dijous, 2 de juliol del 2015

Medtronic touts 1-year data for VenaSeal device

Medtronic logoMedtronic (NYSE:MDT) today touted results from its VeClose clinical trial of its VenaSeal varicose vein treatment, saying the device posted a 96.8% closure rate at 12 months.

Results from the study were presented by principal investigator Dr. Nick Morrison of the Morrison Vein Institute in Scottsdale, Ariz., at the the European Venous Forum 2015 in St. Petersburg, Russia.

VenaSeal won approval from the FDA last February. Medtronic acquired the device when it paid $50 billion for Covidien in January. It uses a medical adhesive administered through a minimally invasive procedure that does not require tumescent anesthesia, Medtronic said.

“The VenaSeal closure system provides patients with a minimally invasive procedure that eliminates the need for surgery, thermal ablation and tumescent anesthesia. As a result, patients are often able to quickly return to normal activities after the procedure,” Morrison said in prepared remarks. “The results show sustained closure with VenaSeal closure system that is comparable to closure rates with radiofrequency at 12 months.”

The VeSeal study compared VenaSeal with another legacy Covidien product, the ClosureFast catheter, Medtronic said.

“The 12 month results of the VeClose trial demonstrates the durability of the system,” Medtronic aortic & peripheral vascular medical director Dr. Mark Turco added. “This, combined with the improved patient comfort and reduced recovery times of the VenaSeal closure system, makes this a clinically-proven, patient-friendly treatment option for patients.”

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Biotronik launches Itrevia MRI-safe quad CRT-D in Japan

Biotronik launches Itrevia MRI-safe quad CRT-D in JapanBiotronik said today that it launched its Itrevia MRI-safe quad cardiac resynchronization therapy defibrillator in Japan, part of a Japanese rollout of new devices for 2015.

The device is equipped with home monitoring connectivity, as well as compatibility with up to 1.5 tesla MRI machines, the German medical device giant said.

“As a producer of superior medical technologies, it is imperative for us to have a presence in the world’s leading technologies market. It also makes sense that the world’s biggest producer of ProMRI technology should have a strong presence in the country where MRI scanning is the most common. Our commitment to producing products that assist both physicians’ and patients’ needs has resonated with the Japanese market, as has our unwavering sense of responsibility when it comes to helping patients live normal lives,” Biotronik Japan managing director Jeffrey Annis said in a press release.

The CRT-D device will allow full MRI scans, something Biotronik said is advisable given the rate of co-morbidities in patients with cardiovascular implantable electronic devices.

“Patients implanted with CIEDs can have a variety of underlying diseases such as sick sinus syndrome, complete AV block, atrial fibrillation with bradycardia, ventricular arrhythmias and/or chronic heart failure. So, it is important that the implanted device is compatible with MRI scans as the risk of stroke is always present,” Dr. Kenji Ando of the Kokura Memorial Hospital said in prepared remarks.

Biotronik said that Japan is the world’s largest MRI market with 47 MRI scanners per 1 million people, more than any other country.

In May, Biotronik launched its CardioMessenger Smart 3G and Iforia 7 DR-T and VR-T DF4 MRI-safe implantable cardiac defibrillators in Japan. The devices are designed to communicate to allow physicians to manage data from patients’ implantable devices, transmitted via the company’s home monitoring system.

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Cambridge Robotics startup aims at Intuitive Surgical

Cambridge Robotics startup aims at Intuitive SurgicalU.K.-based startup Cambridge Medical Robotics said today it is tilting at a growing robotic surgery market and taking aim at market leader Intuitive Surgical (NSDQ:ISRG), according to an interview with Business Weekly.

The startup said it is developing a “next-generation universal robotic system for minimal access – or keyhole – surgery,” and aims to make it more affordable by broadening the range of procedures that can be performed robotically.

The company is headed by former Sargentia CEO Martin Frost, who said the company is taking aim at Intuitive Surgical and their daVinci robot system.

“We are addressing a surgical robotics market dominated by Intuitive Surgical – the major US medical devices company – and one that has now been validated by Google and Johnson & Johnson who announced a couple of months ago that they were collaborating to enter this market to an unspecified timescale,” CEO Martin Frost told Business Weekly.

In 2013, Frost was at the head of a similar startup, called Kinective Surgical, according to an interview with Cabume.

Frost said Kinective Surgical, launched in 2012, aimed to raise $5 million to seek FDA approval for a minimally invasive robotic surgery system. The system was slated to be configurable so purchasers could choose which elements they need, instead of having to buy a full platform, to keep the cost down and make it easier to compete against expensive devices such as the daVinci.

Cambridge Medical Robotics has not released details of their robotic surgical platform, but Frost said the company has 30 patent applications filed in the U.K. and that he is confident of a prototype reveal this year.

The company is supported by Norwegian private foundation Escala Capital, but Frost says the company will need to seek more investors to move forward.

“Our investors, Escala Capital, will and can continue to fund the company but we will be looking to add strategic investors over the next 12 months,” Frost told Business Weekly.

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Diabetes: Study finds bariatric surgery beats diet, exercise

Gastric bandA study designed to compare bariatric surgery with lifestyle interventions found that Type II diabetics treated with gastric bypass or banding procedures fared better than patients who watched their diets and exercised.

Results from “Bariatric Surgery versus Intensive Medical Therapy for Diabetes – 3-Year Outcomes,” which was funded by Johnson & Johnson (NYSE:JNJ) subsidiaries Ethicon and LifeScan, the Cleveland Clinic and the National Institutes of Health, were published online yesterday in the Journal of the American Medical Assn.

The 3-year, 61-patient study randomized obese subjects 1 of 3 arms: Roux-en-Y gastric bypass; laparoscopic adjustable gastric banding; or 1 year of intensive lifestyle intervention. After a year all 3 arms were subject to 2 years of low-level lifestyle intervention, according to the study. The primary endpoints were partial and complete Type II diabetes remission, with secondary endpoints of diabetes medications and weight change.

Forty percent of the gastric bypass arm and 29% of the gastric banding cohort achieved partial or complete remission, compared with no remission for the lifestyle intervention arm, according to the study. No diabetes meds were needed after 3 years for 65% for the bypass group and 33% for the banding group, compared with no change in medication for the lifestyle group.

The study was limited by its small size and short duration, which weren’t adequate to detect differences in complications such as myocardial infarction, stroke, or death, theUniversity of Pittsburgh School of Medicine researchers wrote. The trial’s protocol calls for another round of follow-ups at 5 years, “which should allow additional assessment of even longer-term efficacy and safety,” they wrote.

“Despite these limitations, we conclude that bariatric surgery represents a potentially useful strategy for the management of Type II diabetes, allowing many patients to reach and maintain therapeutic targets of glycemic control that otherwise would not be achievable with intensive medical therapy alone,” they wrote. “Some patients in our study had complete diabetes remission, whereas others had a marked reduction in the need for pharmacologic treatment. The reduction in cardiovascular risk factors was sustained, allowing for reductions in lipid-lowering and antihypertensive therapies. Other benefits of surgery included a significant improvement in the quality of life. The question as to whether the documented benefits will reduce microvascular and macrovascular morbidity and mortality, as shown in nonrandomized studies, can be adequately answered only through larger, multicenter clinical-outcome trials.”

“I do think it adds strongly to the growing body of data that [surgery] should be considered” in treating obesity and diabetes, lead author Dr. Anita Courcoulas told the Wall Street Journal.

The results from Courcoulas and colleagues echo those from an earlier trial comparing intensive medical therapy alone versus medical therapy plus Roux-en-Y gastric bypass or sleeve gastrectomy in 150 obese patients with uncontrolled Type II diabetes.

“We should consider the use of bariatric (metabolic) surgery in all severely obese patients with [Type II diabetes] and start a mass treatment, similar to what was done with coronary artery bypass graft more than 50 years ago,” Dr. Michel Gagner, of Florida International University, wrote in an editorial accompanying the JAMA report.

“I don’t know how many studies we need to do to keep comparing the best medical treatment to surgery, but it’s clear to me that surgery is the only thing that offers resolution to diabetes,” Gagner told the Journal.

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Appeals court clears inspectors in French breast implants case

Breast implant(Reuters) — A French appeals court today overturned a negligence conviction against certification agency TUV Rheinland for its role in approving faulty breast implants produced with counterfeit silicone by manufacturer PIP until its 2010 closure.

In a statement, the Aix-en-Provence appeals court said the German agency had “respected the obligations incumbent upon it as a certifying organization”.

Poly Implant Prothèse, the French company at the centre of the scandal, sold implants globally over almost 2 decades until French regulators discovered it was passing off low-grade industrial silicone as a much pricier medical product.

The counterfeit substance was used in implants given to some 300,000 women. About one-quarter of those subsequently removed were found to have ruptured, regulators said, raising concerns over the long-term health effects of exposure to their contents.

Company founder Jean-Claude Mas was jailed for four years and fined €75,000 ($83,000) in 2013 after a police investigation revealed a sophisticated fraud.

PIP employees would remove evidence of the cheaper silicone gel before annual inspections by TUV Rheinland, it found.

“TUV Rheinland welcomes this verdict,” the agency’s lawyer, Cécile Derycke, said on Thursday.

“The fraud committed by PIP could not have been detected by TUV Rheinland with the tools granted to certification organisations under current regulations.”

($1 = €0.9036)

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dimecres, 1 de juliol del 2015

Alcon wins CE Mark for AcrySof IQ PanOptix trifocal lens

Alcon wins CE Mark for  AcrySof IQ PanOptix trifocal lensAlcon said last month that it won CE Mark approval in the European Union for its AcrySof IQ PanOptix trifocal intraocular lens.

The lens is indicated for use in patients undergoing cataract surgery who need treatment for near, intermediate, and distance vision needs with a single lens, the Switzerland-based company said.

“The AcrySof IQ PanOptix trifocal IOL is a significant innovation which further augments Alcon’s presbyopia correcting portfolio, leveraging Alcon’s market-leading AcrySof IQ IOL platform. It is designed to provide exceptional functional vision from near to intermediate, in addition to providing excellent distance vision,” Alcon surgical head of R&D Franck Leveiller said in prepared remarks.

“Today’s patients undergoing cataract surgery are more likely to seek vision correction options to address various lifestyle tasks such as reading books, using electronic tablets, working on computers and performing outdoor activities without the need for glasses or contact lenses. The AcrySof IQ PanOptix trifocal IOL is an important option that should provide these patients with a full range of vision and thus significantly reduced dependence on glasses,” Dr. Richard Packard of London’s Arnott Eye Associates said in a press release.

Last November, Alcon met with an FDA advisory panel to review the data behind its application for a new indication for its AcrySof IQ ReSTOR intraocular lens. The AcrySof IQ ReSTOR lens is already approved in the U.S. to treat presbyopia and cataracts.

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B. Braun picks up German dialysis firm

B. Braun logoB. Braun Medical said today that its Avitum AG dialyis subsidiary acquired Lauer Membran Wassertechnik, which makes the Aquaboss water treatment system, for an undisclosed amount.

“This latest global acquisition will allow us to expand and grow our business as a full-system supplier of dialysis products and services in the U.S.,” vice president Sam Amory, said in prepared remarks. “We are proud to offer the revolutionary Aquaboss in-center water treatment system to our valued customers.”

Bethlehem, Pa.-based Braun said the deal rounds out its dialysis water treatment offering. The company said it’s sold and distributed Wittlingen, Germany-based Lauer’s device ” in various countries all over the world,” including the U.S.

Lauer, which employs 75 people, is slated to continue under its own umbrella, Braun said.

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