Tag Archives: MEQ

Insurance providers can assess customer health risks in real-time using contactless vital sign monitoring solution from NuraLogix

LAS VEGAS, June 29, 2022 /PRNewswire/ — Insurance providers are now able to evaluate customer health risks in real-time using a revolutionary contactless wellness and vital sign monitoring solution from NuraLogix. 

The application allows insurance providers to quickly perform a customer health check during the online interview process using a web-browser. The NuraLogix technology uses a conventional video camera to extract blood flow information from the face, in a patented process called Transdermal Optical Imaging (TOI™), resulting in more than 30+ medical grade health and wellness measurements.

The NuraLogix technology was available for demonstration at the America’s Health Insurance Plans (AHIP) show in Las Vegas, Nevada from June 21 to 23.

The benefits of integrating a vital sign monitoring system into the insurance evaluation process are numerous: reduced costs of underwriting a policy, no nurses needed to conduct physical examinations or take fluid samples, improved compliance with the terms of lower-cost standard policies to avoid price increases, and more. This technology has also been shown to create a ‘Sentinel Effect,’ reducing fraud and improving the accuracy of questionnaire responses.

The Background

Currently in the insurance industry, providers calculate premiums for users, the amount users pay in exchange for coverage. Insurance premiums are based on a wide variety of factors such as age, gender, risk, type of coverage, location, and more. Providers calculate the likelihood the user will need to use the insurance, for example, younger people are less likely to need medical care, so their premiums are generally cheaper. Integrating the NuraLogix technology into the risk evaluation process allows insurers to calculate premiums using accurate health data of the individual and potentially even provide incentives to get healthier.

About AHIP 2022

America’s Health Insurance Plans (AHIP) is the national association of nearly 1,300 members who provide healthcare insurance to more than 200 million Americans. As a national trade association in the health insurance industry, AHIP lobbies to create a more affordable healthcare system through research and policy. Their conference, AHIP 2022, (Formerly ‘Institute & Expo’) brings together the people, ideas, and solutions that guide greater health.

About NuraLogix

NuraLogix’s technology is based on extensive peer-reviewed research and clinical studies, a fact which differentiates them from their competitors. NuraLogix has conducted multiple clinical studies and published research in many notable publications such as Frontiers in Psychology, Scientific Reports, and the Journal of Natural Sciences (JNS). NuraLogix currently holds 11 patents, with more pending. Their impressive client roster includes Japanese systems integration leader NTT Data; Sanitas, the second largest medical insurance company in Spain; and Lafiya Telehealth, a Nigerian-based health telehealth platform which provides 24/7 virtual healthcare services to residents in remote and rural areas.

To Learn More:

Visit our website:
NuraLogix – https://www.nuralogix.ai/  

Disclaimers:

Note: In the United States, this product is for Investigational Use only. The performance characteristics of this product have not been established.

For Media Inquiries: Chris Lin, Chief Marketing Officer, ChrisLin@nuralogix.ai , Tel: 437-928-2666

Stryker’s debut at World Intelligence Congress: Bringing Stryker’s Advanced Digital Healthcare to China

SHANGHAI, June 24, 2022 /PRNewswire/ — Stryker (NYSE:SYK), a leading medical technologies company, attended the 6th World Intelligence Congress (WIC) in China, showcasing how its Advanced Digital Healthcare solutions brings clinical, operational and financial values for the healthcare market. This is the first time for Stryker to participate in WIC as a strategic partner in healthcare industry, marking a significant milestone for Stryker as it brings more Advanced Digital Healthcare solutions to the China market.

Statistical Communiqué of The People’s Republic of China on the 2021 National Economic and Social Development shows that over 14.2% of the population, or 200,000,000 people are aged 65 and above, increased by 0.7% compared with that in 2020. The aging population in China presented ever pressing demands for China’s health industry, in which digital technology has a key role to play in achieving “health inclusivity” and “cost reduction and efficiency improvement.”

Stryker has a centralized technology organization called Digital, Robotics, and Enabling Technologies (DRE), dedicated to accelerating innovations across the enterprise.  By enabling its innovative products with digital capabilities, Stryker is generating insights to drive improved clinical, operational and financial outcomes across the patient care pathway.


“We are in the world of specialization focused on each stage of the patient care pathway from transport to diagnosis to planning and the OR, to recovery and monitoring, and then rehab and follow up,” says Robert Cohen, President of Digital, Robotics, and Enabling Technologies at Stryker. “We are keen to bring more of our Advanced Digital Healthcare solutions to China.”

One of the highlights of our Advanced Digital Healthcare breakthroughs is Mako SmartRobotics™, a highly advanced robotics technology that transformed the way total knee, partial knee and hip replacements are performed. Mako is able to provide a personalized surgical plan based on your unique anatomy and allow doctors to cut less by cutting precisely. Mako is poised to play a bigger role in making healthcare available for more patients in China through 5G technology. In China, Stryker also provides digital MedSurg solutions in endoscopy: – 1688 andPinPoint, instruments: Core2.0 and Signature and Sonopet, Hololens – Hololens glasses and HI-Integrated surgery room solution.


“China is the second largest healthcare market in the world, and we have been witnessing booming digital healthcare development here. We are committed to working with local partners to bring more technologies to realization and benefit Chinese patients,” says Greg Holman, President of Stryker China.

Stryker has over 85 global digital solutions that span the patient care pathway. We are dedicated to bringing the “best of Stryker” to customers in China, a strategic market for Stryker’s global strategy. Stryker continues to live up to its promise of “grow with China” as it plays a leading role in digital innovation, introducing Advanced Digital Healthcare—innovation that empowers outcomes to China. Stryker is committed to developing healthcare solutions that fit the local market, and expand local partnerships to build an enabling ecosystem. We’re passionate about digital innovation and helping our customers deliver improved outcomes—today and tomorrow.

About Stryker

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Medical and Surgical, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 100 million patients annually. More information is available at www.stryker.com.

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First AI to Refine Medical Coding by Exploring Therapeutic Data

SAN FRANCISCO, June 2, 2022 /PRNewswire/ — Medical AI start-up Aesop Technology announced a new partnership that made their new product, DxPrime, available in the Olive Library. DxPrime provides physicians and clinical documentation improvement (CDI) teams with information about missing and wrongly coded diagnoses and procedures to correct the patient’s chart in just a few clicks. It makes completing discharge summaries, prioritizing work for CDI teams, and medical coding much easier, faster, and less error-prone.

If the patient record is incorrect, you cannot code correctly.

Completeness, precision, and validity of medical documentation are critical for all healthcare stakeholders. Without correct patient records, patients could receive improper discharge instructions and a sub-optimal continuum of care. Providers also can struggle to estimate the length of stay and code insurance claims correctly, resulting in denials and loss of revenue.

Approximately 10% of inpatient claims are denied, of which more than 85% (or about $35 billion) result in unnecessary losses. Many of these denials occur because of errors in the patient record that occur upstream from the claims process. Diagnosis input errors are difficult for physicians to avoid because the knowledge of coding systems is different from what they need to learn to provide great patient care. Modern medicine’s complexity has caused 14,400 diseases to be included in ICD-10, further classified into 68,000 ICD-10-CM and 87,000 ICD-10-PCS codes.

“Physicians, CDI team, and coders have to spend a lot of time poring through medical records to find the key clinical diagnoses among the vast amount of information available,” said Jim Long, CEO of AESOP. “After that, they have to follow a series of inefficient steps on the computer to complete the input process, and search functionality for ICD codes often is not helpful. The whole process is complex, time-consuming, and error-prone.

When the physicians input the improper diagnosis, it also has downstream implications. When using DxPrime, we have helped physicians often notice they did not correctly code complications such as urinary tract infections and respiratory failure. By assisting them in inputting the proper diagnoses, our partners have seen an increase in revenue of 5-10% per inpatient.”

State-of-the-art machine learning assisted physician data entry.

DxPrime provides high-quality suggestions to support physician data entry based on a machine learning model (published in the Healthcare journal) that has been run on top of data from 3.2 Billion patient visits, including vast amounts of structured information. It allows DxPrime to use items from the patient record like lab test results and medications ordered when predicting a diagnosis.

This comprehensive model utilizes artificial intelligence to efficiently compensate for traditional CDSS and NLP weaknesses to find correct or missed diagnoses.

About Aesop Technology

Aesop Technology develops AI-powered technology to enhance patient safety and medical coding quality.

Contact
Jeremiah Scholl, CPO & Co-founder
hi@aesoptek.com
T: +1 415-818-0633
www.aesoptek.com

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Breakthrough Study Validates Artificial Intelligence as a Novel Biomarker in Predicting Immunotherapy Response – Published in Journal of Clinical Oncology


  • Lunit’s latest study provides evidence for Lunit SCOPE IO’s ability to predict immunotherapy response
  • This is the first study that adopted AI technology to define the tumor immune phenotype and to demonstrate its ability in predicting treatment outcomes of anti-PD-L1 therapy

SEOUL, South Korea, March 16, 2022 — Lunit, a leading startup in AI-based cancer solutions, announced today the publication of its study in the Journal of Clinical Oncology (JCO). Findings from the study validate the effectiveness of Lunit’s AI biomarker, Lunit SCOPE IO, in predicting clinical outcomes of immunotherapy in patients with advanced non-small cell lung cancer (NSCLC).

The JCO is an international, peer-reviewed medical journal published by the American Society of Clinical Oncology (ASCO), with an impact factor (IF) of 44.54. This is the first time that research on AI biomarkers has been published in an international SCI-grade journal of JCO’s prestige.

"Immune phenotyping of tumor microenvironment is a logical biomarker for immunotherapy, but objective measurement of such would be extremely challenging," said Professor Tony Mok from the Chinese University of Hong Kong, co-senior author of the journal. "This is the first study that adopted AI technology to define the tumor immune phenotype, and to demonstrate its ability in predicting treatment outcomes of anti-PD-L1 therapy in two large cohorts of patients with advanced non-small cell lung cancer."

Lunit's AI biomarker platform, Lunit SCOPE IO
Lunit’s AI biomarker platform, Lunit SCOPE IO

Immune checkpoint inhibitors (ICI) are a standard therapy method for advanced NSCLC with programmed death ligand-1 (PD-L1) expression. However, outcomes vary depending on the patient’s tumor microenvironment.

Assessing the PD-L1 tumor proportion score (TPS) can bring predictive benefit for patients with high expression (over 50%), who show superior response to ICI therapy over standard chemotherapy. However, ICIs lose their potency in patients with PD-L1 TPS between 1% and 49%, showing outcomes similar to chemotherapy. Therefore, the development of an accuracy-enhanced biomarker to predict ICI response in NSCLC patients with low PD-L1 expression is highly warranted.

While tumor infiltrating lymphocytes (TIL) are promising biomarkers for predicting ICI treatment outcomes apart from PD-L1, clinical application remains challenging as TIL quantification involves a manual evaluation process bound to practical limitations of interobserver bias and intensive labor. Employing AI’s superhuman computational capabilities should open new possibilities for the objective quantification of TIL.

To validate immune phenotyping as a complementary biomarker in NSCLC, researchers divided 518 NSCLC patients into three groups based on their tumor microenvironment: inflamed, immune-excluded, and immune-desert. As a result, clinical characteristics based on each immune phenotype group showed statistically significant differences in progression-free survival (PFS) and overall survival (OS).

Furthermore, analysis of NSCLC patients with PD-L1 TPS between 1% and 49% based on their immune phenotype found that the inflamed group showed significantly higher results in objective response rate (ORR) and progression-free survival (PFS), compared to the non-inflamed groups. This shows Lunit SCOPE IO’s ability to supplement PD-L1 TPS as a biomarker by accurately predicting immunotherapy response for patients with low PD-L1 TPS.

"Lunit has demonstrated through several abstracts the credibility of Lunit SCOPE IO as a companion diagnostic tool to predict immunotherapy treatment outcomes," said Chan-Young Ock, Chief Medical Officer at Lunit. "This study is a proof-of-concept that compiles all of our past research that elucidates Lunit AI’s ability to optimize cancer treatment selection."

Last year, Lunit announced a strategic investment of USD 26 million from Guardant Health, Inc., a leading precision oncology company. Following this major collaboration intended to reshape and innovate the precision oncology landscape, Lunit continues to refine its global position by validating the effectiveness of its AI technology through various studies.

Vocera, now part of Stryker, introduces latest evolution in hands-free communication to help protect and connect healthcare workers


New Minibadge expands intuitive mobile solutions for care team collaboration and safety

KALAMAZOO, Michigan, USA, March 1, 2022 — Vocera, now part of Stryker, a global leading medical technology company, introduced the new Minibadge, a wearable, voice-driven device that enables mobile workers to communicate completely hands-free. The launch of this small, lightweight device, which can integrate with multiple clinical and operational systems, expands communication and collaboration solutions for frontline workers in healthcare and other mission-critical environments. Providing users with additional flexibility, the Minibadge works in conjunction with Vocera smartphone apps, making it fast and easy for users to alternate between mobile devices to fit their communication needs in the moment.

"The Minibadge is a great option for healthcare workers who need to be completely hands-free while communicating and collaborating with colleagues," said David Augsburger, MSN, MBA, RN, CCRN, Director of Clinically Integrated Technology and Systems at Major Health Partners (MHP), where hospital leaders and frontline workers collaborate to find innovative ways to improve the safety and well-being of their patients, families, staff and community.

During human-centered design sessions and beta testing for the Minibadge, MHP team members expressed their delight with the device, emphasizing its ease of use, the long life of the battery, and its small, sleek form factor. MHP team members also praised the intuitive voice recognition of the Minibadge and its dedicated panic button. This discreet button is also a feature of the Smartbadge, which combines smartphone usability with hands-free communication and is deployed enterprise-wide at the hospital.

"The dedicated panic button on both the Minibadge and Smartbadge gives team members a sense of security and peace of mind," Augsburger said. "Plus, the slight vibration of the Minibadge after the discreet one-way distress call is made, lets staff know they are being heard by security and help is on the way." 

Hands-free communication has helped protect and connect hospital workers around the world. It enables those in isolated environments to stay connected, ask for help, request supplies, and access information without having to leave the bedside or remove personal protective equipment (PPE).

"For more than 21 years, Vocera has led the way in hands-free communication, innovating on voice-driven solutions that simplify workflows and improve the safety and well-being of our customers and the people they serve," said Dave Lively, Senior Vice President of Product Management, Vocera. "The Minibadge is a perfect example of that evolution. Its seamless compatibility with smartphones provides a valuable ‘and’ rather than ‘or’ option for organizations—empowering a broader spectrum of team members who need the flexibility to choose the best device for their assignment or task."

Like with the predecessor Smartbadge, care team members can wear the Minibadge under PPE and initiate communication by saying "OK Vocera," followed by simple voice commands, such as "call room 102 nurse," "broadcast code blue," or "schedule a reminder to turn Mr. Jones." The Minibadge also enables team members to make and receive calls, quickly collaborate with colleagues, listen to messages and respond to alarm notifications completely hands-free. Depending on which device works best for their roles and workflows, the Vocera portfolio provides additional choices when it comes to mobility and interoperability.

"The Minibadge aligns to the technologies and solutions we provide as we strive to provide safer care and better outcomes," said Jessica Mathieson, VP/GM of Acute Care, Stryker. "We’re excited to have the Vocera team join us at Stryker."

Healthcare leaders can get a closer look at the Minibadge, Smartbadge, and other voice-driven solutions at the HIMSS Global Conference, March 14-18, 2022, in booth #2347. Attendees also can learn how intelligent, integrated voice capabilities enhance care team experience.  

About Stryker
Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Medical and Surgical, Neurotechnology, Orthopaedics and Spine that help improve patient and hospital outcomes. More information is available at www.stryker.com.

On Feb. 23, 2022, Stryker completed the acquisition of Vocera Communications, a leader in digital care coordination and communication.

Media contact
Meghan Menz
Sr. Director, Communications
meghan.menz@stryker.com

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Leading E-commerce Logistics and Fulfillment Brand NextSmartShip Partners with B2B Medical E-commerce Giant LyncMed

——NextSmartShip Solution for B2B E-commerce Platforms to Extend Global Reach

SHENZHEN, China, Jan. 13, 2022NextSmartShip, a world-leading fulfillment service provider for global e-commerce sellers, signed a strategic partnership agreement with LyncMed, a major global e-commerce platform for medical instruments.

Under this partnership, NextSmartShip will empower LyncMed during its global expansion with industry-leading logistics and fulfillment expertise and the next-gen proprietary SaaS platform – Fulfillship.

Global e-commerce has seen exceptional growth since the pandemic. Besides traditional industry giants like Amazon, new e-commerce platforms such as Shopify, WooCommerce, Wix, Walmart, and other vertical platforms were also propelled into a higher growth trajectory. Fulfillment companies played a fundamental role during this.

NextSmartShip has been the fulfillment partner for many of these platforms and is becoming the best and only option for more e-commerce, especially B2B platforms for their fulfillment solution, thanks to its comprehensive and innovative capabilities as a fully equipped provider throughout all supply chain stages and the in-depth experience serving 1000+ international DTC brands. Featuring:

  • 97% global coverage with 70+ top international carrier partners;
  • Next-gen SaaS platform offering smart functions like routes recommendation, fee estimation, smart inventory distribution, seamless tracking updates etc;
  • Open API kits that allow easy integration into B2B platforms;
  • Dedicated servers which ensure fast, stable, and secure data transmission;
  • Top of the line value-added services, e.g., product assembling and kitting;
  • One-stop experience: pick up at the door of your thousands of vendors (within China) and deliver globally;
  • A seamless payment experience supporting flexible billing models;
  • Highly-rated customer service.

As one of the leading B2B players in a vertical field, LyncMed is committed to bridging different sectors and improving the efficiency of the whole value chain for the medical device industry. Through this new partnership, LyncMed hopes to meet more global requirements with a stable, efficient, complete yet flexible logistic solution powered by NextSmartShip.

"Relying on our advantages in the global fulfillment industry, our innovative solution can help LyncMed build a robust platform that truly empowers global businesses in the medical device industry."

"We have been chosen and recommended as the overall fulfillment solution provider for nearly ten similar supply chain e-commerce platforms globally, including some industry giants. This proves the scarcity of the ‘NextSmartShip Solution’," said William Yu, CEO and founder of NextSmartShip.

"We are much grateful to all our partners for their trust and recognition of our services and solution. We hope to provide a much more seamless and comfortable logistics experience for both sellers and their buyers on these e-commerce platforms so that sellers can truly focus on scaling their business through product development and supply chain management, which are their core advantages."

To view more details, please visit: http://www.nextsmartship.com 

About NextSmartShip

NextSmartShip is a tech-centered GLOCAL logistics powerhouse that strives to help DTC brands of different sizes to elevate their e-commerce business into the next big thing.

With a short history from 2019, the company has been helping thousands of global DTC brands to gain exceptional growth via its professional, stable, and affordable fulfillment services. It now delivers over a million packages per year to international destinations.

***

For media inquiries, please contact: Jackie.Jiang@nextsmartship.com  

 

Medigate and CrowdStrike to Provide Healthcare Organizations with Unified Endpoint Security for Medical IoT Devices


Integration enables comprehensive visibility, enhanced risk management and security enforcement

BROOKLYN, N.Y., Sept. 9, 2021 — Medigate, healthcare’s Best in KLAS IoT Security Provider, today announced it has partnered with CrowdStrike, a leading provider of cloud-delivered endpoint and workload protection, to provide healthcare delivery organizations (HDOs) with the industry’s first consolidated view of threat activity and incident response capability spanning all connected assets.

With the number of medical devices connecting to a hospital’s network increasing on a daily basis, HDOs struggle to maintain visibility of the location and activity of each endpoint that a device may connect to, as well as protect and manage them. Medigate and CrowdStrike solve this challenge by streamlining security responses and improving overall network efficiency.

The CrowdStrike Falcon® platform integrates with the Medigate platform allowing HDOs to perform comprehensive risk management, anomaly detection and enhanced response. The integration provides hospitals with comprehensive visibility into all managed and unmanaged devices along with enhanced threat detection capabilities that power accurate responses.

"We’ve seen a significant number of cyber and ransomware attacks against hospitals in the past year and it will only continue to rise in the future. A hospital’s focus needs to be on patient care, rather than responding to outside threats," said Matthew Polly, vice president of Worldwide Alliances, Channels and Business Development. "Medigate’s unique focus on the healthcare IoT industry is highly effective in helping to reduce attack surfaces. With CrowdStrike and Medigate, HDOs can accurately see, detect, respond and prevent attacks across the IT and clinical landscape to keep their operations and their data – including the patient information – safe."

"Today’s HDOs face specific challenges that need specialized solutions, not only in securing their vital personnel and devices, but in creating processes that ensure the benefits of connected health. By partnering with CrowdStrike, we are delivering on this vision by empowering HDOs to detect and shut-down attacks," said Jonathan Langer, chief executive officer of Medigate. "The endpoint protections our joint solution enables positions HDOs for the safe adoption of telehealth, remote patient monitoring and other networked care initiatives."

Todd Felker, former Director of Information Security at Torrance Memorial Medical Center: "As care delivery continues to fragment, the need for a centrally managed, integrated approach to securing both clinical and non-clinical endpoints is obvious. That’s why the Medigate/CrowdStrike partnership makes so much sense. I’m sure my enthusiasm for the benefits of this partnership are shared across the industry."

For more details on the Medigate and CrowdStrike partnership, check out the "Endpoint Security for Clinical Networks" solution brief.

About Medigate
Connected devices bring complicated risks, so Medigate created a simple platform to orchestrate and augment HDO security. Medigate gives the confidence to see, secure, and manage all the devices connected to the enterprise network and turn the associated data into a powerful resource for asset management and operational efficiency. It means the end of any compromise between security and usability – put simply, it allows HDOs to connect with confidence.

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Clarivate Report Demonstrates that Nations or Institutions with Diverse Research Priorities Respond More Comprehensively to Unprecedented Scientific Challenges


Forward-looking approach offers a valuable new tool for anticipating and preparing for the unexpected

LONDON, June 16, 2021 — Clarivate Plc (NYSE: CLVT), a global leader in providing trusted information and insights to accelerate the pace of innovation, today released a new Global Research Report which examines the ability of nations and institutions to respond to unexpected challenges or opportunities in science, medicine, technology and social sciences based on the diversity of their research activities and expertise.

With the publication of, "Subject diversity in research portfolios", analysts at the Institute for Scientific Information (ISI)™ at Clarivate consider subject diversity in a research context and show trends in national and institutional research portfolios by examining publications from across the G71 and BRICK2 nations from 1981 – 2018. The report finds that subject diversity provides benefit, notably in resilience and responsiveness to unexpected challenges and examines these nations’ ability to provide for their citizens’ needs in responding to a severe unforeseen global challenge – the COVID-19 pandemic. In doing so, Clarivate identifies a new and readily usable analytical approach to evaluate the capacity and competency of research organizations and nations.

The report looks to the Web of Science™ citation index, relying on the familiar Gini coefficient to provide a pragmatic approach to examining research diversity by identifying a stable global baseline for national comparisons, using highly structured data gathered over forty years. By focusing on the category balance or evenness, rapid visual comparisons can be made over time and between entities. The study demonstrates that diversity analysis provides a new forward-looking view of the opportunities for intellectual, and scientific evolution, in contrast to retrospective publication citation analysis, which looks back to achievement.

Bibliometric data have been thoroughly explored as a tool for tracking past performance and outcomes. Understanding and assessing diversity may prove not only to be a useful forward-looking index for research organizations but also to be a critical tool for national and institutional research managers in anticipating and preparing for the unexpected – and deploying an effective response. 

Jonathan Adams, Chief Scientist at the Institute for Scientific Information at Clarivate said: "The association between diversity of research topics and response to challenge and innovation points to a new source of information for those that manage research portfolios and will form a valuable new tool in support of strategic investment planning."

Diversity and research response

COVID-19 presented an unforeseen global research challenge, and the ISI identified 67,756 papers (articles or reviews) indexed in the Web of Science and published in 2020-21 related to COVID-19. Their analysis of these papers suggests that a diverse research base is indeed of potential benefit in enabling a more comprehensive response, as it provides agility and the scope for recombining knowledge in unexpected interdisciplinary situations. Countries with a diverse research base responded with a rapid and comprehensive range of innovative research – but most specialist countries did not. An exception, Brazil, has a narrow research base but one pre-adapted to this particular challenge.

Joel Haspel, SVP Strategy, Science at Clarivate said: "Diversity matters. Research diversity, in all its forms, is an engine of economic progress. It stimulates innovation and contributes to stability and resilience in national portfolios and should be a valuable part of management planning for research and development for countries and institutions."

Notes to editors:

1 G7 nations: Canada, France, Germany, Italy, Japan, United Kingdom, United States
2 BRICK nations: Brazil, Russia, India, Mainland China, South Korea

About Clarivate

Clarivate™ is a global leader in providing solutions to accelerate the lifecycle of innovation. Our bold mission is to help customers solve some of the world’s most complex problems by providing actionable information and insights that reduce the time from new ideas to life-changing inventions in the areas of science and intellectual property. We help customers discover, protect and commercialize their inventions using our trusted subscription and technology-based solutions coupled with deep domain expertise. For more information, please visit clarivate.com.

Media Contact
Rebecca Krahenbuhl, External Communications Manager, Science
media.enquiries@clarivate.com

WhaleTeq Launches First AED Management Platform with DFS200 to Provide Most Effective and Efficient Maintenance Solution

TAIPEI, June 4, 2021 — WhaleTeq, a Taiwan-based Innovative medical device testing solution company, launches the first AED management platform with their latest defibrillator tester, DFS200, to fill in the AED testing and maintenance gap. AED testing and maintenance is of great importance as AED failures can be life-threatening.

AED Management Platform with DFS200 (for reference only)
AED Management Platform with DFS200 (for reference only)

Despite the potential consequences of AED failures, AED aftercare and maintenance is not a standard service provided by most suppliers. The lack of awareness concerning the low availability of AEDs is a significant factor in this neglect. In addition, current maintenance methods are costly and infrequent since they require well-trained professionals to perform manual inspections. Seeing the need for an accessible means to ensure AEDs’ safety and reliability, WhaleTeq endeavored to create an easy and reliable solution to AED maintenance. The introduction of the DSF200 allowed suppliers to ensure their AEDs’ availability on-site with as little time possible.

Their newest AED Field testers, DFS200, provide a straightforward means to ensure all parts of an AED are functional, including the machine and the battery. This new model comes with various ECG patterns for AED defibrillation tests and an embedded battery voltage multimeter. Users can set different output thresholds to ensure the tested device will deliver the appropriate amount of energy for both adults and children during an emergency. Data retrieval and routine creation are two of the main features of DFS200. This field tester can hold a complete history of every measurement the user has made in the device, including AED test results, date and time, along with user notes.

This AED management platform allows users to use and store data on the cloud. This stored data helps identify any potential issues with minimal training. A user can access clear and simple analytics of tested AED with a complete history of testing records in a phone app. Results that need attention are marked so that anyone can easily spot abnormalities. This platform supports the company’s latest field tester DFS200 as well as any IoT-enabled AED. With IoT-enabled AEDs, it can provide daily analytics. All the information will be presented in a straightforward layout to manage customers and devices effortlessly. WhaleTeq designed these features to promote regular testing and maintenance needed to reduce AED failures.

More info: www.whaleteq.com 

About WhaleTeq Co. Ltd

Founded in September 2013, WhaleTeq provides first-class test solutions, including test equipment and associated services for medical devices. We strive to assist their clients in launching their top-quality medical device to the market in the most time and resources efficient way. Our specialty lies in physiologic monitoring systems testing, such as ECG, EEG, PPG, SpO2, respiration monitor testing. We are honored to have worked with renowned medical device providers such as GE, Philips, Siemens, Medtronic, as well as international laboratories such as UL, SGS, TUV and CSA.

Related Links :

http://www.whaleteq.com

PolyU develops biomimetic nanosheet for cancer therapy and imaging

HONG KONG, May 31, 2021 — A research team from the Department of Applied Biology and Chemical Technology (ABCT) of The Hong Kong Polytechnic University (PolyU) has developed a novel type of biomimetic nanosheet with a multi-modal imaging function, which can track tumour development and treatment processes in real-time. By harnessing two emerging cancer therapies, namely immunotherapy and photothermal therapy, the biomimetic nanosheet enables effective and precise treatment of tumours, which will significantly improve the therapeutic outcome of tumours, reduce side effects and increase patients’ survival rates. The research findings have been published in the prestigious international journal Advanced Science.

Professor Wing-tak WONG, Chair Professor of Chemical Technology of the ABCT of PolyU (also the Deputy President and Provost of PolyU), and his team started the research in 2018. Professor Wong said, "The biology and chemical experts of PolyU have been dedicated to new drug development over the years, and have achieved some significant breakthroughs especially in cancer treatment. The newly developed biomimetic nanomaterials developed by PolyU are part of our endeavours in fighting against cancer. By integrating two emerging cancer therapies, immunotherapy and photothermal therapy, with three imaging modalities for the first time, the novel biomimetic nanomaterials provide a practical design blueprint for the development of a new generation of cancer theranostics agents which have high targeting ability, efficacy and safety."

Synergistic therapy- Combining immunotherapy and photothermal therapy

New cancer treatments emerge since conventional cancer treatments like surgical therapy, chemotherapy and radiotherapy have different limitations and side effects. Dr Summy Lo Wai-sum from ABCT said, "Immunotherapy and photothermal therapy are emerging methods which are expected to provide more options for cancer treatment. The biomimetic nanosheets developed by our team allow us to combine these two methods for synergistic therapy. By applying the synergistic therapy in an experiment for colorectal tumour treatment, we found that it is more effective than single therapy and has fewer side effects on the human body."

The research team used 2D nanosheets (FePSe3) to develop a novel multifunctional nanomaterial for cancer theranostics. PD-1 (programmed cell death 1) exists on T cells, whereas PD-L1 (programmed cell death ligand-1) exists on tumour cells. Cancer cells inhibit the activation of the immune system and prevent T cells from attacking cancer cells through conjugating its PD-L1 with PD-1 on T cells. The team therefore loaded the FePSe3 nanosheets with anti-PD-1 peptide (APP), which can block the conjugation between PD-1 on T-cells and PD-L1 on cancer cells to achieve efficient immunotherapy. Without directly attacking the cancer cells, blockage of the interaction between the PD-1 and PD-L1 has been reported to revoke T cell functions, leading to enhanced antitumour immunity.

After coating with cancer cell membranes, the nanosheets will become a biomimetic nanomaterial with tumour cell membrane characteristics that provide effective camouflage, enabling them to target the tumour site efficiently. Once the biomimetic nanosheets are injected into the living bodies, the cell membrane enveloping the nanosheets will preferentially adhere to cancer cells and slowly peel away, revealing the nanomaterial to begin immunotherapy. 

Dr Lo explained, "The innate immune system attacks foreign objects which makes it difficult for the drug-loaded nanomaterials to reach the tumour site. The cancer cell membrane has a tumour-targeting characteristic that will converge homologous cells. It explains why the biomimetic nanosheets become attracted to the cancer cells when they are in close proximity with the cancer cells during blood circulation. In addition, the large specific surface area of the 2D nanomaterials is conducive to improving the drug loading ratio of the anti-PD-1 peptide, which will help with enhancing the therapeutic efficiency, as well as reducing the drug dosage and hence alleviating side effects."

On the other hand, the nanomaterials (FePSe3) chosen possess good photothermal conversion efficiency, and so they can convert near infrared laser irradiation into heat to kill tumour cells directly, thus achieving effective photothermal therapy. The heat can further promote immunotherapy by effectively inhibiting tumour growth, which results in a synergistic effect of immunotherapy and photothermal therapy.

Three imaging modes to help real-time monitoring of cancer treatment

The PolyU-developed biomimetic nanosheets can also achieve the goals of theranostics. By harnessing magnetic, optical and thermal properties, the FePSe3 nanomaterials enable three imaging modalities, namely magnetic resonance imaging (MRI), photoacoustic imaging (PAI) and photothermal imaging (PTI), for real-time tracing and tracking of the tumour sites and the nanosheets, in order to achieve multimodal diagnosis in cancer treatment.

PolyU’s novel nanomaterial can facilitate theranostics by combining diagnosis, therapy and efficacy monitoring. It not only enables the imaging and treatment of tumours, but also the real-time monitoring of treatment outcomes. The PolyU team carried out experiments on mice bearing subcutaneous colorectal tumours to investigate the application in living animals.

The study showed that the tumour volume had significantly reduced after 25 days of synergistic therapy, whereas the survival rate of the mice was three times higher than that of the control groups. The major organs of the mice, including the heart, liver, spleen, lung and kidney, showed no obvious inflammation and damage, demonstrating high biosafety and low toxicity. The research team also utilised the MRI and photoacoustic imaging capabilities of the biomimetic nanosheet to observe the tumour for 24 hours, visualising the targeting and accumulation of the nano-theranostic material at the tumour site. Through photothermal imaging, it was observed that the nanomaterial can produce localised heat under near infrared laser irradiation within a few minutes. The experiment proved that PolyU-developed biomimetic nanosheets, with multi-modal imaging capability, can offer accurate and comprehensive detection and evaluation of tumour development, ultimately achieving theranostics alongside synergistic therapeutic effects. 

Dr Lo said, "In view of the fact that there is a lack of efficient and safe theranostics materials, PolyU’s biomimetic nanomaterial has promising prospects in application. In future, our team will further expand the application of this nanomaterial to other cancer therapies and study the metabolism of the nanosheet in the living body, hoping that more cancer patients can benefit from new theranostic methods."

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