What is a key management strategy for children with cystic fibrosis?

Prepare for the Archer Child Health Cardio/Respiratory Test with detailed flashcards and questions. Each question features helpful hints and explanations to enhance learning. Get exam-ready now!

A key management strategy for children with cystic fibrosis involves the use of chest physiotherapy and mucolytics. Cystic fibrosis is a genetic disorder that leads to the production of thick and sticky mucus, which can obstruct the airways and create a favorable environment for bacterial infections.

Chest physiotherapy helps in clearing mucus from the lungs through various techniques, including postural drainage, percussion, and vibration, making it easier for children to breathe and reducing the risk of infection. Mucolytics, which are medications that thin the mucus, also play a crucial role in making airway clearance more effective. By combining both chest physiotherapy and mucolytics, children can maintain better lung function, decrease lung infections, and improve their overall quality of life.

In contrast, while increased caloric intake and hydration are also important for overall management in cystic fibrosis, the focus on specific respiratory interventions like chest physiotherapy and mucolytics is a fundamental part of managing the pulmonary complications associated with the disease. A regular sleep schedule and routine check-ups are important for overall health but do not directly address the respiratory issues caused by cystic fibrosis. Additionally, minimal physical activity is contrary to promoting lung health, as exercise can enhance respiratory function and overall well-being in these

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