A new study published in BMC Infectious Diseases suggests the antiviral remdesivir (RDV) is associated with reduced mortality among COVID-19 patients based on electronic health records (EHRs) of COVID-19 patients seen in three Spanish hospital systems from January 2021 to March 2022.

The authors used artificial intelligence and natural-language processing tools to find relevant clinical information contained in the EHRs, mostly in the form of unstructured free text, otherwise not available in conventional administrative documentation, the authors said. This allowed the authors to assess the real-world efficacy of RDV outside of the existing trials on the drug conducted in the first year of the pandemic. 

Results reenforce clinical guidelines 

The study compared 812 treated and 2,703 untreated patients. The average age was 72 years. and 57.3% were male. The most prevalent conditions at baseline were high blood pressure (65.8%), heart disease (62.3%), and neurological diseases (50%) for all participants. Patients receiving RDV did, however, have higher rates of obesity (27.5% vs 21.7%).

Overall, the hazard ratio for in-hospital mortality at 28 days was 0.73 (95% confidence interval, 0.56 to 0.96) compared to untreated patients, or a 27% lower risk. Risk difference and risk ratio for 28-day survival was 2.7% and 0.76, respectively, for a 24% lower risk.

Our results are also consistent with those of several non-randomized, retrospective studies which have shown that RDV effectively reduces mortality in hospitalized COVID-19 patients.

"Our results are also consistent with those of several non-randomized, retrospective studies which have shown that RDV effectively reduces mortality in hospitalized COVID-19 patients," the authors concluded. They add that the results "are important to reinforce the concept that adherence to clinical guideline recommendations has prognostic implications in our everyday patients."

A study of South Korean children suggests antibiotic use in girls in the first year of life may be linked to earlier onset of puberty, researchers reported last week at a joint meeting of the European Society of Paediatric Endocrinology and the European Society of Endocrinology.

In the study, researchers from two university hospitals in South Korea analyzed antibiotic use in 322,731 children (135,232 boys and 187,499 girls) from 0 to 12 months, then followed them until age 10 for the boys and age 9 for the girls. The primary outcome was central precocious puberty (CPP), which for girls is defined as onset of puberty before age 8.

Most children in the study (90.4%) received antibiotics during the first year of life. Compared with those who were prescribed antibiotics after the first year, girls who received antibiotics during the first 3 months had a 23% increased risk of CPP (adjusted hazard ratio [aHR], 1.23; 95% confidence interval [CI], 1.12 to 1.36). Girls who were prescribed antibiotics at 6 to 9 months (aHR, 1.21; 95% CI, 1.10 to 1.32) and 9 to 12 months (aHR, 1.15; 95% CI, 1.04 to 1.26) also had an increased risk of CPP. In addition, girls who were prescribed five or more classes of antibiotics had a higher risk of CPP than those who received two or fewer.

No significant association between early antibiotic use and CPP was observed in boys.

Altering of the gut microbiome could play a role

"Our study adds to growing concerns about how antibiotics given in infancy could affect children’s long-term development—possibly by altering the gut microbiome or hormonal balance—but the reasons behind it are still unclear," study co-author Yunsoo Choe, MD, of Hanyang University Guri Hospital said in a press release. "Understanding these biological mechanisms may help guide safer antibiotic use and inform early-life care strategies for children."

Choe added that earlier research by the same team found that exclusive breastfeeding was associated with a lower risk of CPP, which supports the idea that early-life factors affecting the gut microbiome or endocrine-metabolic pathways may influence puberty development.

The US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) on May 9 recommended a pause in the use of Valneva’s chikungunya vaccine (Ixchiq) in people ages 60 and older while officials investigate severe adverse events, some neurologic and cardiac, in vaccine recipients.

Globally, 17 severe adverse events, 2 of them fatal, have been reported in people ages 62 to 89 years who received the vaccine. Six were from the United States. The FDA said it will conduct an updated risk-benefit assessment.

The FDA approved the vaccine in November 2023 for use in people ages 18 and older at increased risk for the mosquito-borne disease. At its meeting in April, CDC vaccine advisors recommended including a precaution about the vaccine’s use in people ages 65 and older. The FDA and CDC said about 80,000 doses have been given globally.

Ixchiq contains a weakened form of the virus, which may cause symptoms of chikungunya. Federal officials said some of the severe adverse events reported are similar to severe complications from the disease.

In a statement today, Valneva supported precautionary measures that groups have announced. It added that most of the reports involved those who had underlying health conditions or were taking other medications. It said a thorough investigation is critical for sorting whether the adverse events are related to use of the vaccine.

Pause follows earlier alert, regulator actions in Europe

The recommended pause for use in people ages 60 and older follows a CDC alert in early March that said it was investigating five hospitalizations in people ages 65 and older who had received the vaccine. 

In late April, French drug regulators updated their recommendations for Ixchiq after reports of adverse reactions in older people with underlying health conditions who were prioritized the receive the vaccine in a large ongoing outbreak in La Reunion and Mayotte. On May 7, the European Medicines Agency announced that its safety committee had launched a review of Ixchiq in older people and said the vaccine must not be used in people ages 65 and older.

Rockingham County, Virginia, is now part of Virginia's chronic wasting disease (CWD) management area (DMA) 2 after West Virginia detected cases within 10 miles of the county border, the Virginia Department of Wildlife Resources (DWR) notes on its website.

During the 2024-25 deer-hunting season, 8,801 deer in Virginia were tested, and 109 of them (1.2%) were positive for CWD, a fatal neurodegenerative disease of cervids such as deer, moose, and elk. No cases were found outside of the state's four DMAs.

Rockingham County is in northwestern Virginia, near Grant County, West Virginia, which reported its first case in March 2025.

Since CWD was first identified in Virginia in 2009, it has been confirmed in Carroll, Clarke, Culpeper, Fairfax, Fauquier, Floyd, Frederick, Loudoun, Madison, Montgomery, Prince William, Pulaski, Rappahannock, Roanoke, Shenandoah, Tazewell, and Warren counties, the DWR said.

Hunters, others, inform management strategies

The department conducts CWD surveillance and develops management strategies with the help of hunters, taxidermists, and processors, among other groups.

It is illegal to feed deer in Virginia for any reason year-round in all counties within 25 miles of a known CWD-positive deer.

"One important management strategy is to prevent artificially concentrating deer at point sources like feeding sites," the DWR wrote. "As such, it is illegal to feed deer in Virginia for any reason year-round in all counties within 25 miles of a known CWD-positive deer."

CWD is caused by abnormally folded infectious proteins called prions, which spread via saliva, feces, and urine shed by infected deer, as well as through prion-contaminated soil. The disease hasn't been shown to pose a risk to humans or domestic animals, but public health agencies advise hunters to have their animal tested before consuming the meat.