A rundown of recent Trump administration vaccine policy changes
The Trump administration continued to reshape U.S. health policy in recent days with several moves that could change what vaccines people can get to protect themselves from common illnesses.
Some of the changes are immediate, others are still being discussed, and Health Secretary Robert F. Kennedy Jr. must still sign off on some.
Doctors' groups have expressed alarm at the moves made by Kennedy, a longtime anti-vaccine activist, and his appointees, who at times have ignored well-established science. Nearly 80 medical groups, including the American Medical Association, issued a statement backing vaccines against common respiratory ailments as 'among the best tools to protect the public.'
'We come together as physicians from every corner of medicine to reaffirm our commitment to these lifesaving vaccines,' the groups wrote.
Here's what to know about some of the recent vaccine policy changes:
Flu shots and thimerosal
On Thursday, a vaccine advisory group handpicked by Kennedy recommended that just about every American get a flu shot this fall.
But the group also said people should avoid shots containing thimerosal, a preservative used only in large multi-dose vials that has been proven to be safe. The ingredient isn't used in single-dose flu shots, the type of syringe used for about 95% of U.S. flu shots last season.
Status: Kennedy must sign off on the recommendations. Read more AP coverage here.
How to get a COVID-19 shot
Universal access to updated COVID-19 shots for the fall remains unclear, even after Kennedy's vaccine advisers were shown data showing how well the vaccines are working.
Kennedy changed CDC guidance last month, saying the shots are no longer recommended for healthy children and pregnant women — even though doctors groups disagree. And the Food and Drug Administration has moved to limit COVID-19 vaccinations among healthy people under age 65.
Status: Upcoming advisory meetings, regulatory decisions and policies from insurers and employers are likely to influence access. Read more AP coverage here.
Expanded warnings on COVID-19 vaccine labels
At the request of the FDA, makers of the two leading COVID-19 vaccines on Wednesday expanded existing warnings about a rare heart side effect mainly seen in young men.
Prescribing information from both Pfizer and Moderna had already advised doctors about rare cases of myocarditis, a type of heart inflammation that is usually mild. The FDA had asked the drugmakers to add more detail about the problem and to cover a larger group of patients.
Status: Labels are being updated now. Read more AP coverage here.
Changes considered for the childhood vaccine schedule
On Wednesday, Kennedy's vaccine advisers said they would be evaluating the 'cumulative effect' of the children's vaccine schedule — the list of immunizations given at different times throughout childhood.
The announcement reflected vaccine skeptics' messaging: that too many shots may overwhelm kids' immune systems. Scientists say those claims have been repeatedly investigated with no signs of concern.
The American Academy of Pediatrics said it would continue publishing its own vaccine schedule for children but now will do so independently of the government advisory panel, calling it 'no longer a credible process.'
Status: The examination is in its early stages. Read more AP coverage here.
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The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.
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New York Times
an hour ago
- New York Times
4th of July Sales Are Already Happening. Here Are the Best Deals Available.
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Health Line
an hour ago
- Health Line
A Liver Ultrasound: What This Procedure Means
Your doctor may recommend a liver ultrasound to check for signs of liver disease, and knowing what to expect can help put you at ease. A liver ultrasound is one of a few tests your doctor can order if they want to check your liver. An ultrasound scan (also known as sonography) is a noninvasive procedure that captures live images of your organs using high-frequency sound waves. A liver ultrasound is an essential tool that helps doctors see your liver and its blood vessels in real time. It's a type of abdominal ultrasound. If your doctor has ordered a liver ultrasound, it might mean they want to confirm or rule out a liver condition. Keep reading to learn what conditions a liver ultrasound can detect, what to expect from the procedure, how accurate it is, how much you might need to pay for it, and other useful information. Why is an ultrasound needed to test for liver disease? Liver disease is a general term that refers to a group of conditions affecting your liver. These conditions may have different causes, but all of them can damage your liver and affect your general health. Some of the most common liver conditions are: hepatitis, or inflammation of the liver steatotic liver disease, formerly known as fatty liver disease, or a buildup of fat in the liver autoimmune liver disorders, which result from your immune system mistakenly attacking the cells in your liver liver cancer liver fibrosis, cirrhosis, and liver failure, which involve scarring and damage from liver disease Doctors usually recommend liver ultrasounds for the following reasons: if you show symptoms of liver disease, such as jaundice or pain in the upper right portion of the abdomen (where the liver is located) if you have high liver enzymes on a blood test called the liver function test as a screening tool for liver conditions The purpose of a liver ultrasound is to visualize your liver and record its blood flow. This helps doctors confirm or rule out liver conditions. What should you see on an ultrasound for liver disease? Liver ultrasounds don't usually require special preparation, but your doctor may ask you not to eat or drink anything several hours before the procedure. During the scan, you'll lie still on a scanning table. An ultrasound technician will place a scanner in different spots around the upper right segment of your abdomen. The resulting images will show up on a computer screen in real time. After the ultrasound is done, a doctor will check the ultrasound images. They will look for the following signs of liver disease: liver inflammation, a sign of hepatitis a buildup of fat associated with steatotic liver disease masses or lesions, which can indicate liver cancer changes in the appearance of the liver, such as nodules, which can signify cirrhosis Is a liver ultrasound accurate? A liver ultrasound is a useful tool in identifying certain types of liver disease. It's often the first test your doctor will order if they suspect a liver condition. It's a quick, safe, painless, and relatively inexpensive test. In the past, doctors relied more heavily on liver biopsy to diagnose, stage, and grade liver disease. However, newer research indicates that new liver ultrasound technologies are able to accurately detect liver disease. What does an ultrasound cost for liver disease? On average, an abdominal liver scan can cost around $1,400. However, most health insurance providers cover this procedure. Liver ultrasound costs will vary based on: where you live whether you have medical insurance the type of ultrasound Frequently asked questions How do you diagnose fatty liver disease? A doctor can diagnose steatotic liver disease using a combination of the following tests: liver ultrasound X-ray, CT, or MRI scans of the abdomen transient elastography (also known as FibroScan), shear wave elastography, or acoustic radiation force impulse imaging, which assesses liver stiffness magnetic resonance elastography (MRE), which combines MRI with low frequency sound waves to create a visual map showing liver stiffness Can you get an ultrasound for alcohol liver disease? Long-term, excessive alcohol use can lead to a buildup of fat in the liver known as alcohol-associated liver disease (ALD), or steatosis. Metabolic dysfunction and alcohol-related liver disease (MetALD), a form of alcohol-related liver disease (ARLD), refers to liver damage due to alcohol use along with other risk factors, such as obesity or diabetes. It causes liver inflammation and scarring and can eventually lead to cirrhosis. Liver ultrasound is one of the tests used to diagnose fat in the liver. Other tests may include: a complete blood count (CBC) a liver function test CT or MRI scans a liver biopsy Is there an ultrasound for liver disease in dogs? Similar to humans, abdominal ultrasounds are commonly used in dogs and cats when a vet suspects a liver condition. Symptoms of liver disease in pets can be subtle but may include: appetite issues orange urine jaundice weight loss excessive drinking or excessive urinating light colored stool Can an abdominal ultrasound check for chronic liver disease and hepatocellular carcinoma surveillance? Certain types of liver disease can increase your risk of developing liver cancer, also known as hepatocellular carcinoma (HCC). Because of that, doctors recommend regular screening for HCC in people with cirrhosis, hepatitis B, or hepatitis C every 6 months.


Associated Press
an hour ago
- Associated Press
RetinalGenix Technologies Contracts with LabCorp to Support DNA/GPS Platform for Advanced Genetic and Retinal Health Screening
APOLLO BEACH, Fla., June 27, 2025 (GLOBE NEWSWIRE) -- RetinalGenix Technologies Inc. OTCQB:RTGN ('RetinalGenix' or the 'Company'), a pioneering developmental-stage company focused on ophthalmic screening, monitoring, pharmacogenetic mapping, and repurposed drug development for early detection and treatment of eye and systemic diseases, has entered into an agreement with LabCorp, one of the nation's largest laboratory services organizations, to support the rollout of the RetinalGenix DNA/RNA/GPS Pharmaco-Genetic Mapping™ platform. This innovative program enables patients to undergo genetic testing and high-resolution retinal imaging anonymously and provide insights into both ocular and systemic diseases. Through this collaboration, patients may visit any USA-based LabCorp location to have blood, tears, nasal secretions, and saliva collected and analyzed using proprietary algorithms developed by the RetinalGenix and DNA/RNA GPS analysis platform. These tests may correlate genetic and retinal biomarkers seeking to establish a new standard for early detection of a wide range of health conditions. Based on tests recommended by RetinalGenix, patients may elect to have their data analyzed using specific algorithms developed by RetinalGenix. This process is paired with DNA/RNA/GPS to correlate with current and future biomarkers found in the eye and the blood. Dr. Larry Perich, DO, Advisor for the DNA/RNA/GPS program, noted, 'As the database of disease-associated biomarkers expands, we expect the value of these platforms for diagnosing both ocular and systemic diseases continues to grow, promising improved outcomes and more accessible care.' Patients maintain full control of their health records, which remain anonymous and confidential. Appointments and test orders are managed via the RetinalGenix online platform, with results securely released to patients upon validation of payment at their chosen LabCorp center. Dr. Taimour Langaee, PhD, oversees the Company's DNA/GPS genotyping/sequencing data processing, genetic and pharmacogenomics data analyses, and clinical genetic association studies between eye diseases and genetic variations. Dr. Langaee said, 'I am excited that this creates great opportunities to further expand our knowledge about the important role of genetics and precision medicine in eye diseases, affecting millions of people and the potential to discover novel genetic variants and treatments.' High-resolution retinal imaging will be introduced by RetinalGenix as a value-added additional service at various locations in the near future. The integration of high-resolution imaging is expected to further boost diagnostic accuracy, allowing even general practitioners and standard eye clinics to assist in patient mass screening. These innovations are designed to make screening more accessible, cost-effective, and capable of detecting disease at earlier, more treatable stages. 'The cost of healthcare is enormous, and patient access is critical. This cost-effective methodology aims to reduce reliance on expensive diagnostic procedures such as MRIs, CT scans, PET Scans, echocardiograms to name a few, helping to alleviate the financial burden on both patients and the healthcare system. Equally important is avoiding the use of high-priced specialists to perform basic eye care services. The company is actively collaborating with regulators to establish CPT codes, which should lower healthcare costs and improve access to necessary evaluations. By doing so, the already overburdened patient assessment process can be streamlined,' stated Jerry Katzman, MD, RetinalGenix Technologies CEO. About RetinalGenix RetinalGenix is an ophthalmic research and development company seeking to revolutionize early disease detection and improve patient outcomes across multiple disease areas by integrating genetic screening, advanced imaging, and therapeutic development. Its proprietary High-Resolution Retinal Imaging and RetinalGenix DNA/RNA/GPS Pharmaco-Genetic Mapping™ technologies are designed to help prevent blindness by detecting initial physiological changes that could indicate future ocular and systemic diseases affecting neurodegenerative, cardiovascular, vascular, and metabolic systems, as well as diabetic conditions, Alzheimer's disease and Parkinson's disease. RetinalGenix is also developing therapeutic drugs for dry age-related macular degeneration (dry AMD) and Alzheimer's disease/dementia. Safe Harbor Statement This press release contains certain forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements are identified by the use of the words 'could,' 'believe,' 'anticipate,' 'intend,' 'estimate,' 'expect,' 'may,' 'continue,' 'predict,' 'potential,' 'project' and similar expressions that are intended to identify forward-looking statements and include statements regarding reducing reliance on expensive diagnostic procedures with the Company's methodology, the planned rollout of the RetinalGenix DNA/RNA/GPS Pharmaco-Genetic Mapping™ platform, the program providing insights into both ocular and systemic diseases, correlating genetic and retinal biomarkers to seek to establish a new standard for the early detection of a wide range of health conditions, the value of platforms for diagnosing both ocular and systemic diseases continuing to grow, promising improved outcomes and more accessible care, the opportunities to further expand our knowledge about the important role of genetics and precision medicine in eye diseases and the potential to discover novel genetic variants and treatments, introducing high-resolution retinal imaging as an additional service in the near future, the integration of high-resolution imaging further boosting diagnostic accuracy, allowing even general practitioners and standard eye clinics to assist in patient mass screening, the innovations making screening more accessible, cost-effective, and capable of detecting disease at earlier, more treatable stages, establishing CPT codes to further lower healthcare costs and improve access to necessary evaluations and streamlining the patient assessment process. These forward-looking statements are based on management's expectations and assumptions as of the date of this press release and are subject to a number of risks and uncertainties, many of which are difficult to predict, that could cause actual results to differ materially from current expectations and assumptions from those set forth or implied by any forward-looking statements. Important factors that could cause actual results to differ materially from current expectations include, among others, the Company's ability to successfully complete research and further development and commercialization of Company products, the timing, cost and uncertainty of obtaining regulatory approvals for the Company's products, the Company's ability to protect its intellectual property, and the risk factors described in the Company's Annual Report on Form 10-K for the year ended December 31, 2024 and the Company's subsequent filings with the SEC, including subsequent periodic reports on Forms 10-Q and 8-K. The information in this release is provided only as of the date of this release, and we undertake no obligation to update any forward-looking statements contained in this release on account of new information, future events, or otherwise, except as required by law. Media Contact: For further information, please contact: RetinalGenix Technologies Inc. Media and Investor Relations [email protected] (800) 331-5446