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Cystic Fibrosis - Coggle Diagram

- - - - Wescor sweat check
    - - Infants under 6months
        
        30-59 mmol/L : CF possible
        
        Above 60mmol/L : Indicates CF
      - Children over 6 months
        
        40-59 mmol/L: CF possible
        
        Above 60 mmol/L : Indicates CF
- - - - Bronchodilators eg Salbutamol
      - Inhaled corticosteroids
    - - Nebulised DNase - Pulmozyme
      - Physio
      - Nebulised hypertonic sodium chloride
  - - - Vit A, D, E, K
    - - Ranitidine + PPI
    - - CF-related diabetes
- - - - Ivacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) potentiator
      - Binds to and potentiates the channel opening ability of CFTR proteins on the cell membrane
      - Indicated for the management of CF in patients with G551D mutation - Residual CFTR expression with reduced channel conductance