Objectives: Cost-effectiveness of percutaneous coronary intervention (PCI) using drug-eluting stents (DES), and coronary artery bypass surgery (CABG) was analyzed in patients with multivessel coronary artery disease over a 5-year follow-up.
Objectives: To report very long-term follow-up of “Full-Metal Jacket” (FMJ) percutaneous coronary interventions (PCI) in long-diffuse coronary lesions with drug-eluting stents (DES).
Introduction: Balloon expandable stents are an integral part in the catheter treatment of congenital heart disease. In the growing child, stents require dilatation to greater diameters over time. The Cook Formula stent is a recent 316 stainless steel open-cell design licensed for peripheral vascular work.
A 38-year-old man presented at the emergency department with severe chest pain. He had no history of recent trauma or fever but had undergone percutaneous coronary intervention (PCI) several times for 3-vessel disease. Repeat in-stent restenosis (ISR) was detected during his last angioplasty 1 year ago. Electrocardiography revealed diffuse ST-segment elevation (Figure 1A), and coronary angiography, which was performed because of his high-risk status, demonstrated an aneurysm extending from the left main (LM) coronary artery to the left anterior descending (LAD) coronary artery (Figure 1B and Online Video 1). However, he refused surgical intervention until 1 month later, when he underwent treatment because of refractory chest pain and bacteremia caused by Staphylococcus aureus. Surprisingly, pre-operative coronary angiography and chest computed tomography revealed 2 rapidly growing mycotic aneurysms involving the LM coronary artery and the mid-LAD coronary artery. The aneurysms measured up to 29 × 56 mm, and 1 of them drained into the other (Figure 1C and Figure 1D, and Online Video 2). The operation revealed destroyed stents floating inside the massive aneurysms (Figure 1E and Figure 1F). Bypass surgery was performed successfully; however, the patient eventually died of multiorgan failure. An aggressive bacterial infection was detected in the pathological specimens (Figure 1G).
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: The study sought a prospective multicenter nonrandomized evaluation of the Direct Flow Medical (DFM) system for the treatment of severe aortic stenosis.
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.
Surgical mitral valve repair (SMVR) is the preferred intervention for patients with either symptomatic severe mitral regurgitation (MR) or asymptomatic severe MR and left ventricular dysfunction (1). The rate of freedom from severe MR 10 years after SMVR, however, is reported to be 70% (2), leading to a considerable number of mitral valve reinterventions, which carry substantial risk, particularly in elderly patients and in those with significant comorbidities.
Transcatheter aortic valve replacement (TAVR) has transformed the care of patients with aortic stenosis. The dissemination of this technology after its approval in the United States in the wake of a pivotal randomized trial (1,) has thus far proceeded in a thoughtful and circumspect manner, guided by a coalition of stakeholders dedicated to the delivery of high-quality, patient-centered care. It is anticipated that a number of transcatheter therapies for mitral regurgitation (MR) will also become available for clinical use in selected patients. As an example, the MitraClip device (Abbott Vascular, Santa Clara, California) was approved October 24, 2013, for the reduction of significant (≥3+), symptomatic, degenerative MR in highly anatomically selected patients considered by an experienced heart team to be at prohibitive risk for mitral valve surgery. Other transcatheter approaches in development include mitral annulus–based therapies, transapical neochordal implants, valve-in-valve and valve-in-annuloplasty ring therapies, and valve replacement therapies.
Objectives: This study sought to determine the pre-operative risk factors related to late bleeding, stroke, and pump thrombosis in patients with HeartMate II (HMII) left ventricular assist devices (LVADs) (Thoratec Corporation, Pleasanton, California) that might influence tailored improvements in patient management.
Objectives: The goal of this study was to examine the impact of reasons for surgical inoperability on outcomes in patients undergoing transcatheter aortic valve replacement (TAVR).
Objectives: The goal of this study was to evaluate the safety and performance of the NeoChord DS1000 system (NeoChord, Inc., Minneapolis, Minnesota).
Objectives: The study sought to evaluate the relationship between procedural volume and outcomes with radial and femoral approach.
Objectives: This study sought to compare radial and femoral approaches in patients presenting with ST-segment elevation myocardial infarction (STEMI) and undergoing primary percutaneous coronary intervention (PCI) by high-volume operators experienced in both access sites.
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