Furosemide-induced high urine output with matched hydration significantly reduced the risk of contrast-induced nephropathy in patients with chronic kidney disease undergoing a coronary procedure, according to a new study.
Furosemide-induced high urine output with matched hydration significantly reduced the risk of contrast-induced nephropathy (CIN) in patients with chronic kidney disease undergoing a coronary procedure, according to a new study.
The study, published in the January issue of Journal of the American College of Cardiology-Cardiovascular Interventions, investigated the effect of furosemide-forced diuresis and intravenous saline infusion matched with urine output, using a novel dedicated device designed for CIN prevention.
Investigators studied 170 consecutive patients with chronic kidney disease undergoing coronary procedures. Patients were randomly assigned to receive either furosemide with matched hydration (FMH) or to standard intravenous isotonic saline hydration (control group).
The FMH group received an initial 250-mL intravenous bolus of normal saline over 30 minutes followed by an intravenous bolus (0.5 mg/kg) of furosemide. Hydration infusion rate was automatically adjusted to precisely replace the patient’s urine output.
When a urine output rate >300 mL/h was obtained, patients underwent the coronary procedure. Matched fluid replacement was maintained during the procedure and for 4 hours post-treatment. The definition of CIN was a ≥25% or ≥0.5 mg/dL rise in serum creatinine over baseline.
Four (4.6%) patients in the FMH group developed CIN versus 15 (18%) patients in the control group. A lower incidence of cumulative in-hospital clinical complications was also observed in FMH-treated patients than in the control group (8% vs 18%). In the FMH group, no device- or therapy-related complications were observed.
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