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Publications
Publications (6)
Introduction
Lung function and weight evolution are important parameters in the follow-up of health condition in CF patients.
Objectives
Aim of this study was to investigate the influence of a 4-week multicomponent rehabilitation program on lung function (FEV1, FVC, LCI and Sraw) and weight in adolescent and adult cystic fibrosis patients.
Method...
CF of mucoviscidose is de meest voorkomende autosomaal recessieve erfelijke aandoening van het Kaukasische ras. Respiratoire en gastro-intestinale symptomen staan bij deze aandoening op de voorgrond. De diagnose wordt bevestigd door een gestegen chloorconcentratie in het zweet. Pancreasenzymen, inhalatiemedicijnen en antibiotica enerzijds en fysiot...
Nebulizers are a potential source of contamination of the respiratory tract. Nevertheless, only a few clear guidelines regarding cleaning and disinfection of nebulizers are available. This survey aims to analyze the common household methods used by cystic fibrosis (CF) patients in Belgium.
A questionnaire about type of nebulizer, methods, and frequ...
