Viera Ďurdíková, Jana Gajanová, Eva Babčanová
The article is especially focused on the non-pharmacological therapy of bronchopulmonary changes in children with cystic fibrosis which belongs to the necessary part of complex therapeutic management of children with cystic fibrosis. This hereditary disease is one of the most often presented congenital diseases and it is responsible for shorter duration of life in Caucasian race. The cystic fibrosis is chronic multi-organ disease. The therapeutic management has to be focused on all affected organs. The bronchopulmonary injury is the most life limited injury. Its development and range do not depend on the type of genetic changes but they depend on the adequate pharmacological treatment and necessary daily rehabilitation.