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Low-dose CT chest scans could help detect pneumonia in at-risk patients while exposing them to only small amounts of radiation, a new study has found. The research, published in Radiology: Cardiothoracic Imaging, shows that ultra-low-dose scans can effectively detect pneumonia in patients with compromised immune systems, enabling doctors to treat the infection before it becomes life-threatening. According to the researchers, these scans expose patients to just 2% of the radiation dose used in a standard CT scan.
"This study paves the way for safer, AI-driven imaging that reduces radiation exposure while preserving diagnostic accuracy,” lead researcher Dr Maximiliano Klug, a radiologist with the Sheba Medical Center in Ramat Gan, Israel, said in a news release. He added that CT scans are the gold standard for detecting pneumonia but there are concerns regarding the risk posed by repeated exposure to radiation. There is a solution- ultra-low-dose CT scan. However, the problem is that these scans can be grainy and hard to read, researchers said.
Study Gives Solution To This
To overcome that, Klug's team developed an AI program that could help "de-noise" low-dose scans, making them sharper and easier to read. Between September 2020 and December 2022, 54 patients with compromised immune systems who had fevers underwent a pair of chest CT scans -- a normal dose scan and an ultra-low-dose scan. The AI program cleaned up the low-dose scan, and then both sets of images were given to a pair of radiologists for assessment. Radiologists had 100% accuracy in detecting pneumonia and other lung problems with the AI-cleaned low-dose scans, but 91% to 98% accuracy in examining the scans that hadn’t been improved through AI, results show.
"This pilot study identified infection with a fraction of the radiation dose," Klug said. "This approach could drive larger studies and ultimately reshape clinical guidelines, making denoised ultra-low dose CT the new standard for young immunocompromised patients.
How Can You Detect Pneumonia?
Pneumonia is a lung infection that causes the air sacs in the lungs to fill with fluid or pus and can be caused by bacteria, viruses, or fungi. The symptoms can range from milk to severe, which includes:
Coughing with or without cough
Fever
Chills
Trouble breathing
Chest pain, especially when breathing deeply or coughing
Sweating or chills
Rapid heart rate
Loss of appetite
Bluish skin, lips, and nails
Confusion.
How to detect Pneumonia in coughing newborns and toddlers?
Pneumonia can severely affect newborns and young children as their lungs are comparatively more sensitive. As per Dr Goyal, young children can cough for various reasons including seasonal infections and tonsillitis, which is very common in this age group. But if they look visibly irritable and have poor sleep patterns, then parents must reach out to an expert. "I am not saying that parents must visit a hospital but any local paediatrician would be able to detect pneumonia in your kid.
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More than five months after the UK’s worst meningitis B outbreak in Kent, scientists say they have identified genetic changes that may explain why the infection caused unusually severe disease.
According to UKHSA data, more than 20 young people, mostly students, were infected in the March outbreak linked to a Canterbury nightclub. All required hospital treatment; nine were admitted to intensive care and two died.
“This investigation shows just how quickly and dramatically these bacteria can change, sometimes acquiring new traits from harmless bacteria circulating nearby, that make them more likely to cause disease,” said Dr Charlene Rodrigues, Consultant in Pathogen Genomics at UKHSA.
Two people died in the outbreak — a 21-year-old University of Kent student and Juliette Kenny, a sixth-form pupil at Queen Elizabeth’s Grammar School in Faversham.
The outbreak is thought to have started at Club Chemistry, a nightclub in Canterbury city centre popular with university students. Scientists believe one person may have brought the infection into the venue, where it then spread through close social contact.
At the time, scientists described the outbreak as “unprecedented” and “explosive” because of its unusual speed and severity.
“The fact this outbreak variant was able to spread to so many young people was due to the social environment, a place where lots of close social mixing takes place,” Dr Rodrigues said.
Scientists from UKHSA, the University of Oxford and academic institutions used bacterial genome sequencing to investigate the outbreak.
UKHSA’s Meningococcal Reference Unit sequenced the bacteria within days of the first case and compared the outbreak strains with tens of thousands of meningococcal genomes in international databases.
They found that the outbreak strain had acquired DNA from less harmful bacteria naturally found in the human throat.
“This process is called ‘horizontal gene transfer’ and allows bacteria to pick up and incorporate small pieces of DNA from other bacteria in their environment, effectively borrowing genetic traits without direct reproduction taking place,” the scientists explained.
The changes appear to have altered how the strain interacts with human cells, making it more effective at causing severe disease and potentially harder for the immune system to recognize.
The same changes may also help explain why the strain has not continued to spread widely since the outbreak was controlled.
The findings were published as a pre-print and presented this week at the UKHSA Conference 2026 in Manchester.
The researchers compared the Kent outbreak with historical outbreaks, including one at the University of Southampton in 1997, and found similarities in how the bacteria evolved.
The team said highly invasive strains can emerge suddenly and unpredictably, meaning similar outbreaks could occur again, although exactly when and where is impossible to predict.
The findings highlight the importance of genomic surveillance, rapid public health responses, vaccination and awareness of meningococcal disease symptoms.
Meningitis is inflammation of the meninges, the protective membranes covering the brain and spinal cord. It can be caused by bacterial, viral, fungal or parasitic infections, as well as non-infectious conditions.
Bacterial meningitis can be severe and may lead to complications including hearing loss, vision problems and death if not treated promptly.
In infants, symptoms may include excessive crying, irritability, feeding difficulties, a bulging soft spot on the head and unusual lethargy.
Two doses of the MenB vaccine offer protection against meningococcal group B disease.
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GLP-1 medications have shown significant promise in treating obesity and type 2 diabetes in adults. Their use has also expanded among children with obesity. However, a new study found that nearly 1 in 6 children, or 17%, treated with GLP-1 medications developed a diagnosed nutritional deficiency within one year.
The research, conducted by scientists at Northwestern University and Ann & Robert H. Lurie Children’s Hospital of Chicago, found that vitamin D deficiency was the most common nutritional deficiency, identified in 12.4% of children within one year of starting GLP-1 treatment.
“As appropriate pediatric use of GLP-1s becomes more widespread, we need to understand the risks during periods of rapid growth and pubertal development,” said senior author Justin Ryder, associate professor of surgery and pediatrics at Northwestern University Feinberg School of Medicine.
“Nutrients such as vitamin D, iron and calcium are of particular concern during adolescence, when deficiencies may have lasting implications for skeletal health and overall development,” the expert added. The study was published in the journal Childhood Obesity.
According to Ryder, nutritional support is key once treatment with a GLP-1 medication is initiated.
However, the study found that only 5% of patients received nutritional counseling within 30 days of starting GLP-1 treatment, while less than 25% received nutritional counseling within six months.
The scientists used national administrative claims data from 2017 to 2022 covering more than 100 million patients. They identified 2,031 GLP-1 users aged 10–17 who met continuous enrollment criteria and had no prior diagnosis of nutritional deficiency.
Among these children, the most commonly prescribed GLP-1 medications were liraglutide (78.6%), dulaglutide (10.4%) and semaglutide (9.1%).
The researchers said proactive nutritional management is important when GLP-1 medications are prescribed to children, rather than waiting until a nutritional deficiency is diagnosed.
The new study comes as the use of GLP-1 medications among younger children has been rising in the US, although their use for obesity in this age group remains limited and varies by medication. The FDA has approved GLP-1 treatment for obesity in adolescents, among those age 12.
A recent study from NYU Langone Health, based on health records from more than 3.5 million children aged 8 to 11 with obesity in the US, found that prescriptions for GLP-1 medications increased more than 300-fold between 2019 and June 2026.
In 2019, about 0.03% of children in the study group had been prescribed a GLP-1 drug. By June 2026, that figure had risen to 9.3%.
The medications included drugs such as Wegovy and Saxenda, made by Novo Nordisk, and Eli Lilly's Zepbound.
Among children receiving GLP-1 medications, 94% had severe obesity, while about 65% had obesity-related health conditions, including high blood pressure or sleep apnea.
The FDA has approved certain GLP-1 medications for obesity in some pediatric age groups, but the approvals and age limits vary by drug. The GLP-1 medications included in the under-12 study are not generally FDA-approved for weight management in children younger than 12.
However, doctors can prescribe medicines off-label when they believe there is a medical reason to do so. Clinical guidelines may also support the use of obesity medications in certain circumstances involving younger children.
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India’s Central Drugs Standard Control Organisation (CDSCO) has issued an advisory cautioning against the indiscriminate use of painkillers and antibiotics.
It warned that inappropriate or prolonged use of these medicines can lead to kidney complications and contribute to antimicrobial resistance.
This comes as a Parliamentary Standing Committee on Health and Family Welfare recently noted that the pooled prevalence of chronic kidney disease (CKD) in India is approximately 13.24%.
The committee suggested that people above 20 undergo kidney function testing every six months.
“NSAIDs/painkillers and antibiotics should not be taken indiscriminately, repeatedly or for prolonged periods without medical advice,” the CDSCO said.
It also suggested them to seek medical advice if pain, fever or other symptoms persist or recur, instead of repeatedly using painkillers or antibiotics on your own.
Further, the CDSCO noted that antibiotics should not be used for self-medication or for conditions where they are not clinically indicated, such as most uncomplicated viral infections.
Prescribed antibiotics should be taken strictly as advised and should not be shared or used from leftover medicines.
“Antibiotics prescribed by a healthcare professional should be taken strictly as advised and should not be shared with other persons or used from leftover medicines.”
Also read: Young Americans Are Developing Kidney Failure Without Usual Risk Factors: What Is CKDu?
Healthcare practitioners have been advised to prescribe NSAIDs and antibiotics only when clinically indicated, after considering the patient’s:
“The lowest effective dose for the shortest appropriate duration should be considered when prescribing NSAIDs, particularly in patients at increased risk of renal impairment.”
Doctors have also been advised to take appropriate precautions when prescribing NSAIDs to people with:
Antibiotics should be prescribed judiciously in line with antimicrobial stewardship principles. Unnecessary combination therapy, inappropriate antibiotic selection, incorrect dosing and unnecessarily prolonged treatment should be avoided.
The CDSCO has asked hospitals and healthcare institutions to:
The regulator has directed pharmacies and retailers to strictly comply with rules governing the sale and distribution of prescription medicines.
The CDSCO said that various drugs, including NSAIDs and antibiotics, are placed under Schedules G, H, H1 and X of the Drugs Rules, 1945.
Most NSAIDs are included in Schedule H and are not to be sold at retail without a prescription from a Registered Medical Practitioner. Similarly, most antibiotics are included in Schedule H1.
They are required to carry the following warnings:
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