Date post: | 18-Dec-2014 |
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ALL PATIENTS 40 DAYS POST MI SHOULD RECEIVE
ICD
DR. AASIT S. SHAH MD, DMJASLOK HOSPITAL AND RESEARCH CENTRE
INTRODUCTION
• Indications for ICD implant have evolved in last few years
• Not meant only for drug refractory ventricular arrhythmias
• Focus has changed from identifying patient who needs ICD to identifying patients who can avoid ICD.
ICD TRIALS
• Multiple RCT’s have shown that ICD is better than antiarrhythmic drugs
• Applicable to patients for secondary prevention and for primary prevention
ICD TRIALS- SECONDARY PREVENTION
• AVID• CASH• CIDS
• 73-83% PTS. HAD CAD• EF 32-45%
•Non-significant results.1 The AVID Investigators. N Engl J Med. 1997;337:1576-1583.2 Kuck Kh, et al. Circulation. 2000;102:748-754.3 Connolly SJ, et al. Circulation. 2000;101:1297-1302.
Secondary Prevention Trials: Reduction in Mortality with ICD Therapy
AVID CASH CIDS0
20
40
60
80Overall Death
Arrhythmic Death
1 2 3
31%
56%
23%*
58%
20%*
33%
% M
orta
lity
Redu
ction
w/
ICD
Rx
ICD TRIALS- PRIMARY PREVENTION
• MADIT• MUSTT• MADIT 2• SCD-HeFT
• Two recent meta-analyses have shown 20-30% net risk reduction for total mortality
1 Moss AJ. N Engl J Med. 1996;335:1933-40.2 Buxton AE. N Engl J Med. 1999;341:1882-90.3 Moss AF. N Engl J Med. 2002;346:877-83.4 Moss AJ. Presented before ACC 51st Annual Scientific Sessions, Late Breaking Clinical Trials, March 19, 2002.
MADIT MUSTT MADIT-II0
20
40
60
80 Overall Death
Arrhythmic Death
1 2 3, 4
54%
75%
55%
73%
31%
61%
27 Months 39 Months 20 Months
% M
orta
lity
Redu
ction
w/
ICD
Rx
PRIMARY PREVENTION
ICD mortality reductions in
primary prevention trialsare equal to or
greaterthan those in
secondaryprevention trials.
MADIT MUSTT MADIT-II0
20
40
60
80Overall Death
Arrhythmic Death
AVID CASH CIDS0
20
40
60
80Overall DeathArrhythmic Death
13, 42
5 76
54%
75%
55%
76%
31%
61%
27 months 39 months 20 months
31%
56%
28%
59%
20%
33%
% M
orta
lity
Redu
ction
w/
ICD
Rx
% M
orta
lity
Redu
ction
w/
ICD
Rx
3 Years 3 Years 3 Years
PRIMARY VS. SECONDARY PREVENTION
1 Moss AJ. N Engl J Med. 1996;335:1933-40.2 Buxton AE. N Engl J Med. 1999;341:1882-90.3 Moss AJ. N Engl J Med. 2002;346:877-834 Moss AJ. Presented before ACC 51st Annual Scientific Sessions, Late Breaking Clinical Trials, March 19, 2002.5 The AVID Investigators. N Engl J Med. 1997;337:1576-83.6 Kuck K. Circ. 2000;102:748-54.7 Connolly S. Circ. 2000:101:1297-1302.
ICD TRIALS
Hence it is clear that ICD therapy for SCD provides greater reduction in SCD mortality than antiarrhythmic drug therapy in high risk patients post MI
The most important risk stratification factor is the ejection fraction
SCD INCIDENCE POST MI
• Incidence of SCD is highest in the early phase post MI- first 30 days.
14703 pts.
HIGHEST SCD IN 1 MTH POST MI-19%
83% OF ALL SCD OCCURRED IN 1 MTH
EF<30% HAD HIGHEST RISK OF SCD-
Hence it is logical that if we provide antiarrhythmic therapy early to our post MI high risk patients, incidence of SCD should reduce.
VALIANT TRIAL
VALIANT TRIAL
EF <30%
<31-40%
>40%
Rates of sudden death or cardiac arrest
ICD TRIALS EARLY AFTER MI
• DINAMIT
• IRIS
• BEST
COMPETING RISK: LESSONS FROM THE NEGATIVE TRIALS
COMPETING RISK
ICD TRIALS EARLY POST MI
• These trials did not show improvement in overall mortality when ICD was implanted 6-40 days post MI.
• There was a reduction in SCd in the ICD group; however non SCD deaths in ICD group also increased.
• This paradox has not been satisfactorily explained
ICD TRIALS EARLY POST MI
• Risk stratification factors
• Deleterious effect of ICD therapy –including appropriate programming
• Other causes of sudden death
• Role of EP study
JACC 2009; 54(22) 2001-2005
ACC 2012 RECOMMANDATION CLASS I A : ICD therapy is indicated in patients with LVEF less than or
equal to 35% due to prior MI who are at least 40 days post-MI and are in NYHA functional Class II or III
CLASS I A : ICD therapy is indicated in patients with LV dysfunction due to prior MI who are at least 40 days post-MI, have an LVEF less than or equal to 30%, and are in NYHA functional Class I
CLASS I B : ICD therapy is indicated in patients with nonsustained VT due to prior MI, LVEF less than or equal to 40%, and inducible VF or sustained VT at electrophysiological study.
AUC
3 4
119
20
2628
37
0
5
10
15
20
25
30
35
40
45
50
MUSTT MADIT MADIT II AVID SAVE Merit-HF 4S AmiodaroneMeta-
analysis (5 Yr) (2.4 Yr) (3 Yr) (3 Yr) (3.5 Yr) (1 Yr) (6 Yr) (2 Yr)
NNTx years = 100 / (% Mortality in Control Group – % Mortality in Treatment Group)
ICD Therapysimvastatin
captopril
Metoprololsuccinate
amiodarone
Drug Therapy
PRIMARY PREVENTION
Number Needed to Treatto Save a Life
CONCLUSIONS
• All patients who match current guidelines should be
offered ICD implant
• Better risk stratification criteria and more
appropriate device programming
• Need more trials and data to identify patients at
high risk for SCD early after MI
THANK YOU!