Home Blog Page 42

CIONIC Unveils Three New Centers of Excellence on the East Coast to Aid Patient Mobility Through the Use of FDA-Cleared Bionic Clothing and Neuromodulation

CIONIC

CIONIC, the pioneering neurotech company that created the FDA-cleared Cionic Neural Sleeve, today announced three new Centers of Excellence at renowned institutions including International Multiple Sclerosis Management Practice (IMSMP) in New York City, Hackensack Meridian Neuroscience Institute at Jersey Shore University Medical Center’s MS Center in Neptune, NJ, and MedStar Health with centers across Maryland, Virginia, and Washington, D.C.

CIONIC, in collaboration with qualified clinicians at the Centers of Excellence, utilizes the Neural Sleeve and proprietary neuromodulation platform to deliver a seamless care experience from the clinical environment to the home or community setting. The Neural Sleeve is the first bionic clothing that analyzes and augments human movement, enabling individuals with multiple sclerosis, stroke, spinal cord injuries, and other neurologic diagnoses to move with more freedom and control.

Individuals interested in experiencing the Neural Sleeve can contact their doctor at these Centers of Excellence to make an appointment to try the Neural Sleeve, or contact CIONIC directly at https://cionic.com/coe. The Cionic Neural Sleeve is a mobility aid that is available by prescription only.

“Digital therapeutics are set to transform healthcare, not only through continuous monitoring of patient metrics, but also by delivering real-time care personalized to individual needs. This will only happen through deep collaboration with healthcare providers,” said Jeremiah Robison, CIONIC Founder & CEO. “We are proud to work with IMSMP, Jersey Shore University Medical Center, and MedStar Health to deliver a unified care experience with the Neural Sleeve from the clinic to the home, setting a new standard for mobility care.”

“For over sixty years, IMSMP has provided individuals living with multiple sclerosis industry-leading care that prioritizes access to the latest research,” said Dr. Saud Sadiq, Medical Director of IMSMP. “Our comprehensive, holistic approach addresses the full continuum of care, which includes making the most advanced technology available to our patients and empowering them to live full and independent lives.” Together with partner organization Tisch MS Research Center of New York, their New York City-based facilities make up the largest independently-funded MS center in the world.

“The work we do at our MS Center focuses on providing care that addresses patient needs at every step of their journey with their illness, from diagnosis through treatment,” said David Duncan, M.D., medical director of the MS Center at Jersey Shore University Medical Center, a National Multiple Sclerosis Society designated Center for Comprehensive MS Care. “By integrating innovative technologies like the Neural Sleeve into patient care, we deliver on our commitment to providing the full breadth of resources available to assist our patients with living active and healthy lives.”

CIONIC Centers of Excellence are leading neurological rehabilitation centers that represent the gold standard for patient care. In strategic collaboration with these centers, patients will have an opportunity to experience the Cionic Neural Sleeve under the guidance and expertise of staff. Current Centers of Excellence include Shirley Ryan AbilityLab, the number-one ranked rehabilitation hospital in the country, according to U.S. News & World Report, UCHealth University of Colorado Hospital, the region’s largest adult academic medical center, Craig Hospital, a world-renowned rehabilitation hospital that exclusively specializes in neurorehabilitation, and Neuro Physical Therapy, a distinguished physical therapy practice.

How the Cionic Neural Sleeve Works

Backed by clinical evidence and FDA-cleared, the award-winning Cionic Neural Sleeve analyzes, predicts, and augments an individual’s movement. It uses a dense array of sensors to measure the firing patterns of individual muscles and the resultant position of the leg during movement. Algorithms running on the sleeve analyze this data in real-time to predict intended movement and determine optimal muscle activation patterns. The Cionic Neural Sleeve then delivers Functional Electrical Stimulation to sequence proper muscle firing for natural movement. It is an adaptive system that provides real-time augmentation and adjustment of the wearer’s movement, updating each time they take a step. The Cionic Neural Sleeve has been recognized in numerous global design and healthcare competitions, including TIME Best Inventions, the Digital Health Hub Awards, Fierce Life Sciences Innovation Awards, Fast Company World Changing Ideas, MedTech Innovation Awards, International Design Excellence Awards, iF DESIGN AWARD, Edison Awards, and more.

Positive 6 Month Results from CroíValve’s TANDEM I Study to Treat Tricuspid Regurgitation Presented at New York Valves 2024

TANDEM I Study
W. Wojakowski , New York Valves Jun 2024

Favorable patient outcomes from the TANDEM I first-in-human clinical trial of the CroíValve DUO™ System for the percutaneous treatment of tricuspid regurgitation (TR) were presented today by Professor Wojciech Wojakowski at the New York Valves 2024 scientific conference. The DUO System is a novel transcatheter coaptation valve that works in tandem with the native tricuspid valve to restore valve function, using an anchor system which leaves the right heart and native valve apparatus untouched.

TR is a severe heart condition that occurs when the tricuspid valve, on the right side of the heart, fails to close properly. This results in blood being pumped backwards into the right atrium and venous system causing debilitating symptoms. It affects over 1.6 million people in the US and is associated with significant morbidity and reduced life expectancy.

The TANDEM I trial is a prospective, non-randomized, multicenter study designed to evaluate the safety and performance of the DUO System in patients with severe symptomatic TR. The study reported on 10 patients enrolled, showing sustained positive outcomes.

Dr Martin Quinn, CMO of CroíValve

“We are encouraged by these data, which demonstrate the DUO’s success in reducing TR and improving patients’ Quality of Life. Our goal is to expand the reach of treatment option for patients with tricuspid valve disease. We are committed to building strong evidence to support emerging therapies like the DUO System, with further clinical studies and patient follow-ups underway.”

Following 30-day outcomes presented last year, the six-month results demonstrated significant TR reduction by an independent core lab assessment, with TR reduced to moderate or less in over 85% of patients, even with massive or torrential TR at baseline. Patients also experienced markedly improved functional and Quality of Life outcomes, with a notable significant increase in both KCCQ score and 6MWT over baseline. The trial reported a 100% survival rate at 6 months. No incidences of arrhythmia or conduction disorder requiring permanent pacing were reported, demonstrating the advantages of avoiding right heart contact. Additionally, this data shows stable long-term device positioning and function, while supporting natural reverse remodeling. The simplified procedural experience was highlighted by an average device time of 43 minutes, even with first use cases.

“The six-month results with the DUO System are highly promising, not only for its clinical safety and efficacy, but also for the procedure’s simplicity and the technology’s broad applicability,” stated Professor Wojtek Wojakowski, Chief, Division of Cardiology and Structural Heart Diseases at the Medical University of Silesia in Poland. “This system offers new hope for patients suffering from severe TR, providing a versatile and predictable treatment option that simplifies the procedural and imaging experience for operators.”

The DUO System is delivered using percutaneous techniques and is secured using a novel anchor system which leaves the right heart and native valve apparatus untouched. The implant procedure is straightforward, uses standard imaging and is suitable for a broad patient cohort as it is independent of annular diameter, coaptation gap, leaflet morphology and visibility.

 

Medical Laser Market to Be Worth $17.3 Billion by 2031

Medical lasers are devices that use precisely focused light sources for treating or removing tissues. Since lasers can focus accurately on tiny areas, they are used for precise surgical works or for cutting through tissue in place of a scalpel. Lasers are commonly employed in many medical disciplines, including dermatology, dentistry, cardiology, neurosurgery, and eye surgery, because of their ability to deliver high-precision treatments while remaining minimally invasive. Laser-based therapies and diagnostic methods represent an area of huge future potential. The increasing number of cosmetic procedures, rising preference for minimally invasive procedures, and increasing prevalence of eye disorders are the major factors supporting the growth of the market.

The growth of medical tourism is expected to provide significant growth opportunities for market players. However, factors such as the high cost of lasers, stringent safety regulations, and risks associated with lasers are expected to hamper the growth of the market.

The medical laser market is segmented by type (device type (solid-state laser devices (neodymium yttrium aluminum garnet laser devices (Nd:YAG), erbium yttrium aluminum garnet laser devices (Er:YAG), holmium yttrium aluminum garnet laser devices (Ho:YAG), alexandrite laser devices, potassium titanyl phosphate laser devices, ruby laser devices), gas laser devices (CO2 laser devices, excimer laser devices, argon laser devices, helium-neon (he-ne) laser devices, krypton laser devices, metal vapor (copper and gold) laser devices), diode laser devices, dye laser devices), fiber type (disposable laser fibers, reusable laser fibers)), application (device application (dermatology, ophthalmology, urology, dentistry, cardiology, gynecology, other device applications), fiber application (general surgeries, urology, dermatology, gynecology, cardiology, dentistry, other fiber applications)). The study also evaluates industry competitors and analyzes the market at the regional and country levels. The study also evaluates industry competitors and analyzes the market at geographical levels.

Get a Glimpse Inside: Request Sample Pages- https://www.meticulousresearch.com/request-sample-report/cp_id=5196

Based on type, the medical laser market is segmented into device type and fiber type. In 2024, the device type segment is expected to account for the larger share of the medical laser market. However, the fiber type segment is projected to register the highest CAGR during the period.

Based on device type, the medical laser devices market is segmented into solid-state laser devices, gas laser devices, diode laser devices, and dye laser devices. In 2024, the solid-state laser devices segment is expected to account for the largest share of around 45% of the medical laser devices market. The large market share of this segment is attributed to the increasing use of solid-state lasers in medical applications, such as treatment processes for scar removal, melisma treatment, and skin resurfacing, which has encouraged various healthcare facilities to adopt these lasers for performing treatments. Various advantages associated with solid-state lasers, such as high efficiency compared to gas lasers, simple construct than to other lasers, and economical nature of solid-state lasers, are driving the growth of this segment.

Based on fiber type, the medical laser fibers market is segmented into disposable laser fibers and reusable laser fibers. In 2024, the disposable laser fibers segment is expected to account for the larger share of around 75% of the medical laser fibers market. The large market share of this segment is attributed to the increasing use of laser fiber in diagnostic procedures, rising demand for non-invasive surgical procedures, the effective cost of disposable laser fibers, and increasing number of urologic and plastic surgery procedures

Have Specific Research Needs? Request a Customized Report- https://www.meticulousresearch.com/request-customization/cp_id=5196

Based on application, the medical laser market is segmented into device application and fiber application. In 2024, the device application segment is expected to account for the larger share of the medical laser market. However, the fiber application segment is projected to register the highest CAGR during the period.

Based on device application, the medical laser devices market is segmented into dermatology, ophthalmology, urology, dentistry, cardiology, gynecology, and other device applications. In 2024, the dermatology segment is expected to account for the largest share of around 30% of the medical laser devices market. The large market share of this segment is attributed to the increasing number of cosmetic surgeries simultaneously increasing the use of medical lasers in these treatments and increasing integration of AI technology for dermatology applications. These lasers are used for various treatments, such as vascular lesions, pigmented lesions and tattoos, hair removal, facial wrinkles, scars, sun-damaged skin, and skin cancers.

Based on fiber application, the medical laser fibers market is segmented into general surgeries, urology, dermatology, gynecology, cardiology, dentistry, and other fiber applications. In 2024, the general surgeries segment is expected to account for the larger share of above 27% of the medical laser fibers market. The large market share of this segment is attributed to the growing prevalence of colon cancer, appendicitis procedures, pancreatic cancer, and small and large intestine cancers. Medical laser fibers perform highly efficient surgeries and reduce the risk of cross-contamination between surgeries, increasing the demand for medical laser fibers.

Based on geography, the medical laser market is segmented into North America, Europe, Asia-Pacific, Latin America, and the Middle East & Africa. In 2024, North America is expected to account for the largest share of around 45% of the medical laser market. The market growth in North America is driven by the presence of major vendors in the region, technological advancements in medical devices, government investments to promote innovation in the healthcare segment and the exponential growth of aesthetic/cosmetic procedures. The aging population in the U.S. is creating the need for major surgeries related to geriatric populations, such as ophthalmic surgeries, including cataracts, glaucoma, cardiovascular surgeries, and urological surgeries, driving the demand for medical lasers in this region.

The key players operating in the medical laser market are Lumenis Ltd. (Israel), Fotona d.o.o. (Slovenia), BIOLASE, Inc. (U.S.), IRIDEX Corporation (U.S.), Cutera, Inc. (U.S.), Alna-Medicalsystem AG & Co. KG (Germany), Bausch & Lomb Incorporated (U.S.), Boston Scientific Corporation (U.S.), Alcon, Inc. (Switzerland), Stryker Corporation (U.S.), Alma Lasers (Israel), biolitec AG (Germany), Bluecore, Inc. (South Korea), Cynosure LLC (U.S.), PhotoMedex (U.S.) and Spectranetics (U.S.) MED-Fibers, INC.(U.S.), Clarion Medical Technologies (Canada), Olympus Corporation (Japan).

Browse In-depth Report Now- https://www.meticulousresearch.com/product/medical-lasers-market-5196

Scope of the Report:

Medical Laser Market Assessment—by Type

  • Device Type
    • Solid-State Laser Devices
      • Neodymium Yttrium Aluminum Garnet Laser Devices (Nd:YAG)
      • Erbium Yttrium Aluminum Garnet Laser Devices (Er:YAG)
      • Holmium Yttrium Aluminum Garnet Laser Devices (Ho:YAG)
      • Alexandrite Laser Devices
      • Potassium Titanyl Phosphate Laser Devices
      • Ruby Laser Devices
    •  Gas Laser Devices
      • CO2 Laser Devices
      • Excimer Laser Devices
      • Argon Laser Devices
      • Helium-Neon (He-Ne) Laser Devices
      • Krypton Laser Devices
      • Metal Vapor (Copper and Gold) Laser Devices
    • Diode Laser Devices
    • Dye Laser Devices
  • Fiber Type
    • Disposable Laser Fibers
    •  Reusable Laser Fibers

Medical Laser Market Assessment—by Application

  • Device Application
    • Dermatology
    • Ophthalmology
    • Urology
    • Dentistry
    • Cardiology
    • Gynecology
    • Other Device Applications
  • Fiber Application
    • General Surgeries
    • Urology
    • Dermatology
    • Gynecology
    • Cardiology
    • Dentistry
    • Other Fiber Applications

 Medical Laser Market Assessment—by Geography

  • North America
    • U.S.
    • Canada
  • Europe
    • Germany
    • U.K.
    • France
    • Italy
    • Spain
    • Rest of Europe
  • Asia-Pacific
    • Japan
    • China
    • India
    • South Korea
    • Rest of Asia-Pacific
  • Latin America
    • Mexico
    • Brazil
    • Rest of Latin America
  • Middle East & Africa
    • UAE
    • Israel
    • Rest of Middle East & Africa

IQAir Introduces New XE Smart Air Purifiers

IQAir, a Swiss air quality technology company, launches their new XE air purifiers, the next generation of their best-selling high-performance air purifiers, in North America.

IQAir XE air purifiers feature a redesigned fan system that is up to three times more energy efficient than previous models. With Wi-Fi smart app integration, the air purifiers can be remotely controlled and fully integrated with IQAir’s AirVisual air quality app and platform. The XEs also include three smart modes, allowing for sensor-based operation and prompting automatic adjustment of the air purifier performance based on measured air quality.

Designed and made in Switzerland, the XE line also includes an advanced particle sensor that measures harmful fine particulate pollutants (PM2.5), for real-time insight of indoor air. PM2.5 includes a wide range of pollutants, including smoke, dust, pollen, mold spores, house dust mites, and pet allergens. The HealthPro XE utilizes IQAir’s patented HyperHEPA filtration, which captures over 99.5% of harmful ultrafine pollution particles and biological contaminants down to 0.003 microns in size. This includes particulate matter equal in size of bacteria and viruses such as those that cause COVID-19, the flu, and even the common cold.

Frank Hammes, Global CEO, IQAir.

“The XE line pairs the newest air quality monitoring technology with our award-winning, ultra efficient filtration. Built-in air quality sensors allow the system to automatically adjust filtration according to indoor air quality. This saves energy, extends filter life, and fully automates the removal of even the smallest particles from the air.”

For the North American market, the enhanced features of the XE air purifiers are incorporated into four of IQAir’s popular air purifiers and are now available on iqair.com/us/:

  • HealthPro Plus XE is priced at $1,199
  • HealthPro Compact XE is priced at $1,099
  • GC MultiGas XE is priced at $1,599
  • GCX MultiGas XE is priced at $2,499

B. Braun Launches ACCEL®: Pioneering Interventional Systems

B. Braun Interventional Systems Inc. (BIS), a member of the B. Braun Group of Companies, announced today the launch of its new ACCEL® All-Purpose and Biliary Drainage Catheters with TrueGlide® Hydrophilic Coating for percutaneous drainage.

The ACCEL All-Purpose and Biliary Drainage Catheters are designed for optimal patient comfort and clinical care. The catheter features large oval holes designed to maximize fluid drainage volume, while the TrueGlide Hydrophilic Coating helps with a smooth catheter insertion.

Dave Mittl, Vice President of BIS

“We are excited to expand our percutaneous drainage portfolio of products with the ACCEL All-Purpose and Biliary Drainage Catheters, now offering a full-system drainage solution to our customers and bringing value to their drainage procedures. Our comprehensive portfolio of sizes and configurations is designed to meet patients’ various drainage needs to help improve outcomes.”

Over the last two decades, BIS has continuously expanded its percutaneous drainage product offerings, responding to the market needs and bringing solutions focused on increasing the value, safety and efficiency of drainage procedures. The latest addition of the all-purpose and biliary drainage catheters completes the portfolio as a full-system drainage solution, providing convenience and options for percutaneous fluid drainage management.

 

Ambulatory EHR Market to be Worth $7.84 billion by 2031 – Exclusive Report

Meticulous Market Research reports: According to a new market research report, “Ambulatory EHR Market Size, Share, Forecast, & Trends Analysis by Deployment Mode (Cloud, On-premise) Type (All-in-one, Modular) Application (Practice, Patient Portal, CPOE, CDS, Referral, Population Health) End User, Practice — Global Forecast to 2031,” published by Meticulous Research, the ambulatory EHR market is expected to reach $7.84 billion by 2031, at a CAGR of 5.3% from 2024 to 2031.

Download Sample Report Now

Ambulatory electronic health record (EHR) software is designed for outpatient care settings, enabling medical professionals to access a patient’s complete medical history stored in an electronic format. This data includes records of treatments and procedures conducted outside of hospital admissions. Ambulatory EHR systems facilitate easier monitoring of a patient’s medical history and long-term care by physicians. Through this software, physicians can gather detailed and relevant information about each patient, resulting in comprehensive personal health records. This extensive database helps doctors gain a deeper understanding of a patient’s health, thereby simplifying potential diagnoses.

The growth of the ambulatory EHR market is driven by supportive government initiatives aimed at promoting EHR adoption, the rising preference for ambulatory care over in-patient services among patients, and the rising need to reduce operational costs in the healthcare sector. Additionally, the integration of artificial intelligence (AI) and machine learning (ML) technologies with ambulatory EHRs and the evolving technological landscape in developing countries are expected to create market growth opportunities. However, IT infrastructure constraints in developing nations, concerns about data security, and high implementation costs may restrain market growth.

The report also includes an extensive assessment of leading players’ product portfolios and geographic presence and the key growth strategies adopted by them over the past three to four years. In recent years, the ambulatory EHR market has witnessed several organic and inorganic strategic developments. The key players profiled in the ambulatory EHR market report are Epic Systems Corporation (U.S.), Cerner Corporation (U.S.), Medical Information Technology, Inc. (U.S.), Computer Programs and Systems, Inc. (U.S.), Allscripts Healthcare Solutions, Inc. (U.S.), athenahealth, Inc. (U.S.), NextGen Healthcare, Inc (U.S.), eClinicalWorks (U.S.), Greenway Health, LLC (U.S.), CureMD Healthcare (US), and AdvancedMD, Inc. (U.S.).

Get a Glimpse Inside: Request Sample Pages- https://www.meticulousresearch.com/request-sample-report/cp_id=5190

Rising Need to Reduce Operating Costs in the Healthcare Sector Driving Market Growth

Many hospitals and health systems are currently dealing with escalating operating costs. Electronic health records are known to improve the efficiency of medical practice. Operating costs can be reduced by lowering transcription costs, reducing time spent on documentation, improving documentation for billing, and limiting or eliminating chart pull, storage, and re-filing costs. Studies indicate that adopting EHRs can result in significant cost savings. Hospitals and practices leveraging EHR software can effectively manage expenditures. For instance, data published in the American Journal of Managed Care suggests that patients admitted to hospitals with EHRs may pay up to USD 730 less than those admitted to hospitals without EHRs, primarily due to enhanced efficiency.

Additionally, substantial financial losses are incurred due to medical errors, encompassing expenses for patients requiring treatment to recover from such errors and the high costs of malpractice lawsuits. According to the Commonwealth Fund, medical errors are estimated to cost between USD 17 billion to USD 29 billion annually. The implementation of EHRs can play a pivotal role in reducing these costs by minimizing errors.

The ambulatory EHR market is segmented by Deployment Mode (Cloud/Web-based Ambulatory EHR, On-premise Ambulatory EHR), Type (All-in-one Ambulatory EHR, Modular Ambulatory EHR), Practice Size (Large Practices, Small to Medium-sized Practices, Solo Practices), Application (Practice Management, Computerized Physician Order Entry (CPOE), Patient Portals, Clinical Decision Support (CDS), Referral Management, and Other Applications), End User (Hospital-owned Ambulatory Centers, Independent Ambulatory Centers), and Geography.

Among the deployment modes covered in this report, in 2024, the cloud/web-based ambulatory EHR segment is expected to account for the larger share of 77.5% of the ambulatory EHR market. This segment’s large market share can be attributed to the advantages of cloud-based deployments, including flexibility, real-time monitoring, data security, and lower implementation costs compared to on-premise deployments. Some of the key companies offering cloud/web-based ambulatory EHRs are Epic Systems Corporation (U.S.), Cerner Corporation (U.S.), Medical Information Technology, Inc. (U.S.), Allscripts Healthcare Solutions, Inc. (U.S.), Greenway Health, LLC (U.S.), eClinicalWorks (U.S.), and CureMD Healthcare (U.S.).

Have Specific Research Needs? Request a Customized Report

Among the types covered in this report, in 2024, the all-in-one ambulatory EHR segment is expected to account for the larger share of the market. This segment’s large market share can be attributed to the benefits offered by all-in-one ambulatory EHRs, such as ease of use, comprehensive functionalities, absence of compatibility issues, and seamless integration of software and hardware.

Among the practice sizes covered in this report, in 2024, the large practices segment is expected to account for the largest share of the market. Large practices are typically conducted within sizable organizations housing over 50-100 physicians. This segment’s large market share can be attributed to the rising need for efficient administration and coordination within such extensive setups and equitable distribution of costs and tasks among staff. Moreover, the acquisition of smaller ambulatory surgical centers by larger players contributes to the segment’s significant market share. For instance, in October 2023, SurgNet Health Partners, Inc. (U.S.) announced the acquisitions of Executive Ambulatory Surgery Center (U.S.) and Lippy Surgery Center (U.S.).

Among the applications covered in this report, in 2024, the practice management segment is expected to account for the largest share of 25.9% of the market. Practice management typically encompasses appointment scheduling, patient demographics, visual resource planning, document management, billing, and claim management—all essential components utilized in the daily operations of ambulatory practices. This segment’s large market share can be attributed to factors such as the widespread adoption by ambulatory surgical centers, primarily due to the advanced features offered by these EHRs, including efficient patient scheduling and streamlined management of billings and claims.

Among the end users covered in this report, in 2024, the hospital-owned ambulatory centers segment is expected to account for the larger share of the market. Hospital-owned ambulatory centers, integrated within hospitals, represent a prevalent clinical model in integrated healthcare systems. This segment’s large market share can be attributed to the robust financial capabilities of these centers, facilitating significant investments in advanced EHRs and the benefits offered by these EHRs, including improved coordination of patients’ medical records and adherence to higher patient safety and quality guidelines. Additionally, the increasing need to streamline unstructured healthcare data further drives the adoption of ambulatory EHRs within these centers.

Geographically, in 2024, North America is expected to account for the largest share of 51.2% of the ambulatory EHR market, followed by Europe and Asia-Pacific. North America’s significant market share can be attributed to factors such as the proliferation of ambulatory surgery centers and the presence of leading EHR providers within the region. Furthermore, supportive government initiatives aimed at promoting EHR adoption contribute to the growth of this regional market. For instance, Canada Health Infoway (CHI) has launched initiatives to promote the adoption and utilization of EHR systems. It aims to establish a national infrastructure that facilitates the sharing of EHR systems across Canada.

However, the Asia-Pacific ambulatory HER market is projected to register the highest CAGR during the forecast period.

Scope of the Report:

Ambulatory EHR Market—by Deployment Mode

  • Cloud/Web-based Ambulatory EHR
  • On-premise Ambulatory EHR

Ambulatory EHR Market—by Type

  • All-in-one Ambulatory EHR
  • Modular Ambulatory EHR

Ambulatory EHR Market—by Practice Size

  • Large Practices
  • Small-to-medium-sized Practices
  • Solo Practices

Ambulatory EHR Market—by Application

  • Practice Management
  • Patient Portals
  • Computerized Physician Order Entry (CPOE)
  • Clinical Decision Support (CDS)
  • Population Health Management
  • Referral Management
  • Other Applications

(Other applications include mobile solutions, health analytics, billing solutions, and telehealth)

Ambulatory EHR Market—by End User

  • Hospital-owned Ambulatory Centres
  • Independent Ambulatory Centres

Ambulatory EHR Market—by Geography

  • North America
    • U.S.
    • Canada
  • Europe
    • Germany
    • France
    • U.K.
    • Italy
    • Spain
    • Denmark
    • Netherlands
    • Sweden
    • Ireland
    • Belgium
    • Rest of Europe (RoE)
  • Asia Pacific
    • China
    • Japan
    • India
    • Rest of APAC (RoAPAC)
  • Latin America
  • Middle East & Africa

Unlock Opportunities: Buy Now- https://www.meticulousresearch.com/Checkout/22865064

Related Reports:

Mid-revenue Cycle Management/ Clinical Documentation Improvement Market by Product & Service [Solutions (Coding, Charge Capture, DRG Group, Pre-Bill Review), Consulting Services], End User (Providers, Payers), and Geography – Global Forecast to 2027

Healthcare Analytics Market by Type (Predictive, Prescriptive), Component (Hardware, Software, and Services), Delivery Mode (Cloud), Application (Clinical, RCM, Claims, Fraud, Risk, PHM), End user (Payer, Provider) and Geography- Global Forecast to 2027

Healthcare Artificial Intelligence Market by Product and Services (Software, Services), Technology (Machine Learning, NLP), Application (Medical Imaging, Precision Medicine, Patient Management), End User (Hospitals, Patients) — Global Forecast to 2027

Global Carotid Artery Stent Market to Grow Substantially at a CAGR of ~3% by 2030

DelveInsight’s Carotid Artery Stent Market Insights report provides the current and forecast market analysis, individual leading carotid artery stent companies’ market shares, challenges, carotid artery stent market drivers, barriers, trends, and key market carotid artery stent companies in the market.

Key Takeaways from the Carotid Artery Stent Market Report

  • As per DelveInsight estimates, North America is anticipated to dominate the global carotid artery stent market during the forecast period.
  • In the product type segment of the carotid artery stents market, the self-expanding stents category had a significant revenue share in the year 2023. This can be attributed to the various applications and advantages associated with the self-expanding stents such as self-expanding stents adapt to the anatomy of the carotid area.
  • Notable carotid artery stent companies such as Boston Scientific Corporation, Cordis, Balton, Medtronic, Terumo Europe NV, Silk Road Medical Inc., InspireMD Inc., and several others, are currently operating in the carotid artery stent market.
  • In October 2023, Boston Scientific Corporation got approval for its Carotid WALLSTENT® Monorail® from USFDA for the treatment of carotid artery disease.
  • In October 2022, Cordis a leader in the development and manufacturing of interventional cardiovascular and endovascular technologies, acquired MedAlliance.

To read more about the latest highlights related to the carotid artery stent market, get a snapshot of the key highlights entailed in the Global Carotid Artery Stent Market Report

Carotid Artery Stent Overview

Carotid artery stenting is a minimally invasive procedure used to treat carotid artery disease, a condition where the carotid arteries, located in the neck, become narrowed or blocked by the buildup of plaque. During the procedure, a slender tube called a catheter is inserted into an artery, usually in the groin, and guided to the carotid artery under X-ray imaging. Once in place, a stent—a small mesh tube—is expanded within the narrowed portion of the artery, pushing aside the plaque and restoring blood flow to the brain. This technique is an alternative to carotid endarterectomy, a surgical procedure that involves opening the carotid artery and removing the plaque.

While carotid artery stenting is less invasive compared to surgery, it’s not without risks. Complications can include stroke, bleeding at the puncture site, or the formation of blood clots. However, for certain patients, such as those deemed high-risk for surgery due to other health conditions, or those with difficult-to-reach blockages, carotid artery stenting can be a valuable treatment option. It offers a shorter recovery time and avoids the need for general anesthesia, making it a preferred choice for some individuals. Close monitoring and careful patient selection are crucial to ensure the best possible outcomes.

Carotid Artery Stent Market Insights

In 2023, North America dominated the carotid artery stents market, mainly due to the increasing incidence of cardiovascular diseases and associated risk factors like obesity, hypertension, and diabetes. Factors like government initiatives, high disposable income, a growing aging population, and advanced healthcare facilities further drive market growth in the region.

According to the Centers for Disease Control and Prevention (CDC) in 2022, around 18.2 million adults in the US suffer from coronary artery disease, with approximately 805,000 experiencing heart attacks annually, a significant portion being first-time occurrences. Moreover, the elderly population, especially those over 50, are particularly susceptible to carotid artery disease due to age-related arterial changes.

The United States Census Bureau’s 2021 report indicates that over 54 million adults aged 65 and older lived in the US, and this demographic is expected to reach 85.7 million by 2050, constituting about 20% of the total population. This aging population contributes to the rising demand for carotid artery stents.

Furthermore, the presence of major industry players like Boston Scientific Corporation, Cordis, and Silk Road Medical Inc. headquartered in North America also bolsters the carotid artery stent market growth in the region. Consequently, the increasing prevalence of cardiovascular diseases and the concentration of key market players are driving the expansion of the carotid artery stent market in North America.

To know more about why North America is leading the market growth in the carotid artery stent market, get a snapshot of the Carotid Artery Stent Market Outlook 

Carotid Artery Stent Market Dynamics

The carotid artery stent market has seen significant dynamics over the past few years, driven by a combination of technological advancements, evolving healthcare policies, and increasing prevalence of carotid artery diseases. Carotid artery stenting has emerged as a minimally invasive alternative to traditional surgical interventions for treating carotid artery stenosis, offering reduced recovery times and fewer complications for patients. As a result, the demand for carotid artery stents has been steadily increasing, particularly among aging populations where vascular diseases are more prevalent.

One of the key drivers shaping the carotid artery stent market dynamics is the growing adoption of endovascular procedures by healthcare providers. With advancements in stent design, materials, and delivery systems, carotid artery stenting has become safer and more effective, leading to its wider acceptance as a treatment option. Moreover, the rise in awareness campaigns about stroke prevention and early detection of carotid artery diseases has further fueled the demand for stenting procedures.

However, despite these advancements, challenges persist in the carotid artery stent market. Issues such as stent thrombosis, restenosis, and embolization remain concerns, necessitating ongoing research and development efforts to improve stent design and minimize complications. Additionally, regulatory hurdles and reimbursement policies can impact carotid artery stent market growth, influencing the adoption rates of carotid artery stenting procedures in different regions.

Looking ahead, the carotid artery stent market is poised for continued growth, driven by factors such as an aging population, increasing prevalence of vascular diseases, and ongoing innovations in stent technology. With a focus on improving patient outcomes and reducing procedural risks, manufacturers and healthcare providers are likely to invest further in research, development, and training initiatives to expand the accessibility and efficacy of carotid artery stenting procedures.

Get a sneak peek at the carotid artery stent market dynamics @ Carotid Artery Stent Market Dynamics Analysis

Report Metrics

Details

Coverage

Global

Study Period

2021–2030

Carotid Artery Stent Market CAGR

~3%

Carotid Artery Stent Market Size by 2030

USD 718.25 Million

Key Carotid Artery Stent Companies

Boston Scientific Corporation, Cordis, Balton, Medtronic, Terumo Europe NV, Silk Road Medical Inc., InspireMD Inc., among others

Carotid Artery Stent Market Assessment

  • Carotid Artery Stent Market Segmentation
    • Carotid Artery Stent Market Segmentation By Product Type: Self-Expanding Stents, Balloon Expandable Stents, and Others
    • Carotid Artery Stent Market Segmentation By End User: Hospitals & Clinics, Ambulatory Surgical Centers, and Cardiac Centers
    • Carotid Artery Stent Market Segmentation By Geography: North America, Europe, Asia-Pacific, and Rest of World
  • Porter’s Five Forces Analysis, Product Profiles, Case Studies, KOL’s Views, Analyst’s View

Which MedTech key players in the carotid artery stent market are set to emerge as the trendsetter explore @ Carotid Artery Stent Companies

Table of Contents 

1

Report Introduction

2

Executive summary

3

Regulatory and Patent Analysis

4

Key Factors Analysis

5

Porter’s Five Forces Analysis

6

Carotid Artery Stent Market Layout

7

Global Company Share Analysis – Key 3-5 Companies

8

Carotid Artery Stent Market Company and Product Profiles

9

Project Approach

10

About DelveInsight

Interested in knowing the carotid artery stent market by 2030? Click to get a snapshot of the Carotid Artery Stent Market Trends

Related Reports

Ischemic Stroke Pipeline

Ischemic Stroke Pipeline Insight – 2024 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key Ischemic Stroke companies, including Athersys, Inc., Tarveda Therapeutics, Lumosa Therapeutics, NC Medial Research Inc, Acticor Biotech, Meridigen Biotech Co., Prolong Pharmaceuticals, Nanjing Yoko Biomedical Co., Ltd., TrueBinding, Inc., GNT Pharma, Roche, DiaMedica Therapeutics Inc, aptaTargets, Bristol-Myers Squibb, NuvOX Pharma, Simcere Pharmaceutical Co., Ltd., Genentech, Inc., NoNO Inc., Pharming Technologies B.V., Biogen, Avilex Pharma, SanBio, ZZ Biotech, Revalesio, Stemedica Cell Technologies, StemCyte, Ninnion, Algernon Pharmaceuticals, Primary Peptides, TMS, Tasly Pharmaceutical, Pharmazz, among others.

Ischemic Stroke Epidemiology

Ischemic Stroke Epidemiology Forecast – 2032 report delivers an in-depth understanding of the disease, historical, and forecasted ischemic stroke epidemiology in the 7MM.

Acute Ischemic Stroke Market

Acute Ischemic Stroke Market Insight, Epidemiology, and Market Forecast – 2032 report delivers an in-depth understanding of the market trends, market drivers, market barriers, and key acute ischemic stroke companies, including Acticor Biotech, DiaMedica Therapeutics, Lumosa Therapeutics, Bristol Myers Squibb, Janssen Pharmaceutical, Genentech, Inc., Athersy, Healios K.K., NoNO Inc., Bayer, ZZ Biotech, Biogen Inc., Revalesio Corporation, AbbVie, TrueBinding, Inc, Silver Creek Pharmaceuticals, among others.

Acute Ischemic Stroke Pipeline

Acute Ischemic Stroke Pipeline Insight – 2024 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key acute ischemic stroke companies, including Genentech, Acticor Biotech, DiaMedica Therapeutics, and NoNO, among others.

About DelveInsight

DelveInsight is a leading Business Consultant, and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance.

AI Based Wound Care Software Market to Record an Exponential CAGR by 2031 – Exclusive Report by InsightAce Analytic

InsightAce Analytic Pvt. Ltd. announces the release of a market assessment report on the “AI Based Wound Care Software Market”- by Types of Service(s) Offered (Isolated Exosomes, Exosome Characterization, Purification, Chromatography, Engineering, Targeted Delivery, Diagnostic Biomarker, and Quality Control), Method of Exosome Manufacturing (Engineering and Targeted Delivery), Scale of Operation (Discovery / Research, Pre-Clinical, Clinical or Commercialized) and Scalability (Small, Mid-Sized or large), Method of Isolation, Method of Purification, Method of Exosome Characterization, Industry Trends, and Global Forecasts, 2022-2035 And Segment Revenue and Forecast To 2031.

The AI Based Wound Care Software Market is estimated to exhibit a CAGR of 7.1% during the forecast period.

Download Free Report Sample Pages: https://www.insightaceanalytic.com/request-sample/2519

 

Report Attribute

Specifications

Growth Rate CAGR

CAGR of 7.1% from 2024 to 2031

Quantitative Units

Representation of revenue in US$ Bn and CAGR from 2024 to 2031

Historic Year

2019 to 2023

Forecast Year

2024-2031

Report Coverage

The forecast of revenue, the position of the company, the competitive market structure, growth prospects, and trends

Segments Covered

By Wound Type, By Application

Regional Scope

North America; Europe; Asia Pacific; Latin America; Middle East & Africa

Country Scope

U.S.; Canada; U.K.; Germany; China; India; Japan; Brazil; Mexico; The UK; France; Italy; Spain; China; Japan; India; South Korea; Southeast Asia; South Korea; Southeast Asia

List of Prominent Players in the AI Based Wound Care Software Market:

  • Pacify Medical
  • Healogics
  • Swift Medical
  • Healthy.io
  • WoundZoom
  • eKare, Inc.
  • Medline
  • WoundMatrix
  • Entec Solution
  • Essity
  • Spectral AI
  • Urgo Medical

Buy 180 Pages Full Report @ https://www.insightaceanalytic.com/buy-report/2519

Market Dynamics:

Drivers:

The growing incidence of chronic wounds, such as diabetic ulcers, pressure ulcers, and venous leg ulcers, necessitates advanced wound care solutions. Chronic wounds are often challenging to manage, requiring continuous monitoring and tailored treatment plans. AI-based solutions reduce the time and effort required for wound assessment and documentation, allowing healthcare providers to focus more on patient care. With an aging global population, the prevalence of conditions that lead to chronic wounds, such as diabetes and immobility, is on the rise. This demographic trend is driving the demand for innovative wound care technologies.

Challenges:

Healthcare providers face the challenge of justifying the cost of AI solutions in terms of improved patient outcomes and cost savings, a task made more difficult without comprehensive reimbursement policies. Additionally, patients in low-income regions may struggle to afford AI-driven wound care solutions, limiting their widespread adoption. Access to advanced healthcare technologies, including AI-based wound care software, is often restricted in rural and underserved areas due to a lack of infrastructure and resources. This digital divide further hampers the ability of these regions to benefit from the advancements in AI-driven healthcare, exacerbating existing disparities in health outcomes.

Regional Trends:

North America accounted for the largest share of the global wound care market, driven by a large patient population with chronic conditions like diabetes, a high incidence of surgical procedures, and a proactive approach to wound care focused on improving healthcare outcomes. This dominance can be attributed to the presence of advanced healthcare infrastructure, high adoption of digital healthcare technologies, and significant investments in research and development. Countries like the United States and Canada have well-established healthcare systems that prioritize innovation and technology integration. Additionally, the rising prevalence of chronic wounds, such as diabetic ulcers and pressure ulcers, in the region has propelled the demand for AI-based solutions for wound assessment, monitoring, and management.

Curious about this latest version of the report? @ https://www.insightaceanalytic.com/enquiry-before-buying/2519

Recent Developments:

  • In February 2024, Spectral AI, an artificial intelligence (AI) startup with a focus on medical diagnostics to enable quicker and more accurate treatment choices for wound care successfully obtained the last phase of UK Conformity Assessed (UKCA) authorization for DeepView AI-Burn, a predictive program intended to help with burn wound diagnosis in the United Kingdom.
  • In November 2023, Urgo Medical, a well-known business that specializes in advanced wound care and imito AG, a knowledgeable supplier of wound care products, announced a collaboration meant to improve wound care. As a result of this partnership, imito AG’s WoundGenius automatic wound measurement technology was used by Urgo Medical to create a new feature called MEASURE in its wound app, Healico.

Segmentation of AI Based Wound Care Software Market

Global AI Based Wound Care Software Market – By Wound Type

  • Chronic Wounds
    • Diabetic Ulcers
    • Pressure Ulcers
    • Venous Ulcers
  • Acute Wounds
    • Traumatic Injuries
    • Surgical Wounds
    • Burns

Global AI Based Wound Care Software Market – By Application

  • Wound Assessment and Monitoring
  • Wound Healing Prediction
  • Wound Documentation and Management
  • Clinical Decision Support
  • Others

North America

  • The US
  • Canada
  • Mexico

Europe

  • Germany
  • The UK
  • France
  • Italy
  • Spain
  • Rest of Europe

Asia-Pacific

  • China
  • Japan
  • India
  • South Korea
  • Southeast Asia
  • Rest of Asia Pacific

Latin America

  • Brazil
  • Argentina
  • Rest of Latin America

 Middle East & Africa

  • GCC Countries
  • South Africa
  • Rest of the Middle East and Africa

MiRus Siegel ™ TAVR: First in Human Results Presented at New York Valves

MiRus Siegel ™ TAVR
MiRus Siegel™ TAVR

MiRus, LLC. reported that Pradeep K. Yadav MD, Director of Structural Interventions, Piedmont Heart Institute, Atlanta presented the initial experience with the MiRus Siegel™ 8-Fr aortic transcatheter heart valve (THV) at the New York Valves conference.

Five sequential patients with severe, symptomatic aortic stenosis (AS) were treated at the Instituto Nacional Del Torax in Santiago, Chile by Drs. C. Dauvergne, J. Sandoval and P. Yadav. Three patients had bicuspid aortic valves and two were tri-leaflet. Three patients had peripheral arterial disease with vascular access < 5.5 mm. There was no mortality or stroke at 30 days and no patients required a permanent pacemaker (PPM) or suffered vascular complications. At 30 days, the mean echo gradient was 6.7 mmHg; four of the five patients had no peri-valvular leak (PVL) and one bicuspid patient had trace PVL.

“The ease of use and hemodynamics were impressive” commented Pradeep K. Yadav, MD. “On the very first case, we comfortably achieved a deployment with 90% aortic and 10% ventricular positioning. The lack of foreshortening is very helpful in precise deployment every time, a feature that implanters will love. Also the frame strength and virtually no recoil, allows cylindrical valve expansion with no waist even in complex bicuspid patients, which contributes to excellent hemodynamics and hopefully durability.”

The Siegel valve represents several firsts in TAVR: 8 French delivery sheath allowing less invasive procedures and broader patient access, particularly for women; the only Nickel-free THV allowing treatment of the 20% of Americans suffering from Nickel allergies; precise delivery due to lack of foreshortening and intrinsic commissural alignment; dry porcine pericardial leaflets with anti-calcification treatment and with the valve pre-mounted on the balloon.

The combination of low delivery system profile and excellent hemodynamics is made feasible by the unique properties of the Rhenium alloys pioneered by MiRus including high yield strength, fatigue resistance and minimal recoil.

“This initial data is striking and potentially heralds a new age for TAVR,” stated Vinod H. Thourani MD, Marcus Chairman of Cardiovascular Surgery and the Marcus Valve Center, Piedmont Heart Institute. “The ability to treat such complex patients with an 8 French system and without Nickel exposure should make TAVR safer and more broadly accessible. From a surgical viewpoint, the very low pressure gradients and low PVL are critically important to implanters and our patients. We are truly on the precipice of surgical-like outcomes with the Siegel THV!!”

Applied Medical Technology Launches IntelAir™, a Nasopharyngeal Airway

Applied Medical Technology, Inc. (AMT), a global leader in manufacturing medical devices, today announced the debut of IntelAir™, a nasal airway support system. The single-use device is intended to ensure airway securement, avoid cannula migration, and maintain a clear airway.

Used during monitored anesthesia to support the soft palate and tongue in sedated patients, the IntelAir™ champions both clinician needs and patient comfort. Its anatomical shape is designed to reduce bleeding and trauma during insertion. The medical-grade silicone bolster and gentle adhesive attach to the nose while protecting the ala against pressure injury. Of interest to clinicians, the device provides protection against tube migration, reliable oxygen delivery, and consistent end tidal monitoring.

We designed the IntelAir™ to fulfill a market need; while some devices focused on patient needs and others on clinician needs, none appropriately served both. With this all-in-one device, users can benefit from the streamlined approach paired with AMT’s commitment to excellence,” reflected Dr. George Picha M.D., Ph.D., F.A.C.S., Founder & CEO of Applied Medical Technology, Inc.

AMT adds the IntelAir™ to its ever-growing surgical line portfolio, which includes suture delivery systems, initial placement kits, smoke evacuators, retractors, and more.

The IntelAir™ is available for sale now with and without tubing in varying lengths.