Search This Blog

Monday, May 5, 2025

Hospital-onset antimicrobial resistant infections increased during COVID-19 pandemic

 Hospital-onset antimicrobial-resistant infections increased across U.S. hospitals during and beyond the COVID-19 pandemic, according to a study published online April 29 in the Annals of Internal Medicine.

Christina Yek, M.D., Ph.D., from the National Institutes of Health Clinical Center in Bethesda, Maryland, and colleagues examined the incidence of antimicrobial-resistant infections in U.S. hospitals during and beyond the pandemic in a retrospective cohort study conducted in 243 U.S. hospitals.

The researchers found that antimicrobial-resistant infections increased from 182 to 193 per 10,000 hospitalizations during the peak of the COVID-19 pandemic (6.5% increase). There was a 31.5% increase in hospital-onset antimicrobial-resistant infections, from 28.9 to 38.0 per 10,000 hospitalizations. Illness severity (intensive care unit admission, , vasopressors, COVID-19 diagnosis), comorbidities (Elixhauser Comorbidity Index), and prior exposure to  were factors associated with hospital-onset antimicrobial resistance (AMR), but no association was seen for hospital factors.

As the pandemic waned, the prevalence of AMR returned to prepandemic levels (182 per 10,000 hospitalizations); however, hospital-onset AMR remained above baseline (32.3 per 10,000 hospitalizations).

"Antibiotic exposure in the preceding three months had incremental and sizable population-level impact on AMR increases, reinforcing the scope of this modifiable factor in potentially mitigating the ongoing crisis," the authors write.

More information: Christina Yek et al, Impact of the COVID-19 Pandemic on Antibiotic Resistant Infection Burden in U.S. Hospitals, Annals of Internal Medicine (2025). DOI: 10.7326/ANNALS-24-03078


https://medicalxpress.com/news/2025-05-hospital-onset-antimicrobial-resistant-infections.html

Vagus nerve stimulation provides long-term benefits for PTSD patients in clinical study

 In a first-of-its-kind clinical study, scientists at the University of Texas at Dallas and Baylor University Medical Center have shown that patients with treatment-resistant PTSD were symptom-free up to six months after completing traditional therapy paired with vagus nerve stimulation (VNS).

The results of the nine-patient Phase 1 trial, conducted by scientists from UT Dallas's Texas Biomedical Device Center (TxBDC) in collaboration with researchers from the Baylor Scott & White Research Institute (BSWRI), are published in Brain Stimulation.

Dr. Michael Kilgard, the Margaret Fonde Jonsson Professor of neuroscience in the School of Behavioral and Brain Sciences, said the outcome highlighted the potential of this approach.

"In a trial like this, some subjects usually do get better, but rarely do they lose their PTSD diagnosis. Typically, the majority will have this diagnosis for the rest of their lives," Kilgard said. "In this case, we had 100% loss of diagnosis. It's very promising."

Prolonged —a component of traditional PTSD treatment—is a form of cognitive behavioral therapy, conducted in a safe and supportive environment, that involves individuals gradually confronting thoughts, memories and situations they have avoided since experiencing a trauma.

In the study, scientists paired this therapy with concurrent delivery of short bursts of stimulation of the vagus nerve via a small device implanted in a participant's neck. After a standard 12-session therapy course, assessments were performed four times during the six months after its conclusion. Benefits persisted during that time for all nine participants.

The study is the largest clinical trial to date using an implanted device for the treatment of PTSD, Kilgard said.

Pioneering work by TxBDC researchers has demonstrated previously that VNS paired with physical rehabilitation can accelerate neuroplasticity—the rewiring of areas of the brain. Their 13-year effort to treat a wide variety of conditions using VNS has resulted in approval by the Food and Drug Administration (FDA) for treating impaired upper-limb movement in stroke patients.

"The common theme in our VNS work is that we're taking therapies that show potential, like prolonged exposure therapy for PTSD, and making them work better," he said.

The National Center for PTSD, part of the Department of Veterans Affairs, estimates that 5% of adults in the U.S. have  in any given year, and that women are twice as likely to develop PTSD at some point in their life. Many PTSD patients fail to respond to therapy or pharmacological intervention, or experience intolerable side effects or relapse, leaving them with no viable prospect for remission.

Kilgard said that PTSD patients are not only found among military veterans, but also among average citizens who have faced traumatic events.

"When you hear PTSD, you may picture a combat zone, but it's much more prevalent than that," he said. "It can stem from any event that inspires fear of death or bodily injury, or death of a loved one."

Co-corresponding author Dr. Seth Hays, associate professor of bioengineering in the Erik Jonsson School of Engineering and Computer Science and director of preclinical research at the TxBDC, has been a part of the VNS project since its earliest studies.

"It's been an incredibly rewarding experience to see this technology evolve from early discovery experiments in the lab to clinical benefits in patients," Hays said. "This whole process truly highlights the value of team-based science."

More than a decade ago, Dr. Robert Rennaker, professor of neuroscience and the Texas Instruments Distinguished Chair in Bioengineering, began to design an innovative implantable VNS device that was much smaller and less expensive than devices already on the market. The most recent wireless version of the device is about the size of a dime.

"The technology we have is above and beyond anything else that's out there. The device is about 50 times smaller than our version from just three years ago," he said. "The 49 people in the Dallas area with our devices have a combined 100 years of experience with it implanted. There have been no issues; the devices are all still functioning. And they don't interfere with typical medical care; you can have an MRI, a CT scan or an ultrasound."

The next step in the PTSD research—a double-blind, placebo-controlled Phase 2 pilot study—is ongoing in Dallas and Austin.

"We hope that it will represent another step toward FDA approval of a treatment that doesn't exist now, and it would be invented, tested and delivered by UT Dallas, as was the case for upper-limb recovery after stroke," Kilgard said.

Licensed clinical psychologist Dr. Mark Powers, a research center director of the Trauma Research Center at BSWRI, is the lead and co-corresponding author of the study. Driven by his desire to improve the quality of life among people who experience psychological trauma, Powers said that VNS has "changed the game" by improving both treatment efficacy and its tolerability.

"VNS has changed my work dramatically," he said. "Our gold-standard treatments for PTSD have about an 85% response rate, with 40% no longer having their diagnosis, and a 20% dropout rate. Soon we could have the option of VNS for people who don't get better with cognitive behavioral therapy alone."

Powers added that his collaboration with UTD has a multidisciplinary synergy that he regards as rare.

"With this alliance, we have people doing the preclinical and the clinical work at the same time, giving each other feedback and ideas," he said. "Neither one of our groups could do this alone."

Other UTD-affiliated study authors included Dr. Jane Wigginton, medical director and co-director of the UT Dallas Clinical and Translational Research Center; Amy Porter, TxBDC director of operations; and Holle Carey Gallaway, TxBDC research biomedical engineer. Researchers from Southern Methodist University, UT Austin and Baylor Scott & White Health also contributed to the study.

More information: Mark B. Powers et al, Vagus nerve stimulation therapy for treatment-resistant PTSD, Brain Stimulation (2025). DOI: 10.1016/j.brs.2025.03.007


https://medicalxpress.com/news/2025-05-vagus-nerve-term-benefits-ptsd.html

US fuel distributor Sunoco to buy Canada Distributor Parkland for $9 billion

 Sunoco LP (SUN) has entered into an agreement with Parkland Corp. (PKI) to acquire the company in a $9.1 billion deal, paving the way for creating the largest independent fuel distributor in the U.S.

Sunoco’s stock was down more than 6% at the time of writing, while Parkland’s shares gained over 8.5%.

Dallas-headquartered Sunoco is a fuel distributor and an operator of energy infrastructure.

Parkland is a Calgary-based company that operates gas stations. It is Canada’s largest independent fuel retailing company.

Parkland’s executive chairman, Michael Jennings, called the deal a “compelling outcome” for the company’s shareholders.

Parkland’s shareholders will get CAD$19.80 ($14.25) in cash and 0.295 Sunoco shares for each share held in the company.

“This transaction delivers immediate value for shareholders, including an attractive 25% premium. Sunoco shares our commitment to growth, customer service, operational excellence, and ongoing investment in Canada,” said Parkland CEO Bob Espey.

The Parkland deal is expected to result in $250 million in annual cost savings by the end of the third year. Sunoco said it would also boost cash flow by 10%.

Sunoco expects the deal to close in the second half of 2025, subject to closing conditions, assent from Parkland’s shareholders, and regulatory approvals.

The company said it had secured a $2.65 billion 364-day bridge loan for the cash consideration.

Earlier in 2024, Sunoco acquired NuStar Energy, an operator of fuel storage and pipelines, in a deal valued at $7.3 billion.

https://in.investing.com/news/stock-market-news/sunoco-to-acquire-canadian-fuel-distributor-parkland-for-91b-4808843

There Will Be Boundaries

 by James Howard Kunstler,

"Fascism is when Dad says 'no'" 

- Aimee Terese on "X"

It’s vain and futile to suppose that the disordered minds of Western Civ’s entrenched Wokester Jacobins might ever be subject to polite persuasion about anything they believe. They believe only in the power of pushing their fellow citizens around, and so, alas, the only persuasion that might conceivably work to stop their infantile assaults on liberty, truth, and decency is to push back harder until they suffer and break.

This is something that most parents with young children instinctively understand. You don’t negotiate with two-year-olds. You tell them how things are and what sort of behavior is required of them, as plainly and simply as possible. Mr. Trump, having been the father of many two-year-olds over time, appears to get this. It has been apparent for years that Mr. Trump’s symbolic role as a father figure is the most deeply resented feature of his role in US politics.

It also appears that many men in this country likewise get this, perhaps because nature conditions them early on to understand that some day they might have to play the role of father, meaning they will have to push back hard against emotional disorder, hysteria, illogic, and untruth, and violence.

Hence, you might see the peril of living in a land with so many fatherless households. This lamentable state of things defines the Democratic Party, where raging, inchoate, resentment-driven Jacobinism dwells, a party now with no leader, a household with no father, no one to regulate its frenzied, power-seeking behavior. This also tells you how the Democratic Party has become the party run by women, and by particular types of women — women who have traded the management of children and households for bureaucratic careerism, women too lacking in feminine appeal to attract mates, women attempting to become the men missing in their lives — and men wishing to become women, or pretending to be women.

And so you see how these disorders play out in the ongoing melodrama of men in women’s sports, a proposition so obviously insane that no healthy society has ever abided it for a moment until the American Jacobins ran with it as a cardinal political irritant to vex their opponents (and really for no other reason). The state of Maine’s governor, Janet Mills, clashed openly with Mr. Trump over his executive order to desist from allowing biological men in women’s sports. The matter is currently making its way through the courts.

This week, a “trans” athlete named Soren Stark-Chessa, beat the field of females in a Maine track-meet by a country mile in the 800-meter and 1600-meter runs. No one, except the political leadership of Maine, was fooled about the fairness of this, of course. Fairness is not the point. Intransigent defiance of reality was the point. It is always the point for Jacobin politicians.

Soren Stark-Chessa in full stride

What is most obviously insane in matters like this, is that the female governor is so eager to punish and humiliate her younger fellow females in order to merely press a political point — that she is the boss of Maine, and nobody can tell her what to do, even if she deranges the cultures of schooling and sports. This illustrates, by the way, a principal difference in the way men’s and women’s brains work. Men typically understand boundaries, where things begin and end. It is a necessary cognitive device for regulating behavior in the household and for acting in the face of danger when required.

Sports is just a microcosm of our politics. The whole gestalt of Woke-Jacobin politics is driven by the wish to dissolve boundaries. That is, it is driven by female minds, and what the Woke-Jacobins might call female-adjacent minds. That is why the open border fiasco was another point-of-principle for the Democratic Party — and why “Joe Biden” the phantom president (actually the shadowy figures behind him) pretended that nothing could be done about it.

Mr. Trump demonstrated that was a lie in a New York minute. 

The damage from four years of a wide-open border is immense, much worse than men running in girls’ races. 

The motive for it is also obvious: to jam as many illegal aliens as possible into the country so as 1) to disorder the next census count in swing states to keep congressional districts safe, and 2) to install a base of new “voters” — qualified to vote or not — who will be eternally grateful to the Democratic Party for letting them flood into the country and gifting them with housing, social services, transportation, free meals, and walking-around money.

And now, a Woke-Jacobin judiciary, assisted by an infrastructure of Lawfare ninjas, led by the outlaw Norm Eisen, and financed by George Soros, and what remains of Soros-adjacent NGOs, is using the courts to keep all those illegally-admitted aliens in place here at all costs. So, you see, they are attempting to dissolve a boundary crucial to the Republic’s survival: who is a citizen and who is not a citizen, and what are the privileges entailed? The objective is to keep this dispute alive in the courts long enough to affect the 2026 midterm elections in the hopes of winning Congress back.

You can also see how this will oblige Mr. Trump to marshal the most aggressive legal force possible to crush this seditious legal insurrection. He has executive powers and perquisites in reserve that he has not used yet, or even revealed.

He will defeat these monsters in the end just as he is methodically disassembling their scaffold of psychopathic ideology and their pipelines of funding. It will really be something to see.

https://www.zerohedge.com/geopolitical/there-will-be-boundaries

Corcept Earnings: $157M Revenue and Breakthrough ALS Survival Data Spark Pipeline Momentum


Revenue of $157.2 million, compared to $146.8 million in first quarter 2024Reiterated 2025 revenue guidance of $900 – $950 million

Net income per common share (diluted) of $0.17, compared to $0.25 in first quarter 2024
Cash and investments of $570.8 million as of March 31, 2025

Corcept Therapeutics Incorporated (NASDAQ: CORT), a commercial-stage company engaged in the discovery and development of medications to treat serious endocrinologic, oncologic, metabolic and neurologic disorders by modulating the effects of the hormone cortisol, today reported its results for the quarter ended March 31, 2025.

Financial Results

“In the first quarter, we had another record number of prescriptions from new and existing prescribers, broadly distributed throughout the country. Growing physician awareness of hypercortisolism has resulted in increased screening and treatment of patients with this devastating disease. Our specialty pharmacy vendor began the quarter unable to fulfill this surge in demand, which negatively affected our first quarter financial results. Pharmacy operations improved substantially in March and April, with each month setting a record for tablets dispensed. We are reiterating our 2025 revenue guidance of $900 – $950 million,” said Joseph K. Belanoff, M.D., Corcept’s Chief Executive Officer.


Corcept’s first quarter 2025 revenue was $157.2 million, compared to $146.8 million in the first quarter of 2024. First quarter 2025 operating expenses were $153.8 million, compared to $117.3 million in the same period last year. Net income was $20.5 million in the first quarter of 2025, compared to $27.8 million in the first quarter of 2024.

Cash and investments were $570.8 million at March 31, 2025, compared to $603.2 million at December 31, 2024. The balance at March 31, 2025 reflects the acquisition of $43.3 million of common stock in the first quarter pursuant to the company’s stock repurchase program, net exercise of employee stock options and net vesting of restricted stock grants.

Clinical Development

“Our New Drug Application (NDA) for relacorilant in hypercortisolism is progressing towards approval by the end of this year. We will submit our NDA next quarter for relacorilant in platinum-resistant ovarian cancer. We expect that relacorilant will have a role in helping treat earlier stages of ovarian cancer and other tumors that express the glucocorticoid receptor and have already begun our next clinical trial, BELLA. Meanwhile, we are making progress in understanding the role of cortisol modulation to treat a broad range of other serious disorders, including ALS and Metabolic Dysfunction-Associated Steatohepatitis (MASH),” added Dr. Belanoff.

Trump Set to Sign Order Encouraging Domestic Drug Production



President Trump is expected to sign an executive order that will boost domestic drug production in the U.S., according to the Washington Post. The order builds on Trump’s goal of returning production and manufacturing to the U.S.

Last month, Trump stated that he would soon enact a “major tariff on pharmaceuticals” that are imported to the U.S. in order to promote domestic drug production. As of now, pharmaceuticals are exempt from the administration’s reciprocal tariffs.

https://www.tipranks.com/news/trump-set-to-sign-order-encouraging-domestic-drug-production

BioNTech’s Ambitious PD-L1/VEGF Plans Currently Rely on Chinese Manufacturing

 

BNT327, a PD-L1/VEGF therapy, is still currently being manufactured in China, but BioNTech is working to establish a diversified supply chain, executives said during the company’s Q1 investor call.

BioNTech has big plans for the investigational PD-L1/VEGF therapy BNT327, which is being tested in a sprawling Phase III program for a variety of cancer types. There’s just one problem: President Donald Trump’s escalating trade war—particularly his targeted tariffs on China.

“Manufacturing is currently supplied [from] China,” Chief Strategic Officer Ryan Richardson said during a first quarter earnings call Monday, adding that BioNTech is “reliant on a China-based CDMO.” Richardson was quick to allay investors’ concerns, however, saying on the call that BioNTech is currently “diversifying our supply base and our plans over the next couple of years are to establish multiple supply nodes, including outside of China.”

The company has acquired multiple assets from Chinese companies. BNT327 came to BioNTech when it bought Chinese partner Biotheus in late 2024 for about $950 million. Multiple antibody-drug conjugates in the biotech’s pipeline also came from Shanghai-based DualityBio for $1.5 billion in biobucks.

BioNTech CFO Jens Holstein said that tariffs could affect BioNTech’s vaccine business. “Potential changes in law or government policy, including tariffs and public health policy, and evolving public sentiment around vaccines and mRNA technology worldwide could further negatively impact our anticipated COVID 19 vaccine revenues and expenses,” he said.

Richardson continued to downplay concerns, however. “We have the ability to produce [Comirnaty, BioNTech’s mRNA-based COVID 19 vaccine] in the United States. We also have the ability to produce it in Europe.”

BNT327 is part of an emerging and closely watched class of cancer therapies addressing two of the most widely targeted pathways in cancer: PD-1, which allows malignant cells to suppress and evade the immune system, and VEGF, which tumors use to create new vasculature to supply nutrients and oxygen.

Uniquely, however, BNT327 targets the PD-L1 ligand, as opposed to the PD-1 receptor, which the current VEGF bispecific frontrunner ivonescimab—developed by Summit Therapeutics and Chinese partner Akeso—targets. Investors questioned BNT327’s particular binding target on the call, noting that anti-PD-L1 antibodies have typically underperformed in the clinic.

In response, Chief Medical Officer Özlem Türeci pointed out that BioNTech “deliberately” chose to target PD-L1 over PD-1, because the ligand “might be superior” to the receptor “in anchoring [BNT327] in the tumor microenvironment, where we want to have the bispecific.”

BioNTech plans to move rapidly with BNT327, according to its investor presentation on Monday. The company is currently running several mid-stage trials in solid tumors, including the Phase II ROSETTA Lung-01 study in small cell lung cancer and the Phase II/III ROSETTA Lung-02 study in non-small cell lung cancer.

Seeking to carve a different niche from Summit and Akeso’s ivonescimab, BioNTech is planning to develop BNT327 into novel cancer types, “a couple of those where we think [we’ll be] positioned, if we can execute well, to be potentially first-to-market,” Richardson said on the call. These include triple-negative breast cancer and small cell lung cancer.

Further down the line, BioNTech is also looking to combine BNT327 with other anti-cancer agents, including antibody-drug conjugates. “And there we think we have a differentiated strategy by virtue of our broad pipeline . . . that we have in-house that could be combined with [BNT327],” Richardson added.

In the first quarter of 2025, BioNTech made €182.8 million (approximately $207 million), representing a €415.8 million, or nearly $472 million, net loss. During the same period last year, BioNTech lost €315.1 million (around $357 million).

Looking ahead to the rest of the year, BioNTech reiterated its 2025 revenue guidance despite continued macro-level pressures. The company anticipates bringing in between €1.7 billion and €2.2 billion (approximately $1.7 billion to $2.5 billion) this year, while R&D expenditure is projected to hit €2.6 billion to €2.8 billion, or roughly $2.95 billion to $3.18 billion.

https://www.biospace.com/business/biontechs-ambitious-pd-l1-vegf-plans-currently-rely-on-chinese-manufacturing