Log in or Sign up for Free to view tailored content for your specialty!
Cystic Fibrosis News
Triple therapy improves chronic rhinosinusitis outcomes in cystic fibrosis
Patients with cystic fibrosis had improved chronic rhinosinusitis outcomes after 1 year of elexacaftor/tezacaftor/ivacaftor therapy, according to results published in JAMA Otolaryngology-Head & Neck Surgery.
Cystic fibrosis triple therapy safe, tolerable for 144 weeks in older children
Elexacaftor/tezacaftor/ivacaftor appeared safe and well tolerated among kids aged 12 years and older with cystic fibrosis and either F508del/minimal function or F508del/F508del genotypes for up to 144 weeks, according to study results.
Log in or Sign up for Free to view tailored content for your specialty!
Yearly MRI offers chronic rhinosinusitis monitoring in pediatric cystic fibrosis
Yearly paranasal sinus MRI imaging allowed physicians to track chronic rhinosinusitis development in children with cystic fibrosis, according to results published in Annals of the American Thoracic Society.
FDA grants orphan drug designation to cystic fibrosis treatment
The FDA granted orphan drug designation to ARCT-032 as a treatment for patients with cystic fibrosis, according to a press release from Arcturus Therapeutics.
Triple therapy shows safety, tolerability for older children with cystic fibrosis
In kids aged 6 years and older with cystic fibrosis and either F508del/minimal function or F508del/F508del genotypes, elexacaftor/tezacaftor/ivacaftor was safe and well tolerated for up to 120 weeks, according to study results.
Aerosol gene therapy safe, heightens CFTR protein levels in cystic fibrosis
Receipt of 4D-710, an aerosolized gene therapy, resulted in high cystic fibrosis transmembrane conductance regulator protein expression levels in patients with cystic fibrosis, according to a company press release.
Q&A: Establishing global standard for exercise testing in patients with cystic fibrosis
For patients with cystic fibrosis, exercise helps with disease management, and exercise tests allow clinicians to assess lung health, muscle strength and treatment response, according to a press release from University of Portsmouth.
Metals, sulfate in water heighten risk for mycobacterial infections in cystic fibrosis
Among patients with cystic fibrosis, increases in sulfate and specific metals in water raised the odds for nontuberculosis mycobacterial infections, according to results published in Environmental Epidemiology.
Late cystic fibrosis care negatively impacts infant weight, height
Infants with cystic fibrosis who received care at 47 days old had decreased weight and height-for-age during infancy compared with infants who received care at 10 days old, according to results published in The Journal of Pediatrics.
Life expectancy lengthened in recent years for patients with cystic fibrosis
Patients with cystic fibrosis had an average survival of 66 years in 2022, which is a notable increase from 26 years in 2008, according to study results from Epic Research.
-
Headline News
Burnout, withdrawal remain ‘alarmingly high’ among physicians and residents
September 17, 20242 min read -
Headline News
Over one-third of adults not planning on receiving recommended vaccines this fall
September 18, 20242 min read -
Headline News
Popular home BP devices unable to provide accurate readings for millions due to sizing
September 19, 20242 min read
-
Headline News
Burnout, withdrawal remain ‘alarmingly high’ among physicians and residents
September 17, 20242 min read -
Headline News
Over one-third of adults not planning on receiving recommended vaccines this fall
September 18, 20242 min read -
Headline News
Popular home BP devices unable to provide accurate readings for millions due to sizing
September 19, 20242 min read