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Thorax 2007;62:360-367; doi:10.1136/thx.2006.060889
Copyright © 2007 BMJ Publishing Group Ltd & British Thoracic Society

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REVIEW SERIES

Exacerbations in cystic fibrosis · 1: Epidemiology and pathogenesis

Christopher H Goss1, Jane L Burns2

1 Department of Medicine, University of Washington Medical Center, Seattle, Washington, USA
2 Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA

Correspondence to:
Correspondence to:
Dr Christopher H Goss
Department of Medicine, University of Washington Medical Center, Campus Box 356522, 1959 NE Pacific, Seattle, Washington 98195, USA; goss{at}u.washington.edu

With the improving survival of patients with cystic fibrosis (CF), the clinical spectrum of this complex multisystem disease continues to evolve. One of the most important clinical events for patients with CF in the course of this disease is an acute pulmonary exacerbation. Clinical and microbial epidemiology studies of CF pulmonary exacerbations continue to provide important insight into the course, prognosis and complications of the disease. This review provides a summary of the pathophysiology, clinical epidemiology and microbial epidemiology of a CF pulmonary exacerbation.


Abbreviations: ARIC, Acute Respiratory Illness Checklist; CF, cystic fibrosis; CFTR, cystic fibrosis transmembrane regulator; FEV1, forced expiratory volume in 1 s; IL, interleukin; MCBT, multiple combination bactericidal testing; RSSQ, Respiratory and Systemic Symptoms Questionnaire; TNF{alpha}, tumour necrosis factor {alpha}


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