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Objective Pulsed-field ablation (PFA) is a new technology of catheter ablation for atrialfibrillation (AF). This research is to investigate the feasibility of a new strategy (transoesophageal echocardiography-guided pulsed field ablation, TEEP) to guide PFA for AF with no contrast and zero fluoroscopy.
Atrialfibrillation (AFib) is a common heart rhythm disorder characterized by an irregular and often rapid heartbeat. What is AtrialFibrillation? Symptoms of AtrialFibrillation Symptoms vary among individuals. Consulting a local cardiologist is crucial for the proper diagnosis and management of AFib.
Ablation index (AI)-guided pulmonary vein isolation (PVI) has enhanced procedural outcomes for atrialfibrillation (AF).1 1 However, patients with persistent AF present higher recurrence rates due to advanced atrial remodeling,2-3 represented by the left atrial low voltage area (LVA), compared to those with paroxysmal AF.
Outcomes of ablation with the FARAPULSE PFA System – a nonthermal treatment in which electric fields selectively ablate heart tissue – will be compared to outcomes following use of anti-arrhythmic drug (AAD) therapy, which is commonly prescribed for patients living with persistent AF. The company now anticipates U.S. Circulation.
Pulsed field ablation (PFA) is safe for treating patients with common types of atrialfibrillation (AF), according to the largest study of its kind on this new technology, led by the Icahn School of Medicine at Mount Sinai.
As cryoballoon technology continues to evolve, the introduction of lower-pressure and selectable-size balloons presents new considerations for both safety and efficacy of cryoablation of atrialfibrillation.
Food and Drug Administration (FDA), has granted approval to Boston Scientific for its FARAPULSE Pulsed Field Ablation System. intermittent) atrialfibrillation (AF) and is a unique new alternative to standard-of-care thermal ablation treatment. said Nick Spadea-Anello, president, Electrophysiology, Boston Scientific. "The
Titled "Real-world Data Affirms Safety and Effectiveness of Low/Zero Fluoroscopy AtrialFibrillationAblation," the study was presented as a late-breaker at the 29th Annual International AF Symposium. This is the most commonly used ablation catheter in the world for RF ablation and is fully integrated with the CARTO 3 System.
Rhythm control therapy and especially atrialfibrillation (AF) ablation are the focus of growing research in patients with AF. Recent findings suggest that reduction of AF burden mediates the beneficial effects of AF ablation on cardiovascular events and quality of life.
BackgroundCatheter ablation is frequently used to manage recurrent atrialfibrillation (AF) resistant to drug therapy, with pulmonary vein isolation (PVI) as a key tactic. The reconnection of pulmonary veins was discovered primarily in the anterior region of the right superior PV and the superior portion of the left superior PV.
Atrialfibrillation (AF) is the most common arrhythmia worldwide, with increasing prevalence resulting from improved awareness, increased life expectancy, and advances in detection technology.
Atrialfibrillation (AF) catheter ablation trials report arrhythmia-free survival using different post-ablation rhythm monitoring protocols, resulting in difficulties in the interpretation of the recurrence rates and comparison of ablation strategies and technologies.
Penn Presbyterian Medical Center Becomes First Hospital in the Northeast to Adopt Advanced Robotic Technology for Heart Treatment 5. Late-breaking Clinical Trial Results from FARADISE, admIRE Study and Advent Trial at Heart Rhythm 2024 Highlight Pulsed Field Ablation Developments for AtrialFibrillation Treatment 8.
Omnipolar technology near-field (OTNF) is an emerging cardiac mapping approach and may provide insights into electroanatomical substrate mapping during atrialfibrillation (AF) ablation.
FDA approval for the navigation-enabled FARAWAVE NAV Ablation Catheter for the treatment of paroxysmal atrialfibrillation and FDA 510(k) clearance for the new FARAVIEW Software, which will combine to provide visualization for cardiac ablation procedures with the FARAPULSE Pulsed Field Ablation System.
16, 2025 Primary results from the DEFINE AFib clinical study show the Medtronic LINQ family of insertable cardiac monitors (ICM), paired with a novel algorithm, were able to detect atrialfibrillation episodes and properly risk stratify patients as high risk prior to an AF-related healthcare utilization 80% of the time. 2024, May 15).
Innovation in medical technology exists to improve patient outcomes, increase surgical efficiency and enhance patient safety. Infrequently, we see medical technology innovation of a paradigmatic nature that changes the way physicians approach disease states and dramatically improve results.
Pulmonary vein (PV) isolation is the cornerstone of radiofrequency (RF) ablation for atrialfibrillation (AF). PV reconnection is the most common cause of recurrent AF following an ablation procedure.
Pulsed field ablation (PFA) and very-high power short-duration (vHPSD) radiofrequency ablation are the most recently introduced technologies for atrialfibrillation (AF) ablation. The procedural performance, safety, and effectiveness of PFA versus vHPSD are currently unknown.
No data have been reported on cooling characteristics and the impact of variant pulmonary vein (PV) anatomy on atrialfibrillation (AF) recurrences after POLARx cryoballoon (CB) ablation.
Pulsed field ablation (PFA) for the treatment of paroxysmal atrialfibrillation (AF) was validated to be safe and effective.1 Widespread adoption of this potentially transformative technology has brought into the focus the economics of AF with new therapies requiring significant capital and disposable investment.
Pulsed field ablation (PFA) is a safe and effective technology for catheter ablation of atrialfibrillation (AF). Multiple PFA-platforms for AF-ablation have been developed. However, evidence comparing the real-word implementation and performance of different PFA-systems is still limited.
The 1st generation HeartLight laser balloon (LB) ablation is highly effective in achieving pulmonary vein isolation (PVI), and the safety and 12-month efficacy are comparable with paroxysmal atrialfibrillation (PAF) ablationtechnologies.
Pulsed field ablation (PFA) has recently been introduced as a novel routine ablationtechnology for paroxysmal atrialfibrillation (AF). It is also used as off-label therapy for persistent AF.
As an energy source, pulsed field ablation (PFA) has generated tremendous excitement for AF treatment, largely due to its safety profile. All of the PFA technologies in clinical use, or being studied in clinical trials employ microsecond-scale pulses.
We have employed digital twin technology to perform extra pulmonary vein (PV) ablation in patients with non-paroxysmal atrialfibrillation (AF). We reported that high dominant frequency (DF) site ablation improved rhythm outcomes, but high maximal slope of action potential restitution curve (Smax) site ablation did not.
Non-thermal pulsed field ablation (PFA) is an novel technology to perform pulmonary vein isolation (PVI) for atrialfibrillation (AF). Different PFA systems are available, but no comparative data exist.
Pulsed field ablation (PFA) is an innovative technology recently adopted for treating atrialfibrillation (AF). Preclinical and clinical studies have reported a reassuring safety profile because of its tissue-specific effect, sparing adjacent tissues.1
The present invention relates to medical methods for transseptal access to the heart using steerable introducers based on the Company’s Morph DNA technology. This additional patent protection for BioCardia’s current and future products in this important existing market enhances shareholder value.
a company primarily focused on leveraging its novel and proprietary CellFX Nanosecond Pulsed Field Ablation (nsPFA) technology for the treatment of atrialfibrillation, announced the completion of the first five procedures in its first-in-human feasibility study with its novel CellFX nsPFA cardiac catheter.
This study investigated myocardial injury and inflammation following pulmonary vein isolation using (1) Standard radiofrequency ablation, (2) very high-power short-duration (vHPSD)-70W, (3) vHPSD-90W, and (4) pulsed-field ablation (PFA). Results Baseline characteristics were well-balanced between groups (age 63.1 ± 10.3 ng/L; p < .001).
Abstract Introduction Catheter ablation of atrialfibrillation (AF) has emerged as the most effective therapy. However, rare anatomical abnormalities such as situs inversus totalis, dextrocardia, or interrupted inferior vena cava can make ablation challenging.
Pulmonary vein isolation (PVI) with cryoballoon (CB) ablationtechnology is widely used to treat drug-resistant atrialfibrillation (AF). During CB ablation, there is a possibility of forming an ice cap of con.
Abstract Introduction Despite advanced ablation strategies and major technological improvements, treatment of persistent atrialfibrillation (AF) remains challenging and the underlying pathophysiology is not fully understood. First, high-density mapping (78% biatrial) with a multipolar mapping catheter was performed.
Pulsed field ablation (PFA) has recently been introduced as a novel ablationtechnology for pulmonary vein isolation (PVI) in patients with atrialfibrillation (AF). High rates of acute PVI have been observed based on electrograms of the PFA device only.
Pulsed field ablation (PFA)-induced electroporation is an application of high-energy, direct-current shocks on myocardium albeit at a considerably lower current density that decreases the risks of arcing and barotrauma.1
Pulsed field ablation (PFA) is a non-thermal ablationtechnology, utilising the mechanism of electroporation to interrupt the cellular membrane and induce myocyte apoptosis.
FDA approval of a laser etched kerfed and irrigated tip catheter to improve catheter stability was based upon bench and efficacy studies among adult patients with atrialfibrillation. The effect of this technology on intralesional catheter stability during accessory pathway (AP) ablation in children is unknown.
Introduction: Pulsed Field Ablation (PFA) technologies are being studied in a number of clinical trials, many with strict inclusion/exclusion criteria-typically younger patients with less comorbidities undergoing de-novo PVI procedures.
Characteristics of acute insufficient lesions during vHPSD ablation were analyzed in the retrospective phase. Based on these data, an optimized approach combining both vHPSD ablation and AI-guided ablation was prospectively tested, resulting in an approximately 90% first-pass PVI rate. 0001) with shorter ablation time ( p =.04).
In the past decade, major advances were made in catheter ablation for arrhythmias and implantation of cardiac implantable electronic devices.1 1 Catheter ablation for atrialfibrillation (AF) and ventricular tachycardia (VT) has become the standard of care for many patients presenting with these arrhythmias.2–4
Abstract Background The newly introduced nonthermal pulsed field ablation (PFA) is a promising technology to achieve fast pulmonary vein isolation (PVI) with high acute success rates and good safety features. Data comparing PFA to VHPSD-PVI is lacking. Two tamponades occurred in the PFA while in VHPSD two pts suffered groin bleedings.
This information allows more focused intracardiac mapping (activation map during VT, center figure) and accelerates the ablation process, reducing time to first ablation, overall procedure duration (right figure), and fluoroscopy use. reduction in time to ablation (133 ± 48 vs. 165 ± 49 min, p = 0.02), a 22.6% vs. 33.2 ± 18.0
The most common arrhythmia, atrialfibrillation , will affect approximately 12.1 Food and Drug Administration (FDA) in July 2023, a new leadless pacemaker system placed in both chambers of the heart and using a novel communication technology is now offering a more minimally invasive option for patients. Approved by the U.S.
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