Chronic Pseudomonas aeruginosa infection definition: EuroCareCF Working Group report
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F11%3A7062" target="_blank" >RIV/00064203:_____/11:7062 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11130/11:7062
Result on the web
<a href="http://www.ncbi.nlm.nih.gov/pubmed/21658646" target="_blank" >http://www.ncbi.nlm.nih.gov/pubmed/21658646</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Chronic Pseudomonas aeruginosa infection definition: EuroCareCF Working Group report
Original language description
Chronic pulmonary infection with P aeruginosa develops in most patients with cystic fibrosis (CF); by adulthood 80% of patients are infected and chronic P. aeruginosa infection is the primary cause of increased morbidity and mortality in CF. Chronic infection is preceded by an intermittent stage of infection. The initial stage is characteristically followed by the gradual emergence of mucoid variants of the colonizing strains and a rise in anti-Pseudomonas antibodies. In addition to optimizing existingtherapeutic strategies, effective new agents need to be identified. Studies in patients with CF are particularly challenging: the progressive nature of the disease and the wide variation in severity influence considerably the outcome of drug testing. A validated, universally accepted, and clinically useful classification of patients infected with P aeruginosa, particularly those chronically infected, is needed that can be used as both a criterion for patient selection for clinical trials
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FC - Pneumology
OECD FORD branch
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Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Cystic Fibrosis
ISSN
1569-1993
e-ISSN
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Volume of the periodical
10
Issue of the periodical within the volume
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Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
4
Pages from-to
"S75"-"S78"
UT code for WoS article
000292068000011
EID of the result in the Scopus database
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