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ABSTRACT: Background
Air travel may imply a health hazard for patients with cystic fibrosis (CF) due to hypobaric environment in the aircraft cabin. The objective was to identify pre-flight variables, which might predict severe hypoxaemia in adult CF patients during air travel.Methods
Thirty adult CF-patients underwent pre-flight evaluation with spirometry, arterial oxygen tension (PaO2), pulse oximetry (SpO2) and cardiopulmonary exercise testing (CPET) at sea level (SL). The results were related to the PaO2 obtained during a hypoxia-altitude simulation test (HAST) in which a cabin altitude of 2438 m (8000 ft) was simulated by breathing 15.1% oxygen.Results
Four patients fulfilled the criteria for supplemental oxygen during air travel (PaO
SUBMITTER: Edvardsen E
PROVIDER: S-EPMC5292785 | biostudies-literature | 2017 Feb
REPOSITORIES: biostudies-literature