Tag Archives: PAD

Peripheral artery disease: dramatically higher rates worldwide

The number of people with peripheral artery disease (PAD) is on the rise, according to a study published in The Lancet. PAD refers to diseases of the blood vessels outside of the heart and brain. Peripheral artery disease causes the blood vessels to narrow, restricting blood flow in the arms, legs, stomach and kidneys… …read more

Source: FULL ARTICLE at Medical News Today

Cordis Acquires Flexible Stenting Solutions, Inc.

By Business Wirevia The Motley Fool

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Cordis Acquires Flexible Stenting Solutions, Inc.

Agreement Expands Treatment Options for Advanced Peripheral Artery Disease

BRIDGEWATER, N.J.–(BUSINESS WIRE)– Cordis Corporation, a worldwide leader in the development of interventional vascular technology, today announced it has completed the acquisition of Flexible Stenting Solutions, Inc., a leading developer of innovative flexible peripheral arterial, venous and biliary stents.

Currently, Cordis markets the S.M.A.R.T.® Vascular Stent worldwide. The addition of Flexible Stenting Solutions’ FlexStent® Self Expanding Stent System provides Cordis with the opportunity to evolve the S.M.A.R.T.® Stent platform to address unmet needs in the treatment of peripheral artery disease (PAD). It also extends the company’s potential to expand therapeutic applications into below-the-knee and venous interventions. An estimated 27 million people in Europe and North America alone suffer from PAD.

“Cordis continues to identify opportunities to enhance its expanding portfolio of less invasive treatment options to address the needs of patients suffering from vascular disease worldwide,” said Shlomi Nachman, Company Group Chairman, Cordis Corporation. “This acquisition will enable Cordis to provide clinicians more options to meet their evolving therapeutic needs and to strengthen our leadership position in the treatment of vascular disease.”

This acquisition marks another milestone in the company’s strategy to strengthen its position in the endovascular market. Recently Cordis received superficial femoral artery (SFA) and proximal popliteal artery (PPA) indications for the S.M.A.R.T.® Stent, the only stent approved in the U.S. for iliac, SFA and PPA vascular indications. In addition, Cordis offers market-leading endovascular technology platforms including percutaneous transluminal angioplasty balloons and chronic total occlusion crossing devices.

“The FlexStent® System is a promising platform designed to optimize flexibility, fracture resistance and radial strength with predictable placement. We look forward to expanding our experience with this new technology platform,” said Prof. Dr. Thomas Zeller, Director Department Angiology at Universitaets-Herzzentrum, Freiburg – Bad Krozingen, Bad Krozingen, Germany.

The FlexStent® System received European CE Mark approval for the treatment of vascular disease (iliac, SFA and popliteal) in January 2009. In the U.S., the device received 510(k) clearance by the Food and Drug Administration (FDA) for the palliative treatment of biliary strictures associated with malignant tumors in September 2009. The FlexStent® System is also being evaluated in an Investigational Device Exemption (IDE) study to evaluate its safety and efficacy in the treatment of patients with atherosclerosis in the SFA, or SFA disease. 1 Data from the OPEN Trial are expected to support a Premarket Approval (PMA) application requesting an …read more
Source: FULL ARTICLE at DailyFinance

Boston Scientific Introduces New Diameter Rubicon Catheters

By Dan Carroll, The Motley Fool

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Medical device maker Boston Scientific announced recently that it has begun launching new sizes of its Rubicon Support Catheter in the United States. New 0.035″ and 0.018″ diameter catheters are aimed to help support guidewires for placing stents and other peripheral vascular products in patients suffering from complications of peripheral arterial disease.

Peripheral arterial disease, or PAD, affects around 27-million people around the globe, according to Boston Scientific. The disease can create blockages in blood vessels, leading to cramps, pain, or even amputation of limbs.

Boston Scientific Peripheral Interventions president Jeff Mirviss commented on the use of the company’s new products, saying: “Support catheters can help physicians treat more patients by facilitating the crossing of complex lesions… By making a full range of diameters of Rubicon Support Catheters available, we are offering more choices to clinicians.”

Previously, Boston Scientific had offered the Rubicon catheter in only a 0.014″ diameter model. The newer widths will allow physicians more flexibility in treating a wider range of symptoms. 

The article Boston Scientific Introduces New Diameter Rubicon Catheters originally appeared on Fool.com.

Fool contributor Dan Carroll has no position in any stocks mentioned. The Motley Fool has no position in any of the stocks mentioned. Try any of our Foolish newsletter services free for 30 days. We Fools may not all hold the same opinions, but we all believe that considering a diverse range of insights makes us better investors. The Motley Fool has a disclosure policy.

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Source: FULL ARTICLE at DailyFinance

ACE Inhibitor Improves Walking In People with Peripheral Artery Disease

By Larry Husten, Contributor Giving an ACE inhibitor to people with peripheral artery disease (PAD) and intermittent claudication reduces pain and increases walking time, according to a new study published in JAMA. Currently the pharmacologic options for this patient population are few and have limited efficacy.
Source: FULL ARTICLE at Forbes Latest