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NOTICIAS


20 junio 2012

Kidney Disease May Point to Risk for MI

MEDPAGE TODAY. Kristina Fiore, Staff Writer

Chronic kidney disease (CKD) could be added to the list of criteria for defining people at highest risk for future coronary events, Canadian researchers found. In a large cohort study, patients with only CKD had a significantly higher rate of myocardial infarction (MI) than those who only had diabetes (5.4 versus 6.9 per 1,000 person-years, P<0.0001), according to Marcello Tonelli, MD, of the University of Alberta, and colleagues.

19 junio 2012

La mujer española fallece un 8% más por enfermedad cardiovascular que el hombre.

NoticiasMedicas.es. Fundacion Española del Corazon

Las enfermedades cardiovasculares (ECV) son la primera causa de muerte en nuestro país, siendo responsables del 31,8% de los fallecimientos. Sin embargo, en las mujeres esta proporción aumenta al 35,18%. Tras las ECV, se encuentran como principales causas de mortalidad femenina los tumores (22,35%) y las enfermedades del sistema respiratorio (9,14%)

19 junio 2012

La soledad y vivir solo podrían acortar la vida. Algunos estudios sugieren que los médicos deben preguntar a los pacientes sobre los sistemas de respaldo

MedlinePlus. HealthDay News

Se dice que el uno es el número más solitario, pero también podría ser el más letal. Dos estudios recientes sugieren que vivir solo o sentir soledad pueden aumentar el riesgo de morir de enfermedad cardiaca o de cualquier causa de una persona. En un estudio, las personas con enfermedad cardiaca que vivían solas eran más propensas a morir que sus contrapartes que no vivían solas. Un segundo estudio mostró que las personas a partir de los 60 años de edad estaban en mayor riesgo de declive funcional y/o muerte si se sentían ignoradas, aisladas o reportaban una falta de compañía. Ambos estudios aparecen en la edición en línea del 18 de junio de la revista Archives of Internal Medicine.

15 junio 2012

APPOSITION IV clinical study starts patients enrolment

Cardiovascular NEWS

Stentys has announced that it has enrolled the first patient in its APPOSITION IV clinical study using its new Self-Apposing Sirolimus-eluting stent. The randomised study will enrol 150 heart attack patients who will be treated with either the Stentys stent or Medtronic s Resolute drug-eluting stent, and will compare stent apposition in both groups at four and nine months after treatment.

14 junio 2012

Svelte Medical Systems Announces Start of the FAASTER Post-Market Registry Study

BioPortfolio

Svelte® Medical Systems today announced the start of the FAASTER (First Assessment of the Acrobat Stenting Technique European Post-Market Registry) study in clinical sites across Europe. FAASTER is a real world, multi-center registry assessing the procedural success and resource utilization associated with the Svelte coronary stent mounted on an Integrated Delivery System (IDS) in relation to target lesion and vessel complexity (as defined by NAVI-score) and selected catheter approach (diagnostic or guiding). Up to 1,500 patients will be evaluated in the study.

14 junio 2012

STENTYS Starts Clinical Trial to Broaden Portfolio with New Drug-Eluting Stent

BioPortfolio

STENTYS S.A. (STNT.PA),a medical technology company commercializing the world s first and only Self-Apposing® Stent to treat Acute Myocardial Infarction (AMI), announced today that it has enrolled the first patient in its APPOSITION IV clinical study using its new Self-Apposing® Sirolimus-eluting stent. The randomized study will enroll 150 heart attack patients who will be treated with either the STENTYS stent or Medtronic s Resolute® drug-eluting stent, and will compare stent apposition in both groups at four and nine months after treatment.

13 junio 2012

FDA Panel Backs Wider Use of Sapien Valve

MEDPAGE TODAY. Emily P. Walker, Washington Correspondent

An FDA advisory panel has voted 11-0, with one abstention, to recommend expanding the indication for the Sapien Transcatheter Heart Valve to include high-risk patients with severe aortic stenosis. The FDAs Circulatory Systems Advisory Committee agreed Wednesday that Edwards Lifesciences Sapien valve is safe and effective for patients who are candidates for aortic valve replacement but who have an open-heart surgery mortality risk of 15% or more. The Sapien was approved in 2011 for inoperable patients, but Edwards is seeking the broader "high-risk" indication, which would allow the device to be a treatment option for a greater number of patients.

13 junio 2012

Cardiosolutions, Inc. Receives FDA 510(k) Clearance for Dexterity(TM) Steerable Introducer

Healthcare Sales & Marketing Network20120613

Cardiosolutions Inc., an emerging leader in structural heart solutions for valvular heart disease, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its Dexterity™ Steerable Introducer, a next generation structural heart access introducer and delivery conduit. The Dexterity™ Steerable Introducer is designed to provide physicians straightforward and uncomplicated access to the heart anatomy by simplifying the cardiac trans-septal procedure and facilitating passage of therapies into the entire left atrium, left ventricle and associated heart structures. The Dexterity™ Steerable Introducer is intended to be used for the advancement and delivery of various cardiovascular catheters into the heart, including the left side of the cardiac anatomy through the inter-atrial septum.

12 junio 2012

Bioresorbable Stents: Just What the Interventionalist Ordered?

CardioSource

Development of more biocompatible polymers, as well as thinner stent struts and polymer coatings, is improving efficacy and safety of second-generation drug-eluting stents (DES). Given the link between certain polymers and chronic inflammatory responses to DES, it is a natural next step to develop either a third-generation bioresorbable polymer on a durable platform or a fourth-generation bioresorbable polymer on a bioresorbable platform.

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