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Three scalp cooling abstracts to be presented at ESMO 2019

Pioneering scalp cooling research from India, Ireland and Italy will be presented at this yearโ€™s ESMO Congress 2019 (European Society for Medical Oncology) taking place in Barcelona, Spain, from 27th September โ€“ 1st October.

Research teams from the three hospitals, who have all used British developed Paxman Scalp Cooling Systems, will present their personal findings at the international exhibition to help raise awareness of the treatment and its clinical efficacy

ESMO 2019 is a global stage for excellence in translational research, presentation of practice-changing data and multidisciplinary discussions. The exhibition attracts clinicians, researchers, patient advocates, and the pharmaceutical industry from all over the world keen to learn about the latest advances in oncology, translating science into better cancer patient care.

The abstract presentations include:

The uptake, patient satisfaction and efficacy of scalp cooling among patients receiving chemotherapy in an Irish oncology day ward. Speaker: William Maher (Cork, Ireland)

Scalp cooler is effective in reducing chemotherapy-induced alopecia among breast cancer patients: a single institution experience. Speaker: Emilia Gianotti (Carpi, Italy)

Randomised controlled trial of Scalp Cooling (SC) for the prevention of Chemotherapy Induced Alopecia (CIA). Speaker: Jyoti Bajpai (Mumbai, India)

Speaking about her research Dr Bajpai, Professor in Medical Oncology from Tata Memorial Hospital, Mumbai, India, said: โ€œHair loss is a well-known side effect of many chemotherapy regimens, with many of our patients reporting it to be the most traumatic aspect of their treatment. There are also culturally many misconceptions and stigma attached to hair loss, for example one woman patient from Uttar Pradesh was thrown out of her house by her husband and in-laws because of her baldness. Her teenaged daughters were also asked to leave with her. The family considered her disease and baldness to be an outcome of past sins. The fear of cancer becomes secondary and the fact that they will lose hair during treatment takes centre stage.โ€

The Paxman Scalp Cooling System is available at a large number of cancer centres in Europe, North- and South America, Asia and Australia. With close to 3,500 delivered systems to over 40 countries, Paxman has established itself as the leading player in its field. The award-winning technology is Shonin, Ninsho and FDA cleared and is proven to help cancer patients keep their hair during chemotherapy treatment.

CEO Richard Paxman added: โ€œWe are delighted that real-life data and research from around the globe will be presented at ESMO by a number of leading clinicians. There have been a number of significant steps recently that have helped bring scalp cooling to the forefront of peopleโ€™s minds, and research presentations like these continue this education and awareness-building. It is an exciting time for scalp cooling, and we are delighted to be part of it.โ€

Scalp cooling provides the only real alternative to hair loss, resulting in a high level of retention or even complete hair preservation, improving patientsโ€™ self-confidence and creating positive attitudes towards treatment.

To find out more, visit the Paxman team at ESMO booth number 418.

About Paxman
The Paxman Scalp Cooling System has been developed by the Paxman family to reduce hair loss in breast cancer patients undergoing chemotherapy. The concept behind the system came when the mother of four, Sue Paxman, experienced first-hand the trauma of chemotherapy-induced hair loss. Paxmanโ€™s scalp-cooling cap is made from lightweight, biocompatible silicone that is soft and flexible, providing a snug yet comfortable fit during treatment. To find out more visit: www.paxmanscalpcooling.com

HIMSS Analytics Survey Sponsored by Dimensional Insight Finds Healthcare Orgs. that Focus on Clinical Outcomes as Key ROI Metric Have Higher Success with Analytics

Survey reveals two-thirds of organizations using analytics in clinical, financial, and operational areas; use of metrics tied to analytics success

Dimensional Insightยฎ, the maker of Diver Platformโ„ข, a data management, analytics, and performance management solution, announced the results of a survey it conducted with HIMSS Analytics of 109 senior healthcare leaders. The survey examined how healthcare organizations implement metrics and measure ROI from their analytics programs. It found that those organizations that focus on clinical outcomes as their key ROI metric โ€“ as opposed to financial returns or staff efficiency โ€“ rank higher across the board in terms of usage of analytics across the organization, average number of metrics used, measured success rate, and overall effectiveness of analytics.

โ€œAs healthcare organizations move to value-based payment models, they are finding that focusing on clinical metrics, including readmission rates, infection control, and patient outcome improvements is critical for success,โ€ says George Dealy, vice president of healthcare solutions at Dimensional Insight. โ€œAnalytics provides tremendous insight into these areas and can benefit healthcare organizations that are navigating this transition.โ€

Key findings from the survey include:

  • Of organizations that are leveraging analytics, 84% are doing so in multiple areas (clinical, financial, operational), while two-thirds are leveraging analytics across the organization.
  • Organizations feel their analytics solutions have been most effective towards improving financial performance, but they have been able to see the most measured success with clinical analytics (77.7%) vs. financial analytics (73.5%) or operational analytics (70.3%).
  • The primary method organizations use to determine ROI is most often financial returns and improvements (41.2%) vs. clinical outcome improvement (37.3%), staff efficiency (12.7%), or measured improvements across the patient journey (3.9%). However, they see the highest measured success rate (75.4%) if they use clinical outcomes improvement as their primary metric.

To learn more, download the full survey results at: https://www.dimins.com/HIMSSsurvey19

 

Terumo BCT Offers $100,000 Research Grant Supporting Patient Access to Care

Terumo BCT Offers $100,000 Research Grant Supporting Patient Access to Care

Terumo BCTโ€™s new USD $100,000 Therapeutic Plasma Exchange (TPE) Innovation Award will help clinical investigators expand the field of data for certain types of autoimmune conditions, known as IgG4mediated diseases.

TPE is as an established therapy for many diseases, according to the American Society for Apheresis (ASFA), but the understanding of how it works is still emerging. As a result, some insurance providers and government programs will not cover this type of care โ€” leaving some patients without potentially beneficial treatments.

“The first step in providing innovative therapies is generating data that helps healthcare providers demonstrate how procedures can help improve health outcomes for their patients,” said Regis Leonard, Vice President, Therapeutic Systems, Terumo BCT. “This new grant will support the important work of investigators who are working to improve the lives of patients.”

TPE takes place on therapeutic apheresis devices, an area of focus for Terumo BCT. The Colorado-based company also works in the fields of blood component and cell therapy technologies. It has customers in about 130 countries.

Impact on Patient Lives Terumo BCT will judge applications for the TPE Innovation Award based on several factors, including how the applicant plans to address the unmet medical need of understanding and treating IgG4-mediated diseases. The award committee also considers patient impact, feasibility and the likelihood of success. The company will accept applications until 31 October 2019. Terumo BCT’s Medical and Clinical Affairs specialists, along with an external committee of experts in the field, will select the winner. Learn more here.

TPE can be performed on Terumo BCT’s Spectra Optiaยฎ Apheresis System*. The device enables healthcare providers to remove plasma from a patient’s blood and replace it with either donated fresh frozen plasma or a mixture containing albumin (a protein found in human blood) to manage a variety of conditions.

TPE is an established therapy for some metabolic, neurologic, hematologic and renal disorders, according to ASFA. For example, ASFA recommends TPE as Category I, or first-line, therapy to manage myasthenia gravis, a chronic autoimmune disease that causes muscle weakness and rapid fatigue. However, many patient groups, including those with IG4-mediated diseases, may not receive TPE as first-line treatment because there is a lack of data demonstrating the efficacy of TPE. Data expansion could potentially allow healthcare providers to provide plasma exchange to their patients with insurance or government reimbursement support.

About Terumo
BCT Terumo BCT is a global leader in blood component, therapeutic apheresis and cell therapy technologies. We believe in the potential of blood and cells to do even more for patients than they do today. Terumo BCTโ€™s Cell Therapy Technologies business enables researchers, developers and manufacturers to create next-generation cell and gene therapies. We do this through flexible, automated solutions that help meet evolving needs for reproducibility, quality and scale through the phases of development, from translational research to current good manufacturing practices (cGMP) for commercial manufacturing. www.terumobct.com If

Avior Bio to advance kidney disease treatment through Sono Tek ultrasonic coating equipment

Avior Bio to advance kidney disease treatment through Sono Tek ultrasonic coating equipment

Sono-Tek Corporation is pleased to announce that Sono-Tek has entered into an agreement with Avior Bio Incorporated for Sono-Tek ultrasonic coating equipment to be used in the Avior product development and future manufacturing process. Avior Bio procured Sono-Tekโ€™s medical device coating machine which will be paid for through a combination of cash and Avior Bio equity. Terms of the transaction were not disclosed.

According to R. Stephen Harshbarger, Sono-Tekโ€™s President, โ€œAvior Bio is developing a powerful technology in the nano and microparticle drug delivery arena. The Speeditโ„ข transmucosal film technology is unlike anything else Sono-Tek has seen among its customers, and Avior is using that technology to develop its first product in the target market of chronic kidney disease (CKD). The founder and CEO of Avior, Dr. Niraj Vasisht, has a proven track record of success. We are excited to have Sono-Tek coating machinery used in the Speeditโ„ข manufacturing process, and to be an early investor in Avior.โ€

The CEO of Avior Bio Incorporated, Dr. Niraj Vasisht, commented, โ€œSono-Tek is well known for its precision medical device coating machinery. Sono-Tekโ€™s ultrasonic spray technology offers Avior the ability to make uniform and well controlled microparticles in support of our patent-pending Speeditโ„ข technology. After working at Sono-Tekโ€™s laboratory with their talented applications engineering team, and upon successful completion of our proof-of-concept trials, we are thrilled that this custom-designed coating machine will enable Aviorโ€™s clinical trial material manufacturing up to Phase II clinical program. Partnering with a long-established coating manufacturer and process application experts will help to expedite our product and process development timelines.โ€

Sono-Tek Corporation is a leading developer and manufacturer of liquid spray products based on its proprietary ultrasonic nozzle technology. Founded in 1975, the Companyโ€™s products have long been recognized for their performance, quality, and reliability. Sono-Tek ultrasonic spray systems are proven in a wide range of precision spray applications worldwide, including implantable medical device coatings such as stents, printed circuit board spray fluxing, semiconductor coatings, solar and fuel cell manufacturing, thin film glass deposition, food and other industrial coatings applied to any width production lines. Sono-Tekโ€™s environmentally friendly ultrasonic spray systems feature up to an 80 percent reduction in spray material, and dramatic reductions in waste and energy consumption.

Avior Bio Incorporated, located in Durham, North Carolina, is a clinical stage, pharmaceutical company developing drugs for distressed neurological conditions. Avior has developed a powerful, patent-pending delivery technology called Speeditโ„ข transmucosal drug delivery technology where nano- and microparticles of drug reside on the surface of an oral transmucosal thin film. Using Speeditโ„ข technology, Avior is positioned to develop products that bring unsurpassed value in efficacy and safety.

Aviorโ€™s lead candidate โ€“ AV104 โ€“ is targeted for treatment of a dermatological morbidity condition manifested by Chronic Kidney Disease associated Pruritus (CKD-aP) resulting in itchy, scaly, excoriated nodules on the skin (Prurigo Nodularis). The condition is often seen in patients undergoing hemodialysis for CKD, and estimates of over 2 million patients suffer from CKD associated Pruritus (CKD-aP) from Stage III to V of the end stage renal disease (ESRD) with no FDA approved therapies currently available.

Avior is seeking approval of AV104 through an NDA submission in 2Q2023 via a 505b2 regulatory roadmap. Avior has been funded by several private investors, including Quality Chemical Laboratories, National Institute of Health, and North Carolina Biotechnology Center (NCBC).

FDA Clears ARTIS icono Family of Angiography Systems From Siemens Healthineers

FDA Clears ARTIS icono Family of Angiography Systems From Siemens Healthineers

The U.S. FDA has cleared the ARTIS icono, a high-precision family of angiography systems from Siemens Healthineers that permit a wide range of minimally invasive procedures to be performed in a single interventional suite. The ARTIS icono biplane system is engineered for optimal utilization in neuroradiology and abdominal imaging, while the ARTIS icono floor is a floor-mounted, single-plane system for vascular, interventional cardiology, surgical, and oncology procedures. Both systems in the ARTIS icono family expand the reach of precision medicine.

At its core, the ARTIS icono platform delivers the new OPTIQ image chain, which fundamentally redesigns image processing for 2D imaging. OPTIQ increases image quality across a wide range of C-arm angles and patient weights, regulating acquisition parameters to automatically achieve optimal image contrast at patient radiation doses that conform to the As Low As Reasonably Achievable (ALARA) guiding principal for radiation safety. The platform also improves the Siemens Healthineers roadmap function, which creates subtracted angiography images for easier navigation of the patientโ€™s vascular system during subsequent fluoroscopy, allowing dose reduction during the fluoro mode.

Additionally, the ARTIS icono platform significantly enhances ease of use through Case Flows, which provide personalized workflow plans to optimize imaging parameters and system positions, in addition to displaying layouts for the entire procedure. Case Flows adapt to user needs, providing flexibility when executing certain sequences. Users can therefore standardize procedures across multiple ARTIS icono labs for improved outcomes and more consistent documentation.

ARTIS icono biplane
The ARTIS icono biplane system is engineered for superior utilization in neurointerventions and interventional radiology, with significantly enhanced 2D and 3D imaging as well as improved visualization of difficult-to-delineate structures.

Recent studies have expanded the window for endovascular stroke therapy from 6 to 24 hours, offering the option of treating more ischemic stroke patients. Stroke treatment and other neuro procedures benefit from new features on the ARTIS icono biplane. A revolutionary form of cone beam CT, syngo DynaCT Sine Spin provides images with fewer cone beam CT artifacts in the basal part of the brain and close to the skull. syngo DynaCT Multiphase produces time-resolved cone beam CT volumes, depicting 10 different time points within 60 seconds without moving the patient to a CT system.

Additionally, syngo DynaCT High Speed can substantially shorten low-contrast 3D imaging from 20 seconds to eight to deliver CT-like images that are less susceptible to movement artifacts. The Twin Spin feature enables clinicians to seamlessly switch between 2D biplanar imaging and 3D imaging, accelerating workflow and simplifying 3D imaging for intraprocedural progress checks.

The ARTIS icono biplane also provides rapid flexibility for multidisciplinary lab use. With the Lateral Plane Switch, the user can shift the detectorโ€™s position from the patientโ€™s right side (for interventional radiology procedures) to the left side (for cardiovascular procedures) in under 90 seconds.

ARTIS icono floor
The ARTIS icono floor is a flexible, multi-axis floor system created for a wide range of disciplines, particularly vascular, interventional cardiology, surgical, and interventional oncology. With ceiling-like flexibility and a footprint of just 269 sq. ft., it provides coverage of patients up to 6 ft. 8 inches without repositioning, as well as lateral coverage of 6.23 ft., which is ideal for radial access. With its additional axis, the ARTIS icono floor can achieve virtually the same angles as a ceiling-mounted system and free space for anesthesia carts, echocardiography systems, and patient monitors without the cost of a ceiling-mounted unit.

โ€œThe ARTIS icono family of angiography systems will have nothing short of a revolutionary impact on our customers and on the delivery of healthcare in general, by setting new standards for image quality and optimized workflow in minimally invasive procedures,โ€ says Lara Barghout, Senior Vice President and Head of Advanced Therapies, Siemens Healthineers North America. โ€œAnd as more hospitals introduce comprehensive stroke services to treat more patients who are eligible for thrombectomies, the ARTIS icono biplane raises the bar in consistent 3D image quality for whole-brain imaging.โ€

Siemens Healthineers enables healthcare providers worldwide to increase value by empowering them on their journey towards expanding precision medicine, transforming care delivery, improving patient experience and digitalizing healthcare. A leader in medical technology, Siemens Healthineers is constantly innovating its portfolio of products and services in its core areas of diagnostic and therapeutic imaging and in laboratory diagnostics and molecular medicine. Siemens Healthineers is also actively developing its digital health services and enterprise services.

In fiscal 2018, which ended on September 30, 2018, Siemens Healthineers generated revenue of โ‚ฌ13.4 billion and adjusted profit of โ‚ฌ2.3 billion and has about 50,000 employees worldwide. Further information is available at .

Apollo Endosurgery Receives FDA Clearance for Polypropylene Suture-Anchor Assembly

Apollo Endosurgery Receives FDA Clearance for Polypropylene Suture-Anchor Assembly

Apollo Endosurgery Inc, a global leader in less invasive medical devices for gastrointestinal and bariatric procedures, announced that it has received 510(k) clearance from the U.S. FDA for its Polypropylene Suture-Anchor Assembly for use specifically with the OverStitch Endoscopic Suturing Systems. This proprietary suture-anchor implant is used as part of Apolloโ€™s OverStitchโ„ข and OverStitch Sx Endoscopic Suturing Systems to pass and anchor suture in the gastrointestinal tract.

Apollo is currently distributing a suture anchor that is manufactured by a third party according to Apollo design specifications. โ€œObtaining 510(k) clearance for our own proprietary suture-anchor component is expected to improve our gross margins, and allow us greater control over the supply of our suture by reducing our dependency on third party suppliers. This will be key as we seek to expand into new OverStitch markets outside the United States,โ€ stated Todd Newton, Apolloโ€™s Chief Executive Officer.

About OverStitch and OverStitch Sx
The OverStitch and OverStitch Sx endoscopic suturing systems enable advanced endoscopic surgery by allowing physicians to place full-thickness sutures from a flexible endoscope. This new technology enables a secure approximation of tissue endoscopically and a wide range of less invasive solutions for physicians who treat defects in both the upper and lower GI tract of their patients. Additionally, physicians are leveraging endoscopic suturing to perform a variety of advanced bariatric procedures. For more information regarding OverStitch go to: www.apolloendo.com.

About Apollo Endosurgery, Inc.
Apollo Endosurgery, Inc. is a medical technology company focused on less invasive therapies to treat various gastrointestinal conditions, ranging from gastrointestinal defect repairs to the interventional treatment of obesity. Apollo’s device-based therapies are an alternative to invasive surgical procedures, thus lowering complication rates and reducing total healthcare costs. Apollo’s products are offered in over 70 countries today and include the OverStitchโ„ข Endoscopic Suturing System, the OverStitch Sxโ„ข Endoscopic Suturing System, and the ORBERAยฎ Intragastric Balloon.

Regroup and IPHCA Partner to Expand Access to Mental Health Care

Regroup and IPHCA Partner to Expand Access to Mental Health Care

Regroup Telehealth, a telepsychiatry company, and the Illinois Primary Health Care Association announced a joint partnership aimed at expanding access to behavioral healthcare across Illinois, Iowa and Missouri.

โ€œTelepsychiatry is an ideal solution to deliver services to patients of community health centers in remote and underserved areas,โ€ said Jordan Powell, president and chief executive officer of IPHCA. โ€œRegroupโ€™s ability to integrate scarce clinicians into IPHCAโ€™s network of community health centers is extremely valuable, and we look forward to seeing an increase in patients utilizing accessible treatment.โ€

IPHCA represents 48 community health center members that operate nearly 380 sites in Illinois, Iowa and Missouri โ€” serving 1.4 million patients annually. Under the partnership, Regroup will connect with IPHCAโ€™s community health centers through marketing and communication channels to educate members on the effectiveness of integrated telepsychiatry solutions. IPHCA positions its members to be the providers of choice within the communities they serve through advocacy, education and technical assistance, emphasizing a high-quality, accessible and integrated health center model of care.

โ€œRegroup is excited to enter into this partnership with IPHCA to increase access to behavioral health services across communities in these states,โ€ said David Cohn, CEO and founder of Regroup. โ€œThrough Regroupโ€™s innovative telepsychiatry technology, high-quality behavioral health professionals can connect with patients who may otherwise not receive care.โ€

About Regroup
In partnership with providers at more than 100 community locations across America, Regroup brings individualized mental health services to thousands of patients often isolated by geographic, economic and social conditions. Regroupโ€™s clinician-focused culture attracts highly qualified psychiatrists, nurse practitioners, therapists and clinical social workers with specialized skills ranging from pediatric and geriatric to medication management and psychotherapy. Our telemedicine technology and administrative expertise seamlessly integrates mental health into partner care plans and workflows, yielding better patient care, shorter wait times and reduced red tape at primary care, community, hospital and correctional clinics. For more information visit www.regrouptelehealth.com.

About IPHCA
IPHCA represents Federally Qualified Health Centers (FQHCs) or community health centersโ€”entities created by Congress to meet the health care needs of underserved communities and high-risk patients. These centers fill a void by providing care for those whom other providers often do not serve. Since FQHCs must, by law, serve the medically underserved regardless of their ability to pay, CHCs are located in geographic regions designated as having a shortage of medical providers who serve this population. In addition, the medically underserved may be low-income, uninsured, homeless, affected by HIV/AIDS, struggling with substance abuse and/or have special needs. IPHCA is committed to fulfilling its mission of helping communities help themselves by advocating and expanding community primary care services across Illinois, and assisting member organizations in fulfilling their goal of community empowerment through health care choice. By advocating on behalf of membersโ€™ interests, IPHCA also advocates for underserved citizens and communities. For more information visit https://www.iphca.org/Home.aspx

Philips teams up with PURE on pioneering tele-ultrasound program linking specialists around the globe with physicians in Rwanda

Philips teams up with PURE on pioneering tele-ultrasound program

Royal Philips a global leader in health technology, and PURE (Point-of-care Ultrasound in Resource-limited Environments), a non-profit organization dedicated to enhancing ultrasound education and use in the developing world, highlighted a unique tele-ultrasound mentorship program to provide much needed diagnostic ultrasound training to health workers in Rwanda. Expert training and mentorship in point-of-care ultrasound imaging supports Rwandaโ€™s front-line primary and emergency care system and improves access to care for its citizens.

Ultrasound is considered to be one of the most important technologies to improve access to care in limited resource settings. This is particularly relevant in many practice settings across Africa, which bears 25% of the global burden of disease but has less than 2% of the health workers [1]. PURE has been working in Rwanda since 2011 to provide ultrasound training. However, there are many barriers to overcome when implementing an ultrasound training program in a resource-scare setting that is thousands of miles away.

Philips Lumify with Reacts tele-ultrasound is helping PURE to breakdown some of those barriers. Leveraging the unique live-streaming tele-ultrasound capabilities of Philipsโ€™ Lumify with Reacts (a portable point-of-care ultrasound solution), the PURE mentoring program in Rwanda connects a team of Europe and US-based physicians that are experts in point-of-care ultrasound with emergency medicine residents at the University Hospital of Kigali. Rwanda is helping to lead in access to universal healthcare coverage and in the development of emergency medicine as a specialty in East Africa. The doctors that are trained by PURE act as ultrasound ambassadors who can train primary care and emergency medical workers throughout the rest of the country and beyond.

โ€œThe Rwandese healthcare system has a rapidly developing emergency care infrastructure but still experiences challenges with limited rapid diagnostic capabilities, yet diagnostic imaging is essential in providing specialist-level care for the majority of acute illnesses and injuries presenting,โ€ said Dr. Trish Henwood, President and Co-Founder of PURE and a specialist in emergency medicine and ultrasound. โ€œThe goal of this new tele-ultrasound mentorship program is to get our mentors and mentees better connected, helping to greatly increase the number of physicians we can train, and sustainably develop ultrasound expertise at the point-of-care throughout Rwanda.โ€

โ€œThe role of point-of-care ultrasound in improving emergency medicine in Rwanda is really important. We have a limited number of radiologists that we can call on to perform scans, and as a result there is often a delay in providing care to patients,โ€ said Dr. Vincent Ndebwanimana, Emergency Care Physician at the University of Rwanda. โ€œNow I can make the emergency diagnosis myself so that I can much better fulfil my responsibility as an emergency physician.โ€

โ€œUltrasound is an important first-line diagnostic tool, but may be limited by the capabilities of the user conducting and interpreting the scan,โ€ said Bich Le, Business Leader Ultrasound, Philips. โ€œAt Philips, we are focused on providing ultrasound tools that aid in answering key clinical questions simply and quickly and we continue to believe that sustainable education is critical to increasing access to ultrasound and improving healthcare globally.โ€

Philipsโ€™ Lumify with Reacts point-of-care ultrasound solution, which works in conjunction with a compatible smartphone or tablet, is the worldโ€™s first ultra-portable ultrasound device with advanced telehealth capabilities. The Reacts communications platform enables two-way audio-visual calls with live ultrasound streaming, so both parties can simultaneously view the live ultrasound image and probe positioning, while discussing and interacting at the same time.

Lumify with Reacts is already an integral part of Philipsโ€™ outreach kit for its Community Life Center program, which aims to improve community and primary health across Africa by providing key tools and services for the continentโ€™s health workers and midwives. Philips is a global leader and trailblazer in connected care solutions that support healthcare systems and improve access to care for millions of people across the world. Its other ground-breaking telehealth solutions include home monitoring systems for chronic disease patients and patient monitoring in electronic intensive care units (eICUs), as well as multiple tele-radiology applications.

About Royal Philips
Royal Philips is a leading health technology company focused on improving people’s health and enabling better outcomes across the health continuum from healthy living and prevention, to diagnosis, treatment and home care. Philips leverages advanced technology and deep clinical and consumer insights to deliver integrated solutions. Headquartered in the Netherlands, the company is a leader in diagnostic imaging, image-guided therapy, patient monitoring and health informatics, as well as in consumer health and home care. Philips generated 2018 sales of EUR 18.1 billion and employs approximately 78,000 employees with sales and services in more than 100 countries.

Privia Health Announces Successful Launch of Initial Health System Partnership

Privia Health Announces Successful Launch of Initial Health System Partnership

Health First has become the first health system to launch a partnership with Privia Health, a national physician-led organization focused on improving the wellness and health of patients and communities. With the addition of Health Firstโ€™s 370 providers, this successful step forward supports the health systemโ€™s move toward value-based care, while expanding Priviaโ€™s presence into Central Florida.

โ€œHealth First is a progressive health system and we are thrilled with the outcomes of our collaborative efforts,โ€ said Shawn Morris, CEO, Privia Health. โ€œIn less than six months, Health First implemented proven systems to provide a high-value care delivery model that complements the superior service provided every day to their patients.โ€

As a result of Privia and Health Firstโ€™s preparations for the partnership, the health system has already achieved significant results, including meeting its annual goal of completing patient Comprehensive Health Assessments (CHAs), a version of annual wellness visits, two months early. Since March, the health systemโ€™s monthly CHA completion rate has nearly doubled, enabling patients and providers to spend more time focusing on wellness efforts and chronic disease management.

Other exciting features include:

Online scheduling โ€“ Allows customers to book an appointment online at their convenience
Enhanced customer portal โ€“ delivers seamless access to customerโ€™s medical records
myPrivia app โ€“ provides customers with easy access to logging into their patient portal, making an appointment and contacting a nurse for help
Integrated technology platform and electronic medical record โ€“ streamlines access of patient information for providers and care teams

โ€œHealth Firstโ€™s partnership with Privia has been one of the most impressive transitions I have witnessed in my career,โ€ said Frank Letherby, CEO, Health First Medical Group. โ€œPrivia is our trusted partner, and their tools, talent and technology are making a positive impact on the lives of our patients and providers. Our success and demonstrated results in this short amount of time validates our decision to work with an established provider with extensive experience partnering with healthcare leaders along the transition to value.โ€

About Privia Health
Privia Health is a national physician organization meeting providers where they are to transform the healthcare delivery experience. Through high-performance physician groups, accountable care organizations, and population health management programs, Privia works in partnership with health plans, health systems and employers to better align reimbursements to quality and outcomes. Our physician-led model, scalable systems and proprietary technology reduce unnecessary healthcare costs, achieve better outcomes, and improve the health of patients we serve. For more information: www.priviahealth.com

About Health First
Founded in 1995, Health First is Brevard Countyโ€™s not-for-profit, community healthcare system. The fully integrated delivery network (IDN) includes health insurance plans, hospitals, a multi-specialty medical group and outpatient and wellness services. As a locally owned, not-for-profit organization, Health First is committed to investing in our community. In 2018, Health First provided more than $171 million in community support. To learn more about Health First and how weโ€™re giving back to our community, please visit HFgivesback.org opens in a new window.

KTP wins national acclaim in helping cancer sufferers

KTP wins national acclaim in helping cancer sufferers

A UK Government agency has delivered a verdict of โ€œoutstandingโ€ on University of Huddersfield research that will aid a global healthcare company to continue its expansion, marketing its innovative scalp cooling caps โ€“ designed to prevent hair loss during cancer treatment โ€“ in several continents and dozens of countries.

The multi-national campus at the University has played its part in helping to ensure that the cold caps produced by Huddersfield Company Paxman are a perfect fit for the subtly different head shapes to be found around the world.

Researcher Dr Ertu Unver, a Principal Enterprise Fellow at the University and an expert in product design, needed anthropometric data to complete his latest Knowledge Transfer Partnership (KTP) with Paxman. Its goal was to design and develop a single-use cooling cap made from silicon that can be mass manufactured using the latest 3D printing technology. The cap has to be both comfortable and very close-fitting. Initially, the caps were designed for typical Caucasian head shapes, but then Paxman started to move into new markets that included Japan, meaning it was vital to have caps that could fit more rounded Asian heads.As part of his extensive data-gathering exercise, Dr Unver sought the collaboration of Japanese students at the University of Huddersfield and scanned their heads, enabling him to produce a 3D model that could be used to develop a range of caps for Asian markets.

Huddersfield-based Paxman has a long-standing collaboration with the townโ€™s University and has now provided backing for a dedicated research centre that investigates the biology of scalp cooling โ€“ how and why it prevents hair loss during chemotherapy โ€“ and the development of new generations of cold caps, harnessing the latest manufacturing technologies such as 3D printing and rapid tooling. The Paxman Scalp Cooling Research & Innovation Centre at the University continues the work carried out by Dr Unver during the recently completed KTP. It received funding from the official agency Innovate UK, which has now awarded its highest grade of Outstanding on the four-year project.

Designing the new cooling caps presented considerable challenges โ€“ especially the complex grooves that carry the cooling fluid and which have to be flat in order to make a perfect contact with the scalp. Breakthroughs made by the research team have now led to two patents being awarded. Prof Kagioglou and Dr Unver were the academic supervisors of the KTP, which also saw postgraduate associates based at Paxman, where they were also supervised by Patrick Burke and Richard Paxman.

Speaking about the partnership Dr Unver, said: โ€œOur collaboration with Paxmanisa fantastic opportunity for the academic team that deliverย the BA/BSc Product Designcourse. To date, the team have received many awards, published journal articles, spoken at conferences and exhibited world-wide. Both the University Dean, Mike Kagioglouand I, are very proud of designing an award winning, Shonin, Ninsho, and the FDA cleared product used in over 50 countries that has been proven to help cancer patients keep their hair during chemotherapy treatment.โ€

The Paxman Scalp Cooling Research & Innovation Centre team will now investigate development of a novel, environmentally friendly ecosystem for 3D-printed, individual cooling caps, ready for mass customisation. The team will also research new medical applications for cooling technologies, such as devices that could curtail CIPN (chemotherapy-induced peripheral neuropathy), which causes damage to patientsโ€™ nervous systems.

Hair loss is a well-known side effect of many chemotherapy regimens, with many patients reporting it to be the most traumatic aspect of their treatment. Scalp cooling provides the only real alternative to hair loss, resulting in a high level of retention or even complete hair preservation, improving patientsโ€™ self-confidence and creating positive attitudes towards treatment.

To find out more about scalp cooling visit www.paxmanscalpcooling.com

About Paxman
The Paxman Scalp Cooling System has been developed by the Paxman family to reduce hair loss in breast cancer patients undergoing chemotherapy. The concept behind the system came when the mother of four, Sue Paxman, experienced first-hand the trauma of chemotherapy-induced hair loss. With more than 3,500 systems delivered into hospitals, clinics and treatment centres around the world, Paxman is the leading supplier of Scalp Cooling technology. Paxmanโ€™s scalp-cooling cap is made from lightweight, biocompatible silicone that is soft and flexible, providing a snug yet comfortable fit during treatment.

About the University of Huddersfield
The University of Huddersfield has a growing reputation as an inspiring, innovative provider of higher education of international renown.ย The University has been the recipient of the Times Higher Education magazineโ€™s awards forย University of the Year,ย Entrepreneurial University of the Yearย andย Outstanding Leadership and Managementย and also a recipient of aย Queenโ€™s Awards for Enterprise.ย Itย recently became one of the fewย universities in the UK to be awarded the โ€˜Goldโ€™ standard in the Governmentโ€™s new Teaching Excellence Framework.ย The Universityโ€™s research activities are continuously acknowledged for its internationally recognised centres of excellence, strategic industry relationships and a commitment to providing state-of-the-art facilities and equipment.

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