Lombard Medical Technologies announced that Lombard Medical has filed a registration statement on Form F-1 with the US Securities and Exchange Commission (SEC) relating to a proposed initial public offering of its ordinary shares. The number of shares to be offered and the price range for the offering have not yet been determined.
The Charing Cross Symposium (5—8 April 2014, Grand Hall Olympia, London, UK) will feature three full days of peripheral arterial disease management topics this year. The programme dedicated to lower limb intervention will start with the peripheral arterial day in the Main Programme on Saturday and continue with the LINC @ CX peripheral intervention programme on Sunday and the CX ilegx Collaboration Day on Monday.
Results from six-month data of the PES BTK-70 study have shown 86.2% primary patency in the treatment of short focal lesions in below-the-knee arteries with the self-expanding paclitaxel-eluting Stentys stent. Nearly 90% freedom from target lesion revascularisation was achieved and there was over 98% limb salvage rate.
Thomas Nolte, vascular surgeon and director of Vascular Center, Herz und Gefäßzentrum, Bad Bevensen, Germany, recently commented on the importance of sealing in the endovascular treatment of abdominal aortic aneurysm.
Spectranetics announced that the EXCITE ISR trial achieved the statistical endpoints of the adjunct analysis. According to a company press release, the trial evaluates laser atherectomy plus percutaneous transluminal angioplasty compared with percutaneous transluminal angioplasty alone for the treatment of in-stent restenosis (ISR) in patients suffering from peripheral artery disease.
W L Gore & Associates (Gore) has announced in a press release that the results of the REVISE clinical study showed that the Gore Viabahn endoprosthesis with Heparin Bioactive Surface is superior to percutaneous transluminal angioplasty - the current standard of care for treating stenoses or thrombotic occlusions.
Recognising that new technologies and techniques are revolutionising how venous disorders are treated, in 2014, for the first time, the Charing Cross Symposium (5–8 April, London, UK) will host three days of venous activities. This year, the CX Office-based Vein Practice Course has been extended over two full days—Sunday and Monday—and will be followed by a day of venous talks in the Venous Consensus Update session of the Main Programme on Tuesday.
A study that compared the durability of thoracic endovascular aortic repair (TEVAR) in two similar clinical trials, one that used early-generation and another that used later-generation stent grafts, found a significantly lower freedom from reintervention rate for patients who received the newer stent grafts.
Vascutek has announced the return to market of the Anaconda bifurcate body stent graft system for patients with abdominal aortic aneurysms. The system was voluntarily recalled in October 2013 following the identification of a potential issue with the release wire in the delivery system.
Cardiovascular Systems has announced that it has received US Food and Drug Administration (FDA) clearance of its new Diamondback 360 60cm Peripheral Orbital Atherectomy Systems (OAS) for the treatment of peripheral arterial disease (PAD).
A recent budget impact model of endovascular interventions in the USA and Germany found not only that drug-eluting balloons are a cost-effective therapy, but also that at current reimbursement rates, payer economics are in conflict with provider economics.
Medtronic has announced the European launch of a new peripheral angioplasty balloon, TOTAL across that targets challenging lesions in the lower-extremity, including below-the-knee arteries associated with critical limb ischaemia.
The most recent ZILVER PTX trial data, presented at the Controversies and Updates in Vascular Surgery (CACVS) congress (23–25 January 2014, Paris, France), demonstrate sustained positive results for the paclitaxel-eluting stent (Cook Medical) vs. bare metal stent in patients with peripheral arterial disease.
Study presenter Michael Werk (Department of Radiology of the Martin-Luteher-Hospital, Hubertus-Hospital, Berlin, Germany) reported that the PACIFIER study was a proof-of-concept trial that was designed to demonstrate the efficacy of In.Pact Pacific drug-coated balloon in reducing restenosis of femoropopliteal stenosis and occlusions compared with standard percutaneous transluminal angioplasty (PTA; uncoated balloons). He added that it was an investigator initiated, multicentre study in which patients were randomised in a one-to-one fashion to receive the In.Pact Pacific balloon (41 patients; 44 lesions) or standard PTA (44 patients; 47 lesions), commenting: “The primary endpoint was six-month late lumen loss.”
A clinical study has demonstrated the feasibility of the Esprit drug-eluting bioresorbable vascular scaffold (Abbott), with no deaths or amputations, in patients with symptomatic atherosclerotic disease of the superficial femoral artery or iliac arteries.
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