Title: CArvedilol Post-infaRct survIval COntRol in LV dysfunctioN
1CArvedilol Post-infaRct survIval COntRol in LV
dysfunctioN
Lancet 2001 357 1385 -90
2Rationale
- Beta blocker trials in acute myocardial
infarction (MI) were conducted mostly during the
1970/80s - no thrombolysis or primary angioplasty
- much less use of aspirin
- no ACE inhibitors
- Generally patients with heart failure were
excluded - left ventricular (LV) function was not assessed
3Objective / Design
- To evaluate the effect of carvedilol on clinical
outcome in patients with LV dysfunction following
an acute MI treated in the modern era - Multicentre, randomised, placebo-controlled,
parallel-group trial in patients with LV ejection
fraction ? 40 with or without heart failure
4Study Organisation
- Steering CommitteeH Dargie (UK), W Colucci (US),
JL Lopez-Sendon (E), W Remme (NL), N Sharpe (NZ) - Endpoint CommitteeJ McMurray (UK) , L Kober
(DK), J Sackner-Bernstein (US), J Soler-Soler
(E), Faiez Zannad (F) - DSMBD Julian (UK), I Ford (UK), B Massie (US), S
Thompson (UK), L Wilhelmson (DK) - CAPRICORN involved 163 investigators in 17
countries (Europe, Israel, North-America,
Australia, New Zealand)
5Global Involvement
6Study Plan
Uptitration
Downtitration
Maintenance
Carvedilol (n975)
(n1959)
Placebo (n984)
Initiation with 6.25 mg or 3.125 mg
bidUptitration to maximum tolerated dose over 2
4 weeks. Target dose 25 mg bid
Optimum therapyat investigatorsdiscretion
Normally 3 5 days but up to 21 days post MI
Time to 633 events Mean follow up 1.3 years
7Inclusion Criteria
- Confirmed acute MI within 3 - 21 days (mean of 10
days) - LV ejection fraction ? 40
- Receiving an ACE inhibitor for ? 48 hours
- All appropriate treatments for MI including
thrombolysis and percutaneous interventions - Patients were usually hospitalized, but may have
been recently discharged
8Endpoints
- Primary Endpoints
- All-Cause Mortality
- All-Cause Mortality or Cardiovascular (CV)
Hospitalisation - Secondary Endpoints
- Sudden Death
- Hospitalisation for Heart Failure
- Additional Analyses
- Recurrent, Non-Fatal MI
- CV Mortality or Recurrent, Non-Fatal MI
- All-Cause Mortality or Recurrent, Non-Fatal MI
9Baseline Characteristics
- Placebo Carvedilol (n 984) (n 975)
- Age (years) 63 63
- Male/ Female () 74 / 26 73 / 27
- Ejection fraction () 32.7 32.9
- Reperfusion for index MI () 47 45
- IV Nitrates for index MI () 73 73
- IV Diuretics for index MI () 33 35
- Aspirin at randomisation () 86 86
- ACE inhibitors at randomisation () 97 98
10Primary Endpoint All-Cause Mortality
- Placebo Carvedilol Hazard Log rank (n
984) (n 975) Ratio P value (95 CI) - 151 (15) 116 (12) 0.77 0.031 (0.60-0.98)
11Primary Endpoint All-Cause Mortality
1
23 ? vs. placeboP 0.031
0.95
0.9
Carvedilol
Proportion event free
0.85
0.8
Placebo
0.75
0.7
0
0.5
1
1.5
2
2.5
Years
12Primary Endpoint All-Cause Mortality or CV
Hospitalisation
- Placebo Carvedilol Hazard Log rank (n
984) (n 975) Ratio P value (95 CI) - 367 (37) 340 (35) 0.92 0.296 (0.80-1.07)
13Primary Endpoint All-Cause Mortality or CV
Hospitalisation
1
8 ? vs. placeboP 0.296
0.9
0.8
Proportion event free
0.7
0.6
Carvedilol
Placebo
0.5
0
0.5
1
1.5
2
2.5
3
Years
14Secondary EndpointsSudden Death and
Hospitalisation for Heart Failure
15Additional AnalysesNon-Fatal MI and Mortality
log rankP value
0.0
0.2
0.4
0.6
0.8
1.0
1.2
1.4
1.6
Hazard Ratio / 95 CI
Am J Cardiol 2004 93(suppl) 13B -16B
16Additional AnalysesNon-Fatal MI
1
41 ? vs. placeboP 0.014
0.98
Carvedilol
Proportion event free
0.96
0.94
Placebo
0.92
0
0.2
0.4
0.6
0.8
1.0
1.2
1.4
1.6
1.8
Years
17Additional AnalysesCV Mortality or Non-Fatal MI
1
30 ? vs. placeboP 0.002
0.9
Carvedilol
Proportion event free
0.8
Placebo
0.7
0
0.5
1
1.5
2
2.5
Years
18Additional AnalysesAll-Cause Mortality or
Non-Fatal MI
1
29 ? vs. placeboP 0.002
0.9
Carvedilol
Proportion event free
0.8
Placebo
0.7
0
0.5
1
1.5
2
2.5
Years
19Tolerability
- Placebo Carvedilol
- Max. dose during maintenance
- 12.5 mg bid 52 / 942 (6) 103 / 940 (11)
- 25 mg bid 784 / 942 (83) 692 / 940 (74)
- Permanent withdrawal 174 / 984 (18) 192 / 975
(20)(excluding deaths) - Patients with ? 1 SAE 429 / 980 (44) 396 /
969 (41)
20Summary
- In patients with LV dysfunction following an
acute MI carvedilol treatment was associated
with - 23 lower risk of all-cause mortality
- 8 lower risk of mortality or CV hospitalisations
- 26 lower risk of sudden death
- 25 lower risk of CV mortality
- 41 lower risk of non-fatal MI
- Carvedilol was well tolerated (withdrawals
comparable to placebo) and target doses for
treatment were reached in the majority of patients
21Conclusions
- CAPRICORN is the only large scale study on the
benefits of ? blocker therapy in patients with LV
dysfunction after acute MI - The benefits of carvedilol treatment were shown
on top of current state-of-the-art therapy for
post MI patients - In the absence of specific contraindications,
carvedilol should be considered in all patients
with LV dysfunction following an acute MI - Carvedilol therapy in post MI patients should be
started early and should be continued long-term
22Antiarrhythmic Effect of Carvedilol after
Myocardial Infarction. Results of the Capricorn
Trial
- J. McMurray et al.
- J Am Coll Cardiol 2005 45 525 -30
23Carvedilol
Placebo
P0.0015
24Carvedilol
Placebo
P0.0003
25Carvedilol
Placebo
Plt0.0001
26Carvedilol
Placebo
Plt0.0001
27 Bibliographie Capricorn
- 1) The Capricorn Investigators. Effect of
carvedilol on outcome after myocardial infarction
in patients with left-ventricular dysfunction
the Capricorn randomised trial. Lancet 2001 357
1385 -90 - 2) J. McMurray et al. Antiarrhythmic Effect of
Carvedilol After Acute Myocardial Infarction.
Results of the Carvedilol Post-Infarct Survival
Control in Left Ventricular Dysfunction
(CAPRICORN) Trial. J Am Coll Cardiol 2005 45
525 -30 - 3) W. Colucci. Landmark Study The Carvedilol
Post-Infarct Survival Control in Left Ventricular
Dysfunction Study (Capricorn). - Am J Cardiol 2004 93(suppl) 13B -16B
- 4) R. Doughty et al. Effects of Carvedilol on
Left Ventricular Remodeling After Acute
Myocardial Infarction. The Capricorn Echo
Substudy. Circulation 2004 109 201 -206 - 5) C. Pratt. Three Decades of Clinical Trials
With Beta-Blockers. The contribution of the
CAPRICORN Trial and the Effect of Carvedilol on
Serious Arrythmias. J Am Coll Cardiol 2005 45
531 -532 - 6) Résumé des Caractéristiques du Produit
- Ces publications sont disponibles à la demande