To use programmed ventricular stimulation at the time of AF ablation to define the prevalence and mechanism of inducible ventricular tachycardia (VT); pace-mapping to define the site of origin of ventricular arrhythmias; and voltage mapping to define low voltage scar substrate in the basal LV in patients with pathogenic TTN variants compared to genotype-negative controls.
Participants will undergo AF ablation according to standard, contemporary techniques. The procedure will be performed under general anesthesia. As part of routine standard of care in patients with early-onset AF or patients who have PVCs, we will also test for inducibility of VT using a standardized pacing protocol. The research protocol will include LV mapping and identification of low voltage substrate using electroanatomical mapping as described below.
Study Type
OBSERVATIONAL
Enrollment
32
To use programmed ventricular stimulation at the time of AF ablation to define the prevalence and mechanism of inducible ventricular tachycardia (VT); pace-mapping to define the site of origin of ventricular arrhythmias; and voltage mapping to define low voltage scar substrate in the basal LV in patients with pathogenic TTN variants compared to genotype-negative controls.
Vanderbilt University Medical Center
Nashville, Tennessee, United States
VT Inducibility
The primary endpoint is induction of sustained VT that is determined to be reentrant or likely-reentrant. Sustained VT will be defined as VT lasting 30 seconds or requiring termination with burst pacing or cardioversion due to hemodynamic instability.
Time frame: At the time of procedure
Presence of ventricular arrhythmias per specific site
The primary endpoint is the occurrence (yes/no) of ventricular arrhythmias (PVCs, NSVT, sustained VT) that are mapped to the basal LV as defined above.
Time frame: At the time of procedure
Low voltage substrate
The primary endpoint is the presence of low voltage (yes/no) in the basal LV.
Time frame: At the time of procedure
Site of origin for ventricular arrhythmias
Secondary analyses will explore the rate of ventricular arrhythmias in other segments of the LV and RV and will compare the site of origin for ventricular arrhythmias in the group of participants with pathogenic variants in other CM genes.
Time frame: At the time of procedure
Evaluation of electrogram potentials
Secondary analyses will explore multicomponent electrograms and fractionated potentials that can be created by scar.
Time frame: At the time of procedure
Presence of low voltage
Other secondary analyses will compare the presence of low voltage and the other secondary endpoints in the group of participants with pathogenic variants in other CM genes.
Time frame: At the time of procedure
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.