ResMed Wins German Patent Violation Situation Introduced by Fisher & Paykel

ResMed’s AirSense 10, AirCurve 10 and Lumis products don’t infringe German utility model patent

MUNICH, March. 12, 2017 /PRNewswire/ — ResMed (New york stock exchange: RMD), the earth’s leading tech-driven medical device company and innovator in sleep-disordered breathing and respiratory system care, today announced that the Munich District Court made the decision that ResMed’s AirSense 10, AirCurve 10, Lumis as well as their humidifiers don’t infringe a Fisher & Paykel German utility model (a brief-term patent), DE 20 2013 012 358 U1.

Although ResMed’s products don’t infringe, ResMed continues its challenge from the validity from the German utility model prior to the German Patent and Trademark Office (GPTO). 

Up to now, no German court finds that ResMed’s products infringe a Fisher & Paykel patent most of the three cases introduced by Fisher & Paykel against ResMed in Germany. By comparison, exactly the same German court concluded in September that Fisher & Paykel’s Simplus, Eson and Eson 2 masks infringe ResMed patents, while remaining the proceedings pending the end result of invalidation proceedings. ResMed has become protecting its very own patents within the European Patent Office.     

“We applaud the German court because of its sensible approach,” stated ResMed global general counsel and chief administrative officer David Pendarvis. “We’re pleased the court found our products don’t infringe, and expect to showing this Fisher & Paykel patent is invalid.” 

This ruling in Germany doesn’t have effect on ResMed and Fisher & Paykel’s patent violation litigation in other jurisdictions.

About ResMed
ResMed (New york stock exchange: RMD) changes lives with award-winning medical devices and cloud-based computer programs that better identify, treat and manage anti snoring, chronic obstructive lung disease (Chronic obstructive pulmonary disease) along with other chronic illnesses. ResMed is really a world leader in connected care, using more than 3 million patients remotely monitored every single day. Our 6,000-strong team is dedicated to allowing the world’s best tech-driven medical device company – improving quality of existence, lowering the impact of chronic disease, and saving healthcare costs in additional than 120 countries.

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As Express Scripts pays $3.6B for eviCore Healthcare, did Amazon . com result in the PBM blink?

Money bag icon on blackboard with hand

Express Scripts intends to covering out $3.6 billion to purchase eviCore Healthcare from several investors. It’s an offer which will see the organization liberate in the prescription medication benefits manager and expand in to the wider arena of medical benefit management for insurers, media reports noted.

EviCore Healthcare pre-approves scans along with other pricey tests for health plans covering 100 million people, based on Bloomberg. Obviously, there’s the flipside of saving health plans money, as Saurabh Jha, a radiologist using the Hospital in the College of Pennsylvania, noted on Twitter:

Pharmacy benefit managers, amongst other things, negotiate prices of covered drugs with pharma companies, use financial incentives to influence patients to reduce-cost generics and manage high-cost niche medications.

The offer might be a method for Express Scripts to safeguard itself from the intimidating competition Amazon . com could offer whether it would transfer to the PBM sector, as CNBC reported captured. However in an announcement from Express Scripts CEO Tim Wentworth, it was not obvious the move through the PBM was reply to Amazon . com, although he did suggest the offer would consolidate its power within the patient benefit management market.

“By further strengthening our independent model and creating numerous possibilities for growth, the purchase of eviCore will provide value for the clients, patients, providers, and shareholders,” he stated within the statement.

Meant for its medical benefits management business, eviCore acquired QPID Health this past year. The company, which functions like a subsidiary of eviCore, created a clinical decision support tool that actually works on the top of providers’ electronic permanent medical record systems. Its Q-Guide is made to be utilized before high-cost, high-volume surgical procedures to provide physicians an easy method to evaluate the requirement for a process using the patient’s risks.

The purchase is anticipated to shut through the finish of the year.

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Boston Scientific Appoints Desiree Ralls-Morrison General Counsel and company Secretary

MARLBOROUGH, Mass., March. 4, 2017 /PRNewswire/ — Boston Scientific Corporation (New york stock exchange: BSX) today announced the appointment of Desiree Ralls-Morrison as senior v . p ., general counsel and company secretary. Ralls-Morrison will join Boston Scientific on November 30, 2017, as part of the manager committee, with responsibility for supplying a lawyer over the company’s global companies and processes, and overseeing the business’s global compliance function.

Ralls-Morrison will succeed Timothy Pratt, executive v . p ., general counsel and company secretary, who announced his intention to retire from the organization in April 2017.  

“Desiree is definitely an accomplished leader within the medical industry with deep knowledge of broad-varying legal matters and enterprise business strategy,” stated Mike Mahoney, chairman and ceo, Boston Scientific. “We expect to her contributions to Boston Scientific and also the company’s ongoing growth.”

Ralls-Morrison most lately held the function of senior v . p ., general counsel, corporate secretary, and mind from the global litigation, government matters and public policy organizations at Boehringer Ingelheim USA. Formerly, she was general counsel for that Manley & Manley consumer group, getting progressed through roles of growing responsibility including senior counsel, assistant general counsel, and v . p . of law for that women’s health, nutritionals and over-the-counter companies.

Earlier in her own career, Ralls-Morrison would be a senior attorney and assistant counsel at Merck & Co, Corporation., focusing largely on regulatory and defective products matters, and just before that, she held litigation roles in the lawyers of Kelley Drye & Warren LLP and Shipman & Goodmand LLP. She presently serves around the Danbury Hospital/New Milford Hospital Board of Company directors and also the Inner-City Foundation for Charitable organization and Education. Desiree earned her juris physician from Harvard School, and her bachelor of arts in financial aspects and political science from Wesleyan College.

About Boston Scientific 
Boston Scientific transforms lives through innovative medical solutions that improve the healthiness of patients all over the world. Like a global medical technology leader in excess of 35 years, we advance science for existence by supplying an extensive selection of high end solutions that address unmet patient needs and lower the price of healthcare. To learn more, visit www.bostonscientific.com and connect on Twitter and Facebook.

CONTACTS:

Kate Haranis
Media Relations
(508) 683-6585 (office)
[email protected] 

Susie Lisa, CFA
Investor Relations
(508) 683-5565 (office)
[email protected]

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Third-generation data will give you the underpinnings of clinical transformation

data, insight, knowledge

In the annual Fall Health 2. in Santa Clara, California, David Brailer, former National Coordinator in the ONC, asserted that health It’s unsuccessful to provide sustained clinical transformation since the focus continues to be on just clinical data that resides in HIPAA-covered institutions like providers and payers.

“It’s not too little software, it isn’t too little data architectures, it isn’t too little business process or capability to do things within the industry or insufficient vision,” he stated of the reason for that failure inside a keynote presentation, Monday. “It’s the information is incomplete.”

He spoken in regards to a “third generation of data” that’ll be answer to prompting lasting clinical transformation leading to behavior change and clinical outcomes.

Where shall we be now? We’re exclusively centered on second-generation data — data relaxing in the electronic permanent medical record, claims data.

“It is commonly very specific in regards to a test or test result,” Brailer stated, alluding to fragmented, episodic nature from the information.

Third-generation data has all of the opposite hallmarks of traditional, clinical data: it’s real time, ubiquitous, streaming, physiologic, originating from things everywhere.

“It’s data that actually surrounds our way of life and not simply our overall health,Inches he stated, showing this slide towards the audience.

“This may be the data which i think will end up being the next vehicle for the capability to take transformation much further,” he stated. “If you appear with the literature there’s immense quantity of data being created that implies that consumers do change their behavior whether they have relevant data.”

But incorporating this data in to the fold of traditional healthcare mores requires answering three rather thorny policy questions:

  • Who’ll own and control this data?

By their nature, such data located on home monitoring devices, sensors, in social networking are live wires that healthcare systems don’t want to touch for anxiety about liability.

Brailer believes that patients should control this data.

  • What rules covers this data?

At this time, you will find simply no rules which are controlling this data unlike the information that’s included in HIPAA.

“All another [groups] that collect the rest of the data aren’t controlled by federal laws and regulations apart from a couple of privacy rules – condition privacy rules specifically in California and New You are able to. But it’s a massive open question about what’s the regulatory schema that protects this data, which brings it altogether, causes it to be helpful and doesn’t transform it into a couple of proprietary stuff that we can’t build from,” he stated.

  • Are tech companies going so that you can be great citizens in healthcare and then view this from the patient/disease perspective and not simply someone perspective?

The above mentioned slide implies that the information that Brailer describes is housed in tech companies — Facbebook, Twitter and so on. Because of the spotlight on these businesses with how their platforms happen to be used this last election cycle, it will likely be interesting to determine how these businesses become stewards from the heathcare data located on their sites.

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Edwards Announces Key Occasions For PCR London Valves 2017

LONDON, Sept. 24, 2017 /PRNewswire/ — Edwards Lifesciences Corporation (New york stock exchange: EW), the worldwide leader in patient-focused innovations for structural cardiovascular disease and demanding care monitoring, today announced key occasions for the organization throughout the PCR London Valves 2017 course, because the meeting celebrates fifteen years of transcatheter aortic valve substitute.

One of the scheduled occasions and knowledge presentations are:

  • Introduction from the Edwards SAPIEN 3 Ultra System – Edwards’ CE Mark-pending system for transcatheter aortic valve substitute includes the brand new SAPIEN 3 Ultra valve, which adds a taller outer skirt towards the proven SAPIEN 3 valve design. Initially added to valve sizes 20, 23 and 26 mm, this latest feature is made to further enhance the SAPIEN 3 valve’s best-in-class outcomes. The valve is provided using the SAPIEN 3 Ultra delivery system, which introduces an “on balloon” design, removing the requirement for valve alignment throughout the procedure, and works with the brand new 14F Axela expanding sheath. The Edwards SAPIEN 3 Ultra Product is likely to receive CE Mark through the finish of the season, and the organization also offers intends to introduce this technique in the U . s . States late in 2018.
  • 6-month outcomes using the Edwards CENTERA Transcatheter Heart Valve System – On Monday, Sept. 25, within the Late-Breaking TAVI Trials session, new outcomes of the self-expanding Edwards CENTERA valve is going to be discussed. Results presented captured around the 30-day outcomes using the CENTERA valve shown a really high rate of survival, a minimal disabling stroke rate along with a low percent permanent pacemaker rate. Additionally, there is a minimal rate of moderate paravalvular leak among patients, with no severe paravalvular leak reported at thirty days after transcatheter valve substitute. The Edwards CENTERA valve is repositionable and retrievable and could be delivered via a low-profile 14-French delivery system that includes a motorized handle that leads to stable valve deployment. The valve is distinctively packaged – fully pre-attached, which facilitates easy and rapid device preparation.
  • Symposium: Transcatheter heart valve therapies for those heart valves: from your innovation technique to mainstream therapy – This backed session on Sunday, Sept. 24, is supposed to evaluate the latest numerous studies involving Edwards’ aortic, mitral, tricuspid and lung valve therapies.
  • Symposium: Edwards Cardioband Transcatheter Valve Repair System: expanding choices for patients – This backed session on Tuesday, Sept. 26, is centered on the present experience and clinical outcomes of the Edwards Cardioband system along with a discussion of Edwards’ innovations for transcatheter valve therapies.

“As PCR London Valves celebrates fifteen years of transcatheter aortic valve substitute, Edwards is proud to possess brought the event and evolution of TAVR like a preferred therapy for patients in need of assistance all over the world,Inch stated Ray L. Wood, Edwards’ corporate v . p ., transcatheter heart valves.

The Edwards SAPIEN 3 Ultra System and CENTERA Transcatheter Heart Valve System aren’t presently readily available for commercial purchase in almost any country.

About Edwards Lifesciences
Edwards Lifesciences, located in Irvine, Calif., may be the world leader in patient-focused medical innovations for structural cardiovascular disease, in addition to critical care and surgical monitoring. Driven with a passion to assist patients, the organization collaborates using the world’s leading clinicians and researchers to deal with unmet healthcare needs, trying to improve patient outcomes and enhance lives. To learn more, visit world wide web.Edwards.com and follow us on Twitter @EdwardsLifesci.

What is the news release includes forward-searching statements inside the concept of Section 27A from the Securities Act of 1933 and Section 21E from the Securities Exchange Act of 1934. These forward-searching statements include, but aren’t restricted to, statements regarding expected future product approvals, dates of business availability and expected benefits and results. Forward-searching statements derive from estimates and assumptions produced by control over the organization and therefore are thought to be reasonable, though they’re inherently uncertain and hard to calculate. Our forward-searching statements speak only by the date which they’re made and we don’t undertake any obligation to update any forward-searching statement to mirror occasions or conditions following the date from the statement.

Forward-searching statements involve risks and uncertainties that may cause leads to differ materially from individuals expressed or implied through the forward-searching statements with different quantity of factors, including although not restricted to, unpredicted outcomes after long term clinical knowledge about the merchandise or unanticipated quality, manufacturing or regulatory delays or issues. These 4 elements are detailed within the company’s filings using the Registration including its Annual Set of Form 10-K for that year ended December 31, 2016. These filings, together with important safety details about our products, might be available at edwards.com.

Edwards, Edwards Lifesciences, the stylized E emblem, Axela, Cardioband, CENTERA, Edwards SAPIEN, Edwards SAPIEN 3, Edwards SAPIEN 3 Ultra, SAPIEN, SAPIEN 3, and SAPIEN 3 Ultra are trademarks of Edwards Lifesciences Corporation. Other trademarks belong to their particular proprietors.

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Henry Schein Joins Texas Healthcare Leaders To Convene Expert-Brought Symposium On Practice Recovery In Wake Of Hurricanes

MELVILLE, N.Y., Sept. 20, 2017 /PRNewswire/ — In reaction to the devastation brought on by Hurricanes Harvey and Irma, Henry Schein, Corporation. (Nasdaq: HSIC) announced today that it’ll join the Texas Dental Association, the Texas Veterinary Medical Association, the Texas Veterinary Medical Foundation, and also the College of Texas Health Science Center at Houston (UTHealth) School of Dentistry for hosting a specialist-brought symposium to assist medical professionals restore and re-open their practices publish-natural disaster.

The big event, titled “Recovery Empowerment Symposium: Emerging in the Storm,” is going to be held Saturday, September 23 from 9 a.m. to three p.m. CT in the Denton A. Cooley, M.D. and Rob C. Cooley, D.D.S. College Existence Center, 7440 Cambridge St., Houston, Texas, 77054, next to UTHealth School of Dentistry. It’s free for those medical professionals.

To join up for that event, check out Go.uth.edu/recovery. Space is restricted. Practitioners influenced by Hurricane Irma and individuals otherwise not able to go to personally can view a livestream from the symposium at go.uth.edu/recoverylivestream. The webcast will subsequently be accessible when needed on Henry Schein’s Route to Recovery Resource Center.

Attendees can meet one-on-one with leading experts in the insurance, legal, claims management, and disaster recovery industries, in addition to dental, medical and animal medical expert associations, to go over a variety of topics related to their own personal and professional recovery, including:

  • How you can access Federal agencies, such as the U.S. Federal Emergency Management Association and also the U.S. Sba
  • How you can access insurance companies
  • Working with banks, financial services, and suppliers and
  • How you can enhance worker morale and keep active in patients.

A continental breakfast and lunch is going to be offered, and you will see a networking session for attendees and loudspeakers in the finish from the symposium, that is being held together with the Ada, the ADA Foundation, the Ama Foundation, American Veterinary Medical Foundation, the nation’s Dental Association, and also the Greater Houston Dental Society.

“We at Henry Schein are content to work with Texas healthcare leaders to supply storm-affected health care professionals using the information and sources they have to obtain practices back ready to go,Inch stated Stanley M. Bergman, Chairman from the Board and Leader Office of Henry Schein. “We feel the data provided in this symposium will have a vital role in assisting practitioners restore their practices and resume their roles as reliable medical service providers within their communities.”

About Henry Schein Cares 
Henry Schein Cares stands on four support beams: engaging Team Schein People to achieve their potential, making certain accountability by extending ethical business practices to any or all levels within Henry Schein, promoting ecological sustainability, and expanding use of healthcare for underserved and also at-risk communities all over the world. Healthcare activities based on Henry Schein Cares concentrate on three primary areas: evolving wellness, building capacity within the delivery of healthcare services, and assisting in emergency readiness and relief.

Firmly rooted inside a deep dedication to social responsibility and the idea of enlightened self-interest championed by Benjamin Franklin, the philosophy behind Henry Schein Cares is really a vision of “succeeding by doing good.” With the work of Henry Schein Cares to boost access to look after individuals in need of assistance, the organization believes that it’s furthering its lengthy-term success. “Helping Health Happen Blog” is really a platform for medical professionals to talk about their volunteer encounters delivering help individuals in need of assistance globally. For more info about how exactly Henry Schein Cares is creating a difference, check out our blog: www.helpinghealthhappen.org.

About Henry Schein, Corporation.
Henry Schein, Corporation. (Nasdaq: HSIC) may be the world’s largest provider of healthcare services and products to office-based dental, animal medical and health practitioners. The company also serves dental laboratories, government and institutional healthcare clinics, along with other alternate care sites. A Fortune 500® Company and part of the S&P 500® and also the Nasdaq 100® indexes, Henry Schein employs greater than 21,000 Team Schein People and serves greater than a million customers.

The organization provides a comprehensive choice of services and products, including value-added solutions for operating efficient practices and delivering high-quality care. Henry Schein operates via a centralized and automatic distribution network, with an array of greater than 120,000 branded products and Henry Schein private-brand products available, in addition to greater than 180,000 additional products like special-order products. The organization also provides its customers exclusive, innovative technology solutions, including practice keeper and e-commerce solutions, in addition to a wide range of monetary services.                                              

Headquartered in Melville, N.Y., Henry Schein has operations or affiliates in 32 countries. The company’s sales arrived at an archive $11.6 billion in 2016, and also have grown in a compound annual rate of roughly 15 % since Henry Schein grew to become an open company in 1995. For more details, visit Henry Schein at world wide web.henryschein.com, Facebook.com/HenrySchein and @HenrySchein on Twitter.

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The pediatric landscape is altering: It’s time for you to jump on board

Bigger medtech companies have typically shied from purchasing the pediatric market, however the landscape is altering. Within the this past year alone, we observed the passage from the twenty-first century Cures Act and also the signing from the Food and drug administration Reauthorization Act (FDARA 2017) into law. The is ripe for innovation which legislative advances present new possibilities for connecting innovators using the investment community.

Also can be achieved?

Before a tool is removed to be used in grown-ups, it undergoes appropriate testing in the intended population to ultimately receive regulatory clearance. Exactly the same isn’t necessarily true in pediatrics since the age groups for pediatric patients is understood to be birth to 21 years old (including subpopulations of newborns, infants, children and adolescents). Because of that ambiguity, it’s entirely possible that the littlest patients, having a low weight, bodily proportions and various physiological and nerve development needs, might not be selected to sign up in each and every pediatric study. Meaning, that pediatricians still end up using adult devices off-label and modifying them quickly in order to save children.

Similarly, parents and people are eager for better solutions. While technology to fix scoliosis by using a brace originates a lengthy way, parents and people are advocating the to trap up by borrowing technology using their company fields. And tech-savvy parents have found methods to hack to their child’s glucose monitor to possess continuous use of information once the child is away in school or in a friend’s house. These a few of the numerous examples. The possibilities for innovation within the pediatric market are unlimited.

How you can enter the pediatric market?

You will find eight Food and drug administration Pediatric Device Consortia across the nation that actually work collaboratively using the Food and drug administration to assist innovators effectively navigate existing laws and regulations, rules and agency guidance to safeguard the safety and health of kids. The consortia provide consultation and a few funding for those phases of pediatric device development – from ideation through marketing. Since 2013, through our consortium, NCC-PDI, and our Sheikh Zayed Institute for Pediatric Surgical Innovation at Children’s National Health System, we’ve supported 67 devices owned by over 40 startups and research labs and awarded funding to 26. Four devices, while being based on NCC-PDI, received market clearance by means of CE mark of approval, 510(k) approval, and IDE.

If you wish to learn to test a pediatric form of your adult device, and have any queries about stepping into pediatrics, speak to a consortium.

How will you become involved now?

Now’s your opportunity to participate the modification. On September 24, 2017, thought leaders in pediatric device space are uniting for that fifth Annual Pediatric Device Innovation Symposium, “Partnering for Breakthroughs in Pediatric Surgery and Care.” It’s a results-driven day which brings together medical device innovators, investors, researchers, clinicians and policy makers to stimulate pediatric device innovation and produce methods to market faster for that benefit of children. This season, we’re co-locating to San Jose, Calif. inside a joint effort using the MedTech Conference operated by AdvaMed.

Our hot-button panel discussions covers topics from funding to rules to promote dynamics – because they connect with the healthiness of our kids. Addititionally there is a pitch competition where as much as six prizes totaling $250,000 is going to be awarded towards the winning presentations.

Keynote loudspeakers are Daniel Kraft, M.D., faculty chair of drugs & Neuroscience, Singularity College and executive director, Exponential Medicine Vasum Peiris, M.D., chief medical officer, Pediatrics and Special Populations, Drug and food Administration  and Alan Flake, M.D., director of Center for Fetal Research, Children’s Hospital of Philadelphia. Additional information regarding the agenda and loudspeakers are available here.

This symposium is the best chance to network with fellow professionals across the nation who’re involved in pediatric device development and motivated through the pursuit to innovate for children.

To join up, visit www.pediatric-device-symposium.org, and join the discussion on twitter using #Innovate4Kids.

Kolaleh Eskandanian may be the Executive Director from the Sheikh Zayed Institute for Pediatric Surgical Innovation at Children’s National Health System and also the National Capital Consortium for Pediatric Device Innovation

Los datos pragmáticos confirman la efectividad a largo plazo en termoplastia bronquial

Pacientes disadvantage asma grave muestran una mejoría clínica sostenida

MARLBOROUGH, Massachusetts, 18 de septiembre de 2017 /PRNewswire/ — Boston Scientific (New york stock exchange: BSX) ha anunciado hoy los resultados de united nations seguimiento a tres años de una cohorte en su estudio realizado disadvantage posterioridad a la aprobación por parte en Administración Estadounidense de Alimentos y Medicamentos (PAS2) consistente dentro del ensayo clínico de evaluación en termoplastia bronquial (BT) en casos de asma grave persistente. Los resultados mostraron que los 190 pacientes que participaron dentro del estudio pragmático lograron una reducción similar en cuanto a exacerbaciones severas, hospitalizaciones y visitas a urgencias, en comparación disadvantage los 190 pacientes tratados disadvantage termoplastia bronquial dentro del ensayo aleatorizado fundamental disadvantage grupo de control Investigación en Intervención del Asma 2 (AIR2).

Los resultados, que fueron publicados en la European Respiratory system Journal, la revista sometida a arbitraje científico en Sociedad Respiratoria Europea, corroboran el ensayo AIR2 y demuestran que los hallazgos se traducen en resultados significativos en la práctica pragmática. Los participantes dentro del estudio PAS2 mostraban síntomas de asma menos controlados que los sujetos del ensayo AIR2, y los resultados del estudio revelan que, tras el último tratamiento disadvantage termoplastia bronquial:

  • El porcentaje de pacientes que experimentaron exacerbaciones severas se redujo del 74 al 40 por ciento
  • El porcentaje de pacientes hospitalizados por al menos united nations síntoma de asma se redujo del 15 al 7 por ciento
  • El porcentaje de pacientes que acudieron a urgencias se redujo del 27 al 11 por ciento y
  • El porcentaje de pacientes que tomaban diariamente medicación corticosteroide de mantenimiento por vía dental se redujo del 19 al 10 por ciento.

“El estudio PAS2 confirma que la termoplastia bronquial es united nations tratamiento eficaz, duradero y seguro en pacientes disadvantage asma grave que presentan united nations peor control sobre la enfermedad al inicio del estudio, en comparación disadvantage pacientes evaluados en ensayos clínicos previos, tales como el AIR2”, afirmó el Dr. Geoffrey Chupp, investigador principal y director del Centro Yale para el Asma y las Enfermedades de las Vías Respiratorias en Escuela de Medicina en Universidad de Yale en New Haven (Connecticut). “El estudio PAS2 es el primer estudio prospectivo a gran escala sobre termoplastia bronquial en united nations contexto de farmacovigilancia, y valida los resultados positivos obtenidos dentro del ensayo AIR2”.

El PAS2 es united nations estudio prospectivo y crime enmascaramiento dentro del que participaron pacientes de manera consecutiva en 27 centros de investigación de Estados Unidos y Canadá. Según las directrices clínicas en Sociedad Respiratoria Europea y la Sociedad Torácica Americana, el 95% de los participantes dentro del PAS2 se consideran asmáticos graves1. En comparación disadvantage los pacientes del ensayo AIR2, los participantes dentro del estudio PAS2 eran de mayor edad, united nations mayor número de ellos tomaban esteroides sistémicos, presentaba united nations índice de masa corporal (IMC) superior, y tomaban dosis más elevadas de esteroides inhalados. A 12 meses previos al tratamiento disadvantage termoplastia bronquial, los participantes dentro del estudio PAS2 también tenían más probabilidades que aquellos del ensayo AIR2 de padecer exacerbaciones severas —75% frente a 52%— y requerir hospitalización —15% frente a 4%—.

“Los resultados del estudio PAS2 confirman que el tratamiento disadvantage termoplastia bronquial tiene united nations gran impacto positivo en la práctica clínica diaria y puede aliviar united nations poco la carga que sufren los adultos aquejados de asma grave”, afirmó Art Butcher, vicepresidente sénior y presidente de Endoscopia de Boston Scientific. “Seguiremos trabajando para que los pacientes tengan acceso y cobertura para este importante y consolidado tratamiento que ha demostrado su capacidad para mejorar calidad de vida en relación al asma”.

El asma afecta a más de 230 millones de personas en todo el mundo y aproximadamente el 10% de los casos pueden considerarse graves2,3. El sistema Alair de termoplastia bronquial cuenta disadvantage la aprobación en Administración Estadounidense de Alimentos y Medicamentos (Food and drug administration) y ha recibido el marcado CE para pacientes adultos que sufren asma grave y no tienen la enfermedad correctamente controlada mediante medicación. Se trata del primer tratamiento no farmacológico basado dentro del uso de dispositivos para el asma grave persistente. Los estudios han revelado en termoplastia bronquial puede reducir los ataques de asma grave durante al menos 5 años4. A principios de este año, se presentaron los resultados iniciales positivos obtenidos del estudio exhaustivo en cohorte en la Conferencia Internacional en Sociedad Torácica Americana celebrada en Washington D. C.

  1. Chung, K. F. “Worldwide ERS/ATS Guidelines on Definition, Evaluation and Management of Severe Bronchial asthma”. TASK Pressure REPORT, ERS/ATS GUIDELINES ON SEVERE Bronchial asthma, Sociedad Torácica Americana, 10 de abril de 2014, world wide web.thoracic.org/statements/sources/allergy-bronchial asthma/Severe-Bronchial asthma-CPG-ERJ.pdf.
  2. OMS. Nota descriptiva núm. 307 sobre asma. Abril de 2017. Disponible en: http://world wide web.who.int/mediacentre/factsheets/fs307/en/index.html
  3. “The Prevalence of Severe Refractory Bronchial asthma AAAAI”. Academia Americana de Alergia, Asma e Inmunología. Journal of Allergy and Clinical Immunology, octubre de 2014. Consulta web: 5 de mayo de 2017. < https://www.aaaai.org/global/latest-research-summaries/New-Research-from-JACI-In-Practice/refractory-asthma>.
  4. Wechsler, M. et al. Journal of Allergy and Clinical Immunology, diciembre de 2013 132(6):1295-302

Acerca de Boston Scientific
Boston Scientific transforma la vida de las personas a través de soluciones médicas innovadoras que mejoran la salud de los pacientes en todo el mundo. Como líder internacional en tecnología médica durante más de 35 años, potenciamos el ámbito de las ciencias biosanitarias al ofrecer una amplia gama de soluciones de alto rendimiento para tratar las necesidades no satisfechas de pacientes y reducir el coste en atención sanitaria. Para obtener más información, visite world wide web.bostonscientific.com y conéctese en Twitter y Facebook.

Declaración cautelar respecto a declaraciones prospectivas

Este comunicado de prensa contiene declaraciones prospectivas conforme al artículo 27A en Ley de Valores de 1933 y el artículo 21E en Ley de Mercados de Valores de 1934. Las declaraciones prospectivas pueden identificarse por la presencia de términos como “prevé”, “espera”, “proyecta”, “cree”, “planea”, “estima”, “pretende” y similares. Estas declaraciones prospectivas se basan en las convicciones, suposiciones y expectativas según la información en que disponemos dentro del momento actual, y no pretenden ser garantía de futuros eventos o desempeños. Estas declaraciones prospectivas incluyen, entre otras, declaraciones relativas a nuestros planes de negocio, ensayos clínicos, aprobaciones normativas y rendimiento e impacto de producto. Si nuestras suposiciones subyacentes resultasen ser incorrectas, o en caso de que se materialicen ciertos riesgos o incertidumbres, los resultados actuales podrían diferir sustancialmente de las expectativas y pronósticos expresados o implícitos en nuestras declaraciones prospectivas. Estos factores, en algunos casos, han afectado y, junto disadvantage otros factores, podrían afectar dentro del futuro a nuestra capacidad para implementar nuestra estrategia de negocio, y pueden provocar que los resultados reales sean sustancialmente diferentes de los mencionados en las declaraciones incluidas en este comunicado de prensa. En consecuencia, se aconseja a los lectores que no depositen una confianza indebida en ninguna de las presentes declaraciones prospectivas.

Los factores que pueden provocar tales diferencias incluyen, entre otros: condiciones económicas, competitivas, de reembolso y normativas futuras introducciones de nuevos productos tendencias demográficas propiedad intelectual litigios condiciones del mercado financiero y decisiones de negocio futuras tomadas por nosotros o la competencia. Todos estos factores boy difíciles o imposibles de predecir disadvantage precisión y muchos de ellos se escapan a nuestro control. Para obtener una lista más exhaustiva y la descripción de estos y otros riesgos e incertidumbres destacados que pueden afectar nuestras operaciones futuras, consulte la Parte I, Punto 1A – Factores de riesgo en nuestro informe anual más reciente del Formulario 10-K presentado ante la Comisión de Bolsa y Valores de Estados Unidos, que podría actualizarse en la Parte II, Punto 1A – Factores de riesgo de nuestros informes trimestrales del Formulario 10-Q presentado o que se presentará dentro del futuro. Renunciamos a cualquier propósito u obligación de actualizar o revisar públicamente cualquiera de las declaraciones prospectivas a fin de plasmar cambios en nuestras expectativas o en determinados eventos, condiciones o circunstancias en las que se asienten dichas declaraciones, o que puedan influir en la probabilidad de que los resultados reales difieran de los contenidos en las declaraciones prospectivas. Esta declaración cautelar es aplicable a todas las declaraciones prospectivas contenidas en este documento.

CONTACTOS:

Catherine Brady 
Relaciones disadvantage Medios 
508-683-4797
[email protected]

Rosie Ireland
Relaciones disadvantage Medios Europeos
+44 ()7585 403359
[email protected]

Susie Lisa, analista financiera certificada
Relaciones disadvantage los Inversores
(508) 683-5565 (oficina)
[email protected]

SOURCE Boston Scientific Corporation

Related Links

http://world wide web.bostonscientific.com

Health insurers on social networking: How five payers compare

Using the rise of technology, many organizations and firms across the nation have started utilizing social networking as a way for connecting with folks and spread news.

Healthcare organizations aren’t any exception. Research conducted recently from Talkwalker, a social networking analytics platform, checked out Twitter data in the nation’s big five health insurers to discover trends within their social networking activities.

Talkwalker examined information from Aetna, Anthem, Cigna, Humana and UnitedHealthcare, which have both an over-all Twitter handle along with a customer care handle.

From August 24 to August 30, there have been 26,700,000 mentions of those insurers.

Hartford, Connecticut-based Aetna required the wedding cake for that top quantity of mentions, dominating 63.1 % from the conversation. Greater than 48 percent of those mentions were negative anyway, and 41.9 % of these were neutral. Only 9.9 % were positive.

These statistics are unsurprising, considering that Aetna was involved in the a debate that week. On August 24, news broke the insurer had accidentally disclosed the Aids statuses as high as 12,000 people. That explains the boost in social networking mentions between August 25 and 26.

Throughout the same week, the rest of the four insurers came nowhere near to Aetna when it comes to mentions on social networking. UnitedHealthcare required up 16.7 % from the conversation, and Humana dominated 11.2 percent from it. Anthem and Cigna lagged behind.

Of these insurers, nearly all social networking mentions were neutral. Particularly, however, 35.4 % of Anthem’s mentions were negative anyway, and 21.4 % of Cigna’s were positive.

But it isn’t about mentions. It is also helpful to consider a macro consider the overall impact each insurer is getting on its audience.

Based on Talkwalker, although Humana may be the tiniest from the insurers, its supporters would be the most engaged. From August 24 to 30, Humana saw 1,671 audience retweets, as the other insurers had figures within the hundreds.

Even though UnitedHealthcare may be the nation’s largest private doctor, Talkwalker thought it was lags behind in social networking interactions.

Photo Credit: lushik, Getty Images

Medical Design & Manufacturing (MD&M) Minneapolis Explores the most recent Trends in Medical Technology Through its Robust Conference Schedule

Printed 30 August 2017

From spark to scale-up: speeding medtech innovation to promote

Medical Design & Manufacturing (MD&M) Minneapolis, the Midwest’s largest medical technology event, will host a strong conference featuring technical sessions, situation studies and panel discussions on up-to-the-minute trends and topics which are affecting the today. Happening November 8-9 in the Minneapolis Convention Center, the MD&M Minneapolis conference may be the premiere program to see expert-brought education.

“Remaining in front of the curve when it comes to industry trends and understanding is from the highest importance to we and us intend to bring the most recent and finest in medical technology towards the Midwest at MD&M Minneapolis,” stated Nina Brown, v . p . of occasions, UBM. “This season we’re excited to pay attention to showcasing all stages from the product process, from research to promote. Hopefully this will give you invaluable information to the attendees.”

Centered on topics dedicated to the introduction of new technology and product processes, the conference is going to be an essential resource to individuals searching to produce effective medical devices, conquer product challenges, and speed new devices to promote. The conference is organized into three concentrated tracks surrounding everyday challenges and breakthroughs present with the. The 2017 conference tracks include:

Track A: Product- Focused regarding how to create medical devices, and encourage them to market faster and fewer expensively.

Track B: R&D and User-Centered Design- Explore the science behind R&D, materials and style, and find out the best way to use what’s a new comer to inspire innovation.

Track C: Hands-On Workshop– Interactive workshops that offer a hands-on learning chance.

The 3 aforementioned conference tracks are explored via a bevy of presentations and panels brought by industry thought leaders representing organizations for example Boston Scientific, the Mayo Clinic, Olympus and much more. Influential people from all of these organizations will explore styles within research, development, engineering, materials, and style in their conference sessions. A new comer to 2017 may be the long awaited plenary session, focused regarding how to sell a concept to upper management. Highlights in the MD&M Minneapolis Conference include:

Plenery Session: How you can Sell Your Idea to Upper Management
Moderator:
Kevin Arnal, Owner, Beach front Design
Panelists:
Rob Cardinal, Director, R&D, Boston Scientific
Jennifer Raeder-Devens, V . P ., R&D, Infection Prevention, Becton Dickinson
Matt Adams, V . P . and Gm, Minnetronix Neuro

Gain understanding of how you can effectively pitch a concept to upper management and take something new to promote the fastest possible way. Persuading colleagues and managers of the need for a concept is really a frequent problem for engineers which session will offer you advice from top-level innovation professionals involved with moving ideas in the lab towards the boardroom.

Situation Study: Developing MR Conditional Devices
Presented by:
John Rondoni, V . P . Product, Operations, and Quality, Inspire Medical Systems
Sandy Wixon, MRI Technology Group Leader, Medtronic CRHF
Terry Forest, Solid Mechanics Laboratory Leader, Food and drug administration Center for Devices & Radiological Health

Presented by industry leaders from two prominent medical device companies and also the Food and drug administration, this session will dive into guidelines for developing MR conditional medical devices. However, there are presently no known health threats from temporary contact with the MR atmosphere, clinicians and people are still worried about the effectiveness of the MR magnetic field and possible lengthy-term health impacts. This situation study will give you great understanding of meeting regulatory standards while developing a top-notch medical device.

MD&M Minneapolis will run alongside five related tradeshows, including MinnPack, Design & Manufacturing Minneapolis, Automation Technology Expo (ATX) Minneapolis, PLASTEC Minneapolis, and Embedded Systems Conference (ESC) Minneapolis. To find out more, check out: mdmminn.mddionline.com

Sign up for MD&M Minneapolis

To join up for MD&M Minneapolis check out: minneapolis.am.ubm.com/2017/registrations/MDM

To join up for any media pass, check out: minneapolis.am.ubm.com/2017/registrations/media

Follow us on social: Facebook, LinkedIn, Twitter, #AdvMfgExpo #ESCconf

Source: Company Pr Release