m. valgimigli university of ferrara italy
DESCRIPTION
MultiStrategy Study design. M. Valgimigli University of Ferrara Italy. Background. Primary angioplasty is the current preferred therapeutic option for patients with ST-segment elevation myocardial infarction (STEMI). - PowerPoint PPT PresentationTRANSCRIPT
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M. ValgimigliM. ValgimigliUniversity of FerraraUniversity of Ferrara
ItalyItaly
MultiStrategyStudy design
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BackgroundBackground
Primary angioplasty is the current Primary angioplasty is the current preferred therapeutic option for patients preferred therapeutic option for patients with ST-segment elevation myocardial with ST-segment elevation myocardial infarction (STEMI).infarction (STEMI).Routine coronary stent implantation in Routine coronary stent implantation in patients with STEMI decreases the need patients with STEMI decreases the need for target vessel revascularization (TVR).for target vessel revascularization (TVR).
Grines CL, et al. N Engl J Med 1999; 341: 1949Grines CL, et al. N Engl J Med 1999; 341: 1949Stone G, et al. Stone G, et al. N Engl J Med 2002; 346: 957N Engl J Med 2002; 346: 957
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STEMI: STEMI: Stent and MortalityStent and Mortality
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STEMI: STEMI: Stent and ReinterventionStent and Reintervention
30 days30 days6 months6 months
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What about external What about external validity?validity?
In some of these trials In some of these trials randomization occurred after randomization occurred after angiography before PCI angiography before PCI In some of these studies In some of these studies randomization occurred after randomization occurred after balloon angioplastyballoon angioplastyIn none of these studies patients In none of these studies patients were recruited without prior were recruited without prior knowledge of coronary anatomyknowledge of coronary anatomy
Mostly excluded patients: Mostly excluded patients:
ShockShock Diffusely diseased or small Diffusely diseased or small
coronary coronary vesselvessel Large thrombus burden Large thrombus burden Severe coronary calcification or Severe coronary calcification or
tortuosity tortuosity Bifurcated lesionsBifurcated lesionsIdeal o
r good st
ent candidates
Ideal or g
ood stent c
andidates
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Participants:Participants: All Patients with STEMI randomly All Patients with STEMI randomly assigned to stenting or balloon Angioplasty. assigned to stenting or balloon Angioplasty. No exclusion criteria were appliedNo exclusion criteria were applied. .
Death or ReinfarctionDeath or Reinfarction
TVR
(%)
TVR
(%)
RR 0.98 (95%CI: 0.78-1.22)RR 0.98 (95%CI: 0.78-1.22)
N=1683N=1683
Heart 2005;91:641–645.
0
5
10
15
20
25
StentBalloon
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LessonsLessons from the BMS from the BMS EraEra
BMS in the setting of STEMI is far BMS in the setting of STEMI is far from being the perfect solution for from being the perfect solution for restenosis and TVR may remain highrestenosis and TVR may remain high
New devices are needed which have New devices are needed which have to be tested in unselected (no to be tested in unselected (no angiographic selection bias) patient angiographic selection bias) patient populationpopulation
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GP IIb/IIIa inhibitorsGP IIb/IIIa inhibitorsThe word to the …The word to the …GuidelinesGuidelines
Primary PCI: Primary PCI: Class IIA indicationClass IIA indication
Class IIA indication with StentClass IIA indication with Stent
Class I indication without StentClass I indication without Stent
Class IIB for tirofiban and eptifibatideClass IIB for tirofiban and eptifibatide
Abci
xim
aAb
cixi
ma
bb
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STEMI UFH - ASAClopidogrel
Tirofiban SHDB
Abciximab stand. regimen
Cypher
BMS
CCU Cath-Lab
Valgimigli et al. Cardiovasc Drugs Ther 04; 18: 225-30
Study designStudy design Inclusion Criteria: STEMI all comers: shock, elderly
included
Exclusion Criteria: Contraindications to Gp IIb/IIIa
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175 Randomized
SHDB Tirofiban(n=87)
Abciximab(n=88)
3 No PCI
1:1
219 Assessed for Eligibility 44 Excluded• 34 Not Meeting Inclusion Criteria• 10 Refused to Participate
3 POBA 74 SES 7 BMS84 PTCA
Clinical Follow-up
Angiographic Follow-up
Pts not eligible Refused to participate
4 POBA 77 BMS2 SES83 PTCA 5 No PCI
3 3 74 7 4 77 2 50 1 62 4 1 64 1 03 2 6 0 3 4 0 50 0 6 3 0 9 1 0
Study ProfileStudy Profile
Valgimigli et al. JAMA 2005; 293: 2109-2117
85% 88%
77% 75%
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30-Day Outcome30-Day Outcome n=175n=175
0
2
4
6
8
10
12
14
MACE Death Re-AMI TVR CVA
P=0.33
P>0.99 P=0.62 P=0.62
P=>0.99
%
Abciximab+BMS Tirofiban+SES
Valgimigli et al. JAMA 2005; 293: 2109-2117
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Death/MI at 8 MonthsDeath/MI at 8 Months
0 50 100 150 200 250
Tim e after I n itial Procedure (days)
40
30
20
10
0
Probability of Events (%
)
A bc + BMS (DEA TH / M I )SHDB Tir + SES (DEATH / M I )
17%
13%
JAMA 2005; 293: 2109-2117
p=0.4
HR 0.71 [95% CI: 0.34-1.5]
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0 50 100 150 200 250
Tim e after I n itial Procedure (days)
40
30
20
10
0
Probability of Events (%
)
A bc + BMS (M A CE) SHDB Tir + SES (M A CE)
18 %
32 %
Death/MI/TVR at 8 MonthsDeath/MI/TVR at 8 Months
HR 0.53 [95% CI: 0.28-0.92]
p=0.043
JAMA 2005; 293: 2109-2117
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8-Month Outcome8-Month Outcome n=175n=175
05
101520253035404550
P=0.043
P=0.8 P=0.6
P=0.01
P>0.99
P=0.004
P=0.005
MACE Death MI TVR CVA 1° EndPointBR
%
Abciximab+BMSTirofiban+SES
50%
19%
Valgimigli et al. JAMA 2005; 293: 2109-117
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STEMI All Comers PatientsSTEMI All Comers PatientsAspirin + Clopidogrel Aspirin + Clopidogrel ++ UFHUFH
Intent-to-stentIntent-to-stentN ~ 730N ~ 730
TirofibanTirofiban AbciximabAbciximab
SESSES BMSBMS
MULTI-STRATEGYTrial Design
SESSES BMSBMS
Università degli Studi di Ferrara - Cattedra di Cardiologia
1:1
1:11:1
Valgimigli M. et al Am Heart J. 2007 Jul;154(1):39-45.
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MULTI-STRATEGY
1.1. Whether Whether tirofiban administered at high bolus tirofiban administered at high bolus dose is non inferior to abciximab on the degree of dose is non inferior to abciximab on the degree of cumulative ST-segment resolution, expressed as cumulative ST-segment resolution, expressed as the proportion of patients reaching ≥ 50% the proportion of patients reaching ≥ 50% recovery, at 90’ after the mechanical recovery, at 90’ after the mechanical intervention.intervention.
2.2. Whether SES implantation –based on the Whether SES implantation –based on the intention-to-treat principle– is superior to BMS on intention-to-treat principle– is superior to BMS on the incidence of major adverse cardiovascular the incidence of major adverse cardiovascular events (MACE) within 8 months, defined as the events (MACE) within 8 months, defined as the composite of death, nonfatal myocardial composite of death, nonfatal myocardial infarction and clinically-driven target vessel infarction and clinically-driven target vessel revascularization (TVR). revascularization (TVR).
Primary objectivesPrimary objectives
Università degli Studi di Ferrara - Cattedra di Cardiologia
Valgimigli M. et al Am Heart J. 2007 Jul;154(1):39-45.
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The effect of tirofiban infusion or SES implantation on The effect of tirofiban infusion or SES implantation on the MACE either singularly considered or as a the MACE either singularly considered or as a composite and on the incidence of stent thrombosis. composite and on the incidence of stent thrombosis.
The effect of tirofiban on the rate of TIMI 3 flow before The effect of tirofiban on the rate of TIMI 3 flow before and after intervention and on partial (and after intervention and on partial (≥≥50%) or 50%) or complete (complete (≥≥70%) cumulative ST segment resolution 70%) cumulative ST segment resolution or in the single lead with greatest ST changes.or in the single lead with greatest ST changes.
The effect of SES implantation on the rate of major The effect of SES implantation on the rate of major cardiovascular events either singularly considered or cardiovascular events either singularly considered or as a composite after thienopyridines discontinuationas a composite after thienopyridines discontinuation
TThe cost-effectiveness profile in STEMI of SES he cost-effectiveness profile in STEMI of SES implantation or tirofiban infusionimplantation or tirofiban infusion
The effect of tirofiban on the rate of bleeding and The effect of tirofiban on the rate of bleeding and thrombocytopeniathrombocytopenia
MULTI-STRATEGYMajor Secondary objectivesMajor Secondary objectives
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MULTI-STRATEGY16 Participating centers
Università degli Studi di Ferrara - Cattedra di Cardiologia
Ferrara, M.ValgimigliFerrara, M.ValgimigliValle Oppio, GF PercocoValle Oppio, GF PercocoArezzo. L. Bolognese Arezzo. L. Bolognese Verona, M. Anselmi Verona, M. Anselmi Bergamo, N. De CesareBergamo, N. De CesareMirano, GP PasquettoMirano, GP PasquettoPavia, E. BramucciPavia, E. BramucciAncona, R. PivaAncona, R. PivaTorino, I. SheibanTorino, I. SheibanTorino, S. ColangeloTorino, S. ColangeloRoma, F. PratiRoma, F. PratiRoma, R. VioliniRoma, R. Violini
ItalyItaly ArgentinaArgentina SpainSpain
Buenos Aires, A. RodriguezBuenos Aires, A. RodriguezOtamendi HospitalOtamendi Hospital
Madrid, R. MorenoMadrid, R. MorenoHuelva, José DíazHuelva, José Díaz
Valgimigli M. et al Am Heart J. 2007 Jul;154(1):39-45.
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STEMI All Comers PatientsSTEMI All Comers PatientsAspirin + Clopidogrel Aspirin + Clopidogrel ++ UFHUFH
Intent-to-stentIntent-to-stentN ~ 730N ~ 730
TirofibanTirofiban AbciximabAbciximab
SESSES BMSBMS
MULTI-STRATEGYTrial Design
SESSES BMSBMS
Università degli Studi di Ferrara - Cattedra di Cardiologia
1:1
1:11:1ACC 2008
ACC 2008
Valgimigli M. et al Am Heart J. 2007 Jul;154(1):39-45.