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4, 2025 Riverain Technologies recently announced it expanded across eight countries in 2024 and added nearly 50 new customers with its ClearRead solutions to clearly, confidently and quickly detect cardiothoracic diseases. tim.hodson Tue, 02/04/2025 - 16:21 Feb.4,
6, 2025 Medtronic plc hasannounced it received CE ( Conformit Europenne ) Mark for the Harmony Transcatheter Pulmonary Valve (TPV) System, a minimally invasive alternative to open-heart surgery for congenital heart disease patients with native or surgically repaired right ventricular outflow tract (RVOT).
We look forward to bringing our AI technology to meet patients and physicians where they are, ultimately benefiting both worldwide.” The companies will also work together to validate the clinical utility of the integrated solution and seek regulatory clearance to bring this technology to market. Under the agreement, InfoBionic.Ai
A new Intelligent thrombo-suction catheter system , is being introduced for treatment of acute pulmonary embolism.This device regulates the force with which thrombus is sucked , with less injury and bleeding and better outcomes. They have become a Integral tool kit in peripheral arterial, venous and also pulmonary thrombosis.We
Superior vena cava (SVC) conduction delay or isolation during right superior pulmonary vein (RSPV) ablation using thermal ablation technologies has been previously described.1,2 1,2 No reports regarding the impact of pulsed-field ablation (PFA) on the SVC exist.
6, 2025 Eko Health, a leader in applying artificial intelligence (AI) for the early detection of heart and lung diseases, recently announcedpublication of a peer-reviewed study evaluating its novel algorithm for the detection of pulmonary hypertension (PH). tim.hodson Mon, 02/10/2025 - 12:43 Feb.
Objective Pulsed-field ablation (PFA) is a new technology of catheter ablation for atrial fibrillation (AF). After a successful transseptal puncture, the PFA catheter (CardiPulse) was delivered to the different pulmonary veins sequentially for standard PFA, and the pulmonary vein electrical isolation (PVI) was observed in real-time.
Ablation index (AI)-guided pulmonary vein isolation (PVI) has enhanced procedural outcomes for atrial fibrillation (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.
a powerful and advanced mechanical thrombectomy system for the removal of venous thrombus and the treatment of pulmonary embolism (PE), effectively completing Penumbras VTE platform. Innovative Valve Technology Element features the HemoLockValve System, designed to ensure hemostasis through dual-valve engineering. CAT TM 16 catheter.
The pivotal trial will study the Vertex Pulmonary Embolectomy System, which incorporates Jupiter’s Endoportal Control platform technology into an endovascular procedure intended to treat Acute Pulmonary Embolism (PE) with an unprecedented level of control and precision. pivotal study (NCT06576427).
BackgroundPercutaneous mechanical thrombectomy (PMT) is increasingly used in the treatment of intermediate and high-risk acute pulmonary embolism (PE), and the treatment of high-risk PE with the aid of veno-arterial extracorporeal membrane oxygenation (VA-ECMO) has also been reported. The mortality rate was 27.3% during the 90-day follow-up.
a developer of cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, reported it has submitted a 510(k) for approval of its patented Morph DNA Steerable Introducer Sheath. mtaschetta-millane Wed, 07/31/2024 - 07:00 July 31, 2024 — BioCardia, Inc. ,
BackgroundCatheter ablation is frequently used to manage recurrent atrial fibrillation (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.
Background Percutaneous pulmonary valve implantation (PPVI) has emerged as a less invasive alternative for treating severe pulmonary regurgitation after tetralogy of Fallot (TOF) repair in patients with a native right ventricular outflow tract (RVOT).
Penn Presbyterian Medical Center Becomes First Hospital in the Northeast to Adopt Advanced Robotic Technology for Heart Treatment 5. Patent Covering the Use of Levosimendan in Pulmonary Hypertension with Heart Failure with Preserved Ejection Fraction (PH-HFpEF) 10. Scientists Suggest a New Method for Diagnosing Heart Diseases 6.
Xeltis synthetic restorative pulmonary heart valve evolves into a fully functioning, natural heart valve through colonization by the patient’s own tissue. Xeltis’ novel technology has already treated over 100 patients across different clinical trials.
The TWOSOME trial randomized paroxysmal atrial fibrillation (AF) patients to either single-tip or single shot pulsed field ablation (PFA) for pulmonary vein isolation (PVI). Only few data investigating silent cerebral lesions (SCL) after novel PFA technology exist.
Conduction delay or isolation of the superior vena cava (SVC) has been previously described during the right superior pulmonary vein (RSPV) ablation using thermal ablation technologies due to the anatomical proximity of the SVC to the RSPV. Currently, there are no reports on the impact of pulsed-field ablation (PFA) on the SVC.
Pulsed Field Ablation (PFA) represents a significant advancement in ablation technology for pulmonary vein isolation (PVI). However, the durability of chronic ablation regions created by the Novel Variable-Loop Circular Catheter (VLCC, VARIPULSE) remains unclear.
Non-thermal pulsed field ablation (PFA) is an emerging technology to perform pulmonary vein isolation (PVI) for atrial fibrillation (AF). Different PFA systems are available, but no comparative outcome data exist.
a company focused on cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases announced that the Unites States Patent Office has granted Patent No: 12,036,371 titled “Method of Accessing the Left Atrium with a Multi-Directional Steerable Catheter,” with a patent term that will expire in 2035.
BackgroundIn recent years, self‐expanding technology to treat pulmonary regurgitation in the native right ventricular outflow tract became Food and Drug Administration approved in the United States and is now routinely used. This paves the way for routine use of VR in patient selection for self‐expanding valve technologies.
In patients with atrial fibrillation (AF), pulsed field ablation (PFA) has emerged as a safe and effective technique for pulmonary vein isolation (PVI). However, first-generation PFA catheters lack integration with 3D mapping technology, meaning fluoroscopy remains the primary method for catheter guidance during PFA-PVI procedures.
No data have been reported on cooling characteristics and the impact of variant pulmonary vein (PV) anatomy on atrial fibrillation (AF) recurrences after POLARx cryoballoon (CB) ablation.
BackgroundAcute pulmonary embolism (APE) is a common and potentially fatal cardiovascular disease that can lead to sudden cardiac arrest in severe cases. For patients with concurrent main pulmonary artery embolism and bleeding, balloon pulmonary angioplasty may be an option.
The AP Fontan operation and the total cavo-pulmonary connection (TCPC) have revolutionised the surgical treatment of patients with functionally univentricular hearts. However, post-surgical arrhythmias contribute considerably to morbidity and mortality and can be difficult to manage.
Cryoballoon (CB) ablation is the mainstay of single-shot pulmonary vein isolation (PVI). However, these two technologies have not been compared. A radiofrequency balloon (RFB) catheter has recently emerged as an alternative.
Pulsed field ablation (PFA) has recently been introduced as a novel ablation technology for pulmonary vein isolation (PVI) in patients with atrial fibrillation (AF). High rates of acute PVI have been observed based on electrograms of the PFA device only.
A company statement reported that its PFA System is indicated for the isolation of pulmonary veins in the treatment of drug-refractory, recurrent, symptomatic, paroxysmal (i.e., The FARAPULSE PFA System is indicated for the isolation of pulmonary veins in the treatment of drug-refractory, recurrent, symptomatic, paroxysmal (i.e.,
Using a combination of deep learning and machine learning technologies, the company develops AI solutions that automatically detect and prioritize life-threatening conditions within seconds, assess them for severity, and seamlessly notify clinicians. CINA-iPE and CINA-ASPECTS are the latest tools from Avicenna.AI
Pulmonary vein isolation (PVI) is the most effective means of maintaining sinus rhythm in atrial fibrillation (AF); point-by-point radiofrequency (RF) catheter ablation is a widely used approach to PVI. While complications are rare with both technologies, the risk of atrioesophageal fistula (AEF) remains a concern.
Non-thermal pulsed field ablation (PFA) is an novel technology to perform pulmonary vein isolation (PVI) for atrial fibrillation (AF). Different PFA systems are available, but no comparative data exist.
Pulmonary vein (PV) isolation is the cornerstone of radiofrequency (RF) ablation for atrial fibrillation (AF). Advances in catheter technology, ablation techniques, and ablation lesion metrics have resulted in improved PV isolation durability. PV reconnection is the most common cause of recurrent AF following an ablation procedure.
Methods In this study, blood samples were collected from 16 patients before and 24h after pulmonary vein isolation (PVI) via a novel investigational PFA-based technology.
Abstract Introduction Through systematic scientific rigor, the CLOSE guided workflow was developed and has been shown to improve pulmonary vein isolation durability. However, this technique was developed at a time when using power-controlled ablation catheters with conventional power ranges was the norm.
Persistent atrial fibrillation (AF) ablation targeting extra-pulmonary vein drivers using various technologies has delivered varying results from no benefit to significant arrhythmia free survival.
BackgroundResearch into the gutlung axis links gut microbiota to pulmonary artery hypertension (PAH). Our findings have implications for advancing gut microbiotabased PAH diagnostic technologies and targeted therapies. Journal of the American Heart Association, Ahead of Print.
The integration of 3D mapping technology, which allows detailed visualization of multielectrode ablation catheters and mapping of the left atrium and pulmonary veins, is anticipated to improve clinical outcomes. The application of pulsed field energy for atrial fibrillation (AF) has seen rapid advancements in recent years.
a company focused on cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, announced that the Unites States Patent Office has granted Patent No: 11,986,611 titled “Radial and Transendocardial Delivery Catheter,” with a patent term that will expire in 2036. Peter Altman , BioCardia CEO.
Pulsed field ablation (PFA) has emerged as a promising energy for pulmonary vein isolation (PVI). Advancements in next generation PFA technologies and waveforms are needed.
Pulsed field ablation (PFA) represents a novel technology for the treatment of atrial fibrillation (AF). While PFA-based pulmonary vein isolation (PVI) has been reported to result in extensive isolation of the left atrial (LA) wall, the specific details and its relationship with creatine kinase (CK) and CK-MB levels remain unclear.
A novel focal 9mm lattice tip catheter, namely Sphere-9, has recently received regulatory approval and is part of a technology that allows the delivery of either pulsed electric field or radiofrequency energy and incorporates a proprietary 3D electroanatomical mapping system.
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