High-resolution computed tomography scores in cystic fibrosis patients colonized with Pseudomonas aeruginosa or Staphylococcus aureus;Escore tomográfico em pacientes com fibrose cística colonizados por Pseudomonas aeruginosa ou Staphylococcus aureus

Jornal Brasileiro de Pneumologia

Volumn 38, Issue 1, 2012, Pages 41-49

  Folescu, Tania Wrobel ^a   Marques, Elizabeth de Andrade ^b   Boechat, Márcia Cristina Bastos ^a   Daltro, Pedro ^a   Higa, Laurinda Yoko Shinzato ^a   Cohen, Renata Wrobel Folescu ^a  

^a INSTITUTO OSWALDO CRUZ   (Brazil)

^b STATE UNIVERSITY OF RIO DE JANEIRO   (Brazil)

Author keywords

Cystic fibrosis; Pseudomonas aeruginosa; Staphylococcus aureus; Tomography

Indexed keywords

ARTICLE; BRONCHIECTASIS; CHILD; COMPUTER ASSISTED TOMOGRAPHY; CYSTIC FIBROSIS; EPIDEMIOLOGY; FEMALE; HUMAN; MALE; METHODOLOGY; MICROBIOLOGY; MUCUS; OBSERVER VARIATION; PSEUDOMONAS INFECTION; RADIOGRAPHY; STAPHYLOCOCCUS INFECTION;

BRONCHIECTASIS; CHILD; CYSTIC FIBROSIS; EPIDEMIOLOGIC METHODS; FEMALE; HUMANS; MALE; MUCUS; OBSERVER VARIATION; PSEUDOMONAS INFECTIONS; STAPHYLOCOCCAL INFECTIONS; TOMOGRAPHY, X-RAY COMPUTED;

EID: 84858611808     PISSN: 18063713     EISSN: 18063756     Source Type: Journal    
DOI: 10.1590/S1806-37132012000100007     Document Type: Article

References (21)

1. Helbich TH, Heinz-Peer G, Eichler I, Wunderbaldinger P, Götz M, Wojnarowski C, et al. Cystic fibrosis: CT assessment of lung involvement in children and adults. Radiology. 1999;213(2):537-44.
2. Rosenfeld M, Ramsey BW, Gibson RL. Pseudomonas acquisition in young patients with cystic fibrosis: pathophysiology, diagnosis, and management. Curr Opin Pulm Med. 2003;9(6):492-7.
3. de Jong PA, Ottink MD, Robben SG, Lequin MH, Hop WC, Hendriks JJ, et al. Pulmonary disease assessment in cystic fibrosis: comparison of CT scoring systems and value of bronchial and arterial dimension measurements. Radiology. 2004;231(2):434-9.
4. Brody AS, Klein JS, Molina PL, Quan J, Bean JA, Wilmott RW. High-resolution computed tomography in young patients with cystic fibrosis: distribution of abnormalities and correlation with pulmonary function tests. J Pediatr. 2004;145(1):32-8.
5. Puderbach M, Eichinger M. The role of advanced imaging techniques in cystic fibrosis follow-up: is there a place for MRI? Pediatr Radiol. 2010;40(6):844-9.
6. Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pediatr. 1998;132(4):589-95.
7. Nissim-Rafinia M, Kerem B, Kerem E. Molecular biology of cystic fibrosis: CFTR processing and functions, and classes of mutation. In: Hodson ME, Geddes DM, Bush A, editors. Cystic Fibrosis. London: Hodder Arnold; 2007. p. 49-58.
8. Gilligan PH, Kiska DL, Appleman MD. Cystic Fibrosis Microbiology. Cumitech 43. Washington, DC: ASM Press; 2006.
9. Leão RS, Pereira RH, Ferreira AG, Lima AN, Albano RM, Marques EA. First report of Paenibacillus cineris from a patient with cystic fibrosis. Diagn Microbiol Infect Dis. 2010;66(1):101-3.
10. Hansell DM, Bankier AA, MacMahon H, McLoud TC, Müller NL, Remy J. Fleischner Society: glossary of terms for thoracic imaging. Radiology. 2008;246(3):697-722.
11. Silva CI, Marchiori E, Souza Júnior AS, Müller NL; Comissão de Imagem da Sociedade Brasileira de Pneumologiae Tisiologia. Illustrated Brazilian consensus of terms and fundamental patterns in chest CT scans. J Bras Pneumol. 2010;36(1):99-123.
12. Judge EP, Dodd JD, Masterson JB, Gallagher CG. Pulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis. Chest. 2006;130(5):1424-32.
13. Fleiss JL. Statistical Methods for Rates and Proportions. New York: Wiley; 1981.
14. Luiz RR. Métodos estatísticos em estudos de concordância. In Medronho RA, Bloch KV, Luiz RR, Werneck GL, editors. Epidemiologia. São Paulo: Atheneu; 2008. p. 343-69.
15. Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet. 1986;1(8476):307-10.
16. Bhalla M, Turcios N, Aponte V, Jenkins M, Leitman BS, McCauley DI, et al. Cystic fibrosis: scoring system with thin-section CT. Radiology. 1991;179(3):783-8.
17. Santamaria F, Grillo G, Guidi G, Rotondo A, Raia V, de Ritis G, et al. Cystic fibrosis: when should high-resolution computed tomography of the chest be obtained? Pediatrics. 1998;101(5):908-13.
18. Taccone A, Romano L, Marzoli A, Girosi D, Dell'Acqua A, Romano C. High-resolution computed tomography in cystic fibrosis. Eur J Radiol. 1992;15(2):125-9.
19. Farrell PM, Collins J, Broderick LS, Rock MJ, Li Z, Kosorok MR, et al. Association between mucoid Pseudomonas infection and bronchiectasis in children with cystic fibrosis. Radiology. 2009;252(2):534-43.
20. Robinson TE, Leung AN, Chen X, Moss RB, Emond MJ. Cystic fibrosis HRCT scores correlate strongly with Pseudomonas infection. Pediatr Pulmonol. 2009;44(11):1107-17.
21. Linnane B, Robinson P, Ranganathan S, Stick S, Murray C. Role of high-resolution computed tomography in the detection of early cystic fibrosis lung disease. Paediatr Respir Rev. 2008;9(3):168-74; quiz 174-5.