Cystic fibrosis secondary prevention: Difference between revisions
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==Secondary Prevention== | ==Secondary Prevention== | ||
In cystic fibrosis secondary prevention include:<ref name="pmid29303286">{{cite journal |vauthors=Fila L |title=[Cystic fibrosis in adults] |language=Czech |journal=Vnitr Lek |volume=63 |issue=11 |pages=834–842 |date= 2018 |pmid=29303286 |doi= |url=}}</ref><ref name="urlCystic Fibrosis and Congenital Absence of the Vas Deferens - GeneReviews® - NCBI Bookshelf">{{cite web |url=https://www.ncbi.nlm.nih.gov/books/NBK1250/ |title=Cystic Fibrosis and Congenital Absence of the Vas Deferens - GeneReviews® - NCBI Bookshelf |format= |work= |accessdate=}}</ref> | |||
* Airway clearance techniques | |||
* Dornase alpha | |||
* Hypertonic saline | |||
* Antibiotics for prevention of airway [[infection]] with resistant bacterial pathogens (especially ''[[Pseudomonas aeruginosa|P. aeruginosa]]'') | |||
* Immunizations including anti-RSV monoclonal antibody | |||
* Physical activity to maintain bone health and improve airway clearance | |||
* Nutritional support for pancreatic insufficiency | |||
* Extra salt and water | |||
* Hot and dry climates | |||
==References== | ==References== | ||
Revision as of 20:33, 2 March 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]
Overview
The prevention of airway infection with resistant bacterial pathogens (especially P. aeruginosa) is essential.
Secondary Prevention
In cystic fibrosis secondary prevention include:[1][2]
- Airway clearance techniques
- Dornase alpha
- Hypertonic saline
- Antibiotics for prevention of airway infection with resistant bacterial pathogens (especially P. aeruginosa)
- Immunizations including anti-RSV monoclonal antibody
- Physical activity to maintain bone health and improve airway clearance
- Nutritional support for pancreatic insufficiency
- Extra salt and water
- Hot and dry climates
References
- ↑ Fila L (2018). "[Cystic fibrosis in adults]". Vnitr Lek (in Czech). 63 (11): 834–842. PMID 29303286.
- ↑ "Cystic Fibrosis and Congenital Absence of the Vas Deferens - GeneReviews® - NCBI Bookshelf".