In the care of a school-age child with cystic fibrosis, which finding is a priority for the nurse to address?

In managing a school-age child with cystic fibrosis, addressing a lack of appetite is crucial because it may indicate a decline in nutritional status, which is essential for the growth and development of the child. Children with cystic fibrosis often have difficulty absorbing nutrients due to pancreatic insufficiency, which can lead to malnutrition if not properly managed.

Inadequate nutrition can exacerbate the child's overall health, making it more challenging to combat respiratory infections or manage symptoms effectively. With a lack of appetite, there’s a risk that the child may not receive sufficient calories and nutrients to support their increased metabolic demands associated with cystic fibrosis.

While other findings such as coughing up mucus, frequent respiratory infections, and night sweats are also important components of cystic fibrosis management, prioritizing nutritional intake allows for a holistic approach to care that supports the child's respiratory health and overall well-being. Ensuring that the child maintains adequate nutrition can lead to improved growth, better lung function, and enhanced quality of life.