Cystic Fibrosis P2

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  • Cystic Fibrosis
    • Age range
      • The median age of diagnosis is 6-8 months old
      • 2/3 of people are diagnosed by 1 year of age
      • The age at diagnosis varies widely
      • Clinical presentation, severity of symptoms, and rate of disease progression varies
    • Treatments
      • Cystic fibrosis cannot be cured
      • There are treatment options to help manage symptoms and reduce complications
      • Antibiotics: Given in the form of inhaled therapy to improve lung function by impeding growth of basctiera
        • Tobramycin
        • Aztreonam
        • Colistin
      • Anti-inflammatory drugs: to prevent inflammation in the airway passage
        • Ibuprofen
      • Mucus thinners: to help patients cough up mucus and improve lung function
        • Acetylcysteine
      • Bronchodilators: to open and relax muscles around the bronchia (lungs)
        • Albuterol
        • Salmeterol
    • Heath and social care staff involved in care
      • Dietitian
      • Nurse
        • Nurse practiitoner
        • Physician assistant
      • Physician
        • Pulmonologist
        • Lung specialist
      • Program coordinator
      • Respiratory therapist
      • Social worker
      • Pharmacist
      • Physical therapist
      • Psychologist
      • Research coordinator

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