Why the study?
The predictors of new supraventricular tachycardia (SVT) and its association with subsequent clinical outcomes in mild heart failure patients needed to be assessed.
Does the development of new-onset SVT increase the risk of ventricular tachyarrhythmic events, HF hospitalizations, and death in patients with mild heart failure?
Does the development of new-onset SVT increase the risk of ventricular tachyarrhythmic events, HF hospitalizations, and death in patients with mild heart failure?
In patients with mild heart failure, the development of new-onset SVT is associated with a significantly increased risk of subsequent ventricular tachyarrhythmias and all-cause mortality.
New SVT may identify higher-risk mild HF patients; leaves open whether it is causal or warrants targeted monitoring in CRT populations.
INTRODUCTION: We aimed to assess the predictors of new supraventricular tachycardia (SVT) and the association of new SVT with subsequent clinical outcomes among mild heart failure (HF) patients. METHODS AND RESULTS: The study population comprised patients enrolled in MADIT-CRT, after exclusion of patients with atrial arrhythmias before enrollment (N = 325). Multivariate analysis was used to identify predictors of new-onset SVT and the association of time-dependent development of SVT with subsequent ventricular tachyarrhythmic events (VTEs), HF-hospitalizations, and death. SVT burden was categorized into three groups based on the number of episodes per patient; (a) Low <10, (b) Intermediate ≥10 but <20, and (c) High ≥20. During mean follow up of 3.4 ± 1.1 years, 41(3%) subjects developed new SVT. African American race, diastolic blood pressure (DBP) >80 mmHg and prior non sustained ventricular arrhythmia were independent predictors for SVT. Multivariate analysis showed that the development of time-dependent SVT was associated with a >4-fold increased risk for VTEs (HR = 4.3; 95% CI: 1.6-11.7; P = .004) and with a >6-fold increased risk for all-cause mortality (HR = 6.5; 95% CI: 2.3-18.7; P < .001), but not with HF hospitalizations (HR = 2.2; 95% CI: 0.7-7.2; P = .17). Intermediate, and high SVT-burden were each independent risk factors for death when compared with Low burden (HR = 9.1; P = .03, and HR = 19.4; P < .001; respectively). CONCLUSIONS: In patients with mild HF, the development of new-onset SVT after device implantation is related to distinct baseline clinical and epidemiologic characteristics and is associated with a significant increase in subsequent adverse outcomes, including VTEs and death.
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Younis et al. (2020) studied this question.
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