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The NOTION trial, a pioneering study, sought to compare the long-term clinical and bioprosthesis outcomes of Transcatheter AorticValve Implantation (TAVI) versus Surgical AorticValve Replacement (SAVR) in patients with severe aorticvalvestenosis (AS) at lower surgical risk.
A significant proportion of patients with severe aorticstenosis (AS) undergoing transcatheter aorticvalve implantation (TAVI) have concomitant coronary artery disease (CAD). The best way to treat these patients is contentious.
The goal of the AVATAR trial was to evaluate aorticvalve replacement (AVR) compared with conservative therapy among patients with asymptomatic severe aorticstenosis.
The goal of the DEDICATE-DZHK6 trial was to evaluate transcatheter aorticvalve implantation (TAVI) compared with surgical aorticvalve replacement (SAVR) among patients with severe aorticstenosis and low to intermediate surgical risk.
Transcatheter aorticvalve replacement (TAVR) is the standard treatment for severe aorticstenosis, but post-TAVR leaflet thrombus, identified by hypoattenuated leaflet thickening (HALT), poses potential risks like cerebral thromboembolic events. had thrombus at any aorticvalve complex. Specifically, 14.2%
Articles were analyzed with bibliometric tools such as CiteSpace and VOSviewer to identify key research trends, core authors, institutions, and research hotspots in AI applications for AVS.ResultsA total of 118 articles were analyzed, showing a significant increase in publications from 2014 onwards.
The goal of the NOTION trial was to compare outcomes after transcatheter aorticvalve replacement (TAVR) versus surgical aorticvalve replacement (SAVR) in unselected patients with severe degenerative aorticstenosis.
The goal of the VIVA trial was to evaluate transcatheter aorticvalve replacement (TAVR) compared with surgical aorticvalve replacement (SAVR) among patients with severe aorticstenosis and a small aortic annulus.
Transcatheter aorticvalve replacement (TAVR) is a relatively new treatment method for aorticstenosis (AS) and has been demonstrated to be suitable for patients with varying risk levels.
Blaha, MD, MPH discuss Prevalence of AorticValve Calcium and the Long-Term Risk of Incident Severe AorticStenosis. In this interview, Richard A. Chazal MD, MACC and Michael J.
The goal of the EARLY TAVR trial was to evaluate transcatheter aorticvalve replacement (TAVR) compared with clinical surveillance among patients with asymptomatic severe aorticstenosis (stage C aorticstenosis).
This concept should be applied when managing older patients with severe aorticstenosis. Although left ventricular wall hypertrophy is expected in patients with aorticstenosis, it should not be assumed that this is caused only by aorticstenosis.
What is the 5-year incidence of valve reintervention after self-expanding CoreValve/Evolut transcatheter aorticvalve replacement (TAVR) versus surgical aorticvalve replacement (SAVR)?
The EARLY TAVR trial results demonstrate that early transcatheter aorticvalve implantation in patients with asymptomatic severe aorticstenosis is superior to clinical surveillance in significantly reducing the composite primary outcome of death, stroke, or unplanned hospitalization for cardiovascular causes.
What are the hemodynamic and clinical outcomes after transcatheter aorticvalve replacement (TAVR) and surgical aorticvalve replacement (SAVR) among patients with severe aorticstenosis (AS) and a small aortic annulus?
The goal of the TAVR UNLOAD trial was to evaluate transcatheter aorticvalve replacement (TAVR) compared with clinical surveillance among patients with chronic systolic heart failure and moderate aorticstenosis (stage B aorticstenosis).
In these panel discussions, host Andrea Price, MS, AACC brings together Marian Hawkey, RN and Misty Theriot, BSN to explore best practices related to structural heart disease.
ABSTRACT Patients with severe aorticstenosis (AS) may develop heart failure (HF), the presence of which has traditionally been deemed as a final stage in AS progression with poor outcomes. The use of transcatheter aorticvalve replacement (TAVR) has become the preferred therapy for most patients with AS and concomitant HF.
The goal of the SOLVE-TAVI trial was to compare the safety and efficacy of the Edwards Sapien S3 valve vs. Medtronics CoreValve among patients undergoing transcatheter aorticvalve replacement (TAVR) for severe aorticstenosis.
The goal of the EVOLVED trial was to assess the safety and efficacy of early aorticvalve replacement compared with conservative management among patients with asymptomatic severe aorticstenosis, normal ejection fraction (EF), and presence of myocardial fibrosis on cardiac magnetic resonance imaging (CMR).
What are clinical outcomes among patients with severe aorticstenosis (AS) and coronary artery disease (CAD) undergoing surgical aorticvalve replacement (SAVR) plus revascularization versus transcatheter aorticvalve replacement (TAVR) plus percutaneous coronary intervention (PCI)?
The goal of the TCW trial was to test the noninferiority and, if positive, superiority, of percutaneous coronary intervention (PCI) with transcatheter aorticvalve implantation (TAVI) compared with surgical aorticvalve replacement (SAVR) and coronary artery bypass grafting (CABG) in severe aorticstenosis (AS) with comorbid coronary artery disease (..)
Aims The majority of patients with severe aorticstenosis (AS) planned for transcatheter aorticvalve implantation (TAVI) are elective outpatients. In the present article, we report the study protocol of the ResKriVer-TAVI trial. Methods ResKriVer-TAVI will enroll AS patients planned for elective TAVI.
Heterogeneity was assessed using I2 statistics. All statistical analyses were conducted using Review Manager (Rev Man, Version 5.4; The Cochrane Collaboration, Copenhagen, Denmark).Results:After to 1.17, p=0.30, I2 3%).
In a cohort of patients with severe aorticstenosis (AS) who underwent aorticvalve replacement (AVR), the degree of myocardial fibrosis provides significant prognostic information in women and men.
Patients with bicuspid aorticvalves (BAV) are predisposed to the development of aorticstenosis. We performed a pairwise meta-analysis, comparing the efficacy of transcatheter aorticvalve replacement (TAVR) versus surgical aorticvalve replacement (SAVR) in patients with BAV.
The goal of the LANDMARK trial was to evaluate transcatheter aorticvalve replacement (TAVR) with the Myval prosthesis compared with a contemporary prosthesis among patients with symptomatic severe aorticstenosis.
Two separate late-breaking clinical trials – EARLY TAVR and EVOLVED – presented at TCT 2024 explore whether early aorticvalve intervention improves outcomes in patients with asymptomatic aorticstenosis (AS).
The goal of the PROTECTED TAVR trial was to evaluate the efficacy of intraprocedural cerebral embolic protection (CEP) in reducing strokes among patients undergoing transfemoral TAVR for aorticstenosis.
The goal of the SMART trial was to evaluate a self-expanding valve compared with a balloon-expandable valve among patients with aorticstenosis and a small aortic annulus undergoing treatment with transcatheter aorticvalve replacement (TAVR).
Case description An 80-year-old woman with severe symptomatic aorticstenosis was scheduled for transcatheter aorticvalve implantation (TAVI), following Heart Team decision. Pre-procedural computed tomography (CT) angiogram revealed an area-derived annulus diameter of 23.7 mm, and calcium spur which extended from.
What are the procedural and clinical outcomes of balloon-expandable valves (BEVs) and self-expanding valves (SEVs) in Sievers type 1 bicuspid aorticvalve (BAV) stenosis?
This technique is now employed in approximately 85% of all isolated aorticvalve replacements. In the past decade, the U.S. has seen a 25-fold increase in the use of TAVR, with more than 100,000 performed annually. Despite this growth, there are notable gaps in the evidence.
In women with symptomatic, severe aorticstenosis (AS), TAVR with the balloon-expandable valve was superior to surgical aorticvalve replacement in terms of the composite rate of death, stroke and rehospitalization at one-year follow-up, according to a pooled analysis of patient-level data from RHEIA and PARTNER 3 trials presented at TCT 2024.
Abstract: Transcatheter aorticvalve replacement (TAVR) is an interventional procedure performed in patients with severe aorticstenosis and often required perioperative antiplatelet therapy. Most previous studies have focused on antiplatelet therapy following TAVR.
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