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  • Image not available. A Good nutrition with appropriate pancreatic enzyme and vitamin supplementation are essential in the management of cystic fibrosis.
  • Image not available. Altered pharmacokinetics of cystic fibrosis patients can impact the dosing and clearance of pharmacologic therapy.
  • Image not available. Airway clearance and antiinflammatory therapies are key components to improve pulmonary health in cystic fibrosis patients.
  • Image not available. Antipseudomonal agents are the cornerstone of antibiotic therapy for chronic lung infections in the cystic fibrosis patient.

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Upon completion of the chapter, the reader will be able to:

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  • 1. Recognize that the mutation most commonly identified in this population is ΔF508.
  • 2. Define the basic genetic defect that causes CF.
  • 3. Discuss the differences between classic and nonclassic clinical presentations of CF.
  • 4. Interpret the use of the sweat chloride tests, and know what values are considered abnormal.
  • 5. List the various goals that pertain to each organ system.
  • 6. Create an airway clearance therapy routine and discuss its components.
  • 7. Explain the importance of antiinflammatory therapies utilized in CF.
  • 8. List the various pathogens and their treatments that commonly colonize the airways of the CF patient.
  • 9. Discuss the pharmacokinetic differences that apply to CF patients.
  • 10. Identify the potential issues that older CF patients may encounter.
  • 11. Explain the rationale behind the use of insulin for the treatment of CF-related diabetes (CFRD).
  • 12. Formulate appropriate counseling regarding antibiotic therapy for the pregnant CF patient.
  • 13. Describe the various controversial therapies for CF patients.
  • 14. Critique new therapies being developed for the treatment of CF.
  • 15. Discuss social and quality-of-life issues that impact the life of a CF patient.

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“Woe to that child which when kissed on the forehead tastes salty. He is bewitched and soon must die.” This European adage accurately describes the fate of an individual diagnosed with cystic fibrosis during ancient times.1

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Cystic fibrosis (CF) is a disease state resulting from a dysfunction in the cystic fibrosis transmembrane receptor (CFTR). It is the most common life-limiting disorder in the white population, with an incidence of 1 in 2,000 to 4,000 live births and a prevalence of 30,000 affected individuals in the United States.27

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Currently with care, affected individuals have an expected life span of 36 years. Multiple organ systems are affected in CF individuals; especially, the lungs, the digestive system, and the reproductive organs. Mortality is most commonly due to chronic organ damage or resistant pulmonary infections.8

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The pharmacist plays an essential role in the development and management of a pharmacotherapeutic care plan for the CF patient.

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CF is an autosomal recessive disease occurring in approximately 1 in 3,500 newborns. In the 1970s, patients only survived into their teen years. By 2006, progress in care had extended survival to 36 years. Institution of care at a young age impacts long-term survival; hence, timing of diagnosis and recognition of signs and symptoms is crucial.2...

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