GT Medical Technologies, Inc.’ GammaTile® Therapy Awarded

2023 Most Promising New Product of the Year by The Phoenix: The Medical Device and Diagnostic Conference for Chief Executive Officers TEMPE, Ariz., Oct. 13, 2023 /PRNewswire/ — GT Medical Technologies, Inc. a medical device company dedicated to improving the lives of patients with brain tumors, today announced that its FDA-cleared GammaTile® Therapy was awarded the 2023 Most Promising New Product of the Year by The Phoenix: The Medical Device and Diagnostic Conference for Chief Executive Officers. Continue Reading GammaTile® Therapy was awarded the 2023 Most Promising New Product of the Year Tweet this GT Medical Technologies CEO Matthew Likens accepts the award for GammaTile® Therapy. Awarded the 2023 Most Promising New Product of the Year by The Phoenix: The Medical Device and Diagnostic Conference for Chief Executive Officers. “We are honored to win this prestigious award from our industry peers,” said GT Medical Technologies CEO Matthew Likens. “It’s rewarding to be recognized by the Phoenix Conference as we all work together to help make the lives of our patients better.” GammaTile® Therapy is a Surgically Targeted Radiation Therapy (STaRT) for patients with newly diagnosed malignant intracranial neoplasms and patients with recurrent intracranial neoplasms. GammaTile® Therapy delivers immediate radiation that eradicates brain tumor cells before they can replicate post-surgery while helping to protect healthy brain tissue. GammaTiles are bioresorbable collagen embedded with radioactive seeds, Cesium 131. The award was announced at the 28th Annual Phoenix Conference on Thursday, October 12, 2023, in Half Moon Bay, Calif. GT Medical Technologies’ GammaTile® Therapy joins past winners for Most Promising New Product of the Year, including the Intracept® System by Relievant, FlowTriever by Inari Medical, the Willow Pump by Willow and the Synthetic Cartilage Implant by Cartiva, The Phoenix Awards are presented for outstanding achievements in the medical device and diagnostic industry to individuals and companies selected by industry CEOs. The conference is an invitation-only gathering of executives from large and small healthcare companies to discuss critical issues regarding the medical device industry. Since GammaTile® Therapy received FDA clearance in 2018 for recurrent brain tumors and in 2020 for newly diagnosed tumors, more than 1,000 patients have benefitted from its innovative design that targets any remaining cancer cells after a tumor is surgically removed. About GT Medical Technologies, Inc. Driven to raise the standard of care and improve the lives of patients with brain tumors, a team of brain tumor specialists formed GT Medical Technologies. FDA-cleared GammaTile Therapy is a Surgically Targeted Radiation Therapy (STaRT) for patients undergoing brain tumor removal surgery of newly diagnosed malignant and recurrent brain tumors. This treatment eliminates the need for one to six weeks of daily external beam radiation therapy, allowing patients to go about their daily lives without the burden of additional trips to the hospital or clinic for ongoing treatment. Since its full market release in the United States in March 2020, GammaTile has been offered in more than 95 hospitals, with more centers being added each month. For more information, visit www.gtmedtech.com and follow @GammaTile on Twitter and LinkedIn. Media Contacts: Lori KaganGT Medical Technologies[email protected] Dawn FallonNew Dawn Communications[email protected] SOURCE GT Medical Technologies

Resistant Salmonella infections linked to worse outcomes

NIAID / NIH / Flickr cc A randomized clinical trial found that nasal mupirocin is more effective than nasal iodophor for reducing Staphylococcus aureus and methicillin-resistant S aureus (MRSA) in intensive care unit (ICU) patients, researchers reported this week in JAMA. In the cluster-randomized noninferiority trial, investigators randomized 801,668 ICU patients at 137 US hospitals to receive universal decolonization with nasal mupirocin (an antibiotic ointment) plus chlorhexidine gluconate (CHG) bathing or nasal iodophore (an antiseptic) plus CHG bathing. While a trial conducted from 2009 to 2011 found that universal decolonization with mupirocin and CHG reduced MRSA clinical cultures by 37% and bloodstream infections by 44% in ICU patients, and CHG bathing has been broadly adopted in ICUs, there have been concerns that widespread use of mupirocin could promote resistance in S aureus. Iodophore is considered a potential alternative. The investigators compared ICU-attributable S aureus cultures, MRSA clinical cultures, and all-cause bloodstream infections in the baseline period—when all hospitals used mupirocin-CHG for universal decolonization—and the intervention period. The noninferiority margin was 10%. Iodophore inferior to mupirocin When comparing the two periods, the relative hazard of S aureus clinical cultures was significantly higher by 18.4% for the iodophor-CHG group (hazard ratio [HR], 1.17; 95% confidence interval [CI], 1.12 to 1.23) compared with the mupirocin-CHG group (HR, 0.99; 95% CI, 0.94 to 1.04). Similarly, MRSA clinical cultures were significantly higher by 14.1% for iodophor-CHG compared with mupirocin-CHG (HR, 1.13 vs 0.99, respectively). For all-cause bloodstream infections, iodophore-CHG was not inferior to mupirocin-CHG (HR, 1.00 vs 1.01, respectively). This large study confirms that clearing the nose of bacteria prevents infection, and that the choice of product matters. In addition, when the investigators compared the results from the current trial to the 2009-2011 trial, they found that mupirocin-CHG decolonization remained as effective at reducing S aureus in ICU patients. “This large study confirms that clearing the nose of bacteria prevents infection, and that the choice of product matters,” lead trial investigator Susan Huang, MD, MPH, of the University of California Irvine (UCI), said in a UCI Health press release. “Mupirocin antibiotic ointment remains the best treatment, and serious ICU infections can be avoided by simply giving patients mupirocin for the first five days of an ICU stay along with daily chlorhexidine bathing.”

Mupirocin outperforms nasal antiseptic against Staph infections

NIAID / NIH / Flickr cc A randomized clinical trial found that nasal mupirocin is more effective than nasal iodophor for reducing Staphylococcus aureus and methicillin-resistant S aureus (MRSA) in intensive care unit (ICU) patients, researchers reported this week in JAMA. In the cluster-randomized noninferiority trial, investigators randomized 801,668 ICU patients at 137 US hospitals to receive universal decolonization with nasal mupirocin (an antibiotic ointment) plus chlorhexidine gluconate (CHG) bathing or nasal iodophore (an antiseptic) plus CHG bathing. While a trial conducted from 2009 to 2011 found that universal decolonization with mupirocin and CHG reduced MRSA clinical cultures by 37% and bloodstream infections by 44% in ICU patients, and CHG bathing has been broadly adopted in ICUs, there have been concerns that widespread use of mupirocin could promote resistance in S aureus. Iodophore is considered a potential alternative. The investigators compared ICU-attributable S aureus cultures, MRSA clinical cultures, and all-cause bloodstream infections in the baseline period—when all hospitals used mupirocin-CHG for universal decolonization—and the intervention period. The noninferiority margin was 10%. Iodophore inferior to mupirocin When comparing the two periods, the relative hazard of S aureus clinical cultures was significantly higher by 18.4% for the iodophor-CHG group (hazard ratio [HR], 1.17; 95% confidence interval [CI], 1.12 to 1.23) compared with the mupirocin-CHG group (HR, 0.99; 95% CI, 0.94 to 1.04). Similarly, MRSA clinical cultures were significantly higher by 14.1% for iodophor-CHG compared with mupirocin-CHG (HR, 1.13 vs 0.99, respectively). For all-cause bloodstream infections, iodophore-CHG was not inferior to mupirocin-CHG (HR, 1.00 vs 1.01, respectively). This large study confirms that clearing the nose of bacteria prevents infection, and that the choice of product matters. In addition, when the investigators compared the results from the current trial to the 2009-2011 trial, they found that mupirocin-CHG decolonization remained as effective at reducing S aureus in ICU patients. “This large study confirms that clearing the nose of bacteria prevents infection, and that the choice of product matters,” lead trial investigator Susan Huang, MD, MPH, of the University of California Irvine (UCI), said in a UCI Health press release. “Mupirocin antibiotic ointment remains the best treatment, and serious ICU infections can be avoided by simply giving patients mupirocin for the first five days of an ICU stay along with daily chlorhexidine bathing.”

New Neurological Disorder Linked to DOT1L Gene Variants

Texas Children’s Hospital A study from the laboratory of Dr. Hugo J. Bellen, a distinguished service professor at Baylor College of Medicine and a principal investigator at the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children’s Hospital, has discovered that gain-of-function variants in the DOT1L gene cause a new disorder. Further studies revealed that the majority of the symptoms in the patients were surprisingly due to an increase in the enzymatic activity of a histone methylase encoded by this gene. This study was published in the American Journal of Human Genetics. “This project originated when the Undiagnosed Diseases Network, SickKids Complex Care Genomics project in Canada headed by Dr. Gregory Costain, and a search of the GeneMatcher database identified nine unrelated individuals with intellectual disability, developmental delays, distinctive facial features, and other overlapping features carried variants in DOT1L gene,” said Dr. Bellen. “We found this intriguing because this gene had not been previously associated with a genetic or neurological disorder.” DOT1L is an evolutionarily conserved gene found in a broad range of species from yeast to man. It encodes an enzyme – lysine methyltransferase (KMT) – that adds methyl groups to a specific amino acid (lysine 79 aka K79) present on a particular histone (H3). Methylation of specific lysine residues within histones acts as a switch to turn ‘on’ or ‘off’ the expression of target genes. So far, only partial loss-of-function DOT1L variants in around half of KMT-encoding genes (16 of 34) have been shown to cause dominant human developmental disorders. “We found the variants in DOT1L cause a dominant disorder through a gain-of-function mechanism, which is different from other KMTs,” said Dr. Bellen. Although DOT1L is involved in several fundamental cellular processes, and its misregulation has been implicated in cancer, prior to this study it was not clear how variants in the DOT1L gene cause a congenital disorder. So, Dr. Zelha Nil, the first author and postdoctoral associate in the Bellen lab, turned to fruit flies to address that question. DOT1L and its fruit fly version, grappa (gpp) have similar protein sequences and are also likely to have overlapping functions. Most disease-causing human variants in DOT1L are located in its enzymatic domain. Furthermore, gpp is expressed in a large subset of neurons and some glial cells. The team generated a fly gpp mutant, which grew slowly and died in larval stages. Using these mutant flies and flies in which gpp RNA was knocked down, they found compelling evidence that gpp is essential for the survival of the flies and required for proper development as well as the development and function of the fly nervous system, and for H3K79 methylation. “We attempted to suppress the lethality of gpp mutant flies by expressing the human DOT1L gene in flies,” Dr. Zelha Nil said. “To our surprise, expressing normal or variant versions of the human DOT1L gene in tissues where it occurs naturally in flies was not sufficient for gpp mutants who had lost both copies of the gene to survive. Surprisingly, flies with a partial loss of gpp that expressed the human DOT1L variants were less viable and had more profound morphological defects than the normal DOT1L expressing flies, suggesting the human DOT1L expression in flies was toxic.” Consistent with this observation, gpp mutant flies and cultured cells expressing variant versions of human DOT1L exhibited significantly higher levels of H3K79 methylation than normal DOT1L, suggesting that elevated levels of methylation are the likely molecular cause of the symptoms seen in the patients. “Based on our studies in flies, it appears that the variants result in excess enzymatic activity of DOT1Lin these patients,” Dr. Bellen said. “While additional studies are needed to unravel the exact mechanism of disease pathogenesis, our study suggests that reducing DOT1L activity is a viable therapeutic strategy that can be developed in the future to treat this new genetic condition.” Others involved in the study were Ashish R. Deshwar, Yan Huang, Scott Barish, Xi Zhang, Sanaa Choufani, Polona Le Quesne Stabej, Ian Hayes, Patrick Yap, Chad Haldeman-Englert, Carolyn Wilson, Trine Prescott, Kristian Tveten, Arve Vøllo, Devon Haynes, Patricia G. Wheeler, Jessica Zon, Cheryl Cytrynbaum, Rebekah Jobling, Moira Blyth, Siddharth Banka, Alexandra Afenjar, Cyril Mignot, Florence Robin-Renaldo, Boris Keren, Oguz Kanca, Xiao Mao, Daniel J. Wegner, Kathleen Sisco, Marwan Shinawi, Undiagnosed Disease Network, Michael F. Wangler, Rosanna Weksberg, Shinya Yamamoto, and Gregory Costain. Their institutional affiliations can be found here. The study was funded by a grant from the NIH Commonfund to the Model Organisms Screening Center of the UDN, the Office of Research Infrastructure Programs of the NIH, the Huffington Foundation, the Jan and Dan Duncan Neurological Research Institute at Texas Children’s Hospital to H.J.B, the Baylor College of Medicine IDDRC, through a grant from the Eunice Kennedy Shriver National Institute of Child Health and Human Development for use of the Microscopy Core facilities, NIHR Manchester Biomedical Research Centre and Canadian Institutes of Health Research (CIHR) grants. /Public Release. This material from the originating organization/author(s) might be of the point-in-time nature, and edited for clarity, style and length. Mirage.News does not take institutional positions or sides, and all views, positions, and conclusions expressed herein are solely those of the author(s).View in full here.

Spain travel warning as holidaymakers return to Ireland with ‘crypto’ parasites

Irish holidaymakers are returning from trips abroad with infections of nasty parasites, the HSE has confirmed in an urgent warning to anyone travelling to or from Spain. The health authority has issued hygiene advice to tackle an increase in cases of a condition called cryptosporidiosis, also known as crypto, with a number of holidaymakers coming home with symptoms including vomiting and diarrhoea. Travellers returning from Spain, especially from Salou in Catalonia, have been reported as having intestinal issues. The most common symptom is ‘watery diarrhoea,’ but the illness can also cause dehydration, weight loss, stomach cramps, fever, and nausea. Read More Related Articles Read More Related Articles The HSE has warned that the infection can come about through careless hygiene practices and is urging holidaymakers to wash their hands after handling food, especially raw meat, or live animals. They’ve also advised travellers to take care when drinking tap water, even going so far as to say not to use ice in drinks, as ice cubes can often be contaminated with dangerous bacteria. Precautions should also be taken around food preparation and consumption, with the HSE telling tourists to avoid undercooked shellfish and dodgy street vendors, and to keep an eye on the cleanliness of restaurants. Those who have had the illness have been asked not to go swimming in shared pools for at least a fortnight after the symptoms have cleared up, as the bug is resistant to chlorine. In a healthy person, the symptoms caused by cryptosporidiosis should clear up in a week or two, but the infection can be much more serious for people with compromised immune systems. And as part of the HSE’s official advice, beer and wine are deemed ‘generally safe’ for consumption as well as bottled mineral water and hot drinks. It’s the latest warning to those travelling out of Ireland and onto the continent, with another warning for Irish holidaymakers urged to avoid bringing bedbugs home from their travels as France deals with a scourge of the creepy crawlies – which now look to be becoming resistant to pesticides.

Stethoscope hygiene: A neglected factor in spreading infections, study shows

CINCINNATI (WKRC) – The next time your healthcare providers listens to your breathing or heart, you might want to ask about stethoscope hygiene. While stethoscopes can be used to listen to your heart or breathing over clothing, it’s sometimes placed on unprotected skin. In certain settings then, this can raise the risk for transferring germs if the stethoscope isn’t disinfected between patients. “You’re exactly right. We walk in the room, we wash our hands, and yet we take something on other people and lay it on your chest,” said Dr. Steve Feagins. Feagins said while most providers know to wipe down a stethoscope with alcohol between patients, observational studies of healthcare providers now show that as few as one in five providers actually do that. The stethoscope has now been associated with more healthcare associated infections, as well as spores, drug resistant bacteria, viruses and even an emerging resistant fungi such as candida auris. The alcohol wipe down gets rid of some of these but not others, such as norovirus or a common hospital infection known as C. diff. “We have these devices that look like ovens, many of you have these for your cell phones, and you put your stethoscopes in their prior to rounds and sometimes after rounds. That kills everything,” said Dr. Feagins. Researchers are also looking into adding barrier protections for a stethoscope as part of standard infection control practice. That means, just like we protect hands and bodies with gloves or gowns, these barriers would protect against germs.

Sulbactam-Durlobactam Combo Outperforms Colistin in Acinetobacter baumannii Infections

Acinetobacter baumannii sign (Adobe Stock 76664998 by fotohansel) (This article first appeared on our sister brand ContagionLive.) Treatment with the combination antibiotic sulbactam-durlobactam (SUL-DUR; Xacduro; Entasis Therapeutics) resulted in lower mortality and higher clinical cure and microbiological eradication compared with colistin in individuals with hospital-acquired Acinetobacter baumannii-calcoaceticus complex (ABC) infections. Data from the phase 3 ATTACK clinical trial (NCT03894046) were presented at IDWeek 2023, held October 11 to 14, in Boston, Massachusetts. SUL-DUR, which is an intravenous drug combining sulbactam, a beta-lactam antibacterial, and durlobactam, a beta-lactamase inhibitor, was recently approved by the FDA for the treatment of hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia caused by Acinetobacter baumannii. The phase 3, randomized, controlled, noninferiority trial compared SUL-DUR versus colistin in individuals with monomicrobial and polymicrobial ABC infections, randomly assigned to receive either 1.0 g sulbactam/1.0 g durlobactam IV infused over 3 hours every 6 hours plus 1.0 g imipenem/1.0 g cilastatin IV infused over 1 hour every 6 hours, or 2.5 mg/kg colistin IV infused over 30 minutes every 12 hours (after an initial loading dose of colistin 2.5 to 5 mg/kg) plus 1.0 g imipenem/1.0 g cilastatin IV infused over 1 hour every 6 hours, with a treatment duration of 7 to 14 days. Overall, treatment with SUL-DUR reduced 28-day all-cause mortality, the primary endpoint, by 13.2% compared with colistin (19%, 12/63 vs 32.3%, 20/62, respectively). Outcomes for individuals in the treatment arm were similar regardless of monomicrobial or polymicrobial ABC infections; however, individuals in the control arm with monomicrobial infections had higher mortality rates and worse clinical and microbiological outcomes than those with polymicrobial infections. Among the 12 participants in the SUL-DUR arm who died, 4 were attributed to the index infection (33.3% each for mono- vs. polymicrobial infection) compared with 10 in the control arm (46.7% monomicrobial vs 60% polymicrobial infection). Notably, 35% of patients treated with colistin who had monomicrobial ABC infection died compared with 17% in the SUL-DUR group. A greater portion of those in the SUL-DUR arm reached clinical cure and favorable microbiological outcome at the time of cure (7+2 days) compared with the colistin group (SUL-DUR: 64% clinical cure [mono] vs. 59% [poly]; Colistin: 35% [mono] vs. 53% [poly]; SUL-DUR: 67% favorable microbiological outcome [mono] vs 70% [poly]; Colistin: 33% [mono] vs 63% [poly]). Further, 57% of co-infecting Gram-negative pathogens in the SUL-DUR arm at baseline were non-susceptible to imipenem; however, adding durlobactam restored susceptibility to 85% of those pathogens, including those with multi-drug resistance. “These results suggest that SUL-DUR plus a carbapenem could be an effective treatment for polymicrobial infections that include ABC,” the authors concluded, noting that “additional clinical data are needed to demonstrate efficacy.” Click here for more coverage of IDWeek 2023. Reference McLeod S, Miller A, Shapiro AB, Rana K, Altarac D. Efficacy of Sulbactam-Durlobactam (SUL-DUR) Compared to Colistin (COL) against Acinetobacter baumannii-calcoaceticus Complex (ABC) Monomicrobial and Polymicrobial Infections in a Phase 3 Trial. Presented at: IDWeek 2023. October 11-14, 2023; Boston, MA. Abstract 85.

Deep Sleep With Pink Noise Increases Benefits to Cardiovascular System

Deep sleep with auditory stimulation poses benefits to the heart, specifically the left ventricle, causing it to contract and relax more vigorously, according to the results of a study from the University of Zurich. Investigators noted that blood is pumped more efficiently through the circulatory system, which will benefit most organs, extremities, and the brain.1 ryanking999 – stock.adobe.com In the study (NCT04166916), published in the European Heart Journal, investigators used echocardiography, or cardiac ultrasound examinations, to show how the left ventricle changes after a auditory stimulation. According to a statement, this is the first time that research has shown an increase in brain waves during deep sleep that improved cardiac function.1 “We were expecting that stimulation with tones during deep sleep would impact the cardiovascular system, but the fact that this effect was so clearly measurable after just 1 night of stimulation surprised us,” Caroline Lustenberger, PhD, Swiss National Science Foundation Ambizione Fellow at the Neural Control of Movement Lab at ETH Zurich, said in the statement.1 There were 18 individuals included in the study, who were non-smokers and had no cardiovascular disease, sleep disorders or comorbidities, or significant concomitant diseases, according to the study authors. They spent 3 non-consecutive nights in a sleep laboratory, in which investigators stimulated the individuals with sounds on 2 nights.1,2 The investigators continuously measured the individual’s brain activity, blood pressure, and heart activity during sleep. The measurements were simultaneously uploaded into a computer to analyze the data.1 When the individual fell into deep sleep, a series of brief tones at frequencies known as pink noise played. The series was 10 seconds of pink noise, followed by 10 seconds of silence, then repeated. Investigators monitored whether the sound enhanced deep sleep and whether it influenced the individual’s heart rate and blood pressure. In the morning, the investigators examined the cardiac function of the individual.1 The study authors reported that the pink noise stimulation during sleep significantly and globally enhanced slow waves, and influenced cardiovascular functions. There were no significant differences in the condition of absolute systolic blood pressure, according to the results; however, after corrections made to baseline data, investigators found a small, but consistent, increase in relative systolic blood pressure.2 Furthermore, the study authors observed a significant increase in the left ventricular, with a significant increase in left ventricular ejection fraction and a significant decrease in the left ventricular E/e′ ratio. They determined that the results indicate improvements in left ventricular systolic and diastolic functions for the pink noise stimulation. Additionally, the blood biomarkers and carotid-femoral pulse wave velocity showed no significant effect on the stimulation overnight.2 “Despite the relatively small group of subjects, the results are significant. We were also able to reproduce the results on 2 separate nights, which in statistical terms makes them very strong,” Lustenberger said in the statement.1 She added that future studies should include those who are female due to sex differences in sleep and cardiovascular health, especially because the menstrual cycle and menopause have major effects on sleep.1 Investigators will also look to research more powerful stimulation methods to determine the impact on the cardiovascular system.1 References Increased deep sleep benefits your heart. News release. EurekAlert. October 5, 2023. Accessed October 13, 2023. https://www.eurekalert.org/news-releases/1003820 Huwiler S, Carro-Domínguez M, Stich FM, Sala R, et al. Auditory stimulation of sleep slow waves enhances left ventricular function in humans. Eur Heart J. 2023;ehad630. doi:10.1093/eurheartj/ehad630

Collating data on droplet properties to trace and localize the sources of infectious particles

<div data-thumb="https://scx1.b-cdn.net/csz/news/tmb/2023/collating-data-on-drop.jpg" data-src="https://scx2.b-cdn.net/gfx/news/2023/collating-data-on-drop.jpg" data-sub-html="Conceptual scheme of the aerosol and droplet pathogen transmission routes along with relevant physicochemical properties of respiratory particles. Credit: Reviews of Modern Physics (2023). DOI: 10.1103/RevModPhys.95.045001″> Conceptual scheme of the aerosol and droplet pathogen transmission routes along with relevant physicochemical properties of respiratory particles. Credit: Reviews of Modern Physics (2023). DOI: 10.1103/RevModPhys.95.045001 A team of atmospheric scientists, chemists and infectious disease specialists at the Max Planck Institute for Chemistry, working with colleagues from the Max Planck Institute for Dynamical Systems, the University of Denver, Georg August University and St. Petersburg State University, has embarked on an effort to collate publicly available information on droplet properties, such as the way they are distributed by size, their composition, and the ways they are emitted, as a means of helping to develop mitigation strategies for fighting infectious agents. In their paper published in the journal Reviews of Modern Physics, the group describes their collating process and why they believe it could help fight non-contact infectious diseases. In the early days of the pandemic, as people around the world locked themselves inside their residences, scientists, including those not in the medical field, looked for ways to help. One such pair of researchers, Christopher Pöhlker, an atmospheric scientist, and his wife, Mira, a cloud scientist, began to wonder about the nature of droplet size—something related to both their fields of work. After getting online and doing some searching, they found little research had been done regarding respiratory droplet size as it relates to airborne disease transmission. That led them to begin a research effort of their own that involved gathering known information and collating it in a way that might prove useful to traditional medical researchers. To that end, they joined up with specialists in other fields to form a team with the goal of parameterizing droplets involved in respiratory infections such as COVID-19. The team first searched for available information regarding infectious droplet size. They then embarked on a mission to create a parameterization scheme that would collate the data. To that end, they created a classification system based on what they describe as modes, where different modes are based on the size of droplets created in various parts of the body. They ultimately defined five types in all, each described by its size (from less than 0.2 µm to 130 µm), rather than a name. Each was also classified by the location where it was created: in the lungs, the mouth, tongue or lips and the larynx–trachea. The researchers also left space for data that correlates droplet size with infection potential—specifics that are still not known. The team concluded by suggesting that human studies will have to be conducted to fully complete their collating process, which they suggest should, when complete, provide medical researchers with a valuable resource as they continue to look for ways to develop anti-transmission measures to combat infectious diseases. More information: Mira L. Pöhlker et al, Respiratory aerosols and droplets in the transmission of infectious diseases, Reviews of Modern Physics (2023). DOI: 10.1103/RevModPhys.95.045001 © 2023 Science X Network Citation: Collating data on droplet properties to trace and localize the sources of infectious particles (2023, October 13) retrieved 13 October 2023 from https://phys.org/news/2023-10-collating-droplet-properties-localize-sources.html This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Blood test shows predictive accuracy for high-grade prostate cancer

EV-Fingerprint, a blood-based biomarker test, can accurately predict patients who have grade group 3 or greater prostate cancer and may reduce unnecessary biopsies, according to data published in Cancer Medicine.1 Investigators found that the test was able to predict which patients had grade group 3 or greater prostate cancer with 95% accuracy. According to a news release on the test, “The technology measures levels of prostate cancer biomarkers in a patient’s blood sample, combines that data with their clinical information, then uses machine learning to generate a risk score that predicts the presence of clinically significant prostate cancer.”2 In total, the study of the test included 415 men who were referred for biopsies on the basis of high PSA levels from June 2014 to January 2017 in Alberta, Canada. Of those, 157 (38%) men had a negative biopsy, 258 (62%) received a diagnosis of any prostate cancer, and 73 (18%) were diagnosed with grade group 3 or greater prostate cancer. Investigators found that the test was able to predict which patients had grade group 3 or greater prostate cancer with 95% accuracy (0.81 area under the curve [AUC]). The negative predictive value of the test was 97%. Overall, 144 (35%) patients included in the study could have avoided the recommended biopsy when using a probability cutoff of at least 7.85%. Grade group 3 or greater prostate cancer would have gone undetected in 4 (5%) men. At a risk threshold of at least 5%, 35 (7%) patients could have avoided an unnecessary biopsy, and no grade group 3 or greater prostate cancer would have been missed. “The ClarityDX Prostate test will reduce the number of unnecessary prostate biopsies, which are invasive, uncomfortable, and carry some risk,” stated John D. Lewis, PhD, in a news release.2 Lewis is the Bird Dogs Chair in translational oncology at the University of Alberta, and the CEO of Nanostics Inc, a University of Alberta spinoff company. In comparison with the online risk calculator PCPTRC 2.0 alone, the EV-Fingerprint test demonstrated a greater specificity in predicting grade group 1 or greater disease, with 20% specificity for EV-Fingerprint compared with 15% with PCPTRC 2.0 alone. Both tests showed an AUC of 0.69 and similar negative predictive values. In predicting grade group 2 or greater prostate cancer, EV-Fingerprint demonstrated a greater AUC but a lower specificity and negative predictive value compared with PCPTRC 2.0 alone. Further, prediction of grade group 3 or greater prostate cancer with EV-Fingerprint demonstrated significantly superior AUC (0.81 vs 0.73), specificity (41% vs 24%), and negative predictive value (97% vs 95%) compared with PCPTRC 2.0 alone. The authors note that a larger prospective study is being conducted for clinical validation of the test in a cohort of men from Canada and the US. According to the news release, Nanostics is also currently seeking Health Canada and US FDA approval of the test.2 References 1. Fairey A, Paproski RJ, Pink D, et al. Clinical analysis of EV-Fingerprint to predict grade group 3 and above prostate cancer and avoid prostate biopsy. Cancer Med. 2023;12(15):15797-15808. doi:10.1002/cam4.6216 2. Blood test for prostate cancer could help avoid unnecessary biopsies. News release. University of Alberta. October 5, 2023. Accessed October 15, 2023. https://www.ualberta.ca/folio/2023/10/blood-test-for-prostate-cancer-could-help-avoid-unnecessary-biopsies.html