LYCOS RETRIEVER 
Cystic Fibrosis: Infections
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Cystic fibrosis is an inherited condition where important membrane linings do not function properly. Thickened, rubbery mucus results in blockage and infection throughout the respiratory tract. The pancreatic and bile ducts are blocked, leading to severe digestive problems. Sweat and other secretions contain increased salt.
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The most consistent aspect of therapy in cystic fibrosis is limiting and treating the lung damage caused by thick mucus and infection with the goal of maintaining quality of life. Intravenous, inhaled, and oral antibiotics are used to treat chronic and acute infections. Mechanical devices and inhalation medications are used to alter and clear the thickened mucus.
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The most common manifestation of cystic fibrosis is frequent respiratory infection. Impaired digestion and malabsorption due to pancreatic insufficiency and blocked liver ducts is often seen as well. Management of this condition requires the help of a qualified doctor.
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