Cystic fibrosis is a genetic metabolic disease (↓ DNase 1) that results in reduced secretions in various organs
• Worst symptoms visible in airways
• Mucus is thick and sticky and leads to recurrent bacterial infections
• Body does not have the ability to clear mucus
Dornase alfa- Hydrolyze proteins in bronchial mucus to improve fluidity.
Also known as hyalin membrane disease • Occurs in premature babies • Surfactants that cover airways and are essential for gas exchange are only formed shortly before birth • Lungs can therefore fall flat (atelectasis) → death • Intensive monitoring of respiratory and circulatory status essential
Treatment-Oxygen to ensure oxygenation
• Ventilation used for positive pressure
• Drug: exogenous surfactant: beractant, poractant alfa
• Corticosteroids such as betamethasone - are also given prophylactically to mother before labour to initiate baby's surfactant production
Oxygen ensures oxygenation , dangers is that Increased oxygen over long term leads to retinal damage and blindness
• In newborns and premature babies
• Respiratory centre in brain not yet fully developed to stimulate continuous breathing • Apnea with bradycardia lasts longer than 15 seconds and occurs repeatedly
• May cause hypoxia and neural damage
Theophylline and caffeine