Titlebook: Cystic Fibrosis in Primary Care; An Essential Guide t Douglas Lewis, MD, FAAFP Book 2020 Springer Nature Switzerland AG 2020 cystic fibrosi

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Electrolyte Abnormalities in CF,logic complication of overly rapid correction. Patients with cystic fibrosis are predisposed to hyponatremia due to increased sodium loss in sweat. Major electrolyte and volume changes can be prevented by proper instruction regarding fluid and sodium replacement during periods of exertion or prolonged heat exposure.

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Psychology and Psychotherapy in CF,. This chapter is aimed at identifying how healthcare teams can provide family-oriented assessment and intervention targeted at increasing coping and resilience throughout the life cycle. To provide rich description, four case studies are highlighted.

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?Mein Auto, mein Haus, meine Bank“egies for managing infectious complications of CF patients include chronic prophylactic antibiotics, use of systemic as well as inhaled antibiotics, mechanical assistance with mucus clearance, and scrupulous infection control measures.

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Spondyloarthropathies and Food Intakeies have been developed and are currently available for about 50% of the CF population within the United States. Further therapeutics, including genetic therapy options, are in various stages of development with the eventual hope of providing CFTR modulating and/or genetic therapy options for all individuals with CF.

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CFTR Physiology,rious organs including lungs, pancreas, intestines, hepatobiliary system, and the reproductive system (O’Sullivan and Freedman Lancet 373:1891–904, 2009). Lung disease is a major cause of mortality and morbidity in patients with CF.