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Northwell Health Reports | Receives System-wide Echocardiography Accreditation

Northwell Health, New York State’s largest health system, achieved system-wide accreditation for its 63 echocardiography sites from the Intersocietal Accreditation Commission (IAC). Northwell joins the 708 IAC-accredited echocardiography sites within New York State underscoring Northwell’s commitment to excellence in quality patient care at all clinical sites.

All Northwell hospitals are committed to optimizing patient outcomes and safety by standardizing care. The three-year IAC accreditation recognizes a commitment to following national standards, which includes high quality imaging equipment that contributes to better clinical outcomes for patients. Alignment of imaging and procedural protocols reduces a need for repeat studies.

“Achieving accreditation for echocardiography across our entire system is truly impressive,” said Jeffrey Kuvin, MD, chair of the Department of Cardiology. “It’s another example of our focus on patient-centered, high-quality cardiovascular care at every Northwell location.”

Receiving system-wide accreditation for all of Northwell’s echocardiography sites benefits patients who can be confident they will receive the same level of care regardless of where they go within the health system.

IAC, founded by medical professionals, is a nationally recognized accrediting organization. To receive accreditation, Northwell underwent a thorough review of its echocardiography operational and technical processes.

“We applaud Northwell Health for achieving accreditation for their 63 locations offering echocardiography services,” said Mary Lally, IAC’s chief executive officer. “The standardization and optimization of echocardiography services leads to reductions in administrative and financial burden, but most importantly, improved patient care.”

For more information or to book an appointment, call (833) 826-0897 or go to: https://www.northwell.edu/cardiovascular-thoracic-services/cardiology/find-care/treatments/non-invasive-heart-testing

Guard Medical Announces FDA 510(k) Clearance for Additional Large Sizes of Its Novel NPseal® NPWT Surgical Dressing

Privately-held company Guard Medical Inc. today announces FDA 510(k) clearance for additional large sizes (surgical wounds up to 25cm) of its next generation Negative Pressure Wound Therapy (NPWT) dressing NPseal for the treatment of closed surgical incisions.

NPseal is an easy-to-use, affordable, and cost-effective NPWT surgical dressing with an integrated pump that establishes and maintains negative pressure with just a few pinches.

“Following the successful clinical results of NPseal with my hip replacement patients, the additional large sizes will expand the use of NPseal to all our patients including knee replacement patients,” stated Asit Shah, MD, PhD, Englewood Orthopedic Associates, Englewood, NJ. “I look forward to dressing my patients’ wounds for success with NPseal.”

“We’re excited to expand our portfolio with the NPseal 20 and NPseal 25. FDA clearance for the additional large sizes allows NPseal to become the dressing of choice for the treatment of closed surgical incisions in orthopedic, cesarean, and cardiothoracic procedures,” stated Machiel van der Leest, CEO of Guard Medical. “We believe that NPseal uniquely fits in the ever-increasing outpatient trend requiring higher patient mobility and self-care.”

NPWT has been shown to reduce Surgical Site Complications (SSC) in a large number of peer reviewed articles. Until now, however, conventional disposable NPWT devices have not achieved wide-spread use due to their high cost and complexity. NPseal dressings uniquely broaden NPWT’s application while driving conversion from the Advanced Wound Dressing and Standard Dressing markets.

Guard Medical Inc. (www.guard-medical.com), a privately-held company, is commercializing easy-to-use, affordable, and cost-effective solutions that enable prophylactic Negative Pressure Wound Therapy (NPWT) wound care of closed surgical incisions. Guard Medical’s simple NPWT technology originated with New York-Presbyterian and Weill Cornell Medicine in response to physicians’ identification of unmet needs related to Surgical Site Infections (SSI). Current investors include Bpifrance and Matignon Investissement et Gestion.

Guard Medical’s vision is to develop NPWT solutions for use on a wide range of surgical wound types and sizes with broad applications for infection prevention, scar mitigation, and enhanced cosmesis.

ZOLL Announces Successful Bid to Acquire Vyaire Medical

ZOLL, an Asahi Kasei company that manufactures medical devices and related software solutions, announced today that it is the winning bidder in an auction to acquire Vyaire Medical’s ventilator business as part of Vyaire’s Chapter 11 bankruptcy proceedings. Completion of the acquisition is subject to court approval at a sale hearing and dependent on a successful closing that is anticipated to occur in the coming weeks.

ZOLL is a global leader in acute critical care and related software and diagnostic tools, and its solutions are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. Since 2014, ZOLL has manufactured ventilation devices and accessories designed for the transport of critically ill patients.

“Respiratory care has been central to ZOLL’s business strategy for many years,” said Jon Rennert, CEO of ZOLL. “If the acquisition is successfully completed, adding Vyaire’s ventilators to ZOLL’s product portfolio will enhance our ability to serve a broader range of clinicians and patients.”

Until new ownership is final, Vyaire ventilator customers should continue to contact Vyaire (for details visit https://www.vyaire.com/contact-us).

Additional Background

On June 10, 2024, Vyaire Medical announced it had voluntarily filed for Chapter 11 bankruptcy protection in the U.S. The Chapter 11 filing allowed Vyaire to continue to operate while seeking to sell its business units, including the Vyaire ventilation business. Since filing for bankruptcy, day-to-day operations at Vyaire have continued with little interruption, and Vyaire has continued to serve its ventilator customers and maintain the team needed to operate safely and efficiently.

Dr Kali Stasi Appointed Chief Medical Officer at SalioGen Therapeutics

Dr Kali Stasi will be responsible for bringing SalioGen Therapeutics development candidate SGT-1001 into the clinic by mid-2025 as a one-time treatment for Stargardt disease and continuing to develop the company’s Gene Coding technology for other inherited retinal diseases and cystic fibrosis.

“Dr Kali Stasi brings to SalioGen three decades of expertise in ophthalmology and a proven track record of advancing genetic medicines from early- and late-stage clinical development through commercialization,” said Jason Cole, CEO of SalioGen Therapeutics. “Her clinical vision and leadership will enhance our ability to continue pushing the boundaries of genetic medicine for patients and families, and we’re excited to welcome Dr. Stasi to our team.”

“SalioGen’s novel Gene Coding technology holds tremendous potential for overcoming the limitations of other genetic medicine approaches, significantly expanding the universe of diseases we can address by integrating full genes with high specificity,” said Dr. Stasi. “I’m very excited to work with the SalioGen team to accelerate the positive impact this technology can have on patients.”

Most recently, Dr Kali Stasi served as Senior Vice President of Clinical Development at Adverum Biotechnologies. In this role, she planned and executed global clinical development programs for vision loss. In her previous position, Dr. Stasi led Tenpoint Therapeutic’s cell therapy program for ophthalmic indications as Senior Vice President of Clinical Development. Before that, Dr. Stasi worked at Novartis Institutes for Biomedical Research as a Translational Medical Director, where she led multiple clinical trials in a pipeline of gene and cell therapies intended to treat retinal diseases. Earlier in her career, Dr. Stasi served four years at the University of Pennsylvania as an Assistant Professor of Ophthalmology.

Dr. Stasi earned her M.D. and Ph.D. in neurodegenerative disease from the University of Patras, Greece. She completed an ophthalmology residency at the University of Rochester, NY, a Cornea and Refractive Surgery Clinical fellowship at Johns Hopkins Wilmer Eye Institute, and a business post-baccalaureate program at Wharton Business School.

Real-world Evidence Solutions Market | To be Worth $6.37 Billion by 2031

Clinical evidence obtained from the examination of real-world data (RWD) is known as real-world evidence (RWE).

The resulting clinical evidence covers the use of a medical product and its possible advantages or disadvantages. Pharmaceutical, biotechnology, and medical device firms, as well as healthcare payers and providers, employ RWE solutions for market access and reimbursement/coverage choices, drug development and approvals, post-market surveillance, and medical device development and approvals.

The market for RWE solutions is expanding due to various causes such as the increasing prevalence of chronic illnesses, the growing emphasis on personalized healthcare, the transition to value-based care, and the increasing use of real-world evidence solutions in drug development and commercialization. Real-world evidence solutions market participants could anticipate substantial development prospects due to the emergence of emerging economies and an increasing emphasis on comprehensive RWE services.

Shift Toward Value-based Care is Driving the Market

The value-based care model has emerged as an alternative and potential replacement for the volume-based/fee-for-service reimbursement model. The strategy seeks to save healthcare costs, enhance population health, and deliver better treatment for individuals. In a value-based care approach where pay-for-value is prioritized, using real-world data aids in demonstrating if the medication produces the same patient outcomes as shown in RCTs.

The CMS has launched several value-based care models, including patient-centric medical homes, the Medicare Shared Savings Program, and the Accountable Care Organization (ACO) model. Private payers have also embraced similar accountable, value-based care models. Since validated outcome indicators based on real-world data are being included in value-based payment contracts, the FDA has come to understand that real-world evidence may make the American healthcare system more efficient and competitive.

Value-based payment plans typically rely on cost information and objective, quantifiable patient outcomes (related to product utilization). In the past, to make decisions about how much to pay for new medications and biologics, payers have required additional information beyond the cost and utilization data from their claims systems and the findings of clinical trials, many of which do not evaluate significant long-term outcomes and resource use.

Value-based care is a difficult, transformative path that is quickly gaining popularity around the globe. Cost-effectiveness trials are designed with the assistance of R&D specialists that adopt a value-based mentality. In the early phases of medication development, the trials aid in assessing the burden of illnesses and creating value propositions based on actual outcomes, such as productivity, absenteeism, quality of life, and frequency of clinical episodes. Employing empirical data and supporting documentation is a is a key element in transitioning to value-based care.

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The key players operating in the global real-world evidence solutions market are IQVIA Holdings Inc. (U.S.), Elevance Health, Inc. (U.S.), ICON plc (Ireland), Clinigen Group plc (U.K.), Cognizant Technology Solutions Corporation (U.S.), Revvity, Inc. (U.S.), F. Hoffmann-La Roche Ltd (Switzerland), Thermo Fisher Scientific Inc. (U.S.), Oracle Corporation (U.S.), SAS Institute Inc. (U.S.), Parexel International Corporation (U.S.), and HealthVerity, Inc. (U.S.).

Among all the components studied in this report, in 2024, the datasets segment is expected to account for the largest share of 53% of the real-world evidence (RWE) solutions market. The datasets segment is further segmented into disparate datasets and integrated datasets. The global real-world datasets market is anticipated to be dominated by the disparate datasets sector by 2024. Data that are clearly different in kind, quality, or character make up disparate datasets. Because of their heterogeneity, these datasets are easily combined to offer businesses business insights. The significant market share of this segment can be mainly ascribed to the growing use of wearable technology, registries, electronic health records/electronic medical records (EHRs/EMRs) in hospitals, technological advancements in medical data storage, and increased access to claims data.

Among all the applications studied in this report, in 2024, the drug development & approvals segment is anticipated to register the highest CAGR of 13.1% during the forecast period. Because RWE studies are much less costly and time-consuming than randomized clinical trials, they offer easier access to long-term efficacy data and help get around some of the practical issues with randomized clinical trials, which is why their significance in drug development is growing. Patient-reported outcome Measures (PROMs) and quality-of-life metrics are becoming often used in clinical trials for medication development. Evidence derived from real-world data is frequently used to guide medication development, providing information on treatment paths and comparator interventions in clinical settings, as well as the natural history and epidemiology of a disease.

Among all the end users studied in this report in 2024, the pharmaceutical, biotechnology, and medical device companies segment is expected to account for the largest share of 39.1% of the real-world evidence (RWE) solutions market. Pharmaceutical businesses are using more and more RWE solutions; these solutions are employed at every stage of the drug development process, from drug discovery to post-marketing surveillance, which accounts for the segment’s significant market share. Furthermore, RWE is used by regulatory agencies like the FDA to evaluate the post-market safety of medicines that have been approved, as well as for medication approval. To reduce the likelihood of medication failure, pharmaceutical companies are implementing RWE technologies.

Among all the regions studied in this report, North America is expected to account for the largest share, 48.9%, of the real-world evidence (RWE) solutions market in 2024The presence of important players, significant R&D expenditures made by pharmaceutical and biotechnology corporations for medication development, and encouraging government initiatives are all factors contributing to this region’s significant market share. The region’s stake is also being increased by the growing adoption of EHR in the healthcare sector. The region is seeing an increase in public-private funding for projects utilizing RWE technology. For example, the U.S. Food and Drug Administration stated in 2023 that four more U01 grant awards would be made for the projects, which included using RWE technologies to cure cancer and to improve the effectiveness of clinical trials (refer to U.S. FDA).

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Scope of the Report:

Real-world Evidence Solutions Market Assessmentby Component

  • Datasets
    • Disparate Datasets
      • EMR/EHR/Clinical Data
      • Claims & Billing Data
      • Pharmacy Data
      • Product/Disease Registries Data
      • Genomics Data
      • Other Disparate Datasets
    • Integrated Datasets
  • Consulting Services

Note: Other Disparate Datasets include data generated from mobile devices, wearable devices, and social media.

Real-world Evidence Solutions Market Assessmentby Application

  • Market Access & Reimbursement/Coverage Decisions
  • Drug Development & Approvals
    • Oncology
    • Neurology
    • Immunology
    • Cardiovascular Diseases
    • Other Therapeutic Areas
  • Post Market Surveillance
  • Medical Device Development & Approvals
  • Other Applications

Note:  1) Other Therapeutic Areas include infectious diseases, musculoskeletal disorders, dermatological diseases, and respiratory diseases.

2) Other Applications include regulatory and clinical decision-making. 

Real-world Evidence Solutions Market Assessmentby End User

  • Pharmaceutical, Biotechnology, and Medical Device Companies
  • Healthcare Payers
  • Healthcare Providers
  • Other End Users

Note: Other end users include academic research institutions, patient advocacy groups, regulators, and health technology assessment agencies.

Real-world Evidence Solutions Market Assessmentby Geography

  • North America
    • U.S.
    • Canada
  • Europe
    • Germany
    • France
    • U.K
    • Italy
    • Spain
    • Switzerland
    • Belgium
    • Rest of Europe (RoE)
  • Asia-Pacific (APAC)
    • China
    • Japan
    • India
    • South Korea
    • Taiwan
    • Singapore
    • Australia
    • Rest of Asia-Pacific (RoAPAC)
  • Latin America
    • Brazil
    • Mexico
    • Rest of Latin America (RoLATAM)
  • Middle East & Africa

More here.

Lloyd Diamond | Appointed Chief Executive Officer at Nitinotes

Lloyd Diamond | Appointed Chief Executive Officer at Nitinotes
Lloyd Diamond as Chief Executive Officer, Nitinotes

Lloyd Diamond has been appointed Chief Executive Officer at Nitinotes effective immediately. (Nitinotes are the developers of EndoZip™, a fully automated endoscopic suturing system aimed at treating obesity).

Lloyd Diamond brings more than 30 years of leadership in the medical device industry, having spearheaded significant advancements in orthopedics, endoscopic, and general surgical devices. Most recently, he served as CEO of Pixium Vision S.A., where he led the development of groundbreaking bionic vision systems and strategic partnerships.

John Barr, Chairman of the Board:

“We are thrilled to welcome Lloyd to lead Nitinotes into its next chapter of innovation and growth. Building upon the foundation established and the exceptional achievements attained, his extensive experience in medical technologies positions him as an outstanding leader to advance our future initiatives.”

Lloyd Diamond succeeds Raz Bar-On, who will continue as GM of Nitinotes Israel, overseeing operations, R&D, and regulatory functions.

Lloyd Diamond said:

“I am honored to join Nitinotes at this pivotal time. With obesity rates rising worldwide and over 1 billion people affected, EndoZip™ provides a critical solution to a significant global health challenge. I look forward to working with the talented team to bring this solution to more patients and healthcare providers worldwide.”

As Nitinotes prepares for pivotal trials in the U.S., the company is also enhancing its operational capabilities to meet global demand and regulatory milestones, specifically focusing on the imminent CE mark approval and the European commercial launch.

About Nitinotes: A Leader in Innovative Obesity Treatment

Nitinotes is a pioneer in medical technology, focusing on an innovative solution for obesity treatment. The company’s flagship product, EndoZip™, offers a minimally invasive approach for obesity class I & II patients, ensuring consistent, safe suturing with the press of a button, representing a significant advancement in the field.

Noctrix Health Announces New CMS Reimbursement Codes and Payment for Nidra Tonic Motor Activation Therapy for Restless Legs Syndrome

Nidra Tonic Motor Activation Therapy

Noctrix Health announced that the Centers for Medicare & Medicaid Services (CMS) have established new reimbursement codes and payment for the company’s flagship product, the NidraTM Tonic Motor Activation system, the first FDA-cleared wearable medical device to treat symptoms of Restless Legs Syndrome (RLS). This milestone marks a pivotal moment in making this breakthrough therapy accessible to millions of patients suffering from debilitating symptoms of RLS, recognizing the critical need for accessible, non-pharmaceutical treatments.

Nidra TOMAC Tonic Motor Activation Therapy, which was authorized for marketing in the United States last year following its designation as a “Breakthrough Device” by the US Food & Drug Administration (FDA), remains the only clinically validated, non-pharmaceutical treatment available for patients with RLS. The CMS decision to issue new codes for NidraTM underscores the recognition of this significant unmet need and facilitates access to this breakthrough therapy for millions of patients who do not respond to pharmaceutical treatments. These patients are left with no other approved or cleared treatment alternatives today and continue to suffer from the debilitating effects of sleep deprivation, poor mental health, and a significantly diminished quality of life.

“Receiving dedicated reimbursement codes from CMS is a monumental achievement for Noctrix Health and a testament to our commitment to improving the lives of patients with Restless Legs Syndrome,” said Shri Raghunathan, President & CEO of Noctrix Health. “We are incredibly grateful for this recognition by CMS, which not only validates the innovative technology behind NidraTM TOMAC therapy but also ensures that more patients will have access to this life-changing treatment. This milestone represents a significant step forward in our mission to provide effective, non-pharmaceutical solutions for those in need.”

Justin Kelly, Senior Vice President of Patient Access at Noctrix Health, added, “The CMS decision to provide dedicated codes E0743 and A4544 for NidraTM TOMAC therapy and supplies is a crucial development in expanding patient access to this groundbreaking treatment. Our team has worked tirelessly to advocate for the needs of RLS patients, and this recognition by CMS is a major victory for them. We look forward to working with healthcare providers and payers to ensure that patients across the country can benefit from this innovative therapy.”

Dr. Mark Buchfuhrer, MD, clinical associate professor at Stanford University and one of the principal investigators who was involved in the foundational clinical studies that led to the FDA marketing authorization of TOMAC therapy, emphasized the importance of this recognition: “RLS is a condition that profoundly impacts the quality of life for millions of patients. The availability of a non-pharmaceutical option like NidraTM, now supported by CMS reimbursement, is a game-changer in our treatment approach. This decision will allow more patients to receive effective care, leading to better outcomes and improved quality of life.”

The two new CMS reimbursement codes (E0743 for the devices and A4544 for the supplies) along with the associated payments will become effective on October 1, 2024, enabling more healthcare providers to offer this innovative treatment to eligible patients. Noctrix Health remains committed to advancing patient care and will continue to work closely with the medical

Beyond the Device: How Remote Monitoring Devices & AI-Enabled Analytics are Shaping the Next Generation of Healthcare | By Stuart Long, CEO, InfoBionic.Ai

Remote Monitoring Devices
Stuart Long, CEO, InfoBionic.Ai

Today’s hospital is an epicenter of medical device innovation, with modern devices showing greater acuity, capabilities, and diagnostic accuracy than any generation before them. While medical devices are essential to care delivery inside the hospital, they are perhaps even more integral to care that is delivered outside of the hospital’s walls.

Along with the rising sophistication of inpatient medical devices, data acuity in remote patient monitoring (RPM) devices is also on the rise. Virtual telemetry, for example, enables the continuous collection of health data like heart rate and blood pressure from nearly anywhere a patient may be located.

The applications of RPM are both numerous and diverse. Insider Intelligence estimates that 70.6 million U.S. patients, or 26.2% of the population, will be using RPM by 2025. But this utilization metric is just the beginning. Wearable RPM devices are growing increasingly sophisticated through the integration of advanced technologies like artificial intelligence (AI) and machine learning (ML), which continue to multiply their potential applications and quantifiable impact. For example, research has shown that the use of RPM devices can significantly reduce systolic blood pressure and diastolic blood pressure compared to typical care and self-monitoring alone for hypertension.

Advanced, AI-enabled RPM devices require us to reframe our understanding of the medical device, expanding our view beyond the physical wearable to include the sophisticated analytics that bring its data to life. In this article, we will explore how the marriage of high-acuity virtual telemetry devices and AI-enabled analytics in cardiology is already transforming the timeliness, efficiency, effectiveness, and accessibility of care while forever redefining the medical device itself.

The Anatomy of the High-Acuity Virtual Cardiac Telemetry Device

 Before we look ‘beyond the device,’ let’s first explore how the powerful capabilities of high-acuity virtual cardiac telemetry devices make effective RPM possible. These innovative devices are drastically different from the traditional cumbersome, wired monitoring equipment of yesterday. Their design ensures the delivery of high-acuity, up-to-the-minute data, which is essential to support AI-enabled analytical models. High-acuity virtual telemetry devices uniquely offer:

  • Near-immediate data transmission. Near real-time data enables providers to act at a moment’s notice and it feeds AI models with a degree of timeliness that is essential to the delivery of proactive, effective care. For example, when supported by near-immediate data transmission, AI-enabled analytics enables multi-class arrhythmia detection with accuracies above 99% in controlled test datasets.
  • Continuous connectivity. Modern virtual cardiac telemetry devices offer reliable Bluetooth or Wi-Fi connectivity as they travel with the patient everywhere they go. Long battery life and low latency minimize delays and eliminate blind spots that have historically hindered the cardiologist’s point of view. Connectivity is directly correlated to data acuity, ensuring that all of the data is captured all of the time.
  • Multiple test types in a single device. These devices give providers full diagnostic autonomy and the ability to choose which diagnostics are right for each patient, with multiple available test types like Holter and Event. They can conveniently combine multiple test types in one single device by integrating various sensors and technologies to simultaneously measure and transmit diverse physiological data such as heart rate, blood pressure, oxygen levels, and more.
  • Unobtrusiveness for the patient. Comfortable and easy to use, next-generation devices empower patients to manage their health more proactively and easily, which leads to better adherence to treatment plans and improved health results. One study found that RPM generates improved compliance and engagement, with 80% of patients considered well-engaged and 70% following the instructions issues by their practitioner.
  • Exceptional data acuity. The ability to capture every single beat provides a level of acuity that has never before been possible in remote cardiac monitoring. But as the acuity of remote data inches ever closer to the acuity of in-hospital data, providers will naturally find themselves with a glut of cardiac data. That brings us to our next point—how to effectively manage and leverage this vast amount of data.

AI as an Extension of the Medical Device

Unsurpassed data volume is a hallmark of the next-gen remote patient monitoring device, which means that the device by itself is not sufficient to derive value in its intended use case. Instead, we must expand our view of the device to include the sophisticated machine learning algorithms that power its models. It is at this intersection of the device and the model where transformation truly occurs.

AI algorithms take the data collected from remote patient monitoring devices and analyze it by first processing and filtering the raw data to eliminate irrelevant or redundant information. They then use machine learning models to identify patterns, trends, and anomalies within the data, such as irregular heartbeats (i.e. signs of arrhythmia) or unusual blood pressure levels. The algorithms compare current data against historical data to detect significant changes and predict potential health issues.

These insights are then presented to cardiologists and other clinicians in an actionable format, including dashboards and alerts, which enable them to make informed decisions, initiate timely interventions, and personalize patient care plans based on near real-time, data-driven insights.

AI-enabled analytics not only solve the data volume challenge presented by high-acuity devices, but they also raise the bar for detection and diagnostic accuracy well beyond what is possible with a human reviewer alone.

High-Acuity Virtual Telemetry Devices Empowered by AI-Enabled Analytics: Exploring the Benefits

The marriage of high-acuity virtual telemetry devices and AI-enabled analytics redefines the medical device forever and unlocks transformative benefits for patients and providers alike.

In fact, the continuous transmission of high-acuity data offered by virtual telemetry devices joins forces with the continuous analysis provided by AI-enabled analytics to enable continuous improvement—which is an essential prerequisite to the widespread transformation of cardiac care. A new generation of AI-enabled RPM devices can surface predictive indicators of cardiac conditions and events, some of which have yet to be recognized or referenced in existing cardiology literature.

Additionally, AI-powered RPM devices can dramatically reduce healthcare costs across all service lines. A Deloitte Center for Health Solutions report estimates that utilizing RPM can provide an annual savings of $1,054 to $1,950 per patient, and when applied across the national population, this could amount to $5.4 to $9.9 billion saved annually. Additionally, AI could save the U.S. up to $360 billion annually if adopted more widely in healthcare, according to a report from McKinsey and Harvard.

Embracing the Future of the Next-Gen Medical Device

The future of patient care is bright, and its luminescence is fueled by a new generation of medical devices that combine both wearable technology and AI algorithms in a fully integrated way.

As we advance into the future, the convergence of AI with high-acuity remote monitoring devices is redefining the medical device itself—transforming it from a mere data collection tool into a powerful catalyst for predictive, personalized care.

In this exciting new era, remote monitoring devices bring the care setting to life wherever the patient is located, while AI acts as a force multiplier, enhancing clinical accuracy, efficiency, and insight. Together, these technologies enable cardiologists and other clinicians to make the most informed, timely, and data-driven decisions, ultimately reshaping the way we understand and deliver healthcare in cardiology and beyond.

To learn more about AI-enabled virtual cardiac telemetry, visit https://infobionic.ai/.

Editor’s Note:  Stuart Long has been the CEO of InfoBionic.Ai since March 2017. He underscores the company’s commitment to widespread market adoption of its transformative wireless remote patient monitoring platform for chronic disease management. With more than 25 years of experience in the medical device market, Stuart brings expertise in achieving rapid commercial growth.

Apheros Secures $1.85M

Apheros Notes: Data centers are the backbone of the digital age, with unprecedented demand for digital infrastructure driven by the surge in the use of AI, machine learning, and supercomputing. However, their energy consumption is skyrocketing.

By 2030, an estimated six percent of global energy consumption will be used specifically for cooling data centers. A shift from traditional cooling methods to more cost- and energy efficient liquid-based solutions is inevitable. Enabling this transition, deep tech startup Apheros is today announcing a $1.85m funding round seizing this critical moment to introduce its innovative metal foam technology, offering a superior solution to this pressing industry challenge.

The pre-seed funding round, led by venture capital firm Founderful, will accelerate development and deployment of Apheros’ revolutionary metal foam-based cooling solutions.

The Apheros patented manufacturing process creates unique foam structures with completely open porosity and unparalleled surface area, surpassing traditional solutions by a factor of thousand, which translates into exceptional heat transfer and flow properties. Ideal for high performance cooling applications, Apheros’ metal foams are easily integrated within its customers’ existing cooling systems. They address customers’ urgent needs of reduced energy consumption and cooling costs.

Apheros AG, founded in August 2023, was developed as an ETH Zurich spin-off to tackle cooling challenges in a wide range of applications including high-performance computing and mobile devices. Apheros is led by a team with a proven track record in innovation, business development and tech transfer. Apheros’ co-founder and CEO Julia Carpenter was recently named one of Switzerland’s Top 10 “Founders to Watch” for her invention of Apheros novel metal foam manufacturing process. Co-founder and CTO Gaëlle Andreatta, has over 16 years of experience in R&D, Tech Transfer, and start-up development.

Julia Carpenter, co-founder and CEO of Apheros commented: “Our technology has the potential to set new industry standards and significantly reduce the environmental impact of cooling solutions worldwide. This funding round will allow us to advance our mission of helping our customers achieve superior thermal performance, increase energy efficiency, and contribute to a greener future. Immediately, we will expand production, increase research and development efforts, and bring state-of-the-art solutions to a broader market.”

Apheros currently targets the thermal management market with a focus on liquid cooling, a segment expanding at a fast pace due to the needs created by the growing demand for High Performance Computing, Artificial Intelligence and Data Centers. More efficient cooling systems are needed to overcome current energy shortages and to reach ambitious climate protection goals. There is a pressing need to introduce higher performing cooling solutions to the market.

Gaëlle Andreatta, co-founder and CTO of Apheros added: “There is a dire need for more efficient cooling solutions. AI development is driving exponential growth in data center energy consumption and inefficient cooling is the main culprit. Our unique metal foams have superior heat exchange and fluid transport properties, especially for liquid and two-phase cooling. With our customers, we are redefining thermal management. ”

Apheros’ vision is to catalyze the transition to a more sustainable future through materials innovation. Apheros will redefine sustainable, high-performance liquid cooling and establish its products as the gold standard for sustainable, high-performance liquid cooling.

Lukas Weder, founding partner at Founderful commented: “We are excited to support Apheros’ mission to revolutionize cooling technology. Apheros’ groundbreaking approach has the potential to significantly reduce energy consumption and set new industry standards. We are confident in the team’s vision and capabilities and look forward to seeing the positive impact they will make on both the industry and the environment “

Preparing for Labor: Tips on Making a Birth Plan

Preparing for Labor: Tips on Making a Birth Plan

Pregnant women often find preparing for childbirth to be an intimidating and nerve wracking time. Developing a birth strategy is just one way to help ease these feelings. Birth plans are  beneficial in controlling anxiety and fostering a more seamless birthing experience.

This article delves into preparing for labor: A good birth plan, including fundamentals, benefits, and essential elements to integrate, equipping you with the knowledge and readiness for childbirth.

What is A Birth Plan?

A birth plan constitutes a written framework outlining your preferences for childbirth. This serves as a guide for your healthcare professionals, outlining your ideal methods for the process of childbirth. Birth plans are designed to ensure recognition and adherence to your choices, even during unexpected circumstances.

Birth planning can vary, extending from a simple preference checklist to an in-depth guide encompassing every facet of childbirth and care after delivery. Ultimately, it functions as a tool for voicing your desires and necessities, guaranteeing a seamless and relaxed childbirth journey.

Benefits Of A Birth Plan

Expectant mothers can experience various advantages in childbirth by having a birth plan. First and foremost, it helps by helping expectant parents feel in control, preventing them from feeling unnecessarily stressed out when giving birth. It also helps improve communication with your healthcare providers, making sure they know your preferences and can respond appropriately. This proactive method assists in making informed choices, leading to a smoother childbirth experience.

Moreover, a birthing plan offers reassurance by ensuring your preferences are recorded and will be taken into account, even in unforeseen circumstances. In general, it enables you to become actively involved in your journey through childbirth.

Internet Tools And Assistance

Pregnant women can discover a plethora of online tools to assist in developing their birth plans. Examples include BabyCenter and The Bump, which provide thorough guides and templates for expecting parents. Furthermore, expert guidance from family healthcare professionals, like those who have completed an online post-master’s FNP program, can be extremely helpful.

Important Components For Your Birth Plan

To guarantee that your preferences are understood, a thorough birth plan should include multiple important components. Start by explicitly declaring your pain management strategies, be it medication, natural treatments, or a mix of these methods. Specify your preferred birthing positions, such as squatting, lying back, or utilizing a birthing ball. Outline your choice of companions for the delivery, be it partners, family members, or doulas.

Offer precise guidelines for the newborn’s urgent post-birth care, like fostering direct physical contact, postponing cord clamping, and beginning breastfeeding. Lastly, it’s crucial to address any particular concerns or needs, like choices in music, lighting, or access to birthing equipment.

By specifying these factors, you can make sure your medical team comprehends and honors your preferences, leading to a more tailored and pleasant childbirth process.

Talking to Your Healthcare Provider About Your Birth Plan

Consulting your doctor or midwife about your childbirth plan is crucial to guarantee adherence to your preferences. Engage in this dialogue with an unbiased perspective, express your likes and dislikes, and be receptive to expert advice. The dialogue aids in identifying potential issues and assists in modifying your approach as necessary.

Remember, adaptability is crucial; unexpected events could unfold, necessitating your medical team to modify their approach for safety reasons. By collaborating with your healthcare provider, you can create a birth strategy tailored to your preferences, and work together for a plan that suits everyone, ensuring the highest quality of care for both you and your infant.

Useful Advice For Developing Your Birth Plan

Developing a birth plan can be simple with the right strategies. Begin by conducting research and collecting data from credible sources, such as medical websites and prenatal classes. Use online birth plan templates to help you as you navigate through the steps. Give top priority to the aspects of your labor and delivery that are most important to you.

Make sure your plan is straightforward and succinct so that your healthcare team can easily comprehend and adhere to it. Also, think about talking about your strategy with fellow moms or becoming a member of online communities for different perspectives and tips. This readiness will boost your confidence and prepare you well for your childbirth journey.

In essence, a carefully planned birth plan can greatly improve your childbirth experience, offering clarity and decreasing stress. Having a thorough birth plan gives you authority and ensures that your wishes are honored. Begin preparing ahead of time, clearly express your desires, and stay adaptable to handle unforeseen circumstances. Keep in mind that the ultimate aim is to ensure a safe and healthy delivery for both you and your baby.