Category: 8. Health

  • How are aid cuts impacting child vaccines? The IRC’s critical response

    How are aid cuts impacting child vaccines? The IRC’s critical response

    Right now, global funding for humanitarian aid is facing unprecedented cuts. In 2024 alone, there was a staggering $25 billion shortfall between the funds needed for United Nations appeals and the contributions received.

    In a major setback to global humanitarian efforts, in early 2025 the U.S. State Department—once the world’s largest aid donor—terminated more than 10,000 foreign aid grants and contracts. This has had far-reaching consequences, including the disruption of many lifesaving vaccination programs.

    These cuts come at a time when millions of children in conflict and crisis-affected areas already lack access to critical immunizations, remaining at risk simply because national health systems can’t reach them.

    The funding crisis deepens 

    Recent policy shifts have impacted vaccination funding around the world, including those led by Gavi, the Vaccine Alliance. 

    Infectious disease outbreaks cost an estimated $60 billion per year globally. These outbreaks know no borders and can impact us all. In contrast, disease prevention through vaccination and routine immunization, particularly when delivered by frontline actors, have proven to be highly effective.

    The impact of aid cuts on immunization

    Of the 13 countries the IRC has identified as the most affected by global aid cuts, 10 rank among the bottom 20 globally for measles immunization rates, highlighting a critical gap in disease prevention. This issue is even more alarming as climate change continues to heighten the risks of infectious diseases, further compromising global health efforts.

    Due to these funding cuts, 300 IRC-supported health facilities have closed or are at risk of closing. 

    The IRC provides about 4.3 million services for communicable diseases around the world—1.7 of these services are delivered to children under 5. These services are essential for preventing and controlling outbreaks in vulnerable communities. Critical immunization programs in Burkina Faso, Nigeria, and Afghanistan are all facing the threat of closure.

    Nearly 80% of outpatient visits at the IRC’s 3,300 health facilities worldwide are for infectious diseases. Our programs are integral to helping vulnerable groups survive and to stop diseases from spreading.

    Photo: Karl Bergbom for the IRC

    A global health security threat

    “Preparing for the next pandemic starts by investing where outbreaks begin,” says Dr. Mesfin Teklu Tessema, Senior Director of Health at the IRC. “Global health security is not a luxury. It is a strategic imperative—one that demands sustained, coordinated investment.”

    Cutting vital immunization programs – as well as primary healthcare services- increases the risk of infectious disease outbreaks that could impact everyone. Without prevention and treatment efforts, diseases are more likely to spread unchecked, mutate and become harder to control.

    With 21 million children around the world currently under-immunized, reaching these underserved communities is critical to preventing outbreaks that threaten both regional and global health security.

    The IRC’s solution: Access to life-saving vaccines for children in missed communities

    The IRC is committed to ensuring children receive a full schedule of life-saving vaccines, making immunization a cornerstone of its child health programs. In 2024 alone, over 700,000 children under the age of one were protected against vaccine-preventable diseases by receiving their third dose of the diphtheria, tetanus, and pertussis (DTP) vaccine. This vital protection allows these children to grow up healthier and free from the threat of preventable illnesses.

    To expand access to essential healthcare, including immunizations, the IRC has implemented strategic initiatives designed to maximize the impact of its efforts. These programs focus on reaching children in some of the world’s most fragile and conflict-affected regions, ensuring even the most vulnerable populations can access the care they need. 

    In 2022, the IRC launched the Reaching Every Child in Humanitarian Settings (REACH) project in partnership with Gavi, the Vaccine Alliance. The aim: leverage the IRC’s unique humanitarian expertise to ensure that even the hardest-to-reach children receive the full national schedule of vaccines. 

    Using flexible methods like mobile clinics, local community teams, and mapping tools, our teams are able to reach people in places where the government health system can’t work properly because of conflict, danger, or climate-related problems.

    Since its launch, the REACH consortium has enabled health workers to administer over 13 million vaccine doses to children across the Horn of Africa, with recent extension into Chad and Nigeria.

    An IRC nurse attends to a child during an IRC community outreach program in Turkan, Kenya.

    An IRC nurse, Nancy, attends to Selina Naoi’s* child, Maria*, during an IRC community outreach program in Turkan, Kenya.

    Photo: Billy Mutai for the IRC

    Reaching children at the last mile

    Using flexible and evidence-based interventions enables us to reach more children with essential vaccines, while ensuring maximum impact per dollar spent. Training and supporting community health workers with local knowledge is central to this approach. In 2024, the IRC supported 15,800 community health workers to help ensure more children are protected by lifesaving vaccines.

    In South Sudan, we worked with community health workers and local leaders to raise awareness about vaccines for diseases like polio, measles and diphtheria. Community health workers were also empowered to share community feedback with health officials and help combat misinformation. 

    IRC staff in South Sudan traverse through a flooded village to reach children with vaccinations in Koch County.

    IRC staff in South Sudan traverse through a flooded village to reach children with vaccinations in Koch County.

    Photo: International Rescue Committee

    How can you support vital vaccine programs?

    Now, more than ever, your support is urgently needed to help humanitarian organizations continue to deliver lifesaving services. 

    The new era of reduced aid will bring difficult decisions. But by investing in IRC’s Primary Healthcare Programs that deliver immunization services that center proven interventions, empower local responders, and implement smart financing strategies, we can ensure that available resources have the maximum impact for those most in need.

    With collective action, we can prevent this funding crisis from becoming an era of unprecedented suffering and instead set a path toward sustainable relief and long-term resilience for the world’s most vulnerable populations.

    Donate: Financial contributions are key for trusted organizations like the IRC that prevent, treat and contain infectious diseases. Your donation can empower our work in the U.S. and more than 40 countries worldwide.

    Get connected: Follow our InstagramLinkedInFacebook, and Bluesky accounts.

    Stay informed: Subscribe to IRC alerts to get the latest on our programming and learn more about how you can make a difference.

    Our continued commitment to delivering vital health care

    Every child deserves the right to health care and protection, regardless of crisis. But due to aid cuts, vulnerable children who are relying on humanitarian aid to survive, could be left with nothing. This is a matter of life or death.

    With over 90 years of experience, the IRC knows how to push through tough times by focusing on what matters most—helping those in crisis, working hand-in-hand with communities and treating people with dignity. Our commitment to supporting the hardest-to-reach communities with lifesaving immunization will not waver.

    *Names changed for privacy reasons.


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  • Easing Fears of Cardiac Testing

    Easing Fears of Cardiac Testing

    It’s common for patients to schedule an office visit due to symptoms like shortness of breath from doing regular tasks, feeling heart palpitations, experiencing mild chest pain, or feeling weak or unusually tired. 

    During your assessment, if you determine that the patient has an irregular heartbeat, a family history of cardiac conditions, or believe further testing is warranted, realize that a patient could be fearful of cardiac testing. To ease the concerns of your patients, it’s important to explain how such testing can diagnose the reason they aren’t feeling quite right and how their treatment team can help them feel better.

    Start With the Why 

    Leaving the trusted environment of a primary care office can be daunting for patients, particularly for those who haven’t had cardiac testing before. But explaining why you’re suggesting the tests can help a patient understand. 

    “The most important step would be to explain how cardiac testing can be important in order to screen for issues before they become serious,” said David Weininger Cohen, MD, a cardiologist with the Leonard M. Miller School of Medicine at the University of Miami in Florida.

    He also suggested recounting what symptoms patients are experiencing and how specific tests can investigate what’s causing them. Also, explaining that some symptoms may not even be tied to cardiac issues could be another strategy to demonstrate the importance of further testing.

    “For instance, chest pain is a symptom that becomes a common reason for visits. Most people usually associate chest pain with heart issues, but there are a lot of structures in the chest that can cause pain, not just the heart — cartilage, esophagus, sometimes part of the stomach, skin, and even nerve endings,” he said. “Ultimately, cardiac testing is important because it allows the physician to discriminate between cardiac and non-cardiac causes for the patient’s symptoms.”

    In addition, reassuring your patients that these experts can diagnose potential issues may also ease their worries, so articulate how such cardiac tests are performed in a controlled environment with trained staff that can anticipate issues and respond quickly if something goes wrong, Weininger Cohen added. 

    Understand Patients Are Fearful of Test Results

    Some patients are afraid of the results as much as the test. 

    “In those cases, I like to reinforce why the test is necessary and why we’re doing it,” said Weininger Cohen. “Additionally, I sometimes go through the possible scenarios depending on the results of each test.” Knowing what lies ahead, depending on what the test shows, can sometimes be reassuring — you’re showing patients you know exactly what the next steps would be. 

    Treat Fears Patient by Patient

    Although there are some general practice strategies to ease fear regarding cardiac testing, personalizing your approach is also important. 

    “The best way to tackle fear of cardiac testing would be to ask the patient exactly what they’re afraid of,” said Weininger Cohen. Some patients are going to be afraid of having pain or discomfort during the test. Some patients are afraid of what the results may be, and some patients are afraid of possible complications. 

    “Usually, the best way to approach the topic is to explain the reason for the test and then address the specific fear the patient has,” he specified.

    For example, the best way to describe an EKG would be to explain that it is a test that is trying to capture the electrical activity of the heart. To achieve that, the person performing it is putting sensors on different parts of the patient’s body to detect the heart’s electrical current from different points, he said. Emphasizing that the test is painless, and that it’s just capturing the natural electrical activity of the heart, should put patients at ease. 

    How Can You Best Describe an Echocardiogram? 

    Most patients understand what an ultrasound is, so advising patients that an echocardiogram is simply an ultrasound study of the heart can calm fears. It may also be helpful to share that in some cases, ultrasounds use enhancing agents, referred to as contrast, to get a look at the different structures of the heart, he said. 

    Some patients could be concerned about radiation. 

    “Both tests are radiation free, and this is something that some patients are very interested in knowing before proceeding, especially if they have been previously exposed to radiation through other diagnostic imaging tests or radiotherapy for cancer treatment,” Weininger Cohen said. Taking the time to explain both an echocardiogram and an EKG can help your patients understand what to expect and reduce worry and the fear of the unknown.

    What to Tell Patients Before Referring to a Cardiologist

    Referring a patient to a specialist like a cardiologist could cause fear. So explain why you’re taking this step. 

    Mustafa M. Ahmed, MD

    “Telling a patient why they need to see a heart expert and how they will add to their overall care can be a helpful first step,” said Mustafa M. Ahmed, MD, a cardiologist and professor of medicine, who’s also vice chief of research of the Division of Cardiovascular Medicine and medical director of the Mechanical Circulatory Support Program at the University of Florida in Gainesville. “Assuring them that they won’t be losing their primary care doctor, but gaining a specialist to consult with both them and the primary care team, is often a good way to frame expectations.”

    Lifestyle Tweaks You Might Suggest 

    In the context of your discussions with patients regarding their symptoms and recommendations for cardiac testing, Ahmed suggested expressing how diet and exercise, as a part of overall lifestyle changes, can be the most impactful way to prevent heart disease. 

    “Gentle guidance and step-by-step encouragement are often helpful,” he said. 

    Also, involving other family members and friends in that journey is another strategy. This may include taking walks, preparing meals together, or embracing a healthier mindset overall.

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  • Increased COVID-19 Testing Skewed Understanding of Respiratory Disease Trends

    Increased COVID-19 Testing Skewed Understanding of Respiratory Disease Trends

    Testing practices during and after the COVID-19 pandemic were found to have significant implications on the post-pandemic understanding of respiratory diseases, according to a study published in the Journal of Infection and Public Health.1 Because of increased COVID-19 testing for healthy individuals, researchers uncovered a potential for overdiagnosis of infectious diseases including respiratory syncytial virus (RSV), influenza, and invasive pneumococcal disease.

    “RSV is a major cause of infant hospitalizations, while influenza tends to affect toddlers and school-aged children more commonly,” wrote authors of the study. “Bacterial infections, though less frequent, remain a concern. Especially, children with complex chronic diseases are more susceptible to invasive infections caused by Streptococcus Pneumonia, known as invasive pneumococcal disease, which is a severe and potentially life-threatening condition.”

    Indeed, researchers’ understanding of how respiratory diseases interact with one another was crucial during times like the COVID-19 pandemic. Even more important for pediatric patients, major pandemic-level events have been found to significantly impact epidemiology patterns of respiratory diseases.2

    The current study’s researchers wanted to place the focus on the pandemic and the non-pharmaceutical interventions (NPIs) that came from it. | image credit: Drobot Dean / stock.adobe.com

    READ MORE: ACIP Votes to Expand RSV Vaccine Recommendation to Include Adults 50 Years and Older

    Along with older adults over 65, children too are deemed at risk of contracting respiratory illnesses; a risk that was significantly increased during the COVID-19 pandemic. According to BMC Pulmonary Medicine, rhinovirus/enterovirus and RSV were the most prominent among children during the COVID-19 era.3

    Many researchers and health care professionals are aware of the complex interplay between various respiratory viruses and how they are manifested in children. However, researchers of the current study wanted to place the focus on the pandemic and the non-pharmaceutical interventions (NPIs) that came from it.

    “A potential consequence of these interventions has been the phenomenon known as ‘immunity debt,’ which refers to the reduction in population immunity due to lack of exposure to common pathogens during the pandemic,” continued the authors.1 “The concept of immunity debt has been hypothesized to explain the post-pandemic surge in respiratory infections, and the focus of this study is to present empirical data scrutinizing and quantifying these patterns.”

    Focusing on the 3 aforementioned respiratory diseases, researchers’ goal was to explore the overall impact NPIs that emerged during the pandemic had on RSV, influenza, and invasive pneumococcal disease. They conducted a national, population-based analysis of children in Denmark over a 10-year period lasting from 2012 to 2022.

    Throughout the time period, researchers scanned microbiology tests and hospital contacts for infection rates and testing patterns before, during, and after the pandemic. All participants included in the study were born in Denmark and between 0 and 17 years old during the study period.

    “The outcomes of interest were the occurrences of tests for 3 different pathogens, specifically RSV, influenza virus, and pneumococcus,” they wrote.1 “Testing for COVID-19 was also included to provide context within the study period. Testing patterns were described based on both the absolute number of tests performed and the percentage of positive tests.”

    Researchers included a total of 1,790,464 unique individuals in the final analysis.

    Overall, COVID-19 restrictions and lockdowns led to decreased cases of respiratory diseases. Once those lockdowns were lifted, respiratory infections experienced a resurgence. With COVID-19 emerging at this time as a notable respiratory illness alongside RSV, the flu, and pneumococcus, testing for respiratory pathogens noticeably increased among children in Denmark.

    “The NPIs for COVID-19 not only limited the spread of the targeted virus but also substantially decreased the incidence of RSV, influenza, and pneumococcus,” wrote the authors.1 “The subsequent lifting of restrictions led to a notable resurgence of these infections, likely attributable to immunity debt arising from reduced pathogen circulation.”

    With further evidence regarding immunity debt uncovered, studies like this are constantly being conducted to further the knowledge of health care professionals and their understanding of COVID-19. Like many of the ongoing studies regarding COVID-19’s impact on health care and respiratory health, evidence from the current study can now be used to inform future policy regarding respiratory viruses, infectious diseases, and how they interact with each other among children.

    “Our study comprehensively described the impact of behavioral changes and immunity debt on infectious disease epidemiology,” concluded the authors.1 “The rising number of tests among healthy children contributes to ongoing discussions regarding overdiagnosis and the implications for health care policy.”

    READ MORE: Respiratory Resource Center

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    References
    1. Jensen A, Stensballe LG. Impact of COVID-19 on testing, positive cases, patient characteristics, and hospital contacts for respiratory syncytial virus, influenza, and pneumococcus in Danish children. J Infect Public Health. 2025;18(2):102660. https://doi.org/10.1016/j.jiph.2025.102660
    2. Dallmeyer LK, Schüz ML, Fragkou PC, et al. Epidemiology of respiratory viruses among children during the SARS-CoV-2 pandemic: a systematic review and meta-analysis. IJID. 2023;138:10-18. https://doi.org/10.1016/j.ijid.2023.10.023
    3. Khales P, Razizadeh MH, Ghorbani S, et al. Prevalence of respiratory viruses in children with respiratory tract infections during the COVID-19 pandemic era: a systematic review and meta-analysis. BMC Pulm Med. 2025;25. https://doi.org/10.1186/s12890-025-03587-z

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  • Cough medicine may help slow down Parkinson’s dementia

    Cough medicine may help slow down Parkinson’s dementia

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    A cough medicine may help slow down dementia progression in people with Parkinson’s disease. Image credit: DEV IMAGES/Getty Images.
    • Parkinson’s disease dementia develops in people who have a Parkinson’s disease diagnosis.
    • Experts are interested in finding the best ways to address and prevent Parkinson’s disease dementia.
    • A randomized clinical trial found that the drug Ambroxol may help stabilize the neuropsychiatric symptoms of Parkinson’s disease dementia, and confirmed the safety of the drug’s use among participants.

    Dementia is a common problem that remains a critical focus of clinical research. One subtype of dementia is Parkinson’s disease dementia, which has to do with the mental changes that occur in some people who already have Parkinson’s disease.

    A study published in JAMA Neurology compared the outcome of the expectorant Ambroxol with a placebo among participants with Parkinson’s disease dementia.

    While primary and secondary outcomes were similar, participants on the placebo experienced worsening neuropsychiatric symptoms compared to symptoms remaining the same in the intervention group.

    The results also showed a possible improvement in cognitive symptoms for people with variants of a particular gene.

    The authors of the current study note the need for disease-modifying interventions for Parkinson’s disease dementia. They note that focusing on a particular enzyme, beta-glucocerebrosidase, has potential, with an increase in this enzyme possibly making things better. They also note that the medication Ambroxol affects this enzyme.

    This study involved examining the safety of Ambroxol, how well participants tolerated the medication, and how it affected cognitive symptoms.

    There were 55 participants in total. All participants were over 50 years old and had confirmed Parkinson’s disease for 1 year or more before developing dementia. All participants also had a study partner, someone who was in contact with them “at least 4 days per week.”

    Participants took either Ambroxol or the placebo for 1 year. Researchers had trouble with recruitment for a low-dose Ambroxol group, so this group was not included in the statistical analyses of primary and secondary outcomes. Overall, there were 22 participants in the high-dose Ambroxol group and 24 participants in the placebo group.

    As a primary outcome, researchers evaluated participants’ conditions using two evaluations: the Clinician’s Global Impression of Change and the Alzheimer Disease Assessment Scale-cognitive subscale version 13.

    They also used other evaluation tools for secondary outcomes, including the Parkinson’s Disease Cognitive Rating Scale, the Clinical Dementia Rating Scale, and the neuropsychiatric inventory. Researchers were able to look at cerebral spinal fluid and plasma biomarkers in some participants as well.

    Throughout the study, some participants withdrew due to adverse events. Eight participants in the Ambroxol group withdrew, and three in the placebo group withdrew.

    Participants in the Ambroxol group saw more gastrointestinal adverse events. The placebo group experienced more psychiatric adverse events and falls than the intervention group.

    In the statistical analyses, the primary and secondary outcomes between the two groups were about the same. Thus, Ambroxol did not appear to have a significant impact on cognition.

    However, researchers did observe that the neuropsychiatric inventory stayed the same for the Ambroxol group, but the placebo group got worse in this area, indicating the placebo group experienced worsening behavioral functioning.

    The authors of the study note that GBA1 gene variants can increase the risk for cognitive decline in people who have Parkinson’s disease, and that “homozygous disease-causing variants in GBA1” can increase the risk for Parkinson’s disease.

    In participants with GBA1 gene variants, those taking the high-dose Ambroxol had decreases in neuropsychiatric inventory scores, three to a level of “clinically meaningful improvement,” and three also had clinically important improved cognitive scores.

    Researchers also observed increased beta-glucocerebrosidase levels among Ambroxol participants at the 26-week mark.

    Study author Stephen H. Pasternak, MD, PhD, FRCPC, a specialist in neurology, explained the following about the study to Medical News Today:

    “Our goal was to test the safety and tolerability of Ambroxol and to assess its effect on cognition. We randomized 55 patients to Ambroxol 1,050 mg/day [milligrams per day] or placebo for 1 year. Ambroxol was well tolerated; we only saw stomach upset as a side effect, and it was mostly mild. Patients on Ambroxol had fewer psychiatric symptoms. Patients on placebo had a worsening of plasma GFAP, a marker of neurodegeneration. A subgroup of patients (with GBA1 mutations) appeared to have improved cognition.”

    Pasternak told MNT that: “We hope that Ambroxol, or drugs like Ambroxol, will be able to prevent the onset of Parkinson’s disease and dementia if it is given early enough.”

    While more research is needed, this study sets up the possibility of using Ambroxol in the future to help people with Parkinson’s disease dementia.

    Daniel Truong, MD, a neurologist, medical director of the Truong Neuroscience Institute at MemorialCare Orange Coast Medical Center in Fountain Valley, CA, and editor-in-chief of the Journal of Clinical Parkinsonism and Related Disorders, who was not involved in this research, explained that with future research this could lead to “a new class of disease-modifying therapy for [Parkinson’s disease dementia].

    Hypothesising on the potential mechanisms of action, Truong explained that:

    “Ambroxol, by enhancing lysosomal function via GCase [beta-glucocerebrosidase], may slow underlying neurodegeneration, especially in GBA1-related PDD [Parkinson’s disease dementia] — marking a shift toward targeted disease modification rather than purely symptomatic treatment.”

    He also noted that this could lead to “repurposing an established drug” as “Ambroxol is already widely used as a mucolytic agent with a known safety profile.”

    “This reduces development time, regulatory barriers, and cost, making it more feasible for rapid clinical adoption — especially in resource-limited settings,” Truong added.

    Still, should the current study findings be confirmed by further research, Pasternak hopes experts may see the drug in a new light.

    “Current therapies for Parkinson’s disease and dementia address symptoms but do not stop the underlying disease. These [new] findings suggest Ambroxol may protect brain function, especially in those genetically at risk. It offers a promising new treatment avenue where few currently exist,” he noted in a press release.

    The study does have a few limitations. It was a fairly small study with mostly white male participants that only went on for one year. It is possible that 1 year was not long enough to evaluate changes in cognitive symptoms since the placebo group did not see declines in cognitive symptoms.

    Researchers also note that the study was limited since it was a phase 2 trial out of a single center.

    They also acknowledge difficulties in recruitment and retention, and note that participants had “limited ability to tolerate the long cognitive assessments.”

    The researchers did not get to conduct statistical analyses to look at differences between high and low doses of Ambroxol. They also note that the low-dose group appeared to have worse cognition. They suggest that future studies should possibly stratify participants by cognitive severity.

    They also acknowledge that it is possible that the Alzheimer Disease Assessment Scale-cognitive subscale version 13 might not have been sensitive enough to detect changes in 1 year in participants who had mild Parkinson’s disease dementia. All participants in this study only had mild to moderate dementia.

    Finally, only eight participants total had GBA1 gene variants, so more research is needed to see if people in this group could experience distinct benefits from Ambroxol. Only three participants with GBA1 gene variants had the minimal clinically important difference in cognitive scores, and researchers acknowledge that “this sample is too small to support any conclusion.”

    Pasternak and his colleagues are planning to conduct a follow-up clinical trial later in 2025. The current research received funding from the Garfield Weston Foundation, a grant-giving nongovernmental organisation in the United Kingdom.

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  • Corticosteroids may reduce effectiveness of immunotherapy in lung cancer

    Corticosteroids may reduce effectiveness of immunotherapy in lung cancer

    Corticosteroids, a commonly prescribed medication to alleviate cancer-related symptoms for non-small cell lung cancer patients treated with immunotherapy, are the main reason certain immunotherapies may fail in treating the disease, according to new research by Keck Medicine of USC. 

    The study, published today in Cancer Research Communications, showed that high doses of steroids, when given before and/or during a specific type of immunotherapy, caused patients’ tumors to shrink less than those of patients not on steroids. Those patients also did not live as long. 

    Steroids were the biggest predictor of why certain immunotherapies may not be effective, even when considering multiple other factors such as stage and progression of the disease.”


    Fumito Ito, MD, PhD, Keck Medicine oncologist and immunologist, lead author of the research

    Additionally, researchers believe they have found the mechanism behind why steroids and some immunotherapies may not mix. 

    “Our findings reveal that steroids stop the body’s natural cancer-fighting cells, T-cells, from maturing. This makes them unable to attack the cancer as vigorously as they usually would, leading to worse outcomes for patients,” said Ito, who is also a member and co-leader of the translational and clinical sciences research program at USC Norris Comprehensive Cancer Center. “While other research has indicated steroids may negatively impact immunotherapy’s efficacy, we are one of the first to pinpoint a probable cause and effect.” 

    Ito and his colleagues also discovered that steroids blocked circulating biomarkers in the body – bits of cells in the bloodstream that signal when cancer is progressing so oncologists can adjust the patient’s treatment. 

    “Without the presence of circulating biomarkers to inform our decisions, oncologists cannot treat the cancer as effectively and patients may miss out on the best treatment for their cancer,” said Ito. 

    Two competing medications 

    The study examined the effect of steroids on a type of immunotherapy known as immune checkpoint inhibitors (ICIs). ICIs help the body’s immune system fight cancer by blocking proteins that prevent T-cells from attacking cancer cells. ICIs are often used to treat non-small cell lung cancer, the most common form of lung cancer. 

    Steroids are often prescribed to alleviate symptoms of the cancer or treatments given for a variety of reasons, such as fatigue and vomiting, or more serious side effects like brain swelling and lung inflammation. Steroids suppress the immune system, which reduces the inflammation that can cause these conditions. 

    How the studies were conducted 

    Ito and fellow researchers retrospectively studied the medical records of 277 patients with Stage II-IV non-small cell lung cancer who were treated with ICIs alone or in combination with other therapies. They compared outcomes (tumor shrinkage and survival rate) between patients prescribed steroids and those who were not at three centers, including USC Norris Comprehensive Cancer Center. 

    They analyzed up to eight years of data to determine that steroids were the sole factor impeding the effectiveness of the immunotherapy. 

    They also determined that the T-cells of significant numbers of patients on steroids were not fully matured and launched a preclinical study using mice to observe the effects of steroids on ICI therapy in real time. This mouse model study led to the discovery that steroids given before/during immunotherapy inhibit T-cells from fully maturing. 

    The future of steroids 

    While the Keck Medicine research indicates steroids can interfere with ICIs, Ito acknowledges that for some patients, steroids may be necessary to manage their cancer-related symptoms. 

    “We know that steroids will continue to play an important role in lung cancer care, but it is important to understand their potential limitations,” said Ito. “Each patient should talk to their oncologist to make sure they have the best possible care plan tailored to their specific needs.” 

    He hopes this research will lead to more studies examining the effect of steroids on immunotherapy so oncologists can make fully informed decisions that will best benefit their patients. 

    Other study authors include Keck Medicine medical oncologists Jorge Nieva, MD and Robert Hsu, MD. 

    The study was supported with grants from the National Cancer Institute, P30CA016056 (RPCCC), P30CA014089 (USC), K08CA197966, R01CA255240, R01CA272827 (F. Ito), R01CA188900, R01CA267690 (B.H. Segal) as well as the Department of Defense Lung Cancer Research Program and the Uehara Memorial Foundation. 

    Source:

    University of Southern California – Health Sciences

    Journal reference:

    Polyakov, L., et al. (2025). Impact of Glucocorticoids on Immune Checkpoint Inhibitor Efficacy and Circulating Biomarkers in Non–Small Cell Lung Cancer Patients. Cancer Research Communications. doi.org/10.1158/2767-9764.crc-25-0051.

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  • New investigation reveals potentially fatal side effects of popular weight-loss drugs

    New investigation reveals potentially fatal side effects of popular weight-loss drugs

    Image credits: Getty Images

    Every coin has two sides and so does every miracle. While it gives a person an advantage, it also gives them a disadvantage. Popular weight-loss drugs like Ozempic have been revolutionary in weight loss with a plethora of celebrities jumping on the bandwagon. However, their side-effects including tooth decay, droopy face, saggy butt and hair loss have not been hidden from the eyes of all.Now, a UK regulator is shedding light on much more serious and potentially fatal side effects of these drugs. The UK’s Medicines and Healthcare products Regulatory Agency’s (MHRA) Yellow Card scheme, the official system for collecting and monitoring reports of suspected side effects or reactions to drugs and devices, has recently received over 400 reports of serious pancreas trouble from users of GLP-1.

    Over 400 reports of serious pancreas trouble from users of GLP-1

    Image credits: Getty Images

    Acute pancreatitis is a sudden and extremely painful inflammation of the pancreas that causes people severe abdominal pain, nausea and fever. In the UK, there have been at least 10 deaths linked to this condition among users of GLP-1. Among the users of Mounjaro, there have been 181 reported cases of acute or chronic pancreatitis with 5 deaths.While the pamphlets on these famous drugs note that pancreatitis is an uncommon reaction that only affects one in 100 users, the condition is deemed serious enough to require an investigation.

    Higher risk of developing pancreatitis while taking GLP-1 drugs?

    Image credits: Getty Images

    “Sometimes genes can influence the side‑effects an individual experiences when taking a medicine,” the MHRA told The Guardian. Thus along with Genomics England, MHRA is launching a new study to see if people’s genes put them at a higher risk of developing pancreatitis while taking GLP-1 drugs. Those who have pancreatitis while using the jabs will be asked to provide a saliva sample and have their genes tested.Novo Nordisk, which produces Ozempic and Wegovy, advised people to take the medications only for their approved indications and under the strict supervision of a healthcare professional. “We continuously collect safety data on our marketed GLP-1 medicines and work closely with the authorities to ensure patient safety. The benefit-risk profile of our GLP-1 medicines remains positive, and we welcome any new research that will improve our understanding of treatments for people living with chronic diseases,” they told the outlet.


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  • Sudden Intense Chest Pain Unlike Prior Pneumothorax

    Sudden Intense Chest Pain Unlike Prior Pneumothorax

    Editor’s Note:
    The Case Challenge series includes difficult-to-diagnose conditions, some of which are not frequently encountered by most clinicians, but are nonetheless important to accurately recognize. Test your diagnostic and treatment skills using the following patient scenario and corresponding questions. If you have a case that you would like to suggest for a future Case Challenge, please email us at ccsuggestions@medscape.com with the subject line “Case Challenge Suggestion.” We look forward to hearing from you.

    Background and Initial Presentation

    A 35-year-old man with a history of two prior spontaneous pneumothoraxes — both managed conservatively — presents to the emergency department with new-onset chest pain and lightheadedness. The pain is described as sudden, intense, and exacerbated by deep breathing. He indicates that it is located in the center of the chest. He denies dyspnea or leg swelling and has no other complaints. When asked, he says this pain is different from his pneumothorax pain, mainly because it is in the center of his chest.

    Physical Examination and Workup

    Vital signs are within normal limits, except for a pulse > 120 bpm. Physical examination reveals diminished breath sounds on the left hemithorax. There are no rales or wheezes and no leg edema.

    Discussion

    Central pleuritic chest pain in a patient with a history of pneumothorax suggests a pulmonary etiology. A chest x-ray is the most appropriate investigation to promptly assess for recurrent pneumothorax, pleural effusion, structural abnormalities, or other intrathoracic pathology.

    ECG or cardiac biomarkers such as troponins are indicated primarily if myocardial ischemia or infarction is suspected. This suspicion would be raised if the patient described his chest pain as squeezing or pressure-like sensation radiating to the neck, jaw, or left arm. The patient’s young age and lack of history of coronary artery disease also make acute coronary syndrome less likely.

    A CBC may provide supplementary information about signs of infection or inflammation, especially if the chest x-ray appears normal, but a CBC alone is unlikely to determine the cause of the patient’s acute pleuritic chest pain.

    On initial testing, chest x-ray, metabolic panel, and troponin level were normal. CBC showed an elevated white blood cell count (16,200/μL). An ECG was also performed (Figure 1).

    Figure 1. ECG performed on patient in ED.

    Despite the central location of symptoms, the patient’s young age, history of pneumothorax, and presence of pleuritic chest pain would have placed pneumothorax high on the initial differential diagnosis. After pneumothorax was ruled out with chest x-ray, PE should have become the leading consideration given the pleuritic pain and the patient’s age group, in which PE is far more common than coronary artery disease. Although anxiety is also common in this age group — as it is in others — it should remain a diagnosis of exclusion, considered only after more serious conditions have been reasonably ruled out.

    While the ECG is not diagnostic of PE, it raises suspicion by demonstrating three supportive findings: tachycardia, incomplete right bundle branch block, and nonspecific ST-segment changes.[1] A subsequent D-dimer test was positive, and chest CT angiography showed extensive bilateral pulmonary emboli, more pronounced on the left side.

    PE typically presents as either unilateral pleuritic chest pain or as dyspnea with or without chest pain.[1] However, PE can present without the typical symptom of chest pain, sometimes being asymptomatic or discovered incidentally during diagnostic workup for other conditions.[1,2,3] Other symptoms of large pulmonary emboli may include syncope, diaphoresis, and cardiac arrest. Other symptoms of smaller emboli may include minor hemoptysis or cough.[1,3]

    Although most patients with PE have at least one identifiable risk factor, up to 20% of patients present without any known risk factor, so the absence of risk factors should not exclude the diagnosis.[1]

    Pain in patients with PE is believed to result from pulmonary infarction, which typically occurs when small to medium emboli lodge distally in the peripheral pulmonary arteries — areas with limited collateral circulation — making them more susceptible to infarction. The absence of chest pain does not exclude PE and may contribute to missed diagnoses, increasing the risk of patient morbidity and mortality.

    PE classically presents with pleuritic chest pain and dyspnea associated with known risk factors, tachycardia, and clear lungs both on auscultation and chest radiography. However, most patients with PE present with one or more atypical features, which may include the absence of pain or any known risk factors and/or normal or nonspecific ECG findings.[1] About 40% of patients with PE have tachycardia.[1]

    Scoring systems such as the PE Rule-out Criteria (PERC) can be useful in evaluating patients with suspected PE, but clinicians must be familiar with both the inclusion and exclusion criteria and should recognize that applying PERC requires a low pretest probability based on clinical judgment and the presence of a more likely alternate diagnosis with adequate supporting evidence.

    When PE cannot be excluded based on clinical assessment, diagnostic testing is warranted, typically beginning with a D-dimer assay. If the D-dimer is positive, imaging with CT pulmonary angiography or a or ventilation-perfusion scan should follow.[2,3] D-dimer should not be ordered reflexively or “just in case,” as this often leads to unnecessary imaging. As Greg Henry advises, ”In medicine and life, don’t ask questions you don’t really want to know the answer to.”

    PE is typically treated with anticoagulants unless they are absolutely contraindicated, in which case a vena cava interruption filter may be used.[2,3,4] The treatment setting and choice of anticoagulant depend on various factors, including PE severity, comorbidities, and bleeding risk.[3] Most patients are admitted for treatment initiation, but some low-risk patients may be discharged with oral anticoagulants.[2] Patients with hypotension or right ventricular strain often require ICU admission for close monitoring and may be treated with thrombolytic therapy or, in some cases, surgical intervention.[1,2,3]

    The absolute contraindication to thrombolytic therapy is a history of intracranial hemorrhage, due to a significantly increased risk of catastrophic bleeding.[1,2,4] Thrombolytic agents can dissolve blood clots, but they also impair hemostasis.

    A history of pneumothorax episodes is not considered an absolute contraindication to thrombolytics in this patient.[1] Anemia is an important clinical factor that significantly increases the risk of bleeding during anticoagulation, but it does not preclude thrombolysis, if not caused by active bleeding or associated with a significant coagulopathy.[1,3,5]

    Hemodynamic instability is not a contraindication but rather an indication for thrombolytic therapy in patients with massive PE. The benefits of restoring circulation outweigh the bleeding risk associated with thrombolysis.[1,2,4]

    Hospital admission on intravenous heparin is reasonable. The patient could deteriorate if additional thrombi embolize. ICU admission is typically reserved for patients who remain unstable or require intravenous fibrinolytics. Discharge may be appropriate for stable patients who meet discharge criteria. For patients who are stable but do not qualify for discharge and have a low risk of decompensation, admission to a general medical floor may be considered.

    Because this patient’s CT angiography showed extensive PE and his vital signs were concerning, thrombolytics were considered. However, after heparin was initiated, his vital signs normalized within a few hours, so he was able to be admitted to a telemetry bed.

    Although most patients with PE meet criteria for outpatient treatment,[3,4] a minority of eligible patients are actually discharged from the emergency department despite having an estimated mortality risk of less than 3%.[1,2] Risk stratification tools such as the Pulmonary Embolism Severity Index and the Hestia criteria can help identify candidates for outpatient treatment. Clinicians should also consider using an online calculator (eg, MDcalc.com). In addition to PE severity, clinicians should evaluate the patient’s bleeding risk on anticoagulation when making disposition decisions.[1,2,3,4]

    Editor’s Note: This article was created using several editorial tools, including generative AI models, as part of the process. Human review and editing of this content were performed prior to publication.

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  • Mediterranean Bacteria May Harbor New Mosquito Solution

    Mediterranean Bacteria May Harbor New Mosquito Solution

    Highlights:

    • Mosquitoes that carry pathogens often develop resistance to insecticides.
    • Biopesticides offer an ecologically friendly way to control the pests and mitigate resistance, but options are limited.
    • Researchers recently identified bacteria in Crete that produce metabolites that quickly kill mosquito larvae in lab tests.
    • The compounds might be useful for the development of new biopesticides, though developing the right formulations and delivery method remains a challenge.

    Washington, D.C.-Mosquito-borne diseases kill more than 700,000 people every year, according to the World Health Organization, and the mosquitos that spread the disease are difficult to control. Most species have developed resistance to all major classes of synthetic insecticides, many of which pose both environmental and health risks.

    Biopesticides, derived from living organisms, may mitigate chemical insecticide resistance and offer an environmentally friendly way forward. This week in Applied and Environmental Microbiology, researchers report that bacterial isolates collected from the Mediterranean island of Crete act as insecticides against Culex pipiens molestus mosquitoes, which can transmit human pathogens such as West Nile virus and Rift Valley fever virus. In lab tests, extracts containing metabolites produced by 3 of the isolates killed 100% of mosquito larvae within 24 hours of exposure.

    Those metabolites might guide the development of biopesticides with minimal ecological side effects, the researchers noted. “They degrade more quickly in the environment and therefore don’t accumulate, and they often don’t kill such a wide range of different insect species as chemical insecticides,” said George Dimopoulos, Ph.D., a molecular entomologist and microbiologist at Johns Hopkins University in Baltimore and at the Institute of Molecular Biology and Biotechnology (IMBB) in Crete. He co-led the new study, conducted in Crete, together with molecular biologist John Vontas, Ph.D., at the IMBB.

    Dimopoulos’ research focuses on mosquitoes that transmit human pathogens, and over the past 15 years his group has found microbes that produce metabolites that interfere with the pathogens that cause malaria and dengue, and some bacteria that can kill mosquitoes. More recently, they have been investigating mosquito-killing bacteria in the Mediterranean region as part of the MicroBioPest project, funded by the European Union.

    For the new work, they collected 186 samples from 65 locations across Crete. The samples included topsoil, soil from around plant roots, plant tissues, water samples and dead insects. They then exposed C. pipiens molestus larvae to water solutions containing some of the most promising isolates found in the samples. More than 100 of the isolates killed all the mosquito larvae within 7 days, and 37 of those killed the larvae within 3 days. Those 37 isolates represented 20 genera, many of which have not previously been identified as potential biopesticides, said Dimopoulos.

    Further analyses showed that the rapid-acting bacteria killed the larvae not through infection but through the production of compounds like proteins and metabolites. This is promising, Dimopoulos noted, because it suggests that an insecticide based on these bacteria would not depend on the microbes staying alive. The findings have implications not only for controlling mosquitoes, but also as safe biopesticides to use for controlling agricultural pests.

    The researchers have now begun studying the chemical nature of those insecticidal molecules more closely and identifying whether they are proteins or metabolites. They’re also mapping out the spectrum of pesticidal activity demonstrated by the bacteria, including screening the isolates against other strains of pathogen-bearing mosquitoes and agricultural pest insects.

    Biopesticides often degrade quickly and require multiple applications, Dimopoulos said, and finding the right way to formulate and deliver the compounds will be a challenge in the future. The new study represents the discovery phase.

    “It’s now entering the basic science phase to understand the molecules’ chemical structures and modes of action, and then we’ll shift to a more applied path, really aiming at prototype product development,” he said. “There is a major push toward developing ecologically friendly insecticides.”

    /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.

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  • Germany Continues Leading Europe’s Poliovirus Detections — Vax-Before-Travel

    Germany Continues Leading Europe’s Poliovirus Detections — Vax-Before-Travel

    (Vax-Before-Travel News)

    According to the health departments of various countries, a cluster of vaccine-derived poliovirus type 2 (cVDPV2) has been detected in wastewater samples collected in Europe.

    As of July 7, 2025, the European Centre for Disease Prevention and Control (ECDC) says these countries include, but are not limited to, the United Kingdom, Finland, Germany, Spain, and Poland.

    Specifically, Germany has reported detections of cVDPV2 in multiple environmental samples throughout 2024 and the first half of 2025.

    In 2024, a strain of variant poliovirus originating from Nigeria was repeatedly detected in wastewater samples from Hamburg, Berlin, Munich, Frankfurt, Stuttgart, Dresden, Cologne, Düsseldorf, and Bonn. 

    In 2025, detections have been from Dresden during weeks 17, 19, 21, and 23, Mainz during weeks 15 and 19, Munich during weeks 21, 22, and 23, and Stuttgart during week 21.

    The cluster exhibits a degree of genomic diversity that more strongly supports the hypothesis of multiple introductions than a single introduction with local transmission within the EU.

    However, the large geographical spread in the EU/EEA, the fact that detections occurred over several months, and the identification of specific genetic sub-clusters suggest at least some degree of local transmission.

    Fortunately, no cases of poliomyelitis have been reported in Europe. 

    The last indigenous case of polio in Germany was in 1990.

    Given the presence of non-vaccinated or under-vaccinated population groups in European countries, and the fact that poliomyelitis has not been eradicated globally, the risk of the virus being reintroduced into Europe remains, affirms the ECDC.

    To alert international travelers visiting Europe during the summer of 2020, the U.S. CDC’s Level 2 – Practice Enhanced Precautions, Travel Health Advisory identifies 41 countries at risk for poliovirus detections.

    According to the CDC, travelers to Germany are at increased risk of exposure to poliovirus.

    The CDC recommends that adults who have previously completed the routine polio vaccine series and are traveling to any destination listed may receive a single, lifetime booster dose of polio vaccine. Polio vaccination services are offered at most health clinics and travel pharmacies in the United States.

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  • Global lifetime estimates of expected and preventable gastric cancers across 185 countries – IARC

    7 Juillet 2025

    A new study by scientists at the International Agency for Research on Cancer (IARC) projects the future burden of gastric cancer, including that attributable to Helicobacter pylori infection – the primary cause of gastric cancer – among a cohort of individuals born in 2008–2017. The expected number of gastric cancer cases, in the absence of intervention, was quantified across 185 countries by combining national age-specific incidence rates from GLOBOCAN 2022 and cohort-specific mortality rates from United Nations demographic projections. The article was published in Nature Medicine.

    Worldwide, assuming no change to the current gastric cancer control measures, 15.6 million gastric cancer cases are expected to occur within these birth cohorts, of which 76% are attributable to H. pylori infection and are therefore potentially preventable. Asia accounted for two thirds of the expected cases, followed by the Americas and Africa. Whereas 58% of future cases were projected in regions with historically high gastric cancer incidence, 42% were expected in lower-incidence regions, driven largely by demographic changes. In particular, a significant increase in the burden of gastric cancer is projected in sub-Saharan Africa, where the future number of cases will be up to 6 times those estimated for 2022.

    Gastric cancer is a disease with high morbidity and poor prognosis, although it is largely preventable. Most gastric cancers are attributable to chronic infection with H. pylori, and this burden worldwide is one of the highest of any cancer-causing infection. Despite ongoing global initiatives aimed at eliminating cervical cancer and viral hepatitis, gastric cancer remains relatively neglected, with limited interest and investment in many parts of the world, leading to public health inaction.

    This study highlights the growing burden of gastric cancer with shifting global profiles. The projections offer policy-makers critical information for cancer control planning at both regional and national levels and underscore the urgent need for the implementation of prevention strategies to reduce the global burden of gastric cancer.

    Park JY, Georges D, Alberts CJ, Bray F, Clifford G, Baussano I

    Global lifetime estimates of expected and preventable gastric cancers across 185 countries

    Nat Med. Published online 7 July 2025;

    https://doi.org/10.1038/s41591-025-03793-6

    Read IARC Press Release 368

    Read the article 

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