Cystic fibrosis lung disease in adult patients

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

As the longevity of all patients with cystic fibrosis (CF) continues to increase (median 2005 survival = 36.8 years), more adult patients will be receiving their medical care from nonpediatric adult-care providers. Cystic fibrosis remains a fatal disease, with more than 80% of patients dying after the age of 18 years, and most deaths resulting from pulmonary disease. The changing epidemiology requires adult-care providers to become knowledgeable and competent in the clinical management of adults with CF. Physicians must understand the influence of specific genotype on phenotypic disease presentation and severity, the pathogenic factors determining lung disease onset and progression, the impact of comorbid disease factors such as CF-related diabetes and malnutrition upon lung disease severity, and the currently approved or standard accepted therapies used for chronic management of CF lung disease. This knowledge is critical to help alleviate morbidity and improve mortality for the rapidly expanding population of adults with CF.

Original languageEnglish (US)
Pages (from-to)64-74
Number of pages11
JournalPostgraduate medicine
Volume120
Issue number1
DOIs
StatePublished - Apr 1 2008

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Cystic Fibrosis
Lung Diseases
Malnutrition
Disease Progression
Epidemiology
Genotype
Morbidity
Physicians
Survival
Mortality
Population

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

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Cystic fibrosis lung disease in adult patients. / Vender, Robert.

In: Postgraduate medicine, Vol. 120, No. 1, 01.04.2008, p. 64-74.

Research output: Contribution to journalArticle

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