Catheter ablation of short-coupled variant of torsade de pointes

The short-coupled variant of torsade de pointes (sc-TdP) was originally described by Leenhardt et al. in 1994 who reported 14 patients with structurally normal hearts, absence of QT interval prolongation, and TdP induced by a premature ventricular contraction (PVC) with late transition left bundle branch block (LBBB) pattern, left superior axis, and a coupling interval of less than 300 ms consistent with a right ventricular (RV) moderator band (MB) origin [1‐3]. However, based on the introduction of imaging techniques such as 3D-mapping [4] and intracardiac echocardiography (ICE) [5], sc-TdP and idiopathic ventricular fibrillation (iVF) from the MB have been characterized as different clinical entities which still translates into different therapeutic approaches [1‐3]: Verapamil is still considered the first-line therapy in sc-TdP [6] whereas catheter ablation is the treatment of choice for iVF from the MB [2, 3]. Over the past 25 years, numerous reports have highlighted the malignant phenotype of sc-TdP and the insufficient pharmacological treatment (failure of amiodarone, β-blocker, Mg²⁺, lidocaine, procainamide, quinidine, and cilostazol) while catheter ablation is not widely adopted [1, 7‐11]. Indeed, one-third of patients with sc-TdP, being treated with either verapamil or β-blockers, die suddenly during a mean follow-up of 7 years [1]. The aim of this study was to assess the precise origin of sc-TdP and to assess the short- and long-term outcomes of catheter ablation of sc-TdP using 3D-mapping and ICE.

We retrospectively reviewed the databases of five institutions for sc-TdP treated with 3D-mapping and radiofrequency (RF) catheter ablation. The patients had to have electrocardiographic evidence of sc-TdP, i.e. PVC-induced polymorphic ventricular tachycardia or PVC-induced VF triggered by a monomorphic PVC with late transition LBBB pattern, left superior axis, and a coupling interval of less than 300 ms. Electrophysiological (EP) studies were performed at the discretion of the individual operators. All patients have given written informed consent for publication and ethics approval was not required.

We identified five patients (mean age 36.6 ± 13 years) with sc-TdP who underwent 3D-mapping and ablation of sc-TdP between 2011 and 2019 at five different institutions. Four patients initially presented with sudden cardiac arrest, one patient experienced recurrent syncope as the first manifestation of the arrhythmia. Two patients developed electrical storm either during or 2 years after initial admission (Table 1). Structural and ischemic heart disease had been excluded by echocardiography and coronary angiography in all patients. Cardiac MRI was unremarkable in three patients. All patients demonstrated late transition, left superior axis PVCs with extremely short coupling intervals ranging from 280 to 240 ms (Fig. 1) triggering recurrent sc-TdP or VF. Anti–arrhythmic drug therapy was ineffective to control the arrhythmia (Table 1) except for Verapamil and Ajmaline. Ajmaline not only led to the suppression of short-coupled PVCs in patient #2 but also to VF termination (Fig. 2). Three-dimensional electro-anatomical activation mapping of the culprit PVC was performed in all patients. Intracardiac echocardiography (ICE) (AcuNav, Siemens Medical Solutions, USA and Soundstar/Cartosound, Biosense Webster, USA) was available in four patients. In the last three patients high-resolution 3D-mapping, i.e. multipolar mapping catheters with close interelectrode spacing (Pentaray, Biosense Webster, USA; Orion, Boston-Scientific, USA; LiveWire, Abbott; USA) and a steerable sheath (Agilis NxT, Abbott, USA) were used. Ectopy was spontaneous in four and induced by atrial pacing in one patient. In all patients, normal bi- and unipolar voltages without any late or fragmented potentials were demonstrated on endocardial voltage maps. In four patients, the culprit PVC was mapped to the free wall insertion of the moderator band (MB) with a preceding Purkinje potential in two patients (Fig. 3 and Suppl. 1) which were effectively targeted with RF ablation. In one patient without distinct MB the culprit PVC was ablated at a right ventricular (RV) papillary muscle. All patients were implanted with a transvenous (2) or subcutaneous (3) implantable cardioverter-defibrillator (ICD) for secondary prevention. Device interrogations confirmed the elimination of sc-TdP in all patients, with no recurrence at mean 2.7 years (range 6 months to 8 years) of follow-up.

To our knowledge, this is the first study using high-resolution 3D-mapping to specify the free wall insertion of the RV MB as the predominant origin of short-coupled PVCs triggering sc-TdP. As the right bundle branch and its Purkinje network run along with the MB and arborize via the MB at the free wall, it is possible to record myocardial as well as Purkinje potentials in this region as seen in our patients. In one patient ablation was performed at an papillary muscle, i.e. at the MB complex. RV Purkinje VF triggers display an uniform morphology which has first been reported by Haïssaguerre et al. who pioneered mapping and ablation of Purkinje-related idiopathic VF (iVF) [12‐14]. In addition, Haïssaguerre et al. provided non-invasive ECG imaging data of RV Purkinje triggers that point to the MB free wall insertion as PVC breakthrough site in these patients [14, 15]. Walton et al. also demonstrated ex vivo that uncoupled myocardial and Purkinje MB cells have different action potential durations facilitating re-entry and short-coupled PVCs in this region [16]. The identical PVC morphology has been found to represent a RV MB origin using ICE in a patient with VF storm [2] and a series of 10 patients with monomorphic VT, VF, and recurrent ICD shocks [3]. According to the recently proposed mechanistic classification of primary arrhythmogenic diseases causing sudden cardiac arrest by Haïssaguerre et al., sc-TdP should be classified as iVF from Purkinje-myocardial sources [17].

Three-dimensional activation mapping is essential for the understanding of complex ventricular arrhythmias and especially in cases of papillary muscle or moderator band sources [18]. However, 3D activation mapping of these endocardial structures may carry certain technical challenges. As seen in one patient, the mapping system may erroneously project internal activation points to the surface geometry (Fig. 3a and Suppl. 1) which can be misleading. Activation mapping of the earliest free wall activation site in sinus rhythm (Fig. 3b) may help to correctly localize the MB free wall junction. The novel point density exclusion (PDX) mapping algorithm (Fig. 3c)—that uses absent 3D mapping points within a ventricular lumen to create an endocavitary geometry—may represent an optimal approach in these cases as it allows to generate a separate internal geometry facilitating precise activation mapping [19]. In addition, as seen in two of our patients, multielectrode mapping catheters with close interelectrode spacing may enhance the detection of Purkinje potentials [20]. To monitor and improve contact and stability during mapping and ablation at the MB free wall junction, the use of ICE integrated into the 3D-mapping system as well as the cryoballoon have been advocated [5, 21]. Finally, pace-mapping, in case of non-inducibility of the clinical PVC, may also yield good results as the Purkinje network is an entirely endocardial structure.

The genesis of sc-TdP is currently incompletely understood. Two recent studies have linked sc-TdP with RyR-2 mutations leading to either a decreased RYR2 function or increased RYR2 leak which may promote triggered activity and early afterdepolarizations via an increased Ca²⁺ release. The PVC morphologies reported in those two studies are also typical of a MB-free wall origin [22, 23]. The induction of short-coupled PVCs with atrial overdrive pacing and suppression with Verapamil and Ajmaline in our patients also support triggered activity as the underlying mechanism of sc-TdP. The Dutch iVF cohort linked to the DPP6 risk haplotype shows identical PVC trigger morphologies (Xiao et al., Supp. Online Figure 1), however, based on a different mechanism. In these patients, the DPP6 mutation results in selectively accelerated Purkinje fiber repolarization which may lead to strong repolarization gradients with adjacent ventricular muscle creating an electrophysiological substrat for re-entry and short-coupled PVCs [24, 25]. The susceptibility of the RV MB free wall junction to generate short-coupled PVCs may also be related to a mechanical stretch of the MB during early diastole `mechanoelectrical feedback’ which may involve stretch-activated ion channels [26]. A link between short-coupled PVCs from the MB and mechanical function is supported by the beneficial effect of mechanical unloading in a single patient with intractable VF due to sc-TdP [8].

We have demonstrated that sc-TdP predominantly originates from the free wall insertion of the RV MB and its Purkinje network and particularly high-resolution 3D-mapping and ICE may be useful to precisely locate the triggering PVC in this region facilitating successful catheter ablation. Catheter ablation of sc-TdP leads to excellent short- and long-term results and should be considered as first-line therapy in patients presenting with recurrent TdP or electrical storm. Our observations support triggered activity as the underlying mechanism of sc-TdP which should be classified as iVF from Purkinje-myocardial sources.