Nirsevimab Administration and RSV Hospitalization in the 2024-2025 Season
Authors conducted a cohort study of the 2024 to 2025 RSV season. They hypothesized that nirsevimab would be associated with reduced RSV-associated hospitalization. These are the results of a retrospective cohort study using the Epic Systems Cosmos dataset, created in collaboration with a community of health care systems using Epic Systems software, representing more than 300 million patients from more than 1,700 hospitals and 40,000 clinics from all 50 states, the District of Columbia, Canada, Lebanon, and Saudi Arabia. A total of 409,723 infants (median [IQR] age, 8 (5-10) months; 209 543 [51.1%] male) were included in the study, of whom 194,422 (47.5%) received nirsevimab. The adjusted hazard ratios for RSV-associated hospitalization after treatment with nirsevimab was 0.23 (95% CI, 0.21-0.26). 73% reduction.
Olfactory Dysfunction After SARS-CoV-2 Infection in the RECOVER Adult Cohort
These results come from a prospective cohort study that included adults enrolled in the Researching COVID to Enhance Recovery (RECOVER)–Adult study. All those with and a random sample of those without self-reported change or loss in smell or taste were offered olfactory testing, performed at 83 sites in 35 U.S. states and territories. Participants included 2,956 enrollees with prior infection (1393 with and 1563 without self-reported change or loss) and 569 without prior infection (nine with and 560 without self-reported change or loss in taste) who underwent olfactory testing a mean (SD) of 671.6 (417.8) days after the index date. Among 1,393 infected participants with self-reported change or loss, (79.8%) had hyposmia on the University of Pennsylvania Smell Identification Test, (UPSIT),including 321 (23.0%) with severe microsmia or anosmia. Among 1,563 infected participants without self-reported change or loss, 1,031 (66.0%) had hyposmia, including 128 (8.2%) with severe microsmia or anosmia. In this cohort, self-reported change or loss in smell or taste was an accurate signal of verified hyposmia, but a high rate of hyposmia among those with no reported change or loss was also observed. Formal smell testing may be considered in those with prior SARS-CoV-2 infection to diagnose occult hyposmia and counsel patients about risks.
FDA Conditionally Approves First Drug for Prevention and Treatment of New World Screwworm Infestations in Cattle September 30, 2025
The U.S. Food and Drug Administration conditionally approved Dectomax-CA1 (doramectin injection) injectable solution for the prevention and treatment of New World screwworm larval infestations, and prevention of NWS reinfestation for 21 days. Dectomax-CA1 is conditionally approved for use only in cattle.
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