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Archive for category: E-News

E-News

Artificial intelligence tool promises earlier detection of deadly form of skin cancer

, 26 August 2020/in E-News /by 3wmedia

New technology being developed by researchers at the University of Waterloo and the Sunnybrook Research Institute is using artificial intelligence (AI) to help detect melanoma skin cancer earlier.
The technology employs machine-learning software to analyse images of skin lesions and provide doctors with objective data on tell-tale biomarkers of melanoma, which is deadly if detected too late, but highly treatable if caught early.
The AI system—trained using tens of thousands of skin images and their corresponding eumelanin and hemoglobin levels—could initially reduce the number of unnecessary biopsies, a significant healthcare cost. It gives doctors objective information on lesion characteristics to help them rule out melanoma before taking more invasive action.
The technology could be available to doctors as early as next year. “This could be a very powerful tool for skin cancer clinical decision support,” said Alexander Wong, a professor of systems design engineering at Waterloo. “The more interpretable information there is, the better the decisions are.”
Currently, dermatologists largely rely on subjective visual examinations of skin lesions such as moles to decide if patients should undergo biopsies to diagnose the disease.
The new system deciphers levels of biomarker substances in lesions, adding consistent, quantitative information to assessments currently based on appearance alone. In particular, changes in the concentration and distribution of eumelanin, a chemical that gives skin its colour, and hemoglobin, a protein in red blood cells, are strong indicators of melanoma.
“There can be a huge lag time before doctors even figure out what is going on with the patient,” said Wong who is also the Canada Research Chair in Medical Imaging Systems. “Our goal is to shorten that process.”
University of Waterloo http://tinyurl.com/ybbq9kek

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Drug trial shows promise for deadly neurological disorder

, 26 August 2020/in E-News /by 3wmedia

Results of a small clinical trial show promise for treating a rare neurodegenerative condition that typically kills those afflicted before they reach age 20. The disease, called Niemann-Pick type C (NPC), causes cholesterol to build up in neurons, leading to a gradual loss of brain function. In the drug trial, researchers have shown that treatment with a type of sugar molecule called cyclodextrin slows progression of the disease.
The study, led by researchers at Washington University School of Medicine in St. Louis and the Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health (NIH).
“We were surprised to see evidence that this therapy could slow progression of the disease and, in some cases, get back some function — speech in particular,” said first author Daniel S. Ory, MD, the Alan A. and Edith L. Wolff Professor of Cardiology at Washington University School of Medicine in St. Louis. “In a neurodegenerative disease, therapies can’t recover neurons that have died. But if some brain cells are dysfunctional rather than dead, it seems this drug can recover some of that function.”
The findings are a result of efforts by the National Center for Advancing Translational Sciences of the NIH to find new treatments for rare and neglected diseases. NPC affects about one in 100,000 births, though Ory noted the disease is under-diagnosed and genetic studies suggest a true incidence of closer to one in 40,000 births.
The cholesterol buildup characteristic of NPC can affect organs other than the brain, such as the liver and spleen, but neurological symptoms often first suggest something is amiss. Age of onset varies considerably, but learning delays and clumsiness may emerge in early childhood, followed by progressive loss of brain function, including loss of motor control, hearing, speech and cognition. Most patients with the condition die 10 to 15 years after the onset of symptoms.
In the combined phase one/two clinical trial, 14 NPC patients who were ages 4 to 23 years and showing neurological symptoms were given cyclodextrin, administered into the spinal column once per month for 12 to 18 months. Another three patients were given cyclodextrin in the spinal column every two weeks for 18 months. Since cyclodextrin does not cross into the brain from the bloodstream, the drug must be injected into the spinal column by lumbar puncture, an outpatient procedure often referred to as a spinal tap. The study did not have a control group that received a placebo, so researchers compared the patients’ progression with historical data collected from past NPC patients.
Doctors used a specialized scoring system to measure disease progression. Called the NPC Neurological Severity Score, it helps assess eye movement, gait, speech, swallowing, fine motor skills, cognition, hearing, memory, and presence and severity of seizures. In each category, patients can score zero to five points, with zero indicating normal function and five indicating severe disability or loss of that category of function.
The historical data from past NPC patients showed that patients’ scores increased — meaning the disease worsened — an average of 2.9 points per year. In contrast, the scores of patients in the trial increased an average of 1.2 points per year, a difference that is statistically significant. The improvements compared with the historical data were seen most in gait, cognition and speech.
“Some of the patients began this trial without the ability to speak, and now they speak,” Ory said. “There is a slowing of the decline, but we were surprised to see trends toward improvement in a few categories. Compared with the historical data, half of the patients in this study saw an improvement or no worsening in the neurological severity score.”
However, hearing loss, a symptom of NPC, was also a major adverse effect of the drug.

Washington University School of Medicine
medicine.wustl.edu/news/drug-trial-shows-promise-rare-deadly-neurological-disorder/
 

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Acupuncture reduces breast cancer joint pain

, 26 August 2020/in E-News /by 3wmedia

In the largest, most rigorous study of its kind, acupuncture was found to significantly reduce the debilitating joint pain experienced by tens of thousands of women each year while being treated for early stage breast cancer, according to SWOG research results.
Investigators from SWOG, the global cancer clinical trials network funded by the National Cancer Institute (NCI), conducted a randomized, blinded, multicentre trial, known as S1200, to test whether acupuncture is effective in alleviating pain caused by aromatase inhibitors, a common treatment for hormone sensitive breast cancers.
Treating this pain effectively, without the use of opioids or other drugs, is a top cancer research priority. Tens of thousands of women each year are treated with aromatase inhibitors (AIs), pills that stop the production of estrogen and essentially starve hormone receptor-positive breast cancer cells. Some women are advised to take these pills daily for up to 10 years. But as a side effect of this therapy, many women – as many as 50 percent – experience joint pain and stiffness. This affects knees, hips, hands, and wrists, and makes it difficult for women to walk, sit, climb stairs, and perform simple tasks like typing or driving.
“Some of my patients have difficulty getting out of a chair,” said Dr. Dawn Hershman, the lead researcher of the study and a SWOG vice chair. “As a result, with no good treatment options for their pain and stiffness, many women stop their cancer treatment. This is probably the most commonly cited reason breast cancer patients stop taking AI medication. So we need a solution – one that doesn’t include opioids or drugs that can be addictive or have serious side effects. We want women to continue their cancer treatment and have a good quality of life.”
SWOG researchers for years have chased a way to relieve AI pain – known as AI-Associated Musculoskeletal Syndrome (AIMSS). Many women don’t want to take pills to relieve symptoms caused by other pills, according to Hershman, leader of the Breast Cancer Program at the Herbert Irving Comprehensive Cancer Centre at NewYork-Presbyterian/Columbia University Irving Medical Centre and professor of medicine and epidemiology at Columbia. In a single-centre study at Columbia, acupuncture showed promise. Hershman wanted to put it to the test in a larger, more rigorous study. Hershman and her team enrolled a total of 226 patients from 11 cancer centres nationwide and randomly assigned them to one of three arms. One group received true acupuncture. Another received sham acupuncture, a method of superficially inserting needles in different, non-therapeutic locations on the body. Finally, another group received no treatment at all.
Patients got twice-weekly treatments for six weeks, then a weekly maintenance treatment for another six weeks. Patients reported on their pain before, during, and after treatment using a variety of methods. The primary endpoint – or key indicator for the trial – was the patient’s level of worst pain using the Brief Pain Inventory (BPI-WP), a patient-reported measure, at the end of the first six weeks of treatment.
Results showed that, on average, patients experienced less pain on the acupuncture arm compared with the sham and treatment-free arms. Patients experienced relief for 24 weeks.
“This work strongly shows that true acupuncture results in better outcomes for women,” said Dr. Katherine Crew, a SWOG executive officer, director of the Clinical Breast Cancer Prevention Program at NewYork-Presbyterian/Columbia University Irving Medical Center and an associate professor of medicine and epidemiology at Columbia and a co-investigator on the study team. “I expect this work to influence medical practice, as well as insurers’ willingness to reimburse for acupuncture during AI treatment.”
SWOGhttps://tinyurl.com/ya58napm

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Sensor sensation

, 26 August 2020/in E-News /by 3wmedia

Microfluidic platforms have revolutionized medical diagnostics in recent years. Instead of sending blood or urine samples off to a laboratory for analysis, doctors can test a single drop of a patient’s blood or urine for various diseases at point-of-care without the need for expensive instruments. Before the sample can be tested however, doctors need to insert specific disease-detecting biomolecules into the microfluidic platform. While doing so, it has to be ensured that these biomolecules are well-bound to the inside of the device to protect them from being flushed out by the incoming sample. As this preparatory step can be time-consuming, it would be advantageous if microfluidic platforms could come pre-prepared with specific biomolecules sealed inside. However, this sealing process requires exposure of the device components to high energy or ‘ionized’ gas and whether biomolecules can survive this harsh process is unknown.
To answer this question, researchers at the Okinawa Institute of Science and Technology Graduate University (OIST) have created a novel sensor that detects biomolecules more accurately than ever before. This sensor was used to demonstrate that biomolecules can be successfully sealed within microfluidic devices. The results have profound implications for healthcare diagnostics and open up opportunities for producing pre-packaged microfluidic platform blood or urine testing devices.
The microfluidic platform device, in which disease-detecting biomolecules can be bound for ready-to-use test kits, is not much bigger than a thumbtack.
Traditionally, metal oxide semiconductor (MOS) sensors are used to detect the binding of biomolecules to a surface by measuring changes in charge. Comprised of a silicon semiconductor layer, a glass insulator layer and a gold metal layer, these sensors are incorporated in an electric circuit with the biomolecule sitting in an electrolyte-filled plastic well on top of the sensor. If you then apply a voltage and measure current, you can work out the charge from the capacitance reading given off. Biomolecules with different charges will give you different capacitance readings, enabling you to quantify the presence of biomolecules.
The novel sensor created by researchers in OIST’s Micro/Bio/Nanofluidics Unit, measures charge using the same technique as conventional sensors but has the additional function of measuring mass. Instead of having a solid gold metal layer, the so-called nano-metal-insulator semiconductor (nMIS) sensor has a layer of tiny gold metal islands. If you shine light on these nanostructures, the surface electrons start oscillating at a specific frequency. When biomolecules are added to these nanoislands, the frequency of these oscillations change proportional to the mass of the biomolecule. Based on this change, you can use this technique to measure the mass of the biomolecule, and confirm whether it survives exposure to ionized gas during encapsulation within the microfluidic platform.   
 “We made a simple sensor that can answer very complex surface chemistry questions,” says Dr. Nikhil Bhalla who worked on the creation of the nMIS sensor.
Measuring two fundamental properties of surface chemical reactions on the same device means that researchers can be far more confident that biomolecules have been successfully encapsulated within the microfluidic platform. A measurement of charge or mass alone could be misleading, making it look like biomolecules have bound to a surface when in fact they have not. Having more than one technique in the same device means that you can switch from one mode to the other to see if you have the same result.
“Scientists have to validate one reaction with multiple techniques to confirm that an observation is authentic. If you’ve got a sensor that enables the detection of two parameters on a single platform, then it is really beneficial for the sensing community,” says Dr. Bhalla.
“By combining these two simple measurement techniques into one compact platform, it opens doors to create portable and reliable sensing technologies in the future”, adds PhD student Shivani Sathish.

Okinawa Institute of Science and Technology Graduate Universityhttp://tinyurl.com/ycy35a79

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Ultrasound for children with abdominal trauma

, 26 August 2020/in E-News /by 3wmedia

Despite evidence showing that the routine use of sonography in hospital emergency departments can safely improve care for adults when evaluating for possible abdominal trauma injuries, researchers at UC Davis Medical Center could not identify any significant improvements in care for pediatric trauma patients. The findings, which resulted from a randomized clinical study involving 925 children with blunt torso trauma who were evaluated in the emergency department at the medical centre, showed no difference in important clinical outcomes. The outcomes assessed were developed for the study mainly based on previous research in injured adults.
The UC Davis team investigated the Focused Assessment with Sonography for Trauma (FAST) to determine whether the use of the FAST examination could safely lead to a decrease in the use of computed tomography (CT) scans for children, and other outcomes. FAST is a bedside ultrasound examination using a portable ultrasound machine. It has not been routinely used in the initial emergency department evaluations of injured children. CT scans represent the “gold standard” in diagnostic imaging for clinicians, including the identification of intra-abdominal injuries, but they also pose a greater radiation risk for children than they do for adults.
“A lot of our work has looked at the appropriate use of CT scans in injured patients,” said James Holmes, professor of emergency medicine and the study’s lead author. “At least in the adult trauma population, there’s evidence that you can use ultrasound to safely decrease CT use. One of the big questions has been whether that holds true for children, too.”
Holmes and his colleagues identified a study cohort of hemodynamically-stable children who presented in the emergency department at UC Davis Medical Center with blunt torso injuries resulting from mechanisms such as motor vehicle collisions and falls greater than 20 feet (6m). Four hundred and sixty patients were randomized to the FAST group and 465 to the no-FAST group, who received the same standard trauma evaluations but without ultrasound.
As in previous studies, the researchers wanted to determine whether the FAST protocol could significantly decrease the length-of-stay for patients in the emergency department, reduce hospital billing charges and still identify injuries when compared to patients who did not receive a FAST examination.
“We were surprised that the routine use of FAST did not show any significant differences,” said Nathan Kuppermann, professor and chair of emergency medicine at UC Davis and the study’s senior author and co-principal investigator. “The use of FAST compared with our standard trauma care did not decrease CT scan use, improve resource use, emergency department length-of-stay, safety or hospital charges.”

UC Davis Health http://tinyurl.com/yceftcp4

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New method helps rule out heart valve infection

, 26 August 2020/in E-News /by 3wmedia

A risk assessment system developed by researchers at Lund University in Sweden shows which patients, with a certain type of streptococcal bacteria in the blood, need to be examined for a heart valve infection – a serious condition requiring prolonged medical treatment.
“Our assessment system can help reduce unnecessary examinations of low-risk patients”, says Torgny Sunnerhagen, one of the researchers behind the study.
If a blood sample shows the presence of what is known as alpha-streptococci, there is a risk that the person suffers from infective endocarditis, a heart valve infection. In order to determine whether or not this is the case, the patient must undergo echocardiography, a type of ultrasound examination of the heart, which can be technically difficult to implement and is often unpleasant.
Previously, there has been a lack of supporting documentation and evidence to help healthcare professionals determine when such an examination is to be performed on patients.
Researchers at Lund University have now developed a risk assessment system, HANDOC, which distinguishes which patients with alpha-streptococci in the blood are at high and low risk respectively of suffering from infective endocarditis.
The study was based on medical records from 340 adult patients in Skåne, whose blood samples showed the presence of alpha-streptococci. In 26 of them, infective endocarditis was confirmed. The researchers mapped the factors that distinguished these patients from those who were not diagnosed with infective endocarditis. Based on the result, an assessment system was constructed.
The researchers observed several factors that differed between patients with alpha-streptococci in the blood who had developed endocarditis, and patients who had not. These factors included which bacterial species had affected the patient, the detection of a heart murmur, how long the patient had been ill, where they had fallen ill (in hospital or not), and whether the patient had any underlying heart disease. The risk assessment system scores these factors and provides evidence of whether or not the patient needs to be investigated for infective endocarditis.
The researchers then tested the assessment system on 399 other patients with these alpha-streptococci and showed that the system had good reliability*. Magnus Rasmussen, associate professor of infection medicine at Lund University and physician in the department for infectious diseases at Skåne University Hospital, hopes that the HANDOC system can lead to faster treatment of patients with streptococcal bacteria in the bloodstream.
“Clinical microbiology has taken strides when it comes to determining bacterial strains, but it’s not always clear what this information will mean to the care of the patients. With this assessment system, we have created an easy-to-use tool systematising how clinicians should treat patients with alpha-streptococci in the blood”, says Magnus Rasmussen.
All patients studied were from, and had been tested within, the same healthcare system.
“The risk is small that this would affect the outcome of the study. We now want to continue and see what happens when HANDOC is applied in healthcare. Will the result be that other types of patients to a greater extent will be examined using echocardiography? We’re also working on developing a similar system for another type of bacteria that can also cause a heart valve infection”, says Torgny Sunnerhagen.
Lund University
www.lunduniversity.lu.se/article/new-method-helps-rule-out-heart-valve-infection

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New smell test could aid early detection of Alzheimer’s and Parkinson’s

, 26 August 2020/in E-News /by 3wmedia

Nisha Pradhan was seven when she began to suspect she was missing out on something. Her sister seemed to have an uncanny knack for predicting what their mother was making for dinner. Pradhan, meanwhile, never had a clue.
“I would just stare at her,” Pradhan says. “She’s younger than me—how does she know more than I do?”
Now 21, Pradhan knows she has a limited ability to detect odour—including the smell of dinner cooking. Her situation is not unique: The sense of smell is often taken for granted, until it malfunctions.
As a patient in a clinical trial being conducted at Rockefeller University, Pradhan is helping scientists develop new smell tests, which promise to help improve diagnosis because they can be used reliably for anyone, anywhere. Because smell disorders can be linked to a variety of health conditions—interfering with appetite, as well as social interaction and sometimes leading to isolation, anxiety, and depression.
“People have their vision and hearing tested throughout their lives, but smell testing is exceedingly rare,” says neuroscientist Leslie Vosshall.
The new tests, developed by Vosshall along with Julien Hsieh, a Rockefeller clinical scholar, and their colleagues could even aid the early detection of neurological disorders that have been linked to problems with olfaction.
People suffer from smell loss for various reasons—a head trauma or sinus infection, for example, or even a common cold—and the cause can be as hard to pinpoint as the condition itself. In Pradhan’s case, she believes she lost much of her sense of smell as a young child, although she’s not sure how. She brought the issue up with her paediatrician, but never received any testing or guidance.
Both the medical community and the people affected by smell loss can be prone to overlook it. “Olfies,” says Pradhan, referring to people with a normal sense of smell, “think not having a sense of smell just affects our ability to detect gas leaks, smoke, and bad body odour. But it deprives us of so much more, including emotions and memories that are so intimate and integral to the human experience.”
A handful of tests already exist for diagnosing people like her. One problem with these tests is that they rely on a patient’s ability to detect and identify single types of odour molecules, such as rose-scented phenylethyl alcohol. However, the ability to detect odours and to recognize them can vary greatly between people. So, someone with an otherwise normal sense of smell may not be able to detect the rose molecule. Meanwhile, another person who can smell roses but is from an area where these flowers are scarce may struggle to put a name to the scent. In either case, there is the potential for misdiagnosis, particularly when testing across different populations and countries.
Hsieh and colleagues set out to eliminate these potential biases with the help of “white smells,” made by mixing many odours together to produce something unfamiliar. Just as a combination of wavelengths of light produces white light, and many frequencies of sound make up white noise, the team generated white smells from assortments of 30 different odour molecules. Their two new tests ask patients to distinguish white smells with overlapping ingredients and to detect white smells at increasingly lower concentrations.
If a person is unable to detect a single component of the test scent, this has little effect on the outcome, and test takers don’t need to identify the odour at all. “We’re really excited about these new tests,” says Vosshall, who is Robin Chemers Neustein Professor and a Howard Hughes Medical Institute investigator. “They focus on the problem of smell itself, because they don’t force people to match smells to words.”
Clinical trials conducted at The Rockefeller University Hospital and Taichung Veterans General Hospital in Taiwan showed that the new tests detected smell loss more reliably than conventional options. The results open up the possibility of a new means to detect smell loss worldwide. It could be used for detection of Alzheimer’s and Parkinson’s diseases, says Hsieh, now a resident at the Geneva University Hospitals in Switzerland.
“The goal is to use changes in the sense of smell, along with other biomarkers, to identify underlying causes of these neurological disorders very early, and so potentially improve treatment,” he says.

Rockefeller University www.rockefeller.edu/news/20624-new-smell-test-aid-early-detection-alzheimers-parkinsons/

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Adding radiation treatments to inoperable lung cancer increases survival by up to one year

, 26 August 2020/in E-News /by 3wmedia

Patients with unresectable, or inoperable, lung cancer are often given a dismal prognosis, with low rates of survival beyond a few years.  Researchers exploring combination therapies have recently discovered improved survival rates by up to one year when patients treated with a newly formulated chemotherapy regimen are also given radiation therapy.
A group of patients with metastatic non-small-cell lung cancer (mNSCLC) who had already been enrolled in a clinical trial were given radiation therapy, in addition to their treatment with a novel chemotherapy formulation, mPEBev, which was designed for its immune-modulating and anti-angiogenic effects. The mPEBev regimen is composed of fractionated cisplatin, oral etoposide, and bevacizumab, a monoclonal antibody that inhibits blood vessel growth in the tumour. Treatments were administered metronomically, spaced out in the safest possible doses to reduce side-effects and toxicity.  
“We had recently established the safety and anti-tumor activity of the mPEBev regimen in metastatic non-small-cell-lung cancer (mNSCLC),” says lead researcher Dr. Pierpaolo Correale, M.D., PhD., Director of the Oncology Unit of the Metropolitan Hospital in Reggio Calabria, Italy. “We hypothesized that in patients undergoing the mPEBev regimen, the use of radiotherapy could provide additional immunostimulation to improve their long-term survival,” Correale says. 
“We found that radiotherapy, together with its direct cytolytic effect on tumour tissue, also elicits systemic immunological events, similarly to cancer vaccines,” adds Prof. Luigi Pirtoli M.D., Full Professor and Director, Radiation Oncology at the University of Siena, Italy. “This response may result in the regression of distant metastases, known as the abscopal effect, as suggested by immunological mechanisms further investigated by our team in previous research.”
Researchers identified candidates for this combination therapy in a retrospective analysis of a subset of 69 patients who received the mPEBev regimen in a recent clinical trial. Forty-five of these patients were also given palliative radiotherapy treatments to one or more metastatic sites.
Survival increased in the group of patients who received radiotherapy by an average of 10 months, with the longest survival of over two years.  [chemotherapy vs chemotherapy  + radiotherapy: 12.1 +/-2.5 (95%CI 3.35-8.6) vs 22.12 +/-4.3 (95%CI 11.9-26.087) months; P=0.015].
Survival correlated with the ability of mPEBev to induce the anticancer immune-response  of peripheral dendritic cells, as well increase the antitumor activity of central-memory and effector memory-T-cells.
These results suggest that tumour irradiation may prolong the survival of NSCLC patients undergoing the mPEBev regimen, presumably by eliciting an immune-mediated effect and providing the rationale for further prospective clinical studies into this combination therapy approach. 

Newswise
www.newswise.com/articles/adding-radiation-treatments-to-inoperable-lung-cancer-increases-survival-by-up-to-one-year

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Siemens Healthineers and Braunschweig Municipal Hospital enter into strategic technology partnership

, 26 August 2020/in E-News /by 3wmedia

Braunschweig Municipal Hospital and Siemens Healthineers are breaking new ground through an innovative medical technology partnership. Together, they have entered into a long-term Asset Management Services (AMS) contract. Braunschweig Municipal Hospital is one of the largest hospitals in northern Germany, with 1,499 beds and 38 clinics and institutes. Siemens Healthineers will assume responsibility for supplying and maintaining all initial and replacement equipment in the areas of radiology, radiotherapy and nuclear medicine. The partnership also includes strategic and operational consulting services to drive continuous improvement initiatives over time. On October 23, in Braunschweig, the parties signed a ten-year contract with a five-year extension option.
“The primary goal of this technology partnership is to assure high-quality and cost-effective medical care for our patients through first-class diagnostic radiological, surgical and radiotherapy services”, explains Ulrich Markurth, mayor of Braunschweig and chairman of the hospital’s supervisory board.
“We are very pleased to be able to contribute as a technology partner in the coming years to further improve the quality of patient care at the Braunschweig Municipal Hospital and its performance capability,” says Dr. Stefan Schaller, head of Siemens Healthineers in Germany. “In addition to the provision of innovative medical technology systems, we support the Braunschweig Municipal Hospital in planning new buildings and optimizing workflows in radiology, cardiology and the emergency department as well as in all steps towards the digitization of healthcare. This holistic package provides the hospital with security of planning, budget certainty and future reliability over the entire duration of the project.”
Matthias Platsch, President of Siemens Healthineers Services adds: “We are delighted to have been chosen as a technology partner for the Braunschweig Municipal Hospital and we are both proud and humbled by the vote of confidence that this important healthcare provider has placed in our new services portfolio. In this, Siemens Healthineers’ first asset management services partnership in Germany, we will combine the strength of our innovative product portfolio with the forward-looking business approach of our enterprise services to help deliver best-value clinical outcomes for patients. Together with the Braunschweig Municipal Hospital, we will transform healthcare delivery by leveraging our combined expertise in established and new care models. With a fresh look at the design and operation of the facility we will significantly improve the patient experience, and the new technologies we will deploy will enable more efficient and more precise clinical diagnosis. We are very excited to play such a role in the future of healthcare in Braunschweig.”
Hospital CEO Dr. Andreas Goepfert explains that the award of the contract for this technology partnership, including the vendor-neutral procurement and management of around 50 new systems (ranging from magnetic resonance and computed tomography, to angiography, X-ray, nuclear medicine and radiotherapy machines) is the result of a Europe-wide call for tenders via an initial selection process and a competitive dialogue. The fundamental premise is that this innovative, end-to-end partnership model – for procurement and management, in particular – will generate savings for the hospital compared to a series of individual, reactive calls for tender.
As a consequence, Siemens Healthineers will be responsible for procurement, installation, maintenance, servicing, an innovation guarantee (through updates and upgrades), and an availability guarantee for all devices. The long-term technology roadmap takes into consideration the hospital’s strategic orientation, especially its current plan to concentrate the hospital at two locations. A Syngo.via Enterprise solution will also give the hospital access to all Siemens Healthineers’ software applications, enabling it to stay at the forefront of digital innovation.
 “The technology partnership in the area of radiology will bring together the heterogeneous imaging device landscape and IT in our radiology department at Braunschweig Municipal Hospital,” forecasts its medical director, Dr. Thomas Bartkiewicz. “That ensures we always stay at the forefront of innovation in diagnostic imaging and imaging-based treatment, while ensuring radiation exposure for patients and employees is kept to a minimum.” Complex interfaces will be removed and the clinical staff will find their day-to-day work routines become noticeably simpler. Nursing director Ulrich Heller adds: “Different operating processes from various device manufacturers will be reduced to a single standardized system.” This will speed up workflows and improve quality of care at the same time. In addition, maintenance plans and contracts that were not previously coordinated will be combined as part of an optimized programme in the future. The result will be a sustainable reduction in maintenance costs.
The ‘Braunschweig Model’ for a technology partnership enables the hospital to respond flexibly to changing requirements and future device needs due to a separate ‘innovation budget’. This includes possible changes in both the scope and the timing of procurement throughout the entire term of the partnership. The fixed quarterly payment fee also provides the hospital with budgetary certainty for the contract duration.
“The technology partnership guarantees predictability of costs whilst providing security of investments in the fields of radiology, radiotherapy and nuclear medicine,” says hospital CEO Goepfert. The long-term technology partnership will enable the hospital to benefit from future technological advances in radiology, including innovative algorithms to improve image reading and computer-assisted diagnostic modules. This will ensure high-quality and cost-effective patient care for the long term.
The AMS also encompasses a number of flagship projects in which the two partners will work closely together in the future. For example, Siemens Healthineers will contribute the know-how in the area of molecular diagnostics built up by its company NEO New Oncology GmbH. Thanks to genome analyses of tumour tissue performed by NEO New Oncology, Braunschweig Municipal Hospital will be able to create customized, targeted treatment recommendations that will facilitate highly promising precision medical treatment for cancer patients. www.siemens.com/healthineers

https://interhospi.com/wp-content/uploads/sites/3/2020/06/logo-footer.png 44 200 3wmedia https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png 3wmedia2020-08-26 14:36:442020-08-26 14:36:53Siemens Healthineers and Braunschweig Municipal Hospital enter into strategic technology partnership

Self-powered paper-based ‘SPEDs’ may lead to new medical-diagnostic tools

, 26 August 2020/in E-News /by 3wmedia

A new medical-diagnostic device made out of paper detects biomarkers and identifies diseases by performing electrochemical analyses – powered only by the user’s touch – and reads out the color-coded test results, making it easy for non-experts to understand.
“You could consider this a portable laboratory that is just completely made out of paper, is inexpensive and can be disposed of through incineration,” said Ramses V. Martinez, an assistant professor of industrial and biomedical engineering at Purdue University. “We hope these devices will serve untrained people located in remote villages or military bases to test for a variety of diseases without requiring any source of electricity, clean water, or additional equipment.”
The self-powered, paper-based electrochemical devices, or SPEDs, are designed for sensitive diagnostics at the “point-of-care,” or when care is delivered to patients, in regions where the public has limited access to resources or sophisticated medical equipment.
The test is initiated by placing a pinprick of blood in a circular feature on the device, which is less than two-inches square. SPEDs also contain “self-pipetting test zones” that can be dipped into a sample instead of using a finger-prick test. The top layer of the SPED is fabricated using untreated cellulose paper with patterned hydrophobic “domains” that define channels that wick up blood samples for testing. These “microfluidic channels” allow for accurate assays that change colour to indicate specific testing results. A machine-vision diagnostic application also was created to automatically identify and quantify each of these “colorimetric” tests from a digital image of the SPED, perhaps taken with a cellphone, to provide fast diagnostic results to the user and to facilitate remote-expert consultation.
The bottom layer of the SPED is a “triboelectric generator,” or TEG, which generates the electric current necessary to run the diagnostic test simply by rubbing or pressing it. The researchers also designed an inexpensive handheld device called a potentiostat, which is easily plugged into the SPED to automate the diagnostic tests so that they can be performed by untrained users. The battery powering the potentiostat can be recharged using the TEG built into the SPEDs. “To our knowledge, this work reports the first self-powered, paperbased devices capable of performing rapid, accurate, and sensitive electrochemical assays in combination with a low-cost, portable potentiostat that can be recharged using a paper-based TEG,” Martinez said.

Purdue University https://www.purdue.edu/newsroom/releases/2017/Q3/self-powered-paper-based-speds-may-lead-to-new-medical-diagnostic-tools.html

https://interhospi.com/wp-content/uploads/sites/3/2020/06/logo-footer.png 44 200 3wmedia https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png 3wmedia2020-08-26 14:36:442020-08-26 14:37:01Self-powered paper-based ‘SPEDs’ may lead to new medical-diagnostic tools
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