Arrhythmic risk stratification in post-myocardial infarction patients with preserved ejection fraction: the PRESERVE EF study

European Heart Journal

3 May 2019
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ESC Journals ARRHYTHMIAS AND DEVICE THERAPY Arrhythmias, General Atrial Fibrillation (AF) PREVENTIVE CARDIOLOGY Risk Factors and Prevention

Abstract

AbstractAims

Sudden cardiac death (SCD) annual incidence is 0.6–1% in post-myocardial infarction (MI) patients with left ventricular ejection fraction (LVEF)≥40%. No recommendations for implantable cardioverter-defibrillator (ICD) use exist in this population.

Methods and results

We introduced a combined non-invasive/invasive risk stratification approach in post-MI ischaemia-free patients, with LVEF ≥ 40%, in a multicentre, prospective, observational cohort study. Patients with at least one positive electrocardiographic non-invasive risk factor (NIRF): premature ventricular complexes, non-sustained ventricular tachycardia, late potentials, prolonged QTc, increased T-wave alternans, reduced heart rate variability, abnormal deceleration capacity with abnormal turbulence, were referred for programmed ventricular stimulation (PVS), with ICDs offered to those inducible. The primary endpoint was the occurrence of a major arrhythmic event (MAE), namely sustained ventricular tachycardia/fibrillation, appropriate ICD activation or SCD. We screened and included 575 consecutive patients (mean age 57 years, LVEF 50.8%). Of them, 204 (35.5%) had at least one positive NIRF. Forty-one of 152 patients undergoing PVS (27–7.1% of total sample) were inducible. Thirty-seven (90.2%) of them received an ICD. Mean follow-up was 32 months and no SCDs were observed, while 9 ICDs (1.57% of total screened population) were appropriately activated. None patient without NIRFs or with NIRFs but negative PVS met the primary endpoint. The algorithm yielded the following: sensitivity 100%, specificity 93.8%, positive predictive value 22%, and negative predictive value 100%.

Conclusion

The two-step approach of the PRESERVE EF study detects a subpopulation of post-MI patients with preserved LVEF at risk for MAEs that can be effectively addressed with an ICD.

Clinicaltrials.gov identifier

NCT02124018

Contributors

Konstantinos A Gatzoulis
Konstantinos A Gatzoulis

Author

National & Kapodistrian University of Athens Athens , Greece

Christos-Konstantinos Antoniou
Christos-Konstantinos Antoniou

Author

Athens Medical Centre Athens , Greece

Panagiotis Korantzopoulos
Panagiotis Korantzopoulos

Author

University of Ioannina Medical School Ioannina , Greece

Vassilios Vassilikos
Vassilios Vassilikos

Author

Hippokration General Hospital of Thessaloniki Thessaloniki , Greece

Konstantinos Trachanas
Konstantinos Trachanas

Author

General hospital of Nikaia Agios Panteleimon Athens , Greece