Identify three priority nursing diagnoses that would address a child with Cystic Fibrosis.

Three priority nursing diagnoses for a child suffering from Cystic Fibrosis include: Impaired Gas Exchange due to decreased lung functions as shown by frequent respiratory infections, Activity Intolerance caused by increased fatigue and/or complications resulting from lack of oxygenation; and Deficient Fluid Volume risk due to excessive sweating or production of thick secretions.

First, the CFTR is malfunctioning, which leads to a buildup of mucus in the lungs, making air passage difficult. The symptoms can include chest pains, coughing and shortness in breath. If left untreated, this can result in further complications. In order to address this issue properly, therapies such as chest physiotherapy or aerosol therapy may be prescribed depending on severity—all designed towards loosening any blockages that may be present within the airways allowing for better oxygenation levels throughout the body.

This is due to fatigue and reduced oxygen. This can affect the quality of life for those patients who are unable to perform everyday activities such as sports and chores. To tackle this problem healthcare providers might suggest increasing physical activity gradually while monitoring vital signs carefully —in order ensure that breathing doesn’t become too labored during exercise sessions.

This is due to the combination of sweating and thickening secretions that are produced by these breathing difficulties. This requires additional hydration during the day either intravenously or orally. Also, electrolytes need to be checked regularly in order to correct any imbalances before they get worse. All these treatments should help promote better health outcomes even after administration has been completed in full—provided everyone follows instructions accordingly and takes proper precautions when needed..