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- W2293093088 endingPage "519" @default.
- W2293093088 startingPage "505" @default.
- W2293093088 abstract "In many countries numbers of adults with cystic fibrosis (CF) exceed that of children, with median survival predicted to surpass 50 years. Increasing longevity is, in part, due to intensive therapies including eradication of early infection and suppressive therapies and pulmonary exacerbations. Initial infections with common CF pathogens are thought to arise from the natural environment. We review the impact of climate and environment on infection in CF. Specifically, several studies indicate that higher ambient temperatures, proximity to the equator and the summer season may be linked to the increased prevalence of Pseudomonas aeruginosa in people with CF. The environment may also play an important role in the acquisition of Gram negative organisms other than P. aeruginosa. There is emerging data suggesting that climatic and environmental factors are likely to impact on the risk of infection with NTM and fungi in people which are found extensively throughout the natural environment." @default.
- W2293093088 created "2016-06-24" @default.
- W2293093088 creator A5004563487 @default.
- W2293093088 creator A5009867982 @default.
- W2293093088 creator A5015707789 @default.
- W2293093088 creator A5020072100 @default.
- W2293093088 date "2016-03-28" @default.
- W2293093088 modified "2023-10-15" @default.
- W2293093088 title "Infection in cystic fibrosis: impact of the environment and climate" @default.
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