Symptomatic patients with aortic stenosis and reduced left ventricular ejection fraction (LVEF) represent a particularly difficult subset of patients to diagnose and to treat. These patients, in fact, pose important diagnostic dilemmas because of the symptoms that may derive primarily from the LV dysfunction, rather than from the stenotic valve, or from the combination of both. According to the current guidelines,1 severe aortic stenosis is characterized by peak aortic jet velocity >4.0 m/s, mean gradient >40 mm Hg, or when the aortic valve area is <1.0 cm2. In the presence of these echocardiographic findings, a symptomatic patient or a patient with reduced LVEF (<50%) is candidate for aortic valve replacement (AVR; class I recommendation).2,3 Yet, patients with LV dysfunction often present with an aortic valve area <1.0 cm2 but with low peak aortic jet velocity (<4.0 m/s). Performance of dobutamine stress echocardiography might help to distinguish those patients with true severe aortic stenosis, who will derive most of the benefit from AVR, from those with moderate aortic stenosis and primary LV dysfunction. In addition, dobutamine stress echocardiography provides strong prognostic information because the lack of contractile reserve is associated with high cardiovascular mortality regardless of treatment.4,5 Myocardial fibrosis is among the factors contributing to the lack of contractile reserve and can be detected and quantified by cardiac MRI. When present, myocardial fibrosis is associated with an adverse prognosis.6,7
Background: Transcatheter aortic valve implantation (TAVI) is known to be associated with silent cerebral injury, which could contribute to cognitive impairment. Considering its increasing use, thorough longitudinal investigation of cognitive trajectory after TAVI is pivotal.
Background: There is scant information on the prevalence and factors associated with preoperative anemia in patients undergoing transcatheter aortic valve implantation (TAVI) and whether it is associated with mortality. We sought to determine the prevalence and factors associated with preoperative anemia in addition to the prognostic effects of the various levels of preoperative hemoglobin level on mortality in patients undergoing TAVI.
Background: Chronic total occlusion (CTO) recanalization is a complex and technically challenging procedure. The J-CTO score has been proposed to stratify case complexity and procedural success rates. However, the score has never been tested outside the setting of the original study. Moreover, its predictive value when using a hybrid antegrade or retrograde approach is unknown. We investigated the performance of the J-CTO score for predicting procedure complexity and success in an independent contemporary cohort.
Background: The drug-eluting absorbable metal scaffold has demonstrated feasibility, safety, and promising clinical and angiographic outcomes at 12 months in human coronary arteries. This study aimed to evaluate the degradation rate and long-term vascular responses to drug-eluting absorbable metal scaffold.
Background: Angioplasty and stent placement in right ventricle-to-pulmonary artery (RV-PA) conduits have been shown to prolong the functional lifespan of a conduit. Safety and efficacy of angioplasty of obstructed RV-PA homografts using ultra-noncompliant (UNC) or ultrahigh-pressure balloons are unknown.
Background: Transcatheter pulmonary valve (TPV) replacement is an emerging therapy intended to restore pulmonary valve function in patients with right ventricular outflow tract conduit dysfunction; the impact of this technique on ventricular strain and synchrony is not known.
Objectives: This study sought to compare the initial success rate of percutaneous coronary intervention (PCI) for chronic total occlusion (CTO) in a native coronary artery (NCA) in patients with and without previous coronary artery bypass grafting (CABG) and to assess predictive factors.
Objectives: This study sought to evaluate the incidence, correlates, and clinical implications of periprocedural myocardial injury (PMI) during percutaneous coronary intervention (PCI) of chronic total occlusions (CTO).
Objectives: This study sought to study the efficacy and safety of newer-generation drug-eluting stents (DES) compared with bare-metal stents (BMS) in an appropriately powered population of patients with ST-segment elevation myocardial infarction (STEMI).
Objectives: This study sought to assess the 2-year outcomes of the population included in the EXAMINATION (Everolimus-Eluting Stents Versus Bare-Metal Stents in ST-Segment Elevation Myocardial Infarction) trial beyond the 1-year prescription period of dual antiplatelet therapy.
Objectives: This study sought to determine whether computational modeling can be used to predict the functional outcome of coronary stenting by virtual stenting of ischemia-causing stenoses identified on the pre-treatment model.
Coronary artery disease (CAD) has become the number 1 pathological process responsible for disease burden in the world. Although traditionally the management of CAD was based on anatomic stenosis, more recently, better outcomes have been associated with revascularization of flow-limiting stenoses as opposed to indications on the basis of purely anatomic obstructions. The reference standard for defining ischemia-related coronary obstructions relies on the measurement of fractional flow reserve (FFR) in the catheterization laboratory during adenosine-induced vasodilation. Indeed, FFR-guided percutaneous coronary intervention (PCI) has become the standard of care for intermediate lesions, with a strong body of evidence now accumulated using this paradigm
Objectives: This study sought to evaluate the feasibility of performing contemporary bifurcation techniques with the Absorb everolimus-eluting bioresorbable vascular scaffold (Abbott Vascular, Santa Clara, California) (BVS).
Objectives: This study sought to perform clinical and imaging assessments of the DESolve Bioresorbable Coronary Scaffold (BCS).
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