Our aim was to examine the relationship of arterial stiffness to measures of atherosclerosis, arterial calcification, and bone mineral density (BMD); the heritability of these measures; and the degree to which they are explained by common genetic influences. Journal of the American College of Cardiology. Vol. 57, No. 13, 2011. Copyright © 2011 by the American College of Cardiology Foundation. Published by Elsevier Inc. ISSN 0735-1097.
The purpose of this study was to compare the safety and efficacy of the Xience V (Abbott Vascular, Santa Clara, California) everolimus-eluting stent (EES) with the Taxus Liberté (Boston Scientific, Natick, Massachusetts) paclitaxel-eluting stent (PES) at 2-year follow-up. Journal of the American College of Cardiology. Vol. 58, No. 1, 2011. Copyright © 2011 by the American College of Cardiology Foundation. Published by Elsevier Inc. ISSN 0735-1097.
The aim of this study was to ascertain the 1-year incidence of stent thrombosis (ST) and major bleeding (MB) in a large, unselected population treated with sirolimus-eluting stents (SES). Journal of the American College of Cardiology. Vol. 57, No. 13, 2011. Copyright © 2011 by the American College of Cardiology Foundation. Published by Elsevier Inc. ISSN 0735-1097
We evaluated the impact of the everolimus-eluting stent (EES) on the frequency of stent thrombosis (ST), target vessel revascularization (TVR), myocardial infarction (MI), and cardiac death in randomized controlled trials comparing the EES to non–everolimus-eluting drug-eluting stents (EE-DES). Journal of the American College of Cardiology. Vol. 58, No. 6, 2011. Copyright © 2011 by the American College of Cardiology Foundation. Published by Elsevier Inc. ISSN 0735-1097.
The purpose of this study was to investigate the efficacy and safety of glycoprotein IIb/IIIa inhibitors (GPIs) during elective percutaneous coronary intervention (PCI). Journal of the American College of Cardiology. Vol. 57, No. 10, 2011. Copyright © 2011 by the American College of Cardiology Foundation. Published by Elsevier Inc. ISSN 0735-1097.
Very late stent thrombosis (VLST) was reported to occur even in patients with bare metal stent (BMS) implantation, although the annual incidence of VLST after BMS was much lower than that after drug-eluting stent implantation. Pathophysiologic mechanisms of VLST after BMS implantation remain largely unknown. Copyright © 2012 American Heart Association. All rights reserved. Print ISSN: 1941-7640. Online ISSN:1941-7632
Our data suggest this procedure to be safe and potentially useful to achieve partial relief on the stenosiswhen it is not achieved by standard balloon dilation. A Larger patient series with a control arm is needed to determine if the use of cutting balloon for resistant pulmonary valve stenosis is effective in the long term. INNOVATION IN CARDIVASCULAR INTERVENTIONS MEETING.
New-generation coronary stents that release zotarolimus or everolimus have been shown to reduce the risk of restenosis. However, it is unclear whether there are differences in efficacy and safety between the two types of stents on the basis of prospectively adjudicated end points endorsed by the Food and Drug Administration. The New England Journal of Medicine. Copyright © 2010 Massachusetts Medical Society. All rights reserved.
Aims: To compare the tissue coverage of a hydrophilic polymer-coated zotarolimus-eluting stent (ZES) vs. a fluoropolymer-coated everolimus-eluting stent (EES) at 13 months, using optical coherence tomography (OCT) in an all-comers population of patients, in order to clarify the mechanism of eventual differences in the biocompatibility and thrombogenicity of the devices. European Heart Journal (2011) 32, 2454–2463. Published on behalf of the European Society of Cardiology. All rights reserved. & The Author 2011.
Pathology studies on fatal cases of very late stent thrombosis have described incomplete neointimal coverage as common substrate, in some cases appearing at side-branch struts. Intravascular ultrasound studies have described the association between incomplete stent apposition (ISA) and stent thrombosis, but the mechanism explaining this association remains unclear. Whether the neointimal coverage of nonapposed side-branch and ISA struts is delayed with respect to well-apposed struts is unknown. Copyright © 2011 American Heart Association. All rights reserved. Print ISSN: 0009-7322. Online ISSN: 1524-4539.
Vessel angulation and large changes in vessel geometry after stent implantation have been associated with an increased risk of target lesion failure (TLF) using bare-metal stents. Second-generation drug-eluting stents (DES)offer superior conformability and inhibition of neointima. The aim of the study is to investigate the relationship between pre and post-implant vessel geometry and the occurrence of TLF at 1 year after treatment with second-generation DES; and to compare the conformability of Resolute and Xience stents. American Heart Journal Volume 162. Copytight © 2011, Mosby, Inc. All rights reserved.
The concluding statement from a first-in-man case report published in Circulation in 2002 was: ‘‘Nonsurgical implantation of a prosthetic heart valve can be successfully achieved with immediate and midterm hemodynamic and clinical improvement’’ [1]. The lead author of this short manuscript was Alain Cribier, and the procedure involved transcatheter placement of a bioprosthetic aortic valve in a desperately ill man with critical aortic stenosis (AS) and no therapy alternatives. At the time, it was impossible to predict the future of this new medical therapy, which at the same time appeared both reckless and revolutionary. In retrospect, 10 years later, this humble concluding statement laid the foundation for a medical breakthrough that has altered the landscape of cardiovascular medicine. The odyssey and the anniversary of transcatheter aortic valve replacement (TAVR) deserve our attention and careful reflection. Archives of Cardiovascular Disease (2012) 105, 129—131. Copyright © 2012 Published by Elsevier Masson SAS.
A new generation of balloon-expandable valves (e.g. Edwards SAPIEN XT) enables the use of a decreased sheath size using the NovaFlexTM delivery system for transfemoral transcatheter aortic valve implantation (TAVI). However, there are few data analysing the efficacy and safety of this new prosthesis. Archives of Cardiovascular Disease (2012) 105, 132—140. Copyright © 2012 Elsevier Masson SAS. All rights reserved.
In April 2002, the first human percutaneous aortic valve implantation was performed in Rouen [1]. Different approaches quickly became feasible and, despite the historical use of the antegrade transseptal approach, the retrograde approach became popular during 2005, with the development of the RetroFlex catheter [2]. Due to the large diameter of the first models of the RetroFlex catheter (22/24 F) and the presence, in numerous patients, of small-calibre vessels or vascular disease, the idea of a transapical approach emerged. In 2005, after an animal feasibility study [3], the first patients were implanted via a small anterolateral mini thoracotomy [4,5]. In July 2007, the first transapical implantation in France was performed in our department. Since this time, 61 patients have been implanted using this approach. We report the 4-year outcomes of these patients. Archives of Cardiovascular Disease (2012) 105, 141—145. Copyright © 2012 Published by Elsevier Masson SAS.
The development of transcatheter aortic valve implantation (TAVI) by our group has been a 20-year odyssey. In 1993, postmortem studies validated the concept of intravalvular stenting in calcific aortic stenosis. The first prototypes of balloon-expandable valves were tested in an animal model in 2000. The first-in-man implantation was performed in Rouen in 2002, rapidly followed by two prospective series in compassionate cases in our centre. TAVI took flight in 2004 in the hands of Edwards Lifesciences, with major improvements in devices and approaches. At the same time, the self-expanding CoreValve was launched. Thousands of highsurgical- risk patients were enrolled in feasibility studies, leading to the Conformité Européenne (CE) mark being granted in 2007 for the two devices. Archives of Cardiovascular Disease (2012) 105, 146—152. Copyright © 2012 Elsevier Masson SAS. All rights reserved.
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