A 57-year-old female underwent successful percutaneous coronary intervention (PCI) of the mid-distal left main coronary artery and the mid left anterior descending artery with 2 non-overlapping sirolimus-eluting stents with durable polymer (SES). Three years later, the patient was evaluated with multislice computed tomography due to recurrent chest pain.
Percutaneous stenting seems to be an attractive and preferred alternative to surgical therapy for treatment of aortic coarctation in the adolescent and young adult. However, percutaneous reconstruction of an interrupted aortic arch is challenging.
Objectives: This study sought to evaluate, through a systematic review of the published data, the main baseline characteristics, management, and clinical outcomes of patients suffering coronary obstruction as a complication of transcatheter aortic valve implantation (TAVI).
Objectives: This report sought to study the impact of the balloon-expandable SAPIEN XT (Edwards Lifesciences, Irvine, California) transcatheter heart valve (THV) stent frame geometry and position on outcomes of transcatheter aortic valve replacement (TAVR).
Aortic valve stenosis and its treatment is not a “black box.” It is not like a genetic disorder resulting in a complex syndrome that requires a very profound understanding and a sophisticated therapeutic approach; it is not like arterial hypertension, with a broad set of competing treatment alternatives and yet a somewhat unpredictable interindividual response to a chosen regimen, with a need for constant monitoring and adjustments. Aortic valve stenosis is a simple mechanical problem that requires a mechanical solution. That is the reason why surgical aortic valve replacement has been the successful gold standard treatment for decades in patients with symptomatic and severe aortic valve disease. This also explains why transcatheter aortic valve replacement (TAVR) could emerge as a suitable therapeutic alternative in the past decade and is now established for inoperable and high-risk surgical candidates
Objectives: This study sought to investigate the blood pressure (BP) response after transcatheter aortic valve implantation (TAVI) and its correlation with short- and mid-term clinical outcomes.
Objectives: This study sought to assess whether the volume of contrast media (CM) influences the occurrence of acute kidney injury (AKI) following transcatheter aortic valve implantation (TAVI).
Objectives: This study sought to predict the value of tumor marker carbohydrate antigen 125 (CA125) before and after transcatheter aortic valve implantation (TAVI) for all-cause death and a composite endpoint of death, admission for heart failure, myocardial infarction, and stroke (major adverse cardiac events [MACE]).
Objectives: The purpose of this study was to assess the comparative effectiveness and long-term safety of transcatheter versus surgical closure of secundum atrial septal defects (ASD) in adults.
Objectives: The aim of this study was to evaluate late safety and efficacy outcomes among patients enrolled in clinical trials comparing Endeavor zotarolimus-eluting stents (E-ZES) (Medtronic, Inc., Santa Rosa, California) with first-generation drug-eluting stents (DES) and bare-metal stents (BMS).
Objectives: This study sought to propose a new technique for the treatment of Medina type 1.1.1 bifurcation lesions.
Objectives: This study sought to assess the vascular response of overlapping Absorb stents compared with overlapping newer-generation everolimus-eluting metallic platform stents (Xience V [XV]) in a porcine coronary artery model.
A 44-year-old woman had a transient ischemic attack in 2010 and a subsequent ischemic stroke (while on a regimen of aspirin therapy) in May 2012 with evidence of an ischemic cerebral lesion at magnetic resonance imaging. Thrombophilic screening tests showed factor V Leiden homozygosis. Transesophageal echocardiography revealed an atrial septum aneurysm without shunt during Valsalva maneuver after injection of agitated saline solution in the right antecubital vein; however, there was a late (after 5 cardiac cycles) appearance of agitated saline microbubbles in the left atrium through a pulmonary vein
Drug-eluting stents have dramatically reduced the rate of in-stent restenosis (1). However, very late stent thrombosis (VLST) is one of the clinical issues with regard to the safety of drug-eluting stents (2,3). To date there are no articles that report VLST evaluated by both angioscopy and optical coherence tomography (OCT). A 50-year-old man presented to the emergency department with chest pain. Five years earlier a 3.0 × 13 mm sirolimus-eluting stent (SES) was implanted in the left anterior descending artery
This review discusses the current safety issues related to U.S. Food and Drug Administration approved atrial septal defect devices and proposes a potential avenue to gather additional safety data including factors, which may be involved in device erosion.
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