Cardiovascular
Medicine
Pulsed Field Ablation for the Treatment of Atrial Fibrillation
Cardiology Angiology
A Promising Novel Ablation Technology
Peer-review

Pulsed Field Ablation for the Treatment of Atrial Fibrillation

Review Article
Cardiology Angiology
Alexander Breitensteina
Additional authors
Laurent Rotenb, Tobias Reichlinb
Issue
2024/02
DOI:
https://doi.org/10.4414/cvm.2024.1297020794
Cardiovasc Med. 2024;27(02):41-46
Affiliations
a Department of Cardiology, University Heart Center, University Hospital Zurich, Switzerland
b Department of Cardiology, Inselspital, University Hospital Bern, University of Bern, Switzerland

Published on 27.03.2024

Abstract

Atrial fibrillation (AF) has become the most common arrhythmia worldwide and its incidence is increasing. Treatment strategies for symptomatic patients include stroke prevention, management of cardiovascular comorbidities, and direct treatment of AF itself. With regard to interventional AF treatment, a novel technique called pulsed field ablation has emerged. Large registry data in more than 15,000 patients have demonstrated a high efficacy in reducing the burden of AF with a very high safety. This review provides an overview of the technical aspects of pulsed field ablation and the published clinical data.
Keywords: Atrial fibrillation; catheter ablation; efficacy; pulsed field ablation; safety

Introduction

With the increasing prevalence of cardiovascular risk factors, atrial fibrillation (AF) has become the most common arrhythmia worldwide [1]. According to recent calculations, it is expected that the number of affected Europeans will triple by 2050 [2]. Patients suffering from AF experience symptoms like palpitations, dyspnea, dizziness and exercise intolerance [3]. Furthermore, registry analyses show an association between AF and higher mortality [4, 5]. AF treatment includes stroke prevention with oral anticoagulation in those at increased risk for thromboembolic events, control of cardiovascular risk factors (e.g., arterial hypertension, obesity, diabetes mellitus type 2), and treatment of AF itself [3]. Regarding the latter, either a rate control (and hence acceptance of AF), or a rhythm control strategy can be adopted. Recently, an early rhythm control strategy has been shown to improve the prognosis of AF patients regarding death, stroke and major cardiovascular events [6]. For rhythm control, either antiarrhythmic drugs or a catheter intervention can be selected. The primary goal of a catheter intervention is pulmonary vein isolation (PVI), since seminal studies have identified the triggers which induce AF to be mainly located in the pulmonary veins [7]. Recent randomized trials showed that catheter interventions using either radiofrequency ablation or cryothermal energy are more effective in reducing AF burden and preventing disease progression than antiarrhythmic drugs [8–10]. Even though there were many advances over the past decades in improving efficacy and outcome of PVI, considerable safety concerns remain, including risk of periinterventional stroke, pericardial tamponade, phrenic nerve palsy, pulmonary vein stenosis and atrio-esophageal fistula. The last three complications are typically linked to thermal ablation energy were the ablative heat or cold wave expands through the myocardial wall potentially damaging the surrounding tissue. Pulsed field ablation (PFA) is a novel nonthermal ablation modality selectively targeting the myocardium. As demonstrated in preclinical as well as clinical studies, PFA significantly reduces the risk for energy-related collateral damage associated with thermal ablation [11, 12].

Pulsed Field Ablation Technology

PFA is a tissue-selective nonthermal cardiac ablation modality [13]. On a cellular level, lesion formation is achieved by applying ultra-rapid (microseconds to nanoseconds) alternating (biphasic) electrical fields, either between two electrical poles of a catheter (bipolar PFA) or between the electrical poles of a catheter and a grounding patch attached to the skin of the patient (unipolar PFA). If the electrical field is strong enough, it leads to irreversible nanopore formation (also referred to as electroporation) in the myocardial cell membrane and subsequent cell death [14]. Of importance is that the myocardial tissue exhibits a higher susceptibility towards electroporation compared to the surrounding tissue like the phrenic nerve or the esophagus. This results in a highly selective ablation of the myocardium by using an optimized PFA waveform [15, 16]. Therefore, PFA has a broad therapeutic window and offers high efficacy (myocardial damage) on one side and excellent safety (little to no collateral damage) on the other side. Indeed, previous preclinical and clinical work confirms the selectivity of PFA towards the myocardium, sparing surrounding nerves, vascular and esophageal tissue [15–17].

General Overview of Interventional Catheter Ablation for AF and other PFA Systems

The primary goal of interventional AF ablation is the isolation of the pulmonary veins. This can be achieved by a point-by-point circumferential ablation or by a single-shot ablation technique, where the ablation catheter is placed at the ostium of the pulmonary vein and it is isolated by energy delivery [18]. Over the last decades, radiofrequency energy was the primary type of energy used for the point-by-point technique, while cryoballoon ablation was the preferred method for single-shot ablations [18]. It was demonstrated, that for paroxysmal AF patients, both approaches are equally efficient [19]. In the emerging field of PFA, different ablation catheters are either already or will soon be approved in clinical use offering both a point-by-point or a single-shot ablation approach (table 1). The Farapulse™ PFA system was the first to receive a CE mark and therefore most available clinical data currently stems from this system.

Workflow of a PFA Procedure Using the FARAPULSE™ System

So far, the largest clinical experience is available for the Farapulse™ PFA system (Boston Scientific Inc., Marlborough, MA, United States). In brief, this system uses a pentaspline catheter with four electrodes on each spline (fig. 1). While all electrodes are used for pulsed field energy application (poles 1–4), the third electrode from the tip is used for electrogram recording and pacing (pole 3). To deliver pulsed field energy, the generator (Farastar™, Boston Scientific Inc.) builds an electrical field of 1,800-2,000 Volts which is then delivered as a bipolar biphasic wave between the electrodes of the catheter [20]. A train of five consecutive bursts of pulsed field energy is applied over a total of 2.5 seconds per application (fig. 2).
Figure 1: Pentaspline ablation catheter in basket (A) and flower (B) configuration.
Figure 2: Energy application during pulsed field ablation and acute isolation of the pulmonary veins.
After femoral venous access, a single transseptal puncture is performed under fluoroscopy guidance to gain access to the left atrium. Next, a 13Fr deflectable sheath (Faradrive™, Boston Scientific Inc.) is placed in the left atrium and the 12Fr multi-electrode pentaspline PFA catheter (Farawave™, Boston Scientific Inc.) is advanced over the sheath. Alternatively, transseptal access can be directly obtained via the 13Fr deflectable sheath [21]. Over a 0.035” J-guidewire, the PFA catheter is advanced towards the ostium of each pulmonary vein. Using the integrated pulling-wire mechanism of the catheter, the shape of the five splines of the catheter can be changed to a basket-like configuration when partially expanded or to a flower-like configuration when fully retracted (fig. 1 and 3). According to early experience, pulmonary vein ablation is best performed in pairs of energy delivery [20]. A first pair of pulsed field energy application is given in basket configuration with the catheter positioned at the ostium (fig. 3). Next, the device is rotated by 36° to cover the area between the splines of the first application and another pair of pulsed field energy applications is given (fig. 3). Then, the shape of the splines is changed to the flower configuration and the catheter is placed more proximal on the pulmonary vein ostia (fig. 3). The same 2×2 set of pulsed field energy applications as in the basket configuration are delivered. Therefore, as a standard, a total of eight energy application is given to each pulmonary vein [20, 22].
Figure 3 : Positioning of the ablation catheter in the left upper pulmonary vein (RAO view).
During the intervention, intravenous heparin is given to maintain an activated clotting time (ACT) of more than 350 seconds. Since the application of pulsed field energy is painful even in the bipolar mode, the intervention must be performed either in deep sedation using a combination of midazolam and propofol, or under general anesthesia [22, 23]. However, it is important to mention that patient preparation prior to the intervention as well as patient management during and after the intervention do not differ from traditional PVI ablation approaches such as cryoballoon or radiofrequency ablations. 3D-mapping of the left atrium (fig. 3) can be performed prior to and after the ablation but is not mandatory nor necessary to confirm PVI. Disappearance of the local electrical signal at the pulmonary vein ostia following application (fig. 2) can be used to judge successful energy delivery, while entry and exit block verified by pacing from the PFA catheter at the end of the ablation procedure serves to control for successful PVI [24]. In contrast to radiofrequency ablation, direct visualization of biological effects at the ablated tissue, such as real-time changes in the local electrogram or a drop in the catheter ablation impedance are not available. However, 3D-mapping is especially helpful in more advanced stages of AF (e.g., persistent, or longstanding-persistent AF), where in addition to PVI, the posterior wall of the left atrium can also be isolated in patients exhibiting extensive electrical scaring on the posterior wall [25].

Procedural Safety of PFA for AF Ablation

As recently confirmed in the CABANA trial, the treatment of AF with catheter ablation is a safe intervention [8]. Complications in the context of catheter ablations can be split into thermal- (related to the energy source chosen for ablation) and non-thermal related complications (resulting from device and sheath handling as well as periinterventional anticoagulation). Independent of catheter design, PFA technology offers a high safety profile since the risk for the feared thermal collateral damage is extremely low [20, 22, 23, 26–28].

Atrio-esophageal Fistula

Atrio-esophageal fistula, a rare but feared thermal complication with a high mortality rate, has not been observed with PFA technology [20, 22, 23]. In patients from the 5S study, during which an esophageal temperature probe was used during the procedure and a postprocedural endoscopy was performed, no relevant rise in intestinal temperature was seen and there was no evidence of thermal-related mucosal injury during endoscopy [22]. Consistently, in the multi-national MANIFEST-PF survey including more than 1,700 patients without any periinterventional esophageal protection strategy, no esophageal injury was reported during the follow-up period [23]. In contrast, the POTTER-AF study reported an incidence of atrio-esophageal fistula of 0.038% after radiofrequency and 0.0015% after cryoballoon ablation with a mortality of 66% [29].

Pulmonary Vein Stenosis

Scar formation after the ablation procedure can result in narrowing of the pulmonary vein lumen if the ablation lesions are set too distally from the antral pulmonary vein ostium. After radiofrequency ablation, pulmonary vein narrowing has been observed in nearly one third of all cases [30], usually without any clinical relevance, while such narrowing has not been seen using PFA technology [26, 27, 30, 31]. The absence of clinically relevant pulmonary vein stenosis was confirmed by the MANIFEST-PF survey [23].

Persistent Phrenic Nerve Palsy

Phrenic nerve palsy is a rare but relevant adverse event usually occurring after single-shot cryoballoon ablation procedures. In the MANIFEST-PF cohort, there was only one case of persistent palsy of the phrenic nerve after PFA [23], while transient palsy was observed in eight patients (0.46%). The latter most likely resulted from electrical hyperpolarization of neural cells and regressed within hours after the procedure. In the PULSED AF pivotal trial [27] as well as in the multicenter inspIRE study [26], no permanent phrenic nerve lesions were observed. The very low risk of permanent nerve palsy is in line with preclinical data confirming preserved nerve fascicles within the ablation area after PFA treatment [32].

Non-thermal Complications

Non-thermal (mechanical) complications following PFA can occur at similar rates as after ablation technologies using thermal energy sources. Pericardial tamponade due to catheter and sheath manipulation occurred in around 1 out of 100 procedures in patients undergoing PFA procedures [20, 22, 23]. Transient ischemic attack or stroke was documented in 0.5% of patients in the MANIFEST-PF survey and in 2 out of 191 patients (1%) in the initial validation phase of the single-center 5S trial (Safe and Simple Single Short Pulmonary Vein Isolation with Pulsed Field Ablation Using Sedation) [22]. These events most likely resulted from air embolism or embolization of small clots emphasizing the need for careful removal of air from the large bore sheath used for the procedure [22]. Silent cerebral lesions were identified in 10 out of 53 patients (19%), which corresponds to the finding in patients undergoing thermal ablation procedures [22]. The most frequent complications in the MANIFEST-PF survey were of vascular origin including groin hematomas (2.44%), of which the majority were managed conservatively [23].
Figure 4: Three-dimensional reconstruction of the left atrium before (A) and after (B) ablation (posterior view).
LIPV: Left inferior pulmonary vein; LSPV: Left superior pulmonary vein; RIPV: Right inferior pulmonary vein; RSPV: Right superior pulmonary vein.

Uncertainties, Limitations and Potential Risks

Selectivity for Myocardial Tissue and Thermal Effects

PFA technology offers PVI with a very low complication rate which is, at least in part, due to the highly specific effect of the applied energy to the myocardial tissue. However, this specificity is not 100% and the risk of collateral damage is not zero. The entire tissue which is exposed to the electrical field during PFA is affected by the applied energy; however, each tissue has a characteristic threshold for irreversible electroporation [18]. According to previous data, this threshold is low for myocardial tissue (thus making the myocardium very susceptible for electroporation), but much higher for red blood cells, vascular smooth muscle cells or endothelium and even higher for nerve fibers. This difference in susceptibility offers a certain degree of selectivity; still, if the cumulative energy applied by PFA exerts a certain level, the selectivity will decrease and damage to other organs can happen. As an example, in a cohort of patients undergoing either radiofrequency ablation or PFA, lesions at the descending aorta, although without any clinical consequence, have been seen on MRI analysis in nearly half of the patients after both interventions [33]. This knowledge of potential decreasing myocardium-selectivity is of paramount importance, because the observed high safety profile of PFA may potentially mislead operators to perform too many PFA applications.
The effect of PFA results primarily from a non-thermal creation of nanopores into the myocardial cell membrane. However, some degree of heating cannot be avoided and previous animal studies have shown a rise in temperature in proximity of the ablation catheter [34]. While the maximal temperature correlated with the applied energy, the rise in the temperature did not exert an effect beyond the myocardium [34, 35] and therefore is unlikely to cause a relevant clinical effect. However, similar to the specificity of PFA to the myocardium, this also applies to the PFA applications being within the tested energy dosages and do not significantly exceed the recommended number of deliveries. Apart from tissue heating, the blood surrounding the ablation catheter may also be affected by a rise in temperature. Because an increase of blood temperature from 50 to 80 °C can cause the formation of soft thrombi, this can lead to silent as well as clinically relevant strokes. Indeed, in the study by Zang et al, the highest temperature between the catheter and the blood during energy application exceeded 70 °C. Since the energy impulses are of short duration, the clinical relevance is unclear, but to minimize the risk of clot formation it is recommended to keep the ACT above 350 seconds during the intervention.

Coronary Vasospasm

Not rarely, patients with AF suffer from atrial flutter (AFL) as well hence, ablation beyond PVI is necessary to treat this population adequately. This includes ablation at the cavotricuspid isthmus (for typical right-sided AFL), at the left atrial roof (for left-sided roof-dependent AFL) or at the mitral isthmus (for perimitral flutter). Anatomically, the cavotricuspid as well the mitral isthmus are located in the proximity of coronary arteries and ablation at this localization can lead to injury of a coronary artery. For PFA, vasospasms have been described both in animal models as well as in humans when coronary angiography was performed concomitantly to the PFA energy application [36, 37]. While the majority was subclinical without a relevant effect, reports of patients who developed ST-segment elevation and subsequent ventricular fibrillation emphasize the potential risk [37, 38]. It remains unclear whether the design of the pentaspline catheter or PFA itself is responsible for the occurrence of vasospasm, since patients who underwent ablation of the cavotricuspid isthmus using a focal PFA catheter (but with the same energy waveform) showed no signs of vasospasms or ST-segment elevation [25]. However, with the currently available PFA system it is recommended to avoid ablation close to the coronary arteries.

Interaction with Cardiac Implantable Devices

This is indeed a not yet fully resolved issue of PFA ablations, but of growing relevance since the number of patients suffering from AF that also have other devices implanted (e.g., pacemaker, left atrial appendage occluder) is rising. Chen and colleagues published a case series of twenty patients with either a transvenous pacemaker or defibrillator undergoing PFA [39]. One of them also had a left atrial appendage device occluder implanted. In all patients, the ablation procedure (with the goal to avoid direct contact between ablation catheter and the device component) could be performed without any side effects and no long-term delirious effects have been identified on device interrogation. This observation is supported by previous experience with electroporation in oncologic patients with an implantable device where also no negative impacts on the device parameters have been observed [40].

Procedural Efficacy for AF Ablation

Durable isolation of the pulmonary veins is the major determining factor for the efficacy and benefit of catheter ablation in AF. The first three human trials with the Farapulse™ PFA system (IMPULSE, PEFCAT and PEFCAT II) have shown that acute PVI was achieved in 100% with 7.2±2.2 applications per vein [20]. Importantly, during the invasive reassessment performed after a median of 84 days, 96% of the pulmonary veins remained durably isolated in patients treated with the optimized biphasic waveform and there were no signs of lesion regression over time [41]. In the MANIFEST-PF survey enrolling 1,758 patients at 24 centers, acute PVI was achieved in nearly all patients (99.9%) [23]. This is similar to the experience from the single-center 5S trial in which all pulmonary veins were isolated at the end of the procedure (99.5% after the first application of pulsed field energy) [22].
In most cases the ablation procedure was performed under deep sedation using intravenous propofol, midazolam and opioid analgesics. Although, in the MANIFEST registry, more than 80% of all interventions were performed without general anesthesia [23]. The procedure duration (skin-to-skin) in the mentioned trials including both paroxysmal as well as persistent AF patients, declined with greater operator experience from 96.2±30.3 minutes (IMPULSE and PEFCAT) [20] to 65 minutes in the MANIFEST-PF survey [23] and to 39±14 minutes in the 5S study [22].

12-months Outcome

The one-year outcome of the IMPULSE, PEFCAT and PEFCAT II trial, enrolling primarily patients suffering from paroxysmal AF, showed freedom from any atrial arrhythmia longer than 30 seconds in 84±5.4% for the optimized biphasic bipolar waveform. These results were supported by the recently published data of the MANIFEST-PF trial, which showed freedom from atrial arrhythmias in 78.1% at one-year [42]. A meta-analysis on PVI with PFA confirmed these findings documenting a recurrence of atrial arrhythmia in only 11% of the population after a follow-up of 9±3 months [43]. There is one randomized trial recently presented at the European Society of Cardiology meeting 2023 in Amsterdam and simultaneously published in the New England Journal of Medicine [31], that demonstrates an equal efficacy of PFA versus cryoballoon or radiofrequency ablation in patients with paroxysmal AF with a low rate of major side effects in both groups. There were two tamponades in the PFA group, one of them leading to death due to long resuscitation and multiple organ failure, and one stroke in the thermal ablation population. Further trials comparing efficacy and safety of PVI with PFA to PVI with thermal ablation are underway (e.g., SINGLE SHOT CHAMPION Study, NCT05534581).

Conclusion

PFA technology is a novel treatment option for cardiac arrhythmias. So far, the efficacy of PFA for the reduction of AF seems to be at least as good as conventional thermal energy sources, and theoretically with a better thermal collateral damage safety profile. PVI can be accomplished rapidly with similar efficacy and without compromising safety in our patients. In the near future, other ablation devices using electroporation will be available for the treatment of AF and other arrhythmias, like ventricular tachycardias, will be addressed using PFA technology.
Dr Alexander Breitenstein
Department of Cardiology
University Heart Center Zurich
University Hospital Zurich
Raemistrasse 100
CH-8091 Zurich
alexander.breitenstein[at]usz.ch
1 Benjamin EJ, Muntner P, Alonso A, Bittencourt MS, Callaway CW, Carson AP, et al.; American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2019 Update: A Report From the American Heart Association. Circulation. 2019 Mar;139(10):e56-528.
2 Colilla S, Crow A, Petkun W, Singer DE, Simon T, Liu X. Estimates of current and future incidence and prevalence of atrial fibrillation in the U.S. adult population. Am J Cardiol. 2013 Oct;112(8):1142-7.
3 Hindricks G, Potpara T, Dagres N, Arbelo E, Bax JJ, Blomström-Lundqvist C, et al.; ESC Scientific Document Group. 2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association of Cardio-Thoracic Surgery (EACTS): The Task Force for the diagnosis and management of atrial fibrillation of the European Society of Cardiology (ESC) Developed with the special contribution of the European Heart Rhythm Association (EHRA) of the ESC. Eur Heart J. 2021 Feb;42(5):373-498. Erratum in: Eur Heart J. 2021 Feb;42(5):507. Erratum in: Eur Heart J. 2021 Feb;42(5):546-7. Erratum in: Eur Heart J. 2021 Oct;42(40):4194.
4 Magnani JW, Norby FL, Agarwal SK, Soliman EZ, Chen LY, Loehr LR, et al. Racial Differences in Atrial Fibrillation-Related Cardiovascular Disease and Mortality: The Atherosclerosis Risk in Communities (ARIC) Study. JAMA Cardiol. 2016 Jul;1(4):433-41.
5 Chamberlain AM, Gersh BJ, Alonso A, Chen LY, Berardi C, Manemann SM, et al. Decade-long trends in atrial fibrillation incidence and survival: a community study. Am J Med. 2015 Mar;128(3):260-7.e1.
6 Kirchhof P, Camm AJ, Goette A, Brandes A, Eckardt L, Elvan A, et al.; EAST-AFNET 4 Trial Investigators. Early Rhythm-Control Therapy in Patients with Atrial Fibrillation. N Engl J Med. 2020 Oct;383(14):1305-16.
7 Haïssaguerre M, Jaïs P, Shah DC, Takahashi A, Hocini M, Quiniou G, et al. Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins. N Engl J Med. 1998 Sep;339(10):659-66.
8 Packer DL, Mark DB, Robb RA, Monahan KH, Bahnson TD, Poole JE, et al.; CABANA Investigators. Effect of Catheter Ablation vs Antiarrhythmic Drug Therapy on Mortality, Stroke, Bleeding, and Cardiac Arrest Among Patients With Atrial Fibrillation: The CABANA Randomized Clinical Trial. JAMA. 2019 Apr;321(13):1261-74.
9 Andrade JG, Wells GA, Deyell MW, Bennett M, Essebag V, Champagne J, et al.; EARLY-AF Investigators. Cryoablation or Drug Therapy for Initial Treatment of Atrial Fibrillation. N Engl J Med. 2021 Jan;384(4):305-15.
10 Andrade JG, Deyell MW, Macle L, Wells GA, Bennett M, Essebag V, et al.; EARLY-AF Investigators. Progression of Atrial Fibrillation after Cryoablation or Drug Therapy. N Engl J Med. 2023 Jan;388(2):105-16.
11 Neven K, van Es R, van Driel V, van Wessel H, Fidder H, Vink A, et al. Acute and Long-Term Effects of Full-Power Electroporation Ablation Directly on the Porcine Esophagus. Circ Arrhythm Electrophysiol. 2017 May;10(5):e004672.
12 Reddy VY, Koruth J, Jais P, Petru J, Timko F, Skalsky I, et al. Ablation of Atrial Fibrillation With Pulsed Electric Fields: An Ultra-Rapid, Tissue-Selective Modality for Cardiac Ablation. JACC Clin Electrophysiol. 2018 Aug;4(8):987-95.
13 Wittkampf FH, van Es R, Neven K. Electroporation and its Relevance for Cardiac Catheter Ablation. JACC Clin Electrophysiol. 2018 Aug;4(8):977-86.
14 Kotnik T, Rems L, Tarek M, Miklavčič D. Membrane Electroporation and Electropermeabilization: mechanisms and Models. Annu Rev Biophys. 2019 May;48(1):63-91.
15 van Driel VJ, Neven K, van Wessel H, Vink A, Doevendans PA, Wittkampf FH. Low vulnerability of the right phrenic nerve to electroporation ablation. Heart Rhythm. 2015 Aug;12(8):1838-44.
16 Koruth J, Kuroki K, Iwasawa J, Enomoto Y, Viswanathan R, Brose R, et al. Preclinical Evaluation of Pulsed Field Ablation: Electrophysiological and Histological Assessment of Thoracic Vein Isolation. Circ Arrhythm Electrophysiol. 2019 Dec;12(12):e007781.
17 Koruth JS, Kuroki K, Kawamura I, Brose R, Viswanathan R, Buck ED, et al. Pulsed Field Ablation Versus Radiofrequency Ablation: Esophageal Injury in a Novel Porcine Model. Circ Arrhythm Electrophysiol. 2020 Mar;13(3):e008303.
18 Ramirez FD, Reddy VY, Viswanathan R, Hocini M, Jaïs P. Emerging Technologies for Pulmonary Vein Isolation. Circ Res. 2020 Jun;127(1):170-83.
19 Kuck KH, Brugada J, Fürnkranz A, Metzner A, Ouyang F, Chun KR, et al.; FIRE AND ICE Investigators. Cryoballoon or Radiofrequency Ablation for Paroxysmal Atrial Fibrillation. N Engl J Med. 2016 Jun;374(23):2235-45.
20 Reddy VY, Neuzil P, Koruth JS, Petru J, Funosako M, Cochet H, et al. Pulsed Field Ablation for Pulmonary Vein Isolation in Atrial Fibrillation. J Am Coll Cardiol. 2019 Jul;74(3):315-26.
21 Kueffer T, Madaffari A, Thalmann G, Mühl A, Galuszka O, Baldinger S, et al. Eliminating transseptal sheath exchange for pulsed field ablation procedures using a direct over-the-needle transseptal access with the Faradrive sheath. Europace. 2023 Apr;25(4):1500-2.
22 Schmidt B, Bordignon S, Tohoku S, Chen S, Bologna F, Urbanek L, et al. 5S Study: Safe and Simple Single Shot Pulmonary Vein Isolation With Pulsed Field Ablation Using Sedation. Circ Arrhythm Electrophysiol. 2022 Jun;15(6):e010817.
23 Ekanem E, Reddy VY, Schmidt B, Reichlin T, Neven K, Metzner A, et al.; MANIFEST-PF Cooperative. Multi-national survey on the methods, efficacy, and safety on the post-approval clinical use of pulsed field ablation (MANIFEST-PF). Europace. 2022 Sep;24(8):1256-66.
24 Kueffer T, Baldinger SH, Servatius H, Madaffari A, Seiler J, Mühl A, et al. Validation of a multipolar pulsed-field ablation catheter for endpoint assessment in pulmonary vein isolation procedures. Europace. 2022 Sep;24(8):1248-55.
25 Reddy VY, Anic A, Koruth J, Petru J, Funasako M, Minami K, et al. Pulsed Field Ablation in Patients With Persistent Atrial Fibrillation. J Am Coll Cardiol. 2020 Sep;76(9):1068-80.
26 Duytschaever M, De Potter T, Grimaldi M, Anic A, Vijgen J, Neuzil P, et al.; inspIRE Trial Investigators. Paroxysmal Atrial Fibrillation Ablation Using a Novel Variable-Loop Biphasic Pulsed Field Ablation Catheter Integrated With a 3-Dimensional Mapping System: 1-Year Outcomes of the Multicenter inspIRE Study. Circ Arrhythm Electrophysiol. 2023 Mar;16(3):e011780.
27 Verma A, Haines DE, Boersma LV, Sood N, Natale A, Marchlinski FE, et al.; PULSED AF Investigators. Pulsed Field Ablation for the Treatment of Atrial Fibrillation: PULSED AF Pivotal Trial. Circulation. 2023 May;147(19):1422-32.
28 Reddy VY, Peichl P, Anter E, Rackauskas G, Petru J, Funasako M, et al. A Focal Ablation Catheter Toggling Between Radiofrequency and Pulsed Field Energy to Treat Atrial Fibrillation. JACC Clin Electrophysiol. 2023 Aug;9(8 Pt 3):1786-801.
29 Tilz RR, Schmidt V, Pürerfellner H, Maury P, Chun KR, Martinek M, et al. A worldwide survey on incidence, management and prognosis of oesophageal fistula formation following atrial fibrillation catheter ablation: the POTTER-AF study. Eur Heart J. 2023 Jul;44(27):2458-69.
30 Kuroki K, Whang W, Eggert C, Lam J, Leavitt J, Kawamura I, et al. Ostial dimensional changes after pulmonary vein isolation: pulsed field ablation vs radiofrequency ablation. Heart Rhythm. 2020 Sep;17(9):1528-35.
31 Reddy VY, Gerstenfeld EP, Natale A, Whang W, Cuoco FA, Patel C, et al.; ADVENT Investigators. Pulsed Field or Conventional Thermal Ablation for Paroxysmal Atrial Fibrillation. N Engl J Med. 2023 Aug;NEJMoa2307291.
32 Koruth JS, Kuroki K, Iwasawa J, Viswanathan R, Brose R, Buck ED, et al. Endocardial ventricular pulsed field ablation: a proof-of-concept preclinical evaluation. Europace. 2020 Mar;22(3):434-9.
33 Cochet H, Nakatani Y, Sridi-Cheniti S, Cheniti G, Ramirez FD, Nakashima T, et al. Pulsed field ablation selectively spares the oesophagus during pulmonary vein isolation for atrial fibrillation. Europace. 2021 Sep;23(9):1391-9.
34 Zang L, Gu K, Ji X, Zhang H, Yan S, Wu X. Comparative Analysis of Temperature Rise between Convective Heat Transfer Method and Computational Fluid Dynamics Method in an Anatomy-Based Left Atrium Model during Pulsed Field Ablation: A Computational Study. J Cardiovasc Dev Dis. 2023 Jan;10(2):56.
35 Caluori G, Odehnalova E, Jadczyk T, Pesl M, Pavlova I, Valikova L, et al. AC Pulsed Field Ablation Is Feasible and Safe in Atrial and Ventricular Settings: A Proof-of-Concept Chronic Animal Study. Front Bioeng Biotechnol. 2020 Dec;8:552357.
36 Neven K, van Driel V, van Wessel H, van Es R, du Pré B, Doevendans PA, et al. Safety and feasibility of closed chest epicardial catheter ablation using electroporation. Circ Arrhythm Electrophysiol. 2014 Oct;7(5):913-9. Erratum in: Circ Arrhythm Electrophysiol. 2014 Dec;7(6):1282.
37 Reddy VY, Petru J, Funasako M, Kopriva K, Hala P, Chovanec M, et al. Coronary Arterial Spasm During Pulsed Field Ablation to Treat Atrial Fibrillation. Circulation. 2022 Dec;146(24):1808-19.
38 Della Rocca DG, Del Monte A, Bala G, Pannone L, Ströker E, Monaco C, et al. Transient Inferior ST-Segment Elevation and Ventricular Fibrillation After Cavotricuspid Isthmus Pulsed-Field Ablation. JACC Clin Electrophysiol. 2023 May;9(5):704-6.
39 Chen S, Chun JK, Bordignon S, Tohoku S, Urbanek L, Schaack D, et al. Pulsed field ablation-based pulmonary vein isolation in atrial fibrillation patients with cardiac implantable electronic devices: practical approach and device interrogation (PFA in CIEDs) [published online 2022 Dec 8]. J Interv Card Electrophysiol. 2023 Nov;66(8):1929-1938.
40 Jarm T, Krmac T, Magjarevic R, Kos B, Cindric H, Miklavcic D. Investigation of safety for electrochemotherapy and irreversible electroporation ablation therapies in patients with cardiac pacemakers. Biomed Eng Online. 2020 Nov;19(1):85.
41 Kawamura I, Neuzil P, Shivamurthy P, Petru J, Funasako M, Minami K, et al. Does pulsed field ablation regress over time? A quantitative temporal analysis of pulmonary vein isolation. Heart Rhythm. 2021 Jun;18(6):878-84.
42 Turagam MK, Neuzil P, Schmidt B, Reichlin T, Neven K, Metzner A, et al. Safety and Effectiveness of Pulsed Field Ablation to Treat Atrial Fibrillation: One-Year Outcomes From the MANIFEST-PF Registry. Circulation. 2023 Jul;148(1):35-46.
43 Shaheen N, Shaheen A, Ramadan A, Nashwan AJ. Efficacy and safety of novel pulsed field ablation (PFA) technique for atrial fibrillation: A systematic review and meta-analysis. Health Sci Rep. 2023 Jan;6(1):e1079.
Conflict of Interest Statement
Dr Breitenstein has received consulting fees and support for attending meetings paid to him directly and to the institution from Abbott, Bayer Healthcare, Biosense Webster, Biotronik, Boston Scientific, Bristo-Myers Squibb, Cook Medical, Daiichi Sankyo, Medtronic, Pfizer and Spectranetics/Philips.
Dr Roten has received speaker honoraria from Abbott, and consulting fees and a research grant for an investigator-initiated trial to the institution from Medtronic.
Dr Reichlin has received research grants from the Swiss National Science Foundation, the Swiss Heart Foundation, the sitem-insel Support Funds, Biotronik, Boston Scientific and Medtronic, all payments made to the institution. He has received speaker and/or consulting fees and/or travel support from Abbott/SJM, Bayer, Biosense-Webster, Biotronik, Boston Scientific, Farapulse, Medtronic and Pfizer-BMS, all payments were made to the institution.
No funding has been received in context of this manuscript.
Author Contributions
Conceptualization: All authors. Writing and original draft preparation: AB. Review and editing: All authors. All authors have read and agreed to the published version of the manuscript.

Published under the copyright license.

"Attribution - Non-Commercial - NoDerivatives 4.0"

No commercial reuse without permission.

See: emh.ch/en/emh/rights-and-licences/

 

 

To the top