Key result
In patients with nonischemic dilated cardiomyopathy, NSVT on Holter and VT inducibility independently predicted sustained ventricular arrhythmias during follow-up (P=0.036).
Why the study?
It was unknown whether spontaneous NSVT on Holter, VT inducibility during electrophysiology study, and LGE on CMR carry independent prognostic value for spontaneous SVA in nonischemic DCM.
Do NSVT on Holter, VT inducibility during electrophysiology study, and LGE on CMR independently predict sustained ventricular arrhythmias in patients with nonischemic dilated cardiomyopathy?
Cohort
Do NSVT on Holter, VT inducibility during electrophysiology study, and LGE on CMR independently predict sustained ventricular arrhythmias in patients with nonischemic dilated cardiomyopathy?
In patients with nonischemic dilated cardiomyopathy, NSVT on Holter and VT inducibility during EP study are independent predictors of sustained ventricular arrhythmias, providing additive prognostic value to LGE on CMR.
May support additive risk stratification with NSVT and inducibility beyond LGE; hypothesis-generating for ICD decisions in nonischemic cardiomyopathy.
BACKGROUND: Spontaneous nonsustained ventricular tachycardia (NSVT) on Holter, VT inducibility during electrophysiology study, and late gadolinium enhancement (LGE) on cardiac magnetic resonance (CMR) have been associated with sustained ventricular arrhythmias (SVAs) in nonischemic dilated cardiomyopathy (DCM). This study aimed to analyze whether these parameters carry independent prognostic value for spontaneous SVA in DCM. METHODS: Between 2011 and 2018, patients with the DCM clinical spectrum and documented SVA, suspected SVA, or considered to be at intermediate or high risk for SVA were enrolled in the prospective Leiden Nonischemic Cardiomyopathy Study. Patients underwent a comprehensive evaluation including 24-hour Holter, LGE-CMR, and electrophysiology study. Holters were assessed for the presence of NSVT (≥3 beats; rate, ≥120 bpm; lasting <30 s) and NSVT characteristics (coupling interval, duration, cycle length, morphology, regularity). Patients were followed at 6 to 12 monthly intervals. RESULTS: =0.036) were independently associated with SVA during follow-up. A bivariable model including only noninvasively acquired parameters also allowed identification of a high-risk subgroup (ie, those with both NSVT and LGE on CMR). The findings remained similar when only patients without prior SVA were included. CONCLUSIONS: In patients with DCM, NSVT on Holter and VT inducibility during electrophysiology study predict SVA during follow-up independent of LGE on CMR. NSVTs may serve as an initiator, and sustained VT inducibility indicates the presence of the substrate for SVA in DCM. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01940081.
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A 2022 study conducted a cohort in Nonischemic dilated cardiomyopathy. Nonsustained ventricular tachycardia (NSVT) and VT inducibility vs. Absence of NSVT and VT inducibility was evaluated on Sustained ventricular arrhythmias (SVA) (p=0.036). In patients with nonischemic dilated cardiomyopathy, NSVT on Holter and VT inducibility independently predicted sustained ventricular arrhythmias during follow-up (P=0.036).
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