Patients with multiple cardiovascular (CV) risk factors are not able to reduce their mortality risk from CV causes with daily n-3 polyunsaturated fatty acid intake, according to a long-term Italian study published May 9 in the New England Journal of Medicine.
Patients with multiple cardiovascular (CV) risk factors are not able to reduce their mortality risk from CV causes with daily n-3 polyunsaturated fatty acid intake, according to a long-term Italian study published May 9 in the New England Journal of Medicine.
More than 12,500 patients with multiple CV risk factors or atherosclerotic vascular disease who had not experienced a myocardial infarction were enrolled in a double-blind, placebo-controlled study. They were followed for a median of 5 years by 860 general practitioners in Italy. Patients were randomly assigned to receive a daily 1-g dose of n-3 fatty acids or olive oil, which served as the placebo.
At the end of 1 year, the rate of death, nonfatal myocardial infarction, and nonfatal stroke was lower than the researchers had expected. The researchers changed the primary end point of the study to death from CV causes or hospitalization following a CV event.
At a median of 5 years, 11.8% of patients had died or been hospitalized for CV causes-the new primary end point. Of the 1,478 patients who died or were hospitalized, a similar percentage had received daily n-3 fatty acids (11.7%) compared with those in the placebo-treated group (11.9%). The adjusted hazard ratio with n-3 fatty acids was 0.97 (95% confidence interval, 0.88 to 1.08; P=.58).
“In a large general-practice cohort of patients with multiple cardiovascular risk factors, daily treatment with n-3 fatty acids did not reduce cardiovascular mortality or morbidity,” the authors concluded.
Navitus to Offer Unbranded Stelara Biosimilar, Remove Stelara from Formulary
March 13th 2025Lumicera Health Services, Navitus’ specialty pharmacy, has made a deal with Teva to offer an unbranded biosimilar that they estimate will save $112,000 and $336,000 per patient per year. Navitus will remove Stelara from formulary on July 1, 2025.
Read More
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More