Discover how Cincinnati Children’s CF WELL program is transforming care for children with cystic fibrosis—addressing educational and mental health needs alongside clinical advances.
Lung transplantation for children has similar survival outcomes whether the organs were donated after circulatory death or via donation after brain death. But hospital stays were longer for those receiving organs after circulatory death, and the time to developing acute cellular rejection was shorter.
New organ transport technology allows organs to come from farther distances, increasing the chances of a match.
Discover how Cincinnati Children’s ADEC team delivers multidisciplinary care for complex airway and esophageal conditions in pediatric patients.
Cincinnati Children’s is pioneering pediatric bronchoscopy with advanced, minimally invasive techniques to improve diagnosis and treatment of complex lung conditions.
New research from Cincinnati Children’s reveals early vascular changes in cystic fibrosis, offering insights for earlier diagnosis and treatment strategies.
Cincinnati Children’s researchers explore gene editing strategies to restore CFTR function—offering hope for CF variants unresponsive to current therapies.
Cincinnati Children’s researchers use advanced MRI to track long-term lung changes in cystic fibrosis, offering new insights into pediatric care.