Key result
Induction of monomorphic or polymorphic ventricular tachycardia during programmed stimulation in patients with structural heart disease did not significantly increase all-cause mortality compared to non-inducible patients, though it was associated with higher major adverse cardiovascular events.
Why the study?
Questions remained regarding sensitive low-risk thresholds and the prognostic relevance of ill-sustained or non-specific tachycardia on programmed ventricular stimulation in structural heart disease.
Does VT inducibility predict sudden death, mortality, and MACE in patients with structural heart disease and syncope or documented arrhythmia?
Observational (n=169)
No
Does VT inducibility predict sudden death, mortality, and MACE in patients with structural heart disease and syncope or documented arrhythmia?
Answers are grounded in this paper and cite their sources.
In patients with structural heart disease, induction of monomorphic or polymorphic VT is associated with a higher risk of MACE and predicts VT recurrence or ICD shock.
INTRODUCTION: Currently available data gives some credence to utility of VT induction studies in patients with stable ischemic cardiomyopathy, there are some unresolved questions as to define sensitive threshold for low-risk and the prognostic relevance of ill sustained or non-specific tachycardia on induction study. We evaluated potential ability of VT inducibility to predict likelihood of SHD (Structural heart disease) patients for subsequent arrhythmic or adverse cardiac events. MATERIAL AND METHODS: All consecutive patients with syncope/documented arrhythmia who had VT induction done were included and patients with VT storm, ACS,uncontrolled HF were excluded. We studied in 4 groups-monomorphic VT, sustained polymorphicVT, ill sustainedVT/VF and no VT/VF induced. The primary-endpoints were - Sudden death, all-cause mortality and secondary-endpoints were - MACE (AICD shock, death,HF, recurrence of VT). We screened 411 patients and included 169 within inducible (n = 79) and non-inducible group (n = 90). RESULTS: There were a higher number of patients with coronary artery disease, LV dysfunction, patients on amiodarone in inducible group and no difference in usage of beta-blockers. Recurrence of VT, composite of MACE was significantly higher in inducible group (p < 0.05). Mortality was not different in 3 groups compared with no VT/VF group. We found that monomorphic VT group had significantly higher MACE as compared to others and also predicted recurrence of VT and AICD shock and showed a trend towards significance for prediction of mortality. Inducible patients on AICD had mortality similar to non-inducible group. CONCLUSION: Induction of monomorphicVT/polymorphicVT with ≤3extrastimuli is associated with a higher number of MACE events on follow up. Induction of monomorphicVT predicts recurrence of VT/ICD shock.
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Singh et al. (2022) conducted an observational in Structural heart disease with syncope or documented ventricular arrhythmia (n=169). Inducible ventricular tachycardia (monomorphic or sustained polymorphic) vs. Non-inducible ventricular tachycardia was evaluated on All-cause mortality (p=0.1932). Induction of monomorphic or polymorphic ventricular tachycardia during programmed stimulation in patients with structural heart disease did not significantly increase all-cause mortality compared to non-inducible patients, though it was associated with higher major adverse cardiovascular events.
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