A pathophysiological process where excessively thick mucus obstructs airways is a leading clinical manifestations commonly seen in cystic fibrosis.
Exocrine gland dysfunction results in the secretion of mucus that is thicker and more sticky than usual. Due to the features of this mucus, expectoration is challenging since it pools in the lungs. In addition to airway blockage, respiratory infections are more common in children with cystic fibrosis. Hyperactive airway disease is linked to irritation of the airways. Pneumonia is connected with inflamed lung parenchyma; this is a subsequent consequence linked to the stasis of secretions. Cystic fibrosis does not directly impact the endocrine glands.
In this condition, a nurse can recognize the excessive secretion of thick mucus as a clinical manifestation of cystic fibrosis.
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