Objectives: The goal of this study was to investigate the differential efficacy of clopidogrel or aspirin monotherapy according to smoking status in patients with atherosclerotic vascular disease.
Despite improvements in medical therapy, the overall prognosis of patients with severe pulmonary arterial hypertension remains poor. Heart-lung transplantation or bilateral lung transplantation is the final pathway for a minority. This paper describes both established and novel percutaneous interventional techniques that may palliate or bridge pulmonary hypertension patients to transplantation.
Objectives: This study sought to evaluate the clinical impact of intraprocedural stent thrombosis (IPST), a relatively new endpoint.
Objectives: This study sought to investigate the clinical outcome of patients treated with percutaneous coronary intervention (PCI) for in-stent restenosis (ISR) randomized to short (6 months) versus long (24 months) dual antiplatelet therapy (DAPT) regimen.
Objectives: The purpose of this study was to assess the occurrence, predictors, and mechanisms of optical coherence tomography (OCT)-detected coronary evaginations following drug-eluting stent (DES) implantation.
Background: Impaired re-endothelialization and stent thrombosis are a safety concern associated with drug-eluting stents (DES). PI3K/p110α controls cellular wound healing pathways, thereby representing an emerging drug target to modulate vascular homoeostasis after injury.
Purpose: While surgical closure of ventricular septal defects (VSD) is still the gold standard, we review our experience with the interventional closure of single and multiple muscular VSD in newborns and infants under 20 kg.
Background: Percutaneous closure of atrial defects (ASD) has evolved as the treatment of choice for the majority of defects and patent oval foramens. The Gore Septal Occluder (GSO) is an innovative device consisting mostly of a folded thin GoreTex tube for use in the closure of septal defects.
Objectives: To determine the incidence and etiology of thrombocytopenia following transcatheter Aortic valve replacement (TAVR).
Objective: To evaluate the impact of learning on outcome with use of two different left atrial appendage (LAA) occlusion devices.
In this issue of JACC: Cardiovascular Interventions, Werner et al. 1 present their experience with the use of a biodegradable balloon expandable stent for use in the superficial femoral artery (SFA). This stent, which is commercially available outside the United States, is composed of poly-L-lactic acid (PLLA) and undergoes degradation in the human body through a process of hydrolysis over a long period of time. In this particular device, structural integrity is maintained for 6 months, following which, degradation begins and can last up to 3 years, at which point no more material is detectable.
It is now almost a decade that we have been discussing optimal treatment of bifurcation lesions, and invariably we come to the unanswered question: 1 or 2 stents?
Objectives: This study sought to investigate the effect of endothelial shear stress (ESS) on neointimal formation following an Absorb bioresorbable vascular scaffold (BVS) (Abbott Vascular, Santa Clara, California) implantation.
Objectives: This study sought to better understand and optimize provisional main vessel stenting with final kissing balloon dilation (FKBD).
We earlier reported late stent malapposition and marked coronary artery aneurysm (CAN) formation at the site of implantation of 2 bare-metal stents (BMS), Multilink Vision (Abbott Laboratories, Abbott Park, Illinois) and Liberte (Boston Scientific Corporation, Natick, Massachusetts), to the proximal left anterior descending artery (LAD) and right coronary artery (RCA), respectively, in a woman treated for stable angina in 2006. The patient also had a Xience drug-eluting stent (DES) (Abbott Laboratories) to her mid RCA with less marked CAN on angiography in 2007 1. Diagnostic coronary angiography and optical coherence tomography (OCT) assessment was performed in 2012, although she remained free of symptoms or hospitalizations. Five years later, coronary angiography showed partial angiographic resolution of the CAN in the 2 BMS segments, with continued aneurysm formation at the Xience DES implantation site
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