Literature DB >> 21460730

Pneumothorax in cystic fibrosis.

Patrick A Flume1.   

Abstract

PURPOSE OF REVIEW: Cystic fibrosis (CF) is a complex genetic disease affecting many organs, although 85% of the mortality is a result of lung disease. The natural history of the lung disease consists of early and persistent infection, an exaggerated inflammatory response, structural airway changes (i.e. bronchiectasis), and progressive airways obstruction, ultimately resulting in respiratory failure. As airways disease worsens, there is an increased likelihood of respiratory complications, such as pneumothorax, that may be serious. This review describes our current understanding of the pathogenesis of pneumothorax in CF and its treatment. RECENT
FINDINGS: The CF Foundation Pulmonary Therapies Committee recently published their recommendations for the treatment of hemoptysis and pneumothorax. As insufficient data exist from which a systematic review of the literature could be used to develop guidelines, the recommendations were derived from a formalized expert panel consensus process.
SUMMARY: We now have recommendations on specific care of the patient with CF who has a pneumothorax.

Entities:  

Mesh:

Year:  2011        PMID: 21460730     DOI: 10.1097/MCP.0b013e328345e1f8

Source DB:  PubMed          Journal:  Curr Opin Pulm Med        ISSN: 1070-5287            Impact factor:   3.155


  2 in total

1.  Pseudotyped AAV vector-mediated gene transfer in a human fetal trachea xenograft model: implications for in utero gene therapy for cystic fibrosis.

Authors:  Sundeep G Keswani; Swathi Balaji; Louis Le; Alice Leung; Anna B Katz; Foong-Yen Lim; Mounira Habli; Helen N Jones; James M Wilson; Timothy M Crombleholme
Journal:  PLoS One       Date:  2012-08-24       Impact factor: 3.240

2.  CF Patient's Pneumothoraxes Unique Genes.

Authors:  Jillian McKee; Joseph Majure; Hans Georg Bock; George Moll
Journal:  Glob Pediatr Health       Date:  2016-06-21
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.