ORLANDO, Fla. — OneBlood is issuing an urgent call for blood donations before Tropical Storm Idalia makes landfall in Florida. Officials said there is a need for all blood types, but there is an increased need for types O negative and O positive as well as platelets. ▶ WATCH CHANNEL 9 EYEWITNESS NEWS “Hurricanes and tropical systems often disrupt blood collections for several days,” said Susan Forbes, OneBlood’s senior vice president of corporate communications and public relations. “The most critical time for blood donations is prior to any storm or hurricane in order to sustain the blood supply during and immediately after the event.” Read: All blood donors regardless of gender, sexual orientation now screened the same way OneBlood encourages all eligible donors to make blood donation part of their storm preparations and visit a donor center or Big Red Bus as soon as possible. For a list of OneBlood locations, click here. New FDA regulations make it easier for LGBTQ+ members to donate blood, 7 years after Pulse tragedy New FDA regulations make it easier for LGBTQ+ members to donate blood, 7 years after Pulse tragedy (Jeff Levkulich, WFTV.com/WFTV) Click here to download our free news, weather and smart TV apps. And click here to stream Channel 9 Eyewitness News live. ©2023 Cox Media Group
Month: August 2023
NEW YORK – Researchers from Quest Diagnostics and collaborators have found that changes in levels of the cardiovascular risk marker free myeloperoxidase (MPO) appear correlated with an individual’s overall mortality risk. The finding, described in a study published last month in PLOS One, indicate that longitudinal measurement of MPO could help physicians assess patients’ mortality risk and response to interventions. It also suggests that MPO could prove useful outside the cardio-metabolic context in which it has most commonly been used, including potentially for identifying patients at elevated risk of conditions like cancer and Alzheimer’s disease, said Marc Penn, senior advisor and medical director of Quest’s cardio metabolic endocrine franchise and first author on the study. MPO is an enzyme released by white blood cells in response to infection and inflammation. It was originally used primarily to help assess patients presenting with symptoms indicative of a potential heart attack but in whom heart injury markers like troponin were negative. This application stemmed from the realization that in such cases, patients were often suffering not from a heart condition, but from a vascular problem, Penn said. “We were looking at heart markers to determine if someone had a vascular problem,” he said, noting that this prompted the question of, “Could we develop a vascular marker for vascular events?” Today, MPO is most commonly used in the ambulatory setting to help assess the likelihood of cardiovascular events in high risk individuals, Penn said, noting that the marker provides information on cardiometabolic health not captured by traditional measures. He cited the example of a patient with LDL cholesterol levels just above optimal and a hemoglobin A1c at the high end of normal. “The patient doesn’t really want to go on a statin, but they measure MPO and it is elevated and maybe then the physician is more adamant about that patient lowering their lipids, lowering weight, [improving] diet and exercise,” he said. While MPO’s value as a marker of cardiovascular risk has been established through a number of studies, researchers had not previously shown that longitudinal changes in MPO levels reflected a change in a person’s risk of cardiovascular events. “The most important finding in this study is that we’ve shown for the first time that if you lower MPO, you lower risk, and if you let MPO go up, you raise risk,” Penn said. To establish that relationship, the researchers collected demographic and lab data (MPO, LDL cholesterol, hemoglobin A1c, and ApoB lipoprotein) from a cohort of 3,658 patients seen between 2011 and 2015 by doctors in the national primary care network MDVIP. They analyzed both the correlation between an individual’s baseline MPO level and their risk of adverse events including myocardial infarction, stroke, coronary revascularization, and all-cause death and the correlation between changes in MPO level and risk of adverse events. Running counter to prior studies, the authors found that at baseline the “risk of cardiovascular death did not differ significantly between patients with high and low MPO” once they had adjusted for age, sex, and other cardiovascular risk factors. Penn said that this was due to the fact that incidences of cardiovascular death was small in the relatively healthy population looked at in the study. The researchers did find, however, that patients with high MPO levels were at elevated risk for death due to non-cardiovascular conditions and had higher levels of all-cause mortality. Additionally, as Penn noted, the study found that decreasing MPO levels were linked to mortality reduction, with, the authors wrote, “a 100 pmol/L decrease in MPO correlated with a 5 percent reduction in mortality over five years.” That finding could allow physicians to better assess whether or not particular interventions are mitigating a patient’s mortality risk, Penn said. “It’s a reflection of vascular health,” he said. For instance, “we’ve known for years that there is a link between gum disease and heart disease. In people with periodontal abscesses, gingivitis, things of that nature, MPOs are very high. Sending someone to the dentist and having their mouth cleaned up actually lowers MPO. Getting on top of inflammatory bowel disease, rheumatoid arthritis, things that are known to be associated with heart disease… MPO reflects that.” “The real goal of this study was, we have a population where we lowered MPO. Does that have an impact on health and outcomes?” he said. “And I think this study shows that it does.” The fact that baseline MPO levels and longitudinal changes in levels were corelated with non-cardiovascular health and death from non-cardiovascular conditions suggests the marker could prove useful in other patient populations. For instance, Penn said that elevated MPO in a patient with no signs of elevated cardiovascular risk could lead doctors to more closely examine them for other potential causes, like cancer or Alzheimer’s disease. He suggested that liquid biopsy-based cancer detection is one area that could benefit from such an approach, given the relatively low sensitivity of such tests. Patients with high MPO but no apparent cardiovascular condition might, for instance, be prioritized for more intensive cancer testing or additional follow-up. Penn said he and his colleagues have not begun any studies exploring the usefulness of MPO in this context but that they are “thinking about looking at patients who have MPO [test results] who go on to get a liquid biopsy to see if higher MPO patients are more likely to have a true positive liquid biopsy.” He noted that the MDVIP network offers its patients liquid biopsies for cancer detection and that he and his collaborators are in discussions with the network about possibly using their patient data to look at correlations between MPO levels and liquid biopsy results. MPO tests cost $50.86 under the current Centers for Medicare and Medicaid Services Clinical Laboratory Fee Schedule and is widely available. Penn said the primary challenge in testing MPO levels is with sample collection and the requirement that samples be spun down within 10 to 20 minutes after collection. “Otherwise, the white blood cells sit in the
Summary: Researchers found a live eight-centimeter Ophidascaris robertsi roundworm in the brain of a 64-year-old Australian woman. The parasitic roundworm, typically found in carpet pythons, was successfully extracted following brain surgery. The patient likely contracted the parasite from touching or consuming a type of native grass, Warrigal greens, contaminated with the python’s fecal matter. This alarming case raises concerns about the increasing risk of zoonotic diseases as human and animal habitats continue to overlap. Key Facts: This is the first-ever human case of Ophidascaris robertsi roundworm, which is common to carpet pythons. The roundworm was found in the woman’s brain, a first for any mammalian species. The patient likely contracted the parasite from Warrigal greens beside a lake where the python had shed the parasite through its feces. Source: Australian National University The world’s first case of a new parasitic infection in humans has been discovered by researchers at The Australian National University (ANU) and the Canberra Hospital after they detected a live eight-centimetre roundworm from a carpet python in the brain of a 64- year-old Australian woman. The Ophidascaris robertsi roundworm was pulled from the patient after brain surgery – still alive and wriggling. It is suspected larvae, or juveniles, were also present in other organs in the woman’s body, including the lungs and liver. “This is the first-ever human case of Ophidascaris to be described in the world,” leading ANU and Canberra Hospital infectious disease expert and co-author of the study Associate Professor Sanjaya Senanayake said. “To our knowledge, this is also the first case to involve the brain of any mammalian species, human or otherwise. “Normally the larvae from the roundworm are found in small mammals and marsupials, which are eaten by the python, allowing the life cycle to complete itself in the snake.” Ophidascaris robertsi roundworms are common to carpet pythons. It typically lives in a python’s oesophagus and stomach, and sheds its eggs in the host’s faeces. Humans infected with Ophidascaris robertsi larvae would be considered accidental hosts. Roundworms are incredibly resilient and able to thrive in a wide range of environments. In humans, they can cause stomach pain, vomiting, diarrhoea, appetite and weight loss, fever and tiredness. The researchers say the woman, from southeastern New South Wales in Australia, likely caught the roundworm after collecting a type of native grass, Warrigal greens, beside a lake near where she lived in which the python had shed the parasite via its faeces. The patient used the Warrigal greens for cooking and was probably infected with the parasite directly from touching the native grass or after eating the greens. Canberra Hospital’s Director of Clinical Microbiology and Associate Professor at the ANU Medical School, Karina Kennedy, said her symptoms first started in January 2021. “She initially developed abdominal pain and diarrhoea, followed by fever, cough and shortness of breath. In retrospect, these symptoms were likely due to migration of roundworm larvae from the bowel and into other organs, such as the liver and the lungs. Respiratory samples and a lung biopsy were performed; however, no parasites were identified in these specimens,” she said. “At that time, trying to identify the microscopic larvae, which had never previously been identified as causing human infection, was a bit like trying to find a needle in a haystack. “In 2022, she began experiencing subtle changes in memory and thought processing and underwent a brain MRI scan which demonstrated an atypical lesion within the right frontal lobe of the brain.” The patient was first admitted to a local hospital in late January 2021 after suffering three weeks of abdominal pain and diarrhoea, followed by a constant dry cough, fever and night sweats. By 2022, the patient was experiencing forgetfulness and depression, prompting an MRI scan. A neurosurgeon at Canberra Hospital explored the abnormality and it was then that the unexpected eight-centimetre roundworm was found. Its identity was later confirmed through parasitology experts, initially through its appearance and then through molecular studies. Associate Professor Senanayake said the world-first case highlighted the danger of diseases and infections passing from animals to humans, especially as we start to live more closely together and our habitats overlap more and more. “There have been about 30 new infections in the world in the last 30 years. Of the emerging infections globally, about 75 per cent are zoonotic, meaning there has been transmission from the animal world to the human world. This includes coronaviruses,” he said. “This Ophidascaris infection does not transmit between people, so it won’t cause a pandemic like SARS, COVID-19 or Ebola. However, the snake and parasite are found in other parts of the world, so it is likely that other cases will be recognised in coming years in other countries.” Associate Professor Karina Kennedy said the important message from this case is about general food safety, particularly when gardening or foraging for food where there may be other wildlife in close proximity. “People who garden or forage for food should wash their hands after gardening and touching foraged products. Any food used for salads or cooking should also be thoroughly washed, and kitchen surfaces and cutting boards, wiped downed and cleaned after use,” she said. The patient continues to be monitored by the team of infectious disease and brain specialists. “It is never easy or desirable to be the first patient in the world for anything. I can’t state enough our admiration for this woman who has shown patience and courage through this process,” Associate Professor Senanayake said. The researchers’ findings have been described in the journal Emerging Infectious Diseases. The research team included scientists and infectious diseases, immunology and neurosurgical doctors from ANU, Canberra Health Services, CSIRO, the University of Melbourne and the University of SydneyThe world’s first case of a new parasitic infection in humans has been discovered by researchers at The Australian National University (ANU) and the Canberra Hospital after they detected a live eight-centimetre roundworm from a carpet python in the brain of a 64- year-old Australian woman. The Ophidascaris
So, laughter really is the best medicine. A mere chuckle is enough to expand cardiac tissue and increase the flow of oxygen throughout the body, thus exercising a weakened heart, according to a new study. Scientists in Brazil set out to prove that “laughter therapy” can improve cardiovascular health and ease symptoms of heart disease. “Our study found that laughter therapy increased the functional capacity of the cardiovascular system,” said lead author professor Marco Saffi, of the Hospital de Clínicas de Porto Alegre in Brazil, via the Guardian. “Laughter therapy could be implemented in institutions and health systems like the NHS [National Health System of the UK] for patients at risk of heart problems.” The research was presented at the annual meeting of the European Society of Cardiology in Amsterdam, the world’s largest heart conference. Scientists in Brazil wanted to see if “laughter therapy” could improve cardiovascular health and ease symptoms of heart disease.Getty Images/iStockphoto Researchers looked at 26 adults, at an average age of 64 who had previously been diagnosed with coronary artery disease. Every week for three months, half of the group viewed comedy programs while the other half watched serious documentaries about topics such as the Amazon rainforest or politics. Results showed that the group who watched comedies had a 10% advancement in the amount of oxygen the heart could pump into the body as well as an improvement in their arteries’ ability to expand. Blood testing also detected notable reductions in inflammatory biomarkers, which can indicate if people are at risk for heart attack or stroke and show how much plaque is built up in blood vessels. “When patients with coronary artery disease arrive at hospital, they have a lot of inflammatory biomarkers,” Saffi said. “Inflammation is a huge part of the process of atherosclerosis when plaque builds up in the arteries.” It’s believed that laughter has this effect because it releases endorphins, which are needed to maintain healthy blood pressure and reduce strain on the heart by keeping stress hormones low. “This study found that laughter therapy is a good intervention that could help reduce that inflammation and decrease the risk of heart attack and stroke,” Saffi said. He suggested that laughter therapy could eventually reduce reliance on medications. Saffi noted that these results don’t have to be a result of TV programs alone — it can also come from live comedy shows or fun evenings with friends and family. “People should try do do things that make them laugh at least twice a week,” Saffi said. “Laughing helps people feel happier overall, and we know when people are happier they are better at adhering to medication.”
A new COVID-19 variant may be more likely to cause breakthrough infection, according to the Centers for Disease Control and Prevention (CDC). The CDC released a risk assessment Wednesday, breaking down information regarding the new variant. “BA.2.86 may be more capable of causing infection in people who have previously had COVID-19 or who have received COVID-19 vaccines,” the assessment read. Meaning, it may be more likely to cause breakthrough infections than previous strains of the virus. The CDC also broke down where the variant has been spotted, how severe an illness it may cause, and whether current treatments are effective against it. Here’s what experts currently know about BA.2.86. Getty Images / AzmanL Nicknamed “Pirola,” BA.2.86 was first identified on July 24, 2023. The World Health Organization recently added the new variant to its list of “currently circulating variants under monitoring,” noting that the strain has a “large number of mutations identified.” So far, nine cases of BA.2.86 have been detected—three in Denmark, two in South Africa, two in the U.S., one in the U.K., and one in Israel. One of the cases in the U.S. was a person in Michigan, with the Michigan Health Department noting in a statement on X (formerly known as Twitter) that the patient who contracted the strain is an older adult with “mild symptoms” who hasn’t been hospitalized. BA.2.86 is a subvariant of Omicron, which has been the dominant strain in the U.S. since late 2021, but “it has many, many more mutations than the mutations of each of the variants before,” Timothy Murphy, MD, senior associate dean for clinical and translational research at the University at Buffalo Jacobs School of Medicine and Biomedical Sciences, told Health. Specifically, BA.2.86 has more than 35 amino acid changes to its spike protein than the recently circulating XBB.1.5, which the fall COVID-19 booster was based on, Murphy said. The CDC pointed out that this change is “roughly of the same magnitude” as the switch between the Delta strain of COVID-19 and the initial Omicron variant, BA.1. It’s the spike protein mutations that make this variant likely to cause breakthrough infections. “The virus uses the spike protein to bind the disease to cells,” Murphy said. “That’s what the vaccines are directed against.” With so many mutations in the spike protein, there is a greater chance that the vaccine and having previously been infected with COVID-19 won’t offer as much protection against BA.2.86 as prior strains of the virus, William Schaffner, MD, an infectious disease specialist and professor at the Vanderbilt University School of Medicine, told Health. “Initially, officials thought that BA.2.86 was not all that much different but, now that they’ve noted there are many mutations, they’ve at least raised the question about whether there may be some immune evasion on the part of this strain,” Schaffner said. The CDC said it’s “too soon to know the real-world impacts on immunity” of BA.2.86. However, the agency noted that many people have immunity, either from previous infection, the vaccine, or both. “It is likely that these antibodies will continue to provide some protection against severe disease from this variant,” the CDC said. While testing for COVID-19 is highly encouraged, new variants can be tricky to accurately test for. “We have no lab data or experimental data whatsoever to say how this will impact immunity,” Murphy said. “It simply hasn’t been studied at this point, but likely will be soon.” Samples of the new strain aren’t broadly available for reliable lab testing at this point, but are expected to happen eventually. Meanwhile, existing treatments for older COVID-19 strains can most likely provide relief for patients who are infected with BA.2.86. According to the CDC, the mutation profile of BA.2.86 suggests that treatments like Paxlovid, Veklury, and Lagevrio will be effective against the variant. “The medications don’t target the spike protein—they go after different proteins in the virus and those do not appear to be any different,” Murphy said. Schaffner agreed. “The treatments for sure ought to work, but we’ll see whether over-the-counter tests continue to be able to detect this new variant as we go forward,” he said. Overall, it’s hard to say how different BA.2.86 is from other variants. The CDC stressed that there have just been nine cases, making it hard to know how infectious this variant is and how severe of an illness it may cause. “There’s really zero information here,” Murphy said. “With nine cases, it’s just not enough to know anything.”
<!– Piqua Baptist Church blood drive set for Sept. 7 – Miami Valley Today
BAKERSFIELD, Calif. (KGET) — The Houchin Community Blood Bank is partnering up with Wiki’s Wine Dive & Grill for an end-of-month promotion. Houchin officials say from Monday, Aug. 28 to Friday, Sept. 1 blood donors who make a successful blood donation can receive one $10 voucher for Wiki’s Wine Dive & Grill. The offer is only available while supplies last. In a news release Shane Hubbard, Creative Development Coordinator at Houchin Community Blood Bank said: With many of our community’s routine donors ineligible to donate blood until the beginning of October, we need blood donors who donate maybe 1 or 2 times a year to step up and help our community. The average donor in Kern County donates less than twice a year,” he said. “If we hope to continue saving lives as a community and keep it strong, we need support from every person who is eligible to donate. And for those who are not eligible, we need help spreading awareness of the need for blood. Shane Hubbard If you would like to participate in this offer schedule your appointment by going to the Houchin Community Blood Bank website or call 661-323-4222.
Prioty Islam, MD, MSc, attending physician, medical oncologist, Leukemia, Division of Hematologic Malignancies, Memorial Sloan Kettering Cancer Center, discusses the exploration of novel roles for BTK inhibitors in the treatment of patients with mantle cell lymphoma (MCL) and chronic lymphocytic leukemia (MCL). Due to recent successes derived from treatment with BTK inhibitors in CLL and MCL, there continues to be interest in furthering their utility by harnessing novel combination regimens, targeting mechanisms, and prognostic features, Islam begins. Advertisement Many clinical trials are evaluating the addition of BTK inhibitors with BCL2 inhibitors, such as an investigation of frontline acalabrutinib (Calquence) and venetoclax (Venclexta), Islam states. This could provide patients with an all-oral, time-limited treatment alternative to either standard continuous BTK inhibitor therapy or the combination of a BCL2 inhibitor and a monoclonal antibody infusion, Islam explains. The goal of further developing novel combination regimens is to improve upon the convenience, tolerability, and efficacy of currently available strategies, she adds. Moreover, there is additional interest in if minimal residual disease (MRD) may inform the duration of BTK inhibitor treatment, Islam continues. Any BTK inhibitors that are currently approved for use are approved with continuous administration until disease progression or intolerance, she says. Some patient subsets may benefit more from a truncated or attenuated treatment course, but this population has not yet been identified, Islam notes. To utilize a time-limited treatment strategy with BTK inhibitors, co-administration of an additional novel therapy may be necessary. This could induce deeper remissions, as complete responses with BTK inhibitor monotherapy are typically uncommon, Islam details. Lastly, an emerging area of research in both MCL and CLL is focused on discovering alternative methods of targeting the BTK protein, Islam says. Current BTK inhibitors are either covalent, in which the agent irreversibly binds to the BTK protein, or noncovalent, in which this bond is reversible. However, there may be other ways to inhibit BTK mutations. For example, several agents currently in development have been designed to degrade the BTK protein, Islam introduces. Because this approach would blockthe BTK signaling pathway in its entirety, this method could also overcome or prevent the development of BTK inhibitor resistance through its varied mechanisms, Islam concludes. Disclosures: Dr Islam reports consulting roles with AbbVie, AstraZeneca, BeiGene, DAVA Oncology, and LOXO Oncology; as well as speaking roles with Targeted Oncology and The Video Journal of Hematologic Oncology (VJHemOnc).
Anna B. Halpern, MD, physician, assistant professor, Clinical Research Division, Fred Hutch; assistant professor, hematology, University of Washington School of Medicine, discusses investigational efforts being developed to expand on the use of ruxolitinib and navitoclax in earlier treatment lines for patients with myelofibrosis. In cohort 3 of the phase 2 REFINE trial (NCT03222609), the combination of ruxolitinib and navitoclax was evaluated in the upfront setting for patients (n=32) who had not been previously exposed to a JAK inhibitor. The study’s primary end point was spleen volume reduction of 35% or greater from baseline at week 24. An exploratory analysis of this cohort was presented at the 2022 ASH Annual Meeting and Exposition, Halpern begins. Findings showed that navitoclax plus ruxolitinib produced a spleen volume reduction of at least 35% at week 24 across specific patient subsets, she details. These subsets consisted of patients 75 years of age or older, those with a high Dynamic International Prognostic Scoring System score, and those with HMR mutations. The percentage of patients who experienced optimal spleen volume reduction in these subgroups are 50%, 33%, and 47%, respectively. Notably, changes in bone marrow fibrosis and reductions in the variant allele frequency (VAF) of the driver gene mutation were seen with the combination regimen in many patients, Halpern continues. Half of patients achieved a greater than 20% reduction in VAF from baseline at week 12 or 24, while a greater than 50% VAF reduction from baseline occurred in 18% of patients. When comparing those with or without HMR mutations, no differences in greater than 20% VAF reduction from baseline to week 12 or 24 were observed between populations. These results indicate the potential disease-modifying ability of ruxolitinib and navitoclax, suggesting that reductions in bone marrow fibrosis and VAF may serve as biomarkers for disease modification, Halpern states. Notably, long-term outcomes cannot be definitively assessed as correlates for leukemia, progression, and survival, she adds. The viability of these 2 biomarker candidates should be assessed more short term, and in larger study populations, Halpern concludes.
Credit: CC0 Public Domain For centuries, we have known that tuberculosis is a social disease. It thrives on poverty and social factors such as malnutrition, poor housing, overcrowding, unsafe work environments and stigma. Globally in 2021 an estimated 2.2 million cases of TB were attributable to undernourishment, 0.86 million to HIV infection, 0.74 million to alcohol use disorders, 0.69 million to smoking and 0.37 million to diabetes. But knowledge about social determinants alone does not always translate into tangible action and progress. A new trial in India, called RATIONS, aimed to determine the effect of nutritional supplementation on new cases of tuberculosis in households of adults with pulmonary TB. The research found that providing food baskets to people with TB and their households could go a long way to prevent and mitigate the disease. No easy silver bullets The TB community has typically looked for biomedical solutions, or “silver bullets”, for a social pathology, and we are struggling to make progress. Since the COVID pandemic, TB mortality and incidence have increased globally, putting TB back on top as the single most deadly infectious killer of humankind. In 2021, 1.6 million people died of TB. In Africa, TB incidence is high (212 per 100,000 population) with a high case fatality rate because of the HIV epidemic. Undernutrition is the most important cause of TB. This has been shown in studies in many countries, including South Africa, where researchers found poor levels of nutrition in patients admitted to a specialized TB hospital. Malnutrition refers to all forms of deficiencies in nutrition, including over-nutrition and obesity. Undernutrition refers more specifically to a deficiency of nutrients. While we know that many patients with TB have poor nutrition, the latest evidence is that undernutrition also plays a key role in TB within households. The results of the Reducing Activation of Tuberculosis by Improvement of Nutritional Status (RATIONS) trial show that improved nutrition in family members of patients with lung TB reduced all forms of TB by nearly 40%, and infectious TB by nearly 50%. This trial recruited 10,345 household members of 2,800 patients with lung TB. All TB patients received a monthly 10kg food basket (rice, pulses, milk powder, oil) and multivitamins for six months. In one group family members received 5kg rice and 1.5kg pulses per person per month, while the other group of family members did not get food baskets. Food worked like a vaccine in this trial, cutting the risk of household members developing TB. Nutrition could also protect against other conditions such as anemia, diarrhea and respiratory infections, but these were not not the main focus of the trial. An accompanying paper, based on the results of the RATIONS trial, showed that severe undernutrition was present in nearly half of all patients. An early weight gain in the first two months was associated with 60% lower risk of TB mortality. The other benefits were higher treatment success and better weight gain. During the six-month follow-up period, a remarkable treatment success rate of 94% was achieved. Getting food to patients How expensive was the intervention? The cost of a food basket was US$13 per TB patient per month and US$4 per household member per month and could be delivered, even in rural areas, using field staff. Even before the RATIONS trial, the Indian government had recognized the need for nutrition support for people with TB, and in 2018 launched “Nikshay Poshan Yojana”, a direct benefit transfer scheme. Under this scheme, each TB patient receives a financial incentive of US$6 per month for the duration of the anti-TB treatment (typically, six months for people with drug-sensitive TB). Emerging data suggests that while the scheme improves the treatment completion rates among patients with TB in India, they often receive their payments late. There is a need to improve the efficiency and provide timely payments. The new RATIONS trial suggests that directly providing food baskets may be another effective strategy. Many countries, including India, have other social security programs, including public distribution systems to provide food grains at subsidized prices. Using existing channels to provide extra food rations to people with TB, and expanding the menu to include proteins such as pulses and millets, is a strategy worth exploring. This could also have positive effects on other diseases such as diabetes. Implications for South Africa South Africa is one of the countries labeled by the World Health Organization as a “high TB burden country”. What does this latest research mean for South Africa? Statistics South Africa reported that in 2021 2.6 million people had inadequate access to food and a further 1.1 million stated they had “severe” inadequate access to food. More than 683,000 children five years and younger experienced hunger. This toxic mix requires prevention of TB by nutritional support, drugs to prevent TB infections and early diagnosis with molecular tests and treatment. With high levels of food insecurity and undernutrition in South Africa, fueled by the highest levels of inequality, it is critical that South Africa includes social benefits for people with TB and those in their households to reduce the prevalence of TB in the country and to meet the Sustainable Development Goals for 2030. Regardless of how social benefits are distributed, action must be based on evidence. We need better tests, cures and vaccines for TB, but they alone cannot end the epidemic. TB patients must be provided with the social benefits that they need and deserve, as a basic human right. Provided by The Conversation This article is republished from The Conversation under a Creative Commons license. Read the original article. Citation: TB research shows a good diet can cut infections by nearly 50% (2023, August 28) retrieved 28 August 2023 from https://medicalxpress.com/news/2023-08-tb-good-diet-infections.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.