Prevent sleep-related traffic accidents! Screen for sleep apnea!
Obstructive sleep apnea syndrome (OSAS), a sleep-related breathing disorder, is not only an independent risk factor for hypertension, but it also raises the risk of both traffic accidents and cardiovascular mortality.
Screen for OSAS with Meditech apneABP, an ambulatory blood pressure monitor with OXY (SpO2) module, which can be used for early recognition in primary care.
Meditech apneABP features and benefits
– full 24-hour blood pressure profile for diagnosing hypertension – full SpO2 profile for diagnosing apneic episodes – full actigraphy profile for monitoring physical activity levels – pulse waveforms for an insight on artery conditions
In around 30% of all patients undergo a polysomnography, no apnea is detected. Meditech apneABP is a reliable and inexpensive tool to screen for apnea in your hypertensive patients in primary care. Read more
With up to twice higher signal levels than 1.5T systems, 3.0T MR systems improve spatial resolution and therefore provide more information on very fine anatomical structures. Typically, 3.0T MRIs are common in academic and research hospitals. Now the SIGNA Pioneer brings the power of 3.0T for clinical use and it is designed for accessibility to a broader range of healthcare providers. The SIGNA Pioneer 3.0T MRI delivers the ease-of-use and flexibility of a 1.5T system, with improved image homogeneity and reproducibility for oncology and spine imaging for example. In addition, ultra-high efficiency gradient technology enables high performance, even during demanding clinical applications such as cardiology or oncology. Using equivalent imaging parameters, physicians can use the signal gain to shorten patients’breath-holds for liver exploration; SIGNA Pioneer also enables free-breathing body imaging for a much improved patient experience but also image quality in very challenging situations. The new MAGiC sequence is a major innovation in neuroimaging enabling clinicians to generate six contrasts in a single scan and in as little as one-third of the total time taken to acquire each contrast separately using conventional techniques. After an acquisition of only approximately 5 minutes, it is now possible to adjust the image contrast in real time, even after completing the scan, by simply moving a dynamic cursor to change conventional MRI acquisition parameters (TE, TR and TI) depending on the disease or the age of the patient. MAGiC also provides quantitative information (maps T1, T2, and proton density) that opens new perspectives for the characterization and monitoring of lesions. This has the potential to provide physicians the ability to detect and characterize earlier and more precisely small or secondary lesions, improving the diagnosis and monitoring of patients with neurodegenerative disorders, and enabling the adjustment of the treatment of cancer patients. Patients with neurodegenerative disease, who cannot remain still during the examinations, can also now benefit from MR. With new advanced 3D motion correction software, SIGNA Pioneer will compensate patient movement to provide the same image quality and comfort for diagnosis despite involuntary movements. An enhanced SilentScan package also dramatically reduces scan noise from excess of 110 decibels (dBA) for conventional MRI scans to just three dBA above ambient noise for most head exams, a major differentiator for patient comfort and to minimize the risk of deteriorating image quality in anxious patients. Read more
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Medtronic has received CE Mark for Micra™ AV Transcatheter Pacing System (TPS), the world’s smallest pacemaker with atrioventricular (AV) synchrony. Micra AV is indicated for the treatment of patients with AV block, a condition in which the electrical signals between the chambers of the heart (the atria and the ventricle) are impaired. Medtronic now offers the only CE Mark approved leadless pacemaker portfolio. First implants of Micra AV recently occurred in Spain by Dr. José Ramón González Juanatey at the University Hospital in Santiago de Compostela.
“This new device not only stimulates but is also able to recognize the electrical activity of the whole heart. Now we can extend this wireless technology to our patients who require dual chamber stimulation and in whom traditional stimulation cannot be performed or is conditioned by previous infections, occlusions of the vessels of the upper extremities, etc.,” said Dr. Juanatey, director, Cardiology and Intensive Cardiac Care Department, full professor of Cardiology, University Hospital, Santiago de Compostela, Spain (past-president, Spanish Society of Cardiology). Historically, patients with AV block have been treated with traditional dual-chamber pacemakers which are implanted in the upper chest, under the skin below the collar bone, and connected to the heart using thin wires called “leads”. Identical in size and shape to the original Micra TPS, Micra AV has several additional internal atrial sensing algorithms which detect cardiac movement, allowing the device to adjust pacing in the ventricle to coordinate with the atrium, providing “AV synchronous” pacing therapy to patients with AV block.
Unlike traditional pacemakers, Micra does not require leads or a surgical “pocket” under the skin, so potential sources of complications related to leads and pockets are eliminated – as are any visible signs of the device.
For more information, visit: www.medtronic.com Read more
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Honeywell’s Systevo Mobile device offers a scalable platform designed to give caregivers critical patient information, such as approved medicines or planned care tasks, through advanced mobile technology. The system can efficiently collect vital sign data, helps to prioritize patient calls on the go, and can escalate issues to other staff members through an efficient alert notification system leveraging data, telephony, SMS or e-mail transmission. Created for demanding hospital environments, the Honeywell Systevo Mobile device features a large display for easy usability, a high-performance barcode scanner, extended battery life for longer shift operation, and is highly resistant to clinical disinfection agents.
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The CIRS Dynamic Cardiac Phantom, Model 008C, is a precision instrument that simulates the realistic motion of an average human heart. It provides known, accurate and repeatable 3D motion of a solid heart model inside the tissue-equivalent thorax phantom. The phantom is designed as a comprehensive image analysis tool for calcification detection, iodine contrast resolution and ECG signal gating. The cardiac phantom is constructed from a tissue equivalent thorax body, moving rod with a solid tissue equivalent heart inside, motion actuator, motion controller and CIRS Motion Control software. The 3D movement of the heart is controlled by CIRS Motion Control software, which is installed on a Windows PC or Laptop. The software comes loaded with three basic motion profiles that are specific to different anatomical parts of the heart and one correlated ECG profile. The software can overlay respiratory motion with cardiac motion to account for total displacement of the heart. The respiratory motion can mimic either breath hold or continuous breathing of a patient. With repeatable and controllable 3D heart motion, this tool could help define protocols in the cardiac field for better and safer patient imaging. The Cardiac Dynamic Phantom joins CIRS’ existing lineup of dynamic phantoms, which includes the Dynamic Thorax Phantom (Model 008A), MRI-LINAC Dynamic Phantom (Model 008M), Dynamic Pelvis Phantom (Model 008P) and Dynamic Platform (Model 008PL). Each of these products is operated using CIRS Motion Control Software. Read more
With Somatom go.Sim and Somatom go.Open Pro, Siemens Healthineers introduces two computed tomography (CT) systems specifically designed to facilitate planning procedures for radiation therapy and provide better images to help calculate radiation plans. The CT images enable radiation oncologists to identify the target tumour. More precise planning means the tumour can be treated with improved accuracy, while providing better protection for surrounding tissue and organs-at-risk. Designed to accommodate patient positioning accessories and increase patient comfort, the 64-slice Somatom go.Sim and the 128-slice Somatom go. Open Pro have an extra-large 85 cm bore. Both systems also feature optional Siemens Healthineers-manufactured patient marking lasers known as Direct Laser. The laser is used to mark the patient’s position for treatment in the CT, which will make subsequent positioning in the linear accelerator both faster and more accurate. Direct Laser are mounted directly onto the gantry and controlled via a mobile tablet. The new GO with Green mobile workflow brings ease of use and walks the radiation therapist through each step of the patient setup process, enabling the therapist to remain at the patient’s side, potentially improving communication and comfort as well as reducing anxiety. The Somatom go. Sim and Somatom go.Open Pro also feature DirectORGANS for OAR (Organs at Risk) contouring. This software automatically addresses the dependency between image quality and the consistency of autocontouring results. DirectORGANS uses a specialized image reconstruction, optimizing the CT images for autocontouring and applying a deep learning-trained contouring algorithm. DirectORGANS may reduce unwarranted variations with high-quality contours that approach the level of consensus-based contours. Unique to the Somatom go.Open Pro CT system is the Direct Intelligent 4D (Direct i4D) technology, which adapts the image acquisition to a patient’s breathing in real time during the scan. Direct i4D is designed to help optimize image quality for each patient, reducing artifacts that are common to 4D image sets and often prompt rescans. In this manner, Direct i4D images can help customers treat more patients with techniques such as stereotactic body radiation therapy (SBRT) that require a high degree of precision to avoid damaging healthy tissue. The SOMATOM go.Sim and SOMATOM go.Open Pro are pending 510(k) clearance, and are not yet commercially available in the United States. Read more
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Advances in technology, and the constant competitive necessity to upgrade workforce skills mean that employees need to be trained continuously. For that reason, Siemens Healthineers expanded its premium subscription for workforce education management, PEPconnections, with a Virtual Library, which provides customers with the ability to add their own learning content to their group. With PEPconnections institutions can easily manage their workforce education, design learning plans, manage, assign and administer online training and professional development activities for employee groups in hospitals and laboratories. Importantly, it does not matter whether the learning activities were developed by Siemens Healthineers, the institution itself, or any other source. Customers now can easily upload their own content as PDFs, videos, documents or links to the Virtual Library. Following upload, items in the Virtual Library are available for general usage or can be assigned to group members through a new or existing learning plan. PEPconnections allows subscribers to manage staff competency and skills – supporting them in transforming care delivery for enhanced patient outcomes. Institutions can benefit from Siemens Healthineers trainings but also have the ability to individualize their learning experience and upload their own content. PEPconnections provides a connection to knowledge in digitalizing healthcare that is designed to increase staff competency, efficiency, and productivity. The basis is PEPconnect – the industry’s first personalized education and performance experience for healthcare professionals worldwide. It provides medical professionals with customized training and professional development opportunities, with learning activities in topics on laboratory diagnostics, medical imaging and minimally-invasive therapy. The activities are designed at Siemens Healthineers by experts in key areas, such as application design, instructional technology and information security. Learners can also construct a learning experience personalized to their needs, and share their learning experience with others via a range of social media channels or groups they are members of within PEPconnect. Almost 300,000 professionals are already using PEPconnect for their training and professional development needs in up to eight different languages. Read more
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The SonoSite EDGE II is a high-resolution, all-digital, 9.0-pound (4.1 kg) ultrasound system with a 12.1in. LED full-bleed glass display. The Edge II boosts improvements in cardiac and abdominal image quality through DirectClear Technology and a new wide-angle display, as well as alignment with the SonoSite pillars. The Edge II features Armored Cable Technology on select transducers, a keypad sealed to the Edge for protection against infection, and persistent knobs for more precise actions. As with our past products, the Edge II is designed with SonoSite’s proprietary Chip Fusion Technology that integrates digital signal processing and multiple system functions into a custom application-specific integrated circuit (ASIC) microchip.
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ndd Medical Technologies (ndd), a leading provider of diagnostic technology enabling healthcare professionals in the early detection of COPD and other chronic lung diseases, has introduced new single patient-use, inline filters for its lung function testing devices, in response to the global COVID-19 pandemic. Ensuring an added level of safety, the new filters can be used with ndd’s portable EasyOne spirometry range, including the EasyOne Air, EasyOne Pro, and EasyOne Pro LAB. EasyOne spirometers are popular among pulmonologists and medical researchers as they provide sensitive, reliable, real-time lung function results and diagnosis of chronic lung diseases, even at the point of care.
The EasyOne product line was originally designed with a strong focus on infection control with easy-to-wipe surfaces, single-use parts for anything that comes into contact with a patient’s breath, and ndd’s unique spirette and flow tube design which protects the flow sensor from cross-contamination. Now, when performing spirometry and testing of the diffusing capacity of the lungs for carbon monoxide (DLCO tests), the new EasyOne inline, single patient-use filters provide “double protection” for technicians and patients by keeping the ambient environment clean, without significantly affecting the EasyOne’s sensitivity.
ndd’s rigorous sensitivity tests have shown that the new inline filters do not significantly affect the device’s sensitivity and show comparable results in 24 waveform testing, (as required by ATS/ERS) and pass testing requirements. World-renowned medical research organizations – such as Johns Hopkins University, University Hospital Zurich and University of Cape Town – are partnering with ndd to assess the long-term lung damage caused by SARS-CoV-2.
Dr Trishul Siddharthan, Assistant Professor of Pulmonary and Critical Care Medicine at Johns Hopkins University, commented: “There is a lot of research underway to investigate the long-term effects of COVID-19. Our research group has been partnering with ndd thanks to the reliability of these spirometers in global settings and the ease of cleaning these devices during the pandemic to ensure safety.”
Prof. Friedrich Thienemann, General Medicine & Global Health research group, University of Cape Town and University Hospital Zurich, also noted: “In order to measure lung functions in resource-constrained settings like South African townships, one needs a device that is portable, point-of-care, easy-to-use, low-maintenance, and reliable without complicated calibration. EasyOne Pro LAB is that device.”
Incorporating ndd’s patented TrueFlow ultrasound technology, the EasyOne translates airflow into ultrasound signals which are measured by the sensors, so the patient’s breath does not come into contact with the sensors. This helps to prevent contamination and minimizes the cleaning required for safe use, while enabling a lifetime of calibration-free accuracy for flow and volume measurements.
To learn more about ndd, visit: www.nddmed.com Read more
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The Trident HD specimen radiography system is a next-generation solution that delivers enhanced image quality, improved workflow and instant sample verification during breast-conserving surgeries and stereotactic breast biopsies. The Trident products are the only specimen radiographs on the market to use amorphous selenium direct capture imaging – the same detector technology used in Hologic’s 3Dimensions mammography system – to generate crisp, clear, high-resolution images. The new Trident HD system, which recently received FDA clearance in the US and a CE Mark in Europe, also features a bigger detector that allows for complete imaging of larger breast surgical specimens, along with a wide range of surgical and biopsy samples. It is a breakthrough solution that delivers superior image quality, helping to streamline workflows and reduce recalls while decreasing procedure times. The Trident HD system eliminates the need for clinicians to transport specimens for imaging and features an ergonomic design that is 37 percent smaller than the original Trident system, making it easy to maneuver in a crowded operating or procedure room. Prior mammography or biopsy images can be displayed on the same Trident HD high-resolution monitor to speed comparison and analysis, resulting in reduced procedure time and improved workflow. Additionally, an intuitive touchscreen interface and wireless integration supports advanced image sharing and seamless transfer of patient records to the facility’s picture archiving and communication system (PACS). Read more
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