Burkholderia cepacia in cystic fibrosis: Novel Australian cluster strain without accelerated respiratory deterioration

Journal of Paediatrics and Child Health

Volumn 37, Issue 2, 2001, Pages 130-136

  Fitzgerald, D A ^a   Cooper, D M ^a   Paul, M ^a   Tiley, S ^a   Kado, J ^a   Cordwell, J ^a   Collins, C ^a  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

Author keywords

Burkholderia cepacia; Cystic fibrosis; FEV1; Growth; Nutrition

Indexed keywords

ADOLESCENT; ARTICLE; AUSTRALIA; BACTERIAL COLONIZATION; BURKHOLDERIA CEPACIA; CHILD; CHILD GROWTH; CHILD NUTRITION; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE COURSE; FEMALE; FORCED EXPIRATORY VOLUME; HUMAN; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; RESPIRATORY TRACT INFECTION; SCHOOL CHILD; STRAIN DIFFERENCE;

ADOLESCENT; BURKHOLDERIA CEPACIA; CHILD; CYSTIC FIBROSIS; FORCED EXPIRATORY VOLUME; HUMANS; NEW SOUTH WALES; NUTRITION ASSESSMENT; RESPIRATORY INSUFFICIENCY; RETROSPECTIVE STUDIES;

EID: 0035046778     PISSN: 10344810     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-1754.2001.00629.x     Document Type: Article

References (39)

1. Pseudomonas cepacia infection in cystic fibrosis: An emerging problem
2. Epidemiology of Pseudomonas cepacia in cystic fibrosis
3. Colonization of the respiratory tract with Pseudomonas cepacia in cystic fibrosis
4. Pseudomonas cepacia in adult cystic fibrosis: Accelerated decline in lung function and increased mortality
5. State of the Art: Cystic fibrosis
6. Effect of Pseudomonas cepacia colonization on survival and pulmonary function of cystic fibrosis patients
7. Pseudomonas cepacia colonization amongst patients with cystic fibrosis
8. Pseudomonas cepacia: Pulmonary infection in patients with cystic fibrosis
9. Pseudomonas cepacia infection in inpatients with cystic fibrosis
10. Genotypic analysis of Burkholderia cepacia isolates from 13 French cystic fibrosis centres
11. Evidence for transmission of Pseudomonas cepacia by social contact in cystic fibrosis
12. Burkholderia cepacia and cystic fibrosis: Do natural environments present a potential hazard?
13. Controlled study of Pseudomonas cepacia and Pseudomonas maltophilia in cystic fibrosis
14. The changing epidemiology of cystic fibrosis
15. Burkholderia cepacia: Medical, taxonomic and ecological issues
16. Molecular epidemiology of Burkholderia cepacia in two Australian cystic fibrosis centres
17. Nutritional assessment and management in cystic fibrosis: A consensus report
18. Gender gap in cystic fibrosis mortality
19. Neonatal screening for cystic fibrosis: A comparison of two strategies for case detection in 1.2 million babies
20. The maximal expiratory flow-volume curve: Normal standards, variability, and effects of age
21. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: Criteria for bacterial strain typing
22. Detection of Pseudomonas (Burkholderia) cepacia using PCR
23. Epidemiology of Burkholderia cepacia infection in patients with cystic fibrosis: Analysis by randomly amplified polymorphic DNA fingerprinting
24. Long term study of one hundred and five patients with cystic fibrosis
25. The relationship between tests of lung function and three chest radiological scoring systems in patients with cystic fibrosis
26. Burkholderia cepacia in cystic fibrosis: Variable disease course
27. Polymerase chain reaction for the detection of Pseudomonas aeruginosa, Stenotrophomonas maltophilia and Burkholderia cepacia in sputum of patients with cystic fibrosis
28. Occurrence of multiple genovars of Burkholderia cepacia in cystic fibrosis patients and the proposal of Burkholderia multivorans sp
29. Burkholderia cepacia: Another twist and a further threat
30. Identification of IS1356, a new insertion sequence, and its association with IS402 in epidemic strains of Burkholderia cepacia infecting cystic fibrosis patients
31. Height and weight in cystic fibrosis: A cross-sectional study
32. Growth status in children with cystic fibrosis based on the national Cystic Fibrosis Patient Registry Data: Evaluation of various criteria used to identify malnutrition
33. Cystic fibrosis: A changing clinical perspective
34. Nutritional benefits of newborn screening for cystic fibrosis
35. Nutritional intervention for weight gain in cystic fibrosis: A meta analysis
36. Predictive value of oropharyngeal cultures for identifying lower airway bacteria in cystic fibrosis patients
37. Bronchoalveolar lavage or oropharyngeal cultures to identify lower respiratory pathogens in infants with cystic fibrosis