Cystic fibrosis is a genetically determined disease. The development of medicine has resulted in an improvement and prolongation of life. Numerous scientific studies support the thesis that maintaining physical performance is a key element of complex treatment. The basis of treatment should be: parallel pharmacological treatment and physiotherapeutic. The aim of this work was to present the physiotherapeutic techniques used in this disease. The main methods of physiotherapeutic treatment include positional drainage, forced exhalation technique, active breathing cycle technique, autogenous drainage, variable bronchial pressure technique and increased respiratory pressure technique. Physiotherapy of the respiratory system is of major importan...
Cystic fibrosis belongs to the most common fatal genetic diseases of Caucasians. The treatment of cy...
Aim of the research. To evaluate effects of the active cycle of breathing techniques on pulmonary fu...
Cystic fibrosis (CF) patients have viscous bronchial secretions, endobronchial infection and, hence,...
Cystic fibrosis is a genetically determined disease. The development of medicine has resulted in an ...
The theme of this thesis is children´s cystic fibrosis and the impact of using the methods of physio...
Physiotherapy remains the cornerstone of cystic fibrosis (CF) management alongside medical treatment...
Cistična fibroza je nasljedna progresivna bolest koja nastaje mutacijom CFTR gena. Dovodi do poteško...
Cistična fibroza teška je kronična bolest koja zahvaća više organa, a najštetnija je za pluća. Nasl...
Cystic fibrosis (CF) is a complex, systemic autosomal recessive disease that affects the functions o...
SUMMARY Twelve children with cystic fibrosis were admitted to a paediatric rehabilitation hospital f...
AbstractIntroductionChest physiotherapy (CP) is used in cystic fibrosis (CF) even if there is no rob...
Respiratory therapy is a part of the treatment of patients with cystic fibrosis (CF). However, there...
Cistična fibroza je nasljedna bolest uzrokovana poremećajem CFTR gena, transmembranskog regulatora p...
The respiratory secretions of patients with cystic fibrosis (CF) cause frequent pulmonary infections...
Physiotherapy management is a key element of care for people with cystic fibrosis (CF) throughout th...
Cystic fibrosis belongs to the most common fatal genetic diseases of Caucasians. The treatment of cy...
Aim of the research. To evaluate effects of the active cycle of breathing techniques on pulmonary fu...
Cystic fibrosis (CF) patients have viscous bronchial secretions, endobronchial infection and, hence,...
Cystic fibrosis is a genetically determined disease. The development of medicine has resulted in an ...
The theme of this thesis is children´s cystic fibrosis and the impact of using the methods of physio...
Physiotherapy remains the cornerstone of cystic fibrosis (CF) management alongside medical treatment...
Cistična fibroza je nasljedna progresivna bolest koja nastaje mutacijom CFTR gena. Dovodi do poteško...
Cistična fibroza teška je kronična bolest koja zahvaća više organa, a najštetnija je za pluća. Nasl...
Cystic fibrosis (CF) is a complex, systemic autosomal recessive disease that affects the functions o...
SUMMARY Twelve children with cystic fibrosis were admitted to a paediatric rehabilitation hospital f...
AbstractIntroductionChest physiotherapy (CP) is used in cystic fibrosis (CF) even if there is no rob...
Respiratory therapy is a part of the treatment of patients with cystic fibrosis (CF). However, there...
Cistična fibroza je nasljedna bolest uzrokovana poremećajem CFTR gena, transmembranskog regulatora p...
The respiratory secretions of patients with cystic fibrosis (CF) cause frequent pulmonary infections...
Physiotherapy management is a key element of care for people with cystic fibrosis (CF) throughout th...
Cystic fibrosis belongs to the most common fatal genetic diseases of Caucasians. The treatment of cy...
Aim of the research. To evaluate effects of the active cycle of breathing techniques on pulmonary fu...
Cystic fibrosis (CF) patients have viscous bronchial secretions, endobronchial infection and, hence,...