Aims Myocardial ischaemia during pharmacological stress echocardiography is a strong prognostic predictor in patients with a left bundle branch block (LBBB). However, the additive value of Doppler-derived coronary flow reserve (CFR) during pharmacological stress testing remains to be investigated in this subset of patients.
Background—With the availability of transcatheter aortic valve replacement, management of coronary artery disease in patients with severe aortic stenosis (AS) is posing challenges. Outcomes of percutaneous coronary intervention (PCI) in patients with severe AS and coronary artery disease remain unknown. We sought to compare the short-term outcomes of PCI in patients with and without AS.
Objectives: This study investigated the role of uncovered stent struts on late stent thrombosis (LST) after drug-eluting stent (DES) implantation with optical coherence tomography (OCT).
Objectives: The purpose of this study was to evaluate the long-term outcomes of the PASSION (Paclitaxel-Eluting Versus Conventional Stent in Myocardial Infarction with ST-Segment Elevation) trial.
Objectives: This study sought to assess whether transradial intervention, by minimizing access-site bleeding and vascular events, improves outcomes in patients with ST-segment elevation myocardial infarction compared with the transfemoral approach.
Objectives: This study investigated the impact of sheath size on the rate of radial artery occlusions (RAO) (primary objective) and other access site complications (hemorrhage, pseudoaneurysm, arteriovenous fistula) as secondary objectives after transradial coronary catheterization.
Objectives: This study sought to evaluate post-dilation strategies in bifurcation stenting.
Objectives: This study sought to describe the presentation, management, and outcomes of patients presenting with angiographic definite stent thrombosis (ST) at coronary bifurcations.
Objectives: This study sought to compare the 1-year safety and efficacy of Cypher Select or Cypher Select Plus (Cordis Corporation, Bridgewater, New Jersey) sirolimus-eluting stents (SES) with the treatment of bare-metal stents (BMS) and drug-eluting stent (DES) in-stent restenosis (ISR) in nonselected, real-world patients.
Objectives: This study sought to quantify the learning curve for the safety and effectiveness of a newly introduced vascular closure device through evaluation of the NCDR (National Cardiovascular Data Registry) CathPCI clinical outcomes registry.
A 70-year-old morbidly obese woman with severe emphysema presented with unstable angina. Coronary angiography revealed high-grade, calcified, ostial left circumflex (LCX) and distal right coronary artery (RCA) lesions. She was deemed a high-risk surgical candidate and underwent stenting of the left main coronary artery into the LCX with a 3.5 × 18-mm Xience V stent (Abbott Vascular, Santa Clara, California). A second 3.5 × 18-mm Xience V stent was overlapped distally to cover a mid LCX lesion, and both stents were post-dilated to 16 atm with a 3.5-mm noncompliant balloon. The RCA lesion was stented with a 3.0 × 12-mm Xience V and post-dilated to 16 atm with a 3.0-mm noncompliant balloon (Figure 1). The patient did well for 6 months until she returned with unstable angina. Angiography revealed restenosis at the ostium of the stented LCX and within the distal RCA stent (Figure 1). During repeat intervention, wiring of the LCX resulted in abrupt closure. The patient developed refractory ventricular fibrillation and died.
Objectives: This study sought to assess the feasibility and safety of percutaneous edge-to-edge mitral valve (MV) repair in patients with an unacceptably high operative risk.
Medical science progress requires a strong educational foundation, and the direct demonstration of knowledge and skills has been a traditional teaching method for practitioners. Advances in communication technology have provided unprecedented opportunities to show patient care in real time. As a result, there has been proliferation of live case presentations to audiences attending professional society conferences and worldwide via the Internet.
Objectives: The goal of this study was to examine the safety and results of interventional procedures performed during the broadcast of live case demonstrations.
Objectives: The purpose of this study was to evaluate the incidence of vascular complications and the predictors of Prostar failure for a “true percutaneous approach” in transfemoral transcatheter aortic valve implantation (TAVI).
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