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Implantable cardiac defibrillator and mortality in non-ischaemic cardiomyopathy: an updated meta-analysis
Ana C Alba1, Farid Foroutan1,2, Juan Duero Posada1
1Department of cardiology, Hear Failure and Transplant Program, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
Insights
Implantable cardiac defibrillators (ICDs) significantly reduce mortality in patients with non-ischaemic cardiomyopathy. This therapy lowers all-cause mortality, cardiovascular mortality, and sudden cardiac death, offering a vital preventative measure.
Area of Science:
- Cardiology
- Electrophysiology
- Preventive Medicine
Background:
- The efficacy of implantable cardiac defibrillators (ICDs) in non-ischaemic cardiomyopathy with systolic dysfunction is debated.
- Systematic reviews and meta-analyses are crucial for synthesizing evidence on ICD benefits.
Purpose of the Study:
- To determine the effect of ICD therapy on all-cause mortality.
- To evaluate ICD impact on cardiovascular mortality.
- To assess ICD influence on sudden cardiac death in non-ischaemic cardiomyopathy.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs).
- Searched multiple databases (MEDLINE, Embase, PubMed, Cochrane) up to October 2016.
- Used random-effect models and GRADE system to assess evidence quality and effects.
Main Results:
- ICD therapy reduced all-cause mortality (HR 0.78) with high-quality evidence.
- Cardiovascular mortality was significantly lowered by ICDs (RR 0.77).
- Sudden cardiac death risk decreased substantially with ICDs (RR 0.45).
Conclusions:
- Primary prevention with ICDs is effective in non-ischaemic cardiomyopathy.
- ICD therapy demonstrably reduces all-cause and cardiovascular mortality.
- ICDs significantly decrease the incidence of sudden cardiac death in this patient group.
Objectives:
The benefit of implantable cardiac defibrillator (ICD) in symptomatic patients with systolic dysfunction and non-ischaemic cardiomyopathy remains controversial. We conducted a systematic review and meta-analysis to determine the effect of ICD in patients with non-ischaemic cardiomyopathy on (1) all-cause mortality, (2) cardiovascular mortality and (3) sudden cardiac death.
Methods:
We searched citations in meta-analyses published until 2012, and in MEDLINE, Embase, PubMed and Cochrane databases from 2012 to October 2016. We included randomised controlled trials (RCTs) evaluating the effect of ICD therapy on all-cause and cardiovascular mortality and sudden cardiac death in patients with non-ischaemic cardiomyopathy. Independent reviewers evaluated study eligibility, abstracted data and assessed risk of bias in duplicate. We used random-effect models to meta-analyse relative risks (RR) and hazard ratios (HR) across studies, the Grades of Recommendation, Assessment, Development, and Evaluation system to quantify absolute effects and quality of evidence, and I2 to evaluate heterogeneity.
Results:
We identified six RCTs including 1715 patients experiencing 421 deaths. ICD therapy was associated with reduced overall mortality (HR 0.78, 95% CI 0.66 to 0.92, I2 = 0%, risk difference 4.7%, high quality), cardiovascular mortality (RR 0.77, 95% CI 0.60 to 0.98, I2 = 39%, risk difference 3.3%, high quality) and sudden cardiac death (RR 0.45, 95% CI 0.29 to 0.70, I2 = 0%, risk difference 4.1%, high quality). The benefit of ICD was not influenced by the use of amiodarone in the comparison group, the duration of follow-up, by use of β-blockers and ACE inhibitors/angiotensin receptor blocker or cardiac resynchronisation therapy.
Conclusion:
Primary prevention ICD therapy reduces all-cause and cardiovascular mortality and sudden cardiac death in patients with non-ischaemic cardiomyopathy.
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