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1.
Monaldi Arch Chest Dis ; 77(3-4): 122-8, 2012.
Article in English | MEDLINE | ID: mdl-23461248

ABSTRACT

BACKGROUND AND AIM: Lung function abnormalities are the main factors responsible for the high mortality of cystic fibrosis (CF) patients. It is not yet clear whether Burkholderia cepacia infection causes more pronounced loss of lung function than pseudomonas aeruginosa infection. Our primary objective was to compare the lung function of adult CF patients with different chronic pulmonary infections. Our second objective was to compare the microbiology using patients' genetic status. METHODS: Fifty-two adult CF patients were divided into 3 groups according to their chronic pulmonary infection profile. All subjects underwent clinical evaluation, pulmonary function tests (PFT) and genetic analysis. RESULTS: The PFT parameters of chronically infected patients were significantly different from those of subjects without pulmonary infection (p < 0.0001). FVC was significantly more altered in patients infected with B. cepacia complex (p < 0.0001); in contrast, FEF25-75% was significantly more altered in patients with P. aeruginosa infection (p < 0.0001). In the groups with chronic P. aeruginosa infection and chronic B. cepacia complex infection, 58.1% and 10% of patients were homozygous for AF508, respectively. In addition to chronic infections, pancreatic insufficiency was also associated with lung function deterioration. CONCLUSION: Chronic pulmonary infection and pancreatic insufficiency are critical processes in lung function deterioration in adult CF patients. Although chronic B. cepacia complex infection causes a more pronounced lung volume reduction, chronic P. aeruginosa infection causes a more pronounced obstruction of small airways. Our results also suggest that deltaF508-homozygous patients are more susceptible to chronic P. aeruginosa infection.


Subject(s)
Cystic Fibrosis/physiopathology , Lung/physiopathology , Respiratory Tract Infections/physiopathology , Adult , Bacteria/isolation & purification , Chronic Disease , Cross-Sectional Studies , Cystic Fibrosis/microbiology , Female , Forced Expiratory Volume , Humans , Male , Respiratory Tract Infections/microbiology
2.
J Hosp Infect ; 60(1): 51-5, 2005 May.
Article in English | MEDLINE | ID: mdl-15823657

ABSTRACT

Ralstonia pickettii and Burkholderia cepacia complex isolates are causes of healthcare-associated infection related to contamination of intravenously administered products. Based on microbiological and epidemiological data and molecular typing by pulsed-field gel electrophoresis, we report the occurrence of two outbreaks of R. pickettii and B. cepacia complex bloodstream infections. The first outbreak occurred from August 1995 to September 1996, and the second outbreak occurred from 28 March to 8 April 1998, affecting adults and neonates, respectively. Infusion of contaminated water for injection was the source of infection.


Subject(s)
Bacteremia/etiology , Burkholderia Infections/etiology , Burkholderia cepacia complex , Cross Infection/etiology , Drug Contamination , Gram-Negative Bacterial Infections/etiology , Injections/adverse effects , Ralstonia , Water Microbiology , Adult , Bacteremia/epidemiology , Brazil/epidemiology , Burkholderia Infections/epidemiology , Burkholderia cepacia complex/classification , Burkholderia cepacia complex/genetics , Burkholderia cepacia complex/isolation & purification , Cross Infection/epidemiology , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Disease Outbreaks/statistics & numerical data , Electrophoresis, Gel, Pulsed-Field , Fatal Outcome , Female , Genotype , Gram-Negative Bacterial Infections/epidemiology , Humans , Infant, Newborn , Infection Control , Male , Molecular Epidemiology , Phylogeny , Ralstonia/classification , Ralstonia/genetics , Ralstonia/isolation & purification , Seasons
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