Respiratory bacterial infections in cystic fibrosis

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Respiratory bacterial infections in cystic fibrosis. / Ciofu, Oana; Hansen, Christine R; Høiby, Niels.

In: Current Opinion in Pulmonary Medicine, Vol. 19, No. 3, 05.2013, p. 251-8.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ciofu, O, Hansen, CR & Høiby, N 2013, 'Respiratory bacterial infections in cystic fibrosis', Current Opinion in Pulmonary Medicine, vol. 19, no. 3, pp. 251-8. https://doi.org/10.1097/MCP.0b013e32835f1afc

APA

Ciofu, O., Hansen, C. R., & Høiby, N. (2013). Respiratory bacterial infections in cystic fibrosis. Current Opinion in Pulmonary Medicine, 19(3), 251-8. https://doi.org/10.1097/MCP.0b013e32835f1afc

Vancouver

Ciofu O, Hansen CR, Høiby N. Respiratory bacterial infections in cystic fibrosis. Current Opinion in Pulmonary Medicine. 2013 May;19(3):251-8. https://doi.org/10.1097/MCP.0b013e32835f1afc

Author

Ciofu, Oana ; Hansen, Christine R ; Høiby, Niels. / Respiratory bacterial infections in cystic fibrosis. In: Current Opinion in Pulmonary Medicine. 2013 ; Vol. 19, No. 3. pp. 251-8.

Bibtex

@article{70501c681d02423db482ed4e47835b47,
title = "Respiratory bacterial infections in cystic fibrosis",
abstract = "PURPOSE OF REVIEW: Bacterial respiratory infections are the main cause of morbidity and mortality in patients with cystic fibrosis (CF). Pseudomonas aeruginosa remains the main pathogen in adults, but other Gram-negative bacteria such as Achromobacter xylosoxidans and Stenotrophomonas maltophilia as well as nontuberculous mycobacteria have been shown to play an important role in the lung disease. The purpose of this review is to summarize the knowledge on disease and treatment of infection with CF-related pathogens.RECENT FINDINGS: The role of the paranasal sinuses as a source of infection and site of bacterial adaptation has been recognized. This review will focus on the different conditions encountered by the bacteria in sinuses and lung, as well as the principles of treatment in the different infection sites.SUMMARY: Chronic, pulmonary infections remain the single most prominent cause of the increased morbidity and mortality in CF. After the increasing efficiency of anti-P. aeruginosa treatment, newer pathogens have been identified, with individual clinical characteristics. Microbiological surveillance is very important in keeping the patients stable. Samples from both the lower and upper respiratory tract (nasal sampling) should be investigated and both infection sites should be treated.",
keywords = "Anti-Infective Agents, Bacterial Infections, Chronic Disease, Cystic Fibrosis, Humans, Lung, Paranasal Sinuses, Pseudomonas aeruginosa, Respiratory Tract Infections",
author = "Oana Ciofu and Hansen, {Christine R} and Niels H{\o}iby",
year = "2013",
month = may,
doi = "10.1097/MCP.0b013e32835f1afc",
language = "English",
volume = "19",
pages = "251--8",
journal = "Current Opinion in Pulmonary Medicine",
issn = "1070-5287",
publisher = "Lippincott Williams & Wilkins, Ltd.",
number = "3",

}

RIS

TY - JOUR

T1 - Respiratory bacterial infections in cystic fibrosis

AU - Ciofu, Oana

AU - Hansen, Christine R

AU - Høiby, Niels

PY - 2013/5

Y1 - 2013/5

N2 - PURPOSE OF REVIEW: Bacterial respiratory infections are the main cause of morbidity and mortality in patients with cystic fibrosis (CF). Pseudomonas aeruginosa remains the main pathogen in adults, but other Gram-negative bacteria such as Achromobacter xylosoxidans and Stenotrophomonas maltophilia as well as nontuberculous mycobacteria have been shown to play an important role in the lung disease. The purpose of this review is to summarize the knowledge on disease and treatment of infection with CF-related pathogens.RECENT FINDINGS: The role of the paranasal sinuses as a source of infection and site of bacterial adaptation has been recognized. This review will focus on the different conditions encountered by the bacteria in sinuses and lung, as well as the principles of treatment in the different infection sites.SUMMARY: Chronic, pulmonary infections remain the single most prominent cause of the increased morbidity and mortality in CF. After the increasing efficiency of anti-P. aeruginosa treatment, newer pathogens have been identified, with individual clinical characteristics. Microbiological surveillance is very important in keeping the patients stable. Samples from both the lower and upper respiratory tract (nasal sampling) should be investigated and both infection sites should be treated.

AB - PURPOSE OF REVIEW: Bacterial respiratory infections are the main cause of morbidity and mortality in patients with cystic fibrosis (CF). Pseudomonas aeruginosa remains the main pathogen in adults, but other Gram-negative bacteria such as Achromobacter xylosoxidans and Stenotrophomonas maltophilia as well as nontuberculous mycobacteria have been shown to play an important role in the lung disease. The purpose of this review is to summarize the knowledge on disease and treatment of infection with CF-related pathogens.RECENT FINDINGS: The role of the paranasal sinuses as a source of infection and site of bacterial adaptation has been recognized. This review will focus on the different conditions encountered by the bacteria in sinuses and lung, as well as the principles of treatment in the different infection sites.SUMMARY: Chronic, pulmonary infections remain the single most prominent cause of the increased morbidity and mortality in CF. After the increasing efficiency of anti-P. aeruginosa treatment, newer pathogens have been identified, with individual clinical characteristics. Microbiological surveillance is very important in keeping the patients stable. Samples from both the lower and upper respiratory tract (nasal sampling) should be investigated and both infection sites should be treated.

KW - Anti-Infective Agents

KW - Bacterial Infections

KW - Chronic Disease

KW - Cystic Fibrosis

KW - Humans

KW - Lung

KW - Paranasal Sinuses

KW - Pseudomonas aeruginosa

KW - Respiratory Tract Infections

U2 - 10.1097/MCP.0b013e32835f1afc

DO - 10.1097/MCP.0b013e32835f1afc

M3 - Journal article

C2 - 23449384

VL - 19

SP - 251

EP - 258

JO - Current Opinion in Pulmonary Medicine

JF - Current Opinion in Pulmonary Medicine

SN - 1070-5287

IS - 3

ER -

ID: 117485562