The public health department's crucial decision to negotiate with leading firms to halve the price of drug-eluting stents has helped well over 100 poor patients in just a fortnight.
The US Coronary Stent Industry Outlook to 2018 – Bioabsorbable Stents to Drive the Future Growth” provides a comprehensive analysis of the various aspects such as the market size of the US Coronary Stent industry, market segments i.e. drug eluting and bare metal stents and future outlook of the industry. The report also covers the market share of major players in the US.
The new generation of biodegradable drug eluting stent is developed by SINOMED to solve the persistent safety problems of late stent thrombosis in the 1st generation of DES products. The perfect combination of innovative design and fine processing lays a solid technical foundation for outstanding clinical performance of the product.
Hurley Medical Center is the only medical center in Genesee County and one of six in the state to use a new kind of drug-coated stent, the Zilver PTX drug-eluting peripheral stent designed to treat peripheral artery disease.
Citic Private Equity Funds Management Co. is considering buying full control of medical devices maker Biosensors International Group Ltd., said two people with knowledge of the deliberations.
Alternatives means of delivering drugs such as paclitaxel could have a similar effect to drug-eluting stents without the invasive procedure, according to a new study to be published in the journal Nanomedicine: Nanotechnology, Biology and Medicine.
SANTA ROSA -- Medtronic, Inc. (NYSE: MDT) on Tuesday reported its Cardiac and Vascular group, which is based in Santa Rosa, reported global sales of $2.119 billion, an increase of 1 percent over the year. The Minneapolis-based company as a whole, however, reported that its third quarter net profit dropped 23 percent, largely related to the discontinuation of a high blood pressure treatment that failed to make it out of trial.
Interruption of dual antiplatelet therapy (DAPT) in patients with second-generation zotarolimus-eluting stents (ZES) is unlikely to lead to stent thrombosis as long as it occurs at least 1 month after implantation, according to a retrospective study published online February 7, 2014, ahead of print in the European Heart Journal. However, earlier interruption is associated with a high risk of adverse events.
Reportstack Announces the Publication of its Research Report - Global Drug-eluting Stent Market 2014-2018. The following companies are the key players in Global Drug-eluting Stent Market: Abbott Laboratories, Boston Scientific Corp., Medtronic Inc., and Terumo Corp. “Increasing demand for minimally-invasive procedures has been witnessed among members of the rapidly aging population across the world, and this is expected to boost the growth of the Global DES market.
Use of a Fully Covered Self-Expanding Metal Stent (SEMS) for the Treatment of Dysphagia due to Severe Torturous Presbyesophagus. Andrew Mazulis, MD, Sarosh B...
Professor Michael Haude, M.D., of Medical Clinic I at the Lukaskrankenhaus in Neuss, Germany, discusses Genous™, OrbusNeich's pro-healing endothelial progenitor cell capture technology
Prof. Stephen W.L. Lee, M.D., of the Queen Mary Hospital, University of Hong Kong, China, discusses the need for novel devices that improve patient outcomes....
Stents are used to keep coronary arteries open after a procedure called angioplasty. Some stents contain medicine that is released over time. It was thought ...
Dr. Valeri Gelev of Tokuda Hospital in Sofia, Bulgaria, discusses the problem of delayed arterial healing associated with drug eluting stents. #EuroPCR2013
CSWN talks with Gregg W. Stone, MD, of Columbia University and New York Presbyterian Hospital, about trends in the stent thrombosis with drug-eluting stents....
TCTAP 2013 Wrap-up Interview "Drug-Eluting Stents" 9:45 AM - 10:15 AM, Thursday, April 25 Moderator: Ron Waksman Interviewees: Bernard Chevalier, Stephen G. Ellis & Renu Virmani.
With the accelerated aging, the prevalence of cardiovascular diseases in China increased year by year. According to statistics of National Health and Family Planning Commission of the People’s Republic of China, in 2012 cardiovascular disease deaths in China reached 3.5 million. The fast growing number of heart patients stimulated rapid growth in Chinese demand for interventional cardiac operation and coronary stent. China's PCI (percutaneous coronary intervention) surgeries increased from 25,000 cases in 2002 to about 531,000 cases in 2012; the number of coronary stent implantation rose from 40,000 units in 2002 to approximately 640,000 units in 2012. In 2007-2012 China's cardiovascular stent market size grew at an AAGR of 20.3%.
Primary Percutaneous Coronary Intervention (PCI) has made huge leaps of improvement in the last two decades, with the ever goal being permanent sufficient flow in the coronary artery. From balloon angioplasty alone to subsequent Bare Metal Stent (BMS) implantation, measures have been made to achieve this aim. The introduction of the Drug Eluting Stent (DES) proved an ever better outcome: the antiproliferative drug coated struts seemed to cause an end to the last barrier of coronary reclosure: neo-intimal hyperproliferation inside the stent. However, contradicting results with regard to stent safety and effectiveness have been published and therefore we sought to compare the BMS with the DES in a real world STEMI-registry. Primarily, we aimed to investigate the DES ability in preventing target lesion revascularizations (TLR) as a result of in-stent restenosis. Our secondary endpoint was to compare both safety and effectiveness of both stent types.
Dr. George Georgiou of the Nicosia General Hospital, Cyprus, discusses the challenges associated with drug eluting stents, including late catch-up phenomenon and late thrombosis.
Yock talks about the costs versus the charges of medical stents. A cynical approach is that the actual metal stents themselves cost 80-90 cents to make and their charge is about $1200. However, there is an enormous amount of R&D effort.
Dr. Zambahari of the Institut Jantung Nagara National Heart Institute in Kuala Lumpur, Malaysia, describes how the COMBO Dual Therapy Stent addresses the problem of late stent thrombosis associated with current monotherapy drug eluting stents.
Advancing the clinical practice of interventional cardiovascular medicine, India Medtronic today announces the availability of the U.S. Food and Drug Administration (FDA) approved Resolute Integrity™ Drug-Eluting Stent (DES) for the treatment of coronary artery disease (CAD) in India.
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