Objectives: This study sought to identify how many patients suitable for transcatheter aortic valve implantation (TAVI) would have a contraindication for the transaortic (TAo) approach due to ascending aortic calcification.
Objectives: This study investigated the outcome for all patients undergoing catheter valve perforation for pulmonary atresia with intact ventricular septum (PAIVS) 21 years after the first procedure at their center.
Objectives: The authors report the feasibility and 30-day outcomes of transfemoral aortic valve replacement (TAVR), using the Edwards SAPIEN (Edwards Lifesciences, Irvine, California) and Edwards SAPIEN XT (Edwards Lifesciences) prosthesis, implanted using exclusively local anesthesia and fluoroscopic guidance.
Randomized, controlled trials (RCTs) have convincingly proven that in patients with advanced (New York Heart Association functional class III/IV) systolic (left ventricular [LV] ejection fraction ≤35%) heart failure and wide QRS complex (QRS ≥120 ms), cardiac resynchronization therapy (CRT) improves functional status and quality of life (1), decreases heart failure hospitalizations (2), and prolongs survival (3). However, the lack of response to CRT in a substantial portion of patients (one-third) has been a consistent finding (4).
Objectives: This study sought to determine the efficacy of patient pelvic lead shielding for the reduction of operator radiation exposure during cardiac catheterization via the radial access in comparison with the femoral access.
Objectives. The purpose of this study was to determine atheroma progression in patients with spotty calcification.
Objectives: The study sought to describe the authors experience with mitral transapical transcatheter valve-in-valve implantation (TVIV).
The patent foramen ovale (PFO) is a normal interatrial communication during fetal life that persists after birth in approximately 1 of every 4 adults. PFO is a potential route for embolic transit from the systemic venous circulation to the brain. Though there is compelling circumstantial evidence implicating PFO, the precise role of PFO in the pathogenesis of cryptogenic stroke is not yet established. Several randomized trials of transcatheter PFO closure versus medical management are ongoing. Results of these trials may improve our ability to select the best treatment for individual patients. Further well-designed studies are necessary to address several unresolved issues related to PFO stroke and PFO migraine pathophysiology, and to identify the patients who would most likely benefit from PFO closure. The purpose of this review is to summarize contemporary understanding, discuss current treatments, and explore some of the knowledge gaps pertaining to the clinical significance of PFO.
Objectives: The goal of this study was to assess serial changes in patient health-related quality of life (HRQOL) over time and identify predictors of patient benefit.
Objectives: This study sought to assess quality of life parameters in a subset of patients enrolled in the PROTECT AF (Percutaneous Closure of the Left Atrial Appendage Versus Warfarin Therapy for Prevention of Stroke in Patients With Atrial Fibrillation) trial.
Objectives: This study sought to assess the relationship of coronary angiography, intravascular ultrasound (IVUS) and fractional flow reserve (FFR) between major epicardial vessel (MV) and side branch (SB) ostial lesions.
Objectives: The purpose of this study was to assess the prognostic impact of intraprocedural thrombotic events (IPTE) during percutaneous coronary intervention (PCI).
Objectives The study sought to determine whether rapid access to medical care and reperfusion results in a better prognosis in patients with in-hospital compared with out-of-hospital stent thrombosis (ST) in patients with ST-segment elevation myocardial infarction (STEMI) in the HORIZONS-AMI (Harmonizing Outcomes with Revascularization and Stents in Acute Myocardial Infarction) trial.
Objectives: This study sought to test the hypothesis that colchicine treatment after percutaneous coronary intervention (PCI) can lead to a decrease in in-stent restenosis (ISR).
Stent thrombosis is an uncommon but serious complication of coronary artery stenting that frequently presents as death or nonfatal myocardial infarction (MI), often with ST-segment elevation. Apprehension regarding stent thrombosis influences which patients are candidates for coronary interventions and alters the strategy by which stents are deployed (1). Adjunctive pharmacology is profoundly altered due to these potential consequences: both the routine administration and duration of dual antiplatelet therapy (DAT) and other anticoagulants center on the prevention of stent thrombosis (2).
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