI primary angioplasty in myocardial
infarctionLong term effect of PCI as compared to
streptokinase for AMI395 pt
  • Mortality over 5 ys was 13 in the angioplasty,
    24 in the streptokinase
  • TVR lt30 ds in PCI 12.4 and in thrombolytic
    42.8
  • TVR gt30 ds in PCI 34.1 and in thrombolytic
    28.3
  • Re-MI in first 30 days 0.5 in angioplasty and
    9 in streptokinase.
  • Re-MI After 30 days 6 in the angioplasty vs.
    12 in streptokinase



  • NEJM 1999

17
STENTIM-2Comparison of PTCA and Stenting in
AMI-2 in 211 pt
  • Re-infarction 4 in PTCA and 3.6 in stent
  • Repeat revascularization 5.4 in PTCA and 5 in
    stent
  • In-hospital event free survival 94.6 in PTCA
    and 95 in stent
  • Six-month event free survival 72.7 in PTCA and
    82 in stent
  • Six-month revascularization 26.4 in PTCA and
    16.8 in stent
  • One year revascularization 28.2 in PTCA and
    17.8 in stent
  • Restenosis 39.6 in PTCA and 25.3 in stent


  • JACC 2000

18
GUSTO IV ACSeffect of GP IIb/IIIa inhibitor
in7800 pt
  • primary endpoint death or myocardial infarction
    at 30 days.
  • FINDINGS 30- day death and MI 8.0 patients on
    placebo

  • 8.2 abciximab on 24 h

  • 9.1 on 48 h abciximab died
  • This study indicates that abciximab is not
    beneficial as first-line medical treatment in
    patients admitted with acute coronary syndromes.


  • Lancet. 2001 Jun

19
GUSTO-IV PilotEarly PCI after reteplase/-
abciximab
  • 30-day composite end point in early PCI
  • (death, re-infarction, urgent revascularization)
    (5.6)
  • Death 3.4,
  • Re-vascularization 1.6
  • Re-infarction 1.2
  • 30-day composite end point in no early PCI
  • (death, re-infarction, urgent revascularization)
    (16)
  • Re-vascularization 9.3
  • Re-infarction 4.9


  • JACC 200036

20
STATStenting vs. Thrombolysis in AMI Trial
in123 pt
  • Primary end point at 6-month 24.2 in stent vs.
    55.7 in t-PA
  • Re-infarction 6.5 in stent and 16.4 in t-PA
  • Stroke 1.6 in stent and 4.9 in t-PA
  • TVR 14.5 in stent and 49.5 in t-PA
  • Recurrent UA 9.7 in stent and 26.2 in t-PA


  • JACC 2001

21
IMPACT-AMIt-PA /- IIb/IIIa integrin receptor
blockade
  • The primary end point was TIMI grade 3 flow at
    90-minute angiography. Secondary end points were
    time to ST-segment recovery, an in-hospital
    composite (death, reinfarction, stroke,
    revascularization procedures, new heart failure,
    or pulmonary edema), and bleeding variables
  • The highest Integrilin dose groups had more
    complete reperfusion (TIMI grade 3 flow, 66
    versus 39 for placebo-treated patients P.006)
  • Shorter median time to ST-segment recovery (65
    versus 116 minutes for placebo P.05).
  • Mortality 5.6 in integrin treated and 3.6 in
    placebo treated group
  • Death and re-infarction 8 in integrin treated
    and 7.3 in placebo treated
  • The groups had similar rates of the composite end
    point (43 versus 42 for placebo-treated
    patients)


  • Circulation 199795

22
RAPPORTReoPro and Primary PTCA Organization and
Randomization Trial
  • The primary end point was death, reinfarction, or
    any (urgent or elective) target vessel
    revascularization (TVR) at 6 months
  • abciximab significantly reduced the incidence of
    death, reinfarction, or urgent TVR at all time
    points assessed 9.9 versus 3.3, at 7 days
  • 11.2 versus 5.8, at 30 days and 17.8
    versus 11.6, at 6
  • months
  • The effect of abciximab with respect to
    death or reinfarction 4.7 versus 1.4, at 7
    days 5.8 versus 3.2, at 30 days and 12.0
    versus 6.9, at 6 months


  • Circulation 199898

23
TIMI-14 (Substudy)Thrombolysis in Myocardial
Infarction-14 (alteplase, abciximab) alone or
abciximab reduced dose of lytics
  • ST segment resolution 59 in combination of tPA
    abciximab vs. 37 in full dose tPA alone
  • 30-day mortality 1.1 with complete ST
    resolution
  • 4.7 with
    incomplete ST resolution
  • 7.1 with no ST
    resolution


  • Circulation 2000101

24
ISAR-2Intracoronary Stenting and Antithrombotic
Regimen-2coronary stenting /- abciximab
  • 30-day MACE 5 in abciximab and 10.5 in heparin
    groups
  • 30-day death 2 in abciximab and 4.5 in heparin
    groups
  • 30-day MI 0.5 in abciximab and 1.5 in heparin
    groups
  • 30-day TVR 3 in abciximab and 5 in heparin
    groups
  • At one year there was 5.7 absolute reduction in
    cardiac events
  • At six-month restenosis 31.1 in abciximab and
    30.6 in heparin groups


  • JACC 200035
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