| Abstrakt: |
There is increasing evidence that close monitoring and early intervention lead to better outcomes in patients with, cystic fibrosis. At each office visit, spirometry should be per-formed and sputum culture specimens should be obtained; if the patient cannot produce sputum, a throat culture can be done instead. New respiratory symptoms or other evidence of worsening lung disease should prompt antibiotic therapy, in-creased airway clearance, and adjunctive anti-inflammatory medication as appropriate. Close attention should be paid to the patient's diet, appetite, stooling pattern, and growth measurements. Adolescents should be given additional information about their medications and adjunctive therapies to encourage them to take on a larger role in their own care. [ABSTRACT FROM AUTHOR] |
