Improved survival of patients with coronary artery disease and low ejection fraction with ICD implantation versus conventional therapy in a real world survey
© Aschenbrenner et al.; licensee BioMed Central Ltd. 2012
Received: 19 January 2012
Accepted: 27 July 2012
Published: 27 July 2012
Coronary artery disease (CAD) is associated with an increased risk for sudden cardiac death. Randomized controlled trials have shown that implantable cardioverter defibrillators (ICD) improve life expectancy unless they are implanted within the first days after an acute myocardial infarction and guidelines recommend their use. We aimed to validate that these results also apply to patients of a typical community hospital in Germany.
This was a retrospective analysis of patients undergoing coronary angiography in the Lippe-Detmold Hospital between 2003 and 2006. They had to have significant CAD and an ejection fraction (EF) ≤ 35% and no acute myocardial infarction within 28 days of implantation and no history of ventricular fibrillation.
213 patients were included; 70 of which received an ICD. Patients with an ICD implantation were younger (64.8 ± 9.9 vs. 67.9 ± 9.8 years; p = 0.034), had single vessel CAD more frequently (22.9 vs. 11.2%; p = 0.025) and a lower EF (26.7 ± 6.3 vs. 29.1 ± 4.6%; p = 0.006). Hospital readmissions were comparable between the ICD and the control group (68.6 vs. 72.0%; p = 0.602). ICD therapy was associated with a considerable survival benefit compared to conventional therapy (HR 0.52; 95%CI 0.29-0.93; p = 0.027) in a Cox-Proportional Hazards Regression analysis.
Appreciating the potential limitations of retrospective studies, we found that ICD use was associated with improved survival in patients with significant CAD and an EF <= 35% typical for a large tertiary hospital.
KeywordsImplantable cardioverter defibrillator Cohort study Myocardial infarction
Coronary artery disease (CAD) is associated with an increased risk for angina, acute myocardial infarction (MI), reduced left ventricular ejection fraction (LVEF), congestive heart failure, and sudden cardiac death . Although considerable progress has been made with respect to improving prognosis  approaches utilizing antiarrhythmic pharmacotherapy have been misleading [3–6], and sudden cardiac death remains a major threat to patients wellbeing. MADIT II documented that ICD use was associated with improved survival in CAD patients with prior MI and reduced LV function (EF ≤ 30%)  while DINAMIT reported no benefit with respect to overall mortality in patients with ICD implantation within days after an acute myocardial infarction .
ICD therapy is recommended by the recent guidelines for the primary prevention of ventricular arrhythmias and sudden cardiac death in patients with LV dysfunction due to prior MI who are at least 40d post-MI and have an LVEF ≤ 30-40%, NYHA II and a good reasonable expectation of survival with a good functional status for more than 1 year (Level of Evidence A) . In clinical practice, ICDs appear to reduce all cause and arrhythmic death to a similar degree as in primary prevention trials . We aimed to validate the results of the aforementioned trial in clinical practice by a retrospective documentation of patients with ICD implantation between 2003 and 2006.
This was a retrospective analysis of patients undergoing coronary angiography in the cardiology unit of the Lippe-Detmold Hospital, a tertiary care hospital, between January 8th 2003 and December 18th 2006. Ethic committee approval as well as patient informed consent was not obtained due to the retrospective design of the study.
Patients included had undergone coronary angiography because of significant CAD and an EF ≤ 35% on monoplane evaluation and had an indication for the primary prevention of ventricular arrhythmias and sudden cardiac death . Exclusion criteria were acute myocardial infarction less than 28 days ago, known cancer (because of the limited life expectancy), and cardio-pulmonary resuscitation due to ventricular fibrillation.
Follow-up data for a duration of at least 30 months were collected from hospital charts when patients were readmitted or via contact by telephone. The following variables were obtained: date of birth, gender, the presence of CAD and the number of vessels diseased, LVEF, the presence of diabetes and concomitant medication. During follow-up data on readmissions to the hospital and the reasons for referral, the adequacy of shocks and overall duration of survival were gathered.
This data were analyzed with Aabel 20/20 data vision 3® from Gigawiz Ltd Co. Descriptive statistics were applied, based on available data and significance calculated using the two-tailed unpaired t-Test. Kaplan-Meier estimates used to compare survival and the p-value calculated by the log-rank test. Further a proportional hazards model was built considering variables displaying significant differences at baseline (p < 0.05).
(n = 143)
(n = 70)
Age in years, mean (±SD)
67.9 ± 9.8
64.8 ± 9.9
Gender, women, n (%)
26 (18.2 %)
6 (8.6 %)
Coronary artery disease (CAD)
1-vessel CAD, n (%)
16 (11.2 %)
16 (22.9 %)
2-vessel CAD, n (%)
3-vessel CAD, n (%)
Left ventricular ejection fraction (LVEF), %
29.1 ± 4.6
26.7 ± 6.3
LVEF, women, %
29.4 ± 4.5
28.7 ± 7.7
LVEF, men, %
29.0 ± 4.7
26.5 ± 6.1
LVEF, 1-vessel CAD, %
29.4 ± 4.2
26.3 ± 7.0
LVEF, 2-vessel CAD, %
28.7 ± 4.7
25.2 ± 7.1
LVEF, 3-vessel CAD, %
29.3 ± 4.7
28.1 ± 5.0
Diabetes, n (%)
Pharmacotherapy, n (%)
Complications after inclusion and ICD therapy
Complications after inclusion
(n = 143)
(n = 70)
Hospital Admissions, n (%)
Rhythm disorders, n (%)
Heart failure, n (%)
Time from EF to ICD / CRT (months)
33.1 ± 20.7
2.3 ± 4.4
Late ICD implantation, n (%)
CRT-D implantation, n (%)
CRT-D upgrade, n (%)
ICD therapy (n = 70)
(n = 56)
(n = 14)
ICD shock, n (%)
Inappropriate* shocks, n (%)
No ICD shocks, n (%)
Outcomes of patients in our registry
Detmold ICD +
Detmold ICD –
(n = 70)
(n = 143)
Coronary artery disease with an EF ≤ 35 %, no MI within the last 28 days, without known cancer or history of ventricular fibrillation
HR Total mortality
HR 0.52 (95%CI 0.29-0.93); p = 0.027
Heart failure related hospitalization
Guideline recommendations for the primary prevention of ventricular arrhythmias and sudden cardiac death such as that of the ACC/AHA/ESC  rely on information derived from randomized, controlled trials. These trials have a high internal validity for the patient group actually included, but may lack such validity for a substantial proportion of patients in clinical practice. Therefore we aimed to validate these trials in the patient population of our community hospital in Detmold. Overall 213 patients were retrospectively documented and prospectively evaluated for survival and appropriateness of shocks. We found that ICD use was associated with a considerable improvement of survival which was statistically significant.
Clinical characteristics of patients in the MADIT II trial
MADIT II ICD +
MADIT II ICD –
(n = 742)
(n = 490)
Prior myocardial infarction more than 28 days ago and an EF ≤ 30%
64 ± 10
65 ± 10
Female Gender (%)
LVEF (% ± SD)
23 ± 5
23 ± 6
HR Total mortality
HR 0.69 (95%CI 0.51-0.93); p = 0.016
Heart failure related hospitalization
Survival benefit in perspective
Both MADIT-II and our observation document improvements in overall survival which may reach about 31% such as in MADIT-II . This is also compatible with SCD-HeFT, which reported a risk reduction of 23% (HR 0.77; p = 0.007) and an absolute decrease in mortality of 7.2% after five years in the overall population. Patients in SCD-HeFT were included based on NYHA class II or III heart failure and a LVEF ≤ 35% and followed for a median of 45.5 months. In comparison MADIT reported a risk reduction of 54% for patients with prior MI, and LVEF ≤ 35% (absolute risk 38.6 vs. 15.8%) and a documented episode of asymptomatic unsustained ventricular tachycardia; and inducible, non suppressible ventricular tachyarrhythmia on electrophysiologic study . Against this background the risk reduction of 48% in our cohort appears high. This might have been due to confounders that we were not able to fully account for. For example there were more patients with triple vessel disease in the control compared to the ICD group (60.1 vs. 44.3%; p = 0.006).
The difference to our data on those of MADIT II is reasonable given that patients with previous proof of arrhythmia were specifically included. None of the patients in the ICD group and 9.8% of the control group died of primary arrhythmia which illustrates a stronger risk reduction for arrhythmic death. Data are however hard to compare due to substantial differences in antiarrhythmic drug use. For example MUST reported a reduced 5 year rate of cardiac arrest or arrhythmic death by 27% (HR 0.73) among patients with CAD, a LVEF ≤ 40% and asymptomatic, not sustained ventricular tachycardia .
Heart failure and inappropriate shocks
An increased risk for heart failure was documented in our observation and also in the MADIT-II trial (Tables 1 and 4). Recently an analysis of risk factors for recurrent heart failure in the MADIT-II trial was published : Risk factors for a first HF hospitalization included treatment with an ICD (HR 1.31; p = 0.05), NYHA class > II (HR 1.95; p < 0.001), female gender (HR 1.38; p = 0.05), atrial fibrillation (HR 1.90; p = 0.001), QRS >120 ms (HR 1.41; p = 0.01), diabetes mellitus (HR 1.51; p = 0.003), heart rate ≥80 (HR 1.35; p = 0.04), diuretic therapy (HR 1.82; p < 0.001), and the presence of prerenal azotemia (blood urea nitrogen:creatinine >20; HR 1.45; p = 0.01). The occurrence of one HF event after enrolment was associated with a 2.8-fold (p < 0.001) increase in the risk of death, whereas after the occurrence of a second event there was a 6.7-fold (p < 0.001) increase in the risk of subsequent mortality.
Inappropriate shocks (those not due to ventricular fibrillation) were also more frequent in patients dying within the observational period (although not significant). This has been associated to the presence of atrial fibrillation (odds ratio 6.2) in a recent analysis of 549 patients with heart failure and ICDs . In a Chinese single center study documenting 34 patients between 2005 and 2009 reasons for inappropriate ICD discharge were documented . They found these to be again related mainly to supraventricular tachyarrhythmias, especially atrial fibrillation. We were however not able to verify this association because of the low number of cases in our observation.
These data reproduce those found in prior randomized controlled trials. Although this is encouraging a number of limitations have to be acknowledged in addition to the ones mentioned before: 1) This was a retrospective study with all limitations inherent in such designs such as: significant bias that may affect the assignment to the treated group or the control group, incompleteness of data which were not fully captured to answer the question under investigation, difficulty in assessing a temporal or even causal relationship, reliance on the quality of data available with no possibility of verification. 2) The set of data obtained for the patients under investigation was limited so that data interfering with the outcome such those on renal function, biomarkers or the presence of atrial fibrillation were not considered in the analysis. 3) We were not able to report on different causes of death (such as arrhythmic) and only report overall survival. 4) Third the study is small allowing no detailed analyses and multiple adjustments due to limited power. 5) There is a slight imbalance in the degree of heart failure, age and the number of vessels diseased which may not have been adequately accounted for. 6) We obtained no reasons why one group was offered an ICD and the other group not thought both had an indication for ICD use.
Appreciating the potential limitations of retrospective studies we found that, in patients with ischemic heart disease and left ventricular dysfunction, typical for those in the community setting, ICD use was associated with an improved survival. The benefits were however offset by heart failure and inappropriate shocks which may justify the further research into more advanced devices such as biventricular pacemakers.
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