Association of lung function, chest radiographs and clinical features in infants with cystic fibrosis

European Respiratory Journal

Volumn 42, Issue 6, 2013, Pages 1545-1552

  Rosenfeld, Margaret ^a   Farrell, Philip M ^b   Kloster, Margaret ^a   Swanson, Jonathan O ^a   Vu, Thuy ^c   Brumback, Lyndia ^d   Acton, James D ^e   Castile, Robert G ^f   Colin, Andrew A ^g   Conrad, Carol K ^h   Hart, Meeghan A ⁱ   Kerby, Gwendolyn S ^j   Hiatt, Peter W ^k   Mogayzel, Peter J ^l   Johnson, Robin C ^m   Davis, Stephanie D ^m,n  

^a SEATTLE CHILDREN S HOSPITAL   (United States)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^c UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF WASHINGTON   (United States)

^e CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^f THE OHIO STATE UNIVERSITY COLLEGE OF MEDICINE   (United States)

^g UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^h STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

ⁱ CASE WESTERN RESERVE UNIVERSITY   (United States)

^j UNIVERSITY OF COLORADO   (United States)

^k Center for Applied Health Research Baylor Scott White Research Institute   (United States)

^l JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^m UNIVERSITY OF NORTH CAROLINA   (United States)

ⁿ INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL FEATURE; COHORT ANALYSIS; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE ASSOCIATION; FEMALE; FORCED EXPIRATORY FLOW; FORCED EXPIRATORY VOLUME; FUNCTIONAL RESIDUAL CAPACITY; HUMAN; HYPERINFLATION; INFANT; LONGITUDINAL STUDY; LUNG DISEASE; LUNG FUNCTION; LUNG FUNCTION TEST; MAJOR CLINICAL STUDY; MALE; PATIENT MONITORING; PRIORITY JOURNAL; STAPHYLOCOCCUS AUREUS; THORAX RADIOGRAPHY;

COUGH; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; FUNCTIONAL RESIDUAL CAPACITY; HUMANS; INFANT; LONGITUDINAL STUDIES; LUNG; MALE; RADIOGRAPHY, THORACIC; REPRODUCIBILITY OF RESULTS; RESPIRATORY FUNCTION TESTS; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS AUREUS; UNITED STATES;

EID: 84890063721     PISSN: 09031936     EISSN: 13993003     Source Type: Journal    
DOI: 10.1183/09031936.00138412     Document Type: Article

References (36)

1. Davis SD, Rosenfeld M, Kerby GS, et al. Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints. Am J Respir Crit Care Med 2010; 182: 1387-1397.
2. Pillarisetti N, Williamson E, Linnane B, et al. Infection, inflammation, and lung function decline in infants with cystic fibrosis. Am J Respir Crit Care Med 2011; 184: 75-81.
3. Mott LS, Park J, Murray CP, et al. Progression of early structural lung disease in young children with cystic fibrosis assessed using CT. Thorax 2012; 67: 509-516.
4. Hoo AF, Thia LP, Nguyen TT, et al. Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening. Thorax 2012; 67: 874-881.
5. Linnane BM, Hall GL, Nolan G, et al. Lung function in infants with cystic fibrosis diagnosed by newborn screening. Am J Respir Crit Care Med 2008; 178: 1238-1244.
6. Peterson-Carmichael SL, Harris WT, Goel R, et al. Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis. Pediatr Pulmonol 2009; 44: 503-511.
7. Nixon GM, Armstrong DS, Carzino R, et al. Early airway infection, inflammation, and lung function in cystic fibrosis. Arch Dis Child 2002; 87: 306-311.
8. Grosse SD, Rosenfeld M, Devine OJ, et al. Potential impact of newborn screening for cystic fibrosis on child survival: a systematic review and analysis. J Pediatr 2006; 149: 362-366.
9. Martinez TM, Llapur CJ, Williams TH, et al. High-resolution computed tomography imaging of airway disease in infants with cystic fibrosis. Am J Respir Crit Care Med 2005; 172: 1133-1138.
10. Kozlowska WJ, Bush A, Wade A, et al. Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis. Am J Respir Crit Care Med 2008; 178: 42-49.
11. Brumback LC, Davis SD, Kerby GS, et al. Lung function from infancy to preschool in a cohort of children with cystic fibrosis. Eur Respir J 2013; 41: 60-66.
12. Stick SM, Brennan S, Murray C, et al. Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening. J Pediatr 2009; 155: 623-628.
13. Borowitz D, Robinson KA, Rosenfeld M, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr 2009; 155: Suppl., S73-S93.
14. Rosenfeld M, Farrell PM, Kloster M, et al. Association of physiologic measures and clinical characteristics in a multicenter cohort of infants with CF. Pediatr Pulmonol 2011: Suppl. 34, 333.
15. Farrell PM, Rosenstein BJ, White TB, et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr 2008; 153: S4-S14.
16. American Thoracic Society, European Respiratory Society. ATS/ERS statement: raised volume forced expirations in infants. Am J Respir Crit Care Med 2005; 172: 1463-1471.
17. Stocks J, Godfrey S, Beardsmore C, et al. Plethysmographic measurements of lung volume and airway resistance. Eur Respir J 2001; 17: 302-312.
18. Castile R, Filbrun D, Flucke R, et al. Adult-type pulmonary function tests in infants without respiratory disease. Pediatr Pulmonol 2000; 30: 215-227.
19. Jones M, Castile R, Davis S, et al. Forced expiratory flows and volumes in infants: normative data and lung growth. Am J Respir Crit Care Med 2000; 161: 353-359.
20. Li Z, Lai HJ, Kosorok MR, et al. Longitudinal pulmonary status of cystic fibrosis children with meconium ileus. Pediatr Pulmonol 2004; 38: 277-284.
21. McKone EF, Emerson SS, Edwards KL, et al. Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study. Lancet 2003; 361: 1671-1676.
22. Green DM, McDougal KE, Blackman SM, et al. Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients. Respir Res 2010; 11: 140.
23. Koscik RE, Kosorok MR, Farrell PM, et al. Wisconsin cystic fibrosis chest radiograph scoring system: validation and standardization for application to longitudinal studies. Pediatr Pulmonol 2000; 29: 457-467.
24. Brasfield D, Hicks G, Soong S, et al. The chest roentgenogram in cystic fibrosis: a new scoring system. Pediatrics 1979; 63: 24-29.
25. Farrell PM, Li Z, Kosorok MR, et al. Bronchopulmonary disease in children with cystic fibrosis after early or delayed diagnosis. Am J Respir Crit Care Med 2003; 168: 1100-1108.
26. Sanders DB, Li Z, Brody AS, et al. Chest computed tomography scores of severity are associated with future lung disease progression in children with cystic fibrosis. Am J Respir Crit Care Med 2011; 184: 816-821.
27. Sanders DB, Li Z, Rock MJ, et al. The sensitivity of lung disease surrogates in detecting chest CT abnormalities in children with cystic fibrosis. Pediatr Pulmonol 2012; 47: 567-573.
28. de Jong PA, Tiddens HA. Cystic fibrosis specific computed tomography scoring. Proc Am Thorac Soc 2007; 4: 338-342.
29. Aziz ZA, Davies JC, Alton EW, et al. Computed tomography and cystic fibrosis: promises and problems. Thorax 2007; 62: 181-186.
30. Ren CL, Rosenfeld M, Mayer OH, et al. Analysis of the associations between lung function and clinical features in preschool children with cystic fibrosis. Pediatr Pulmonol 2012; 47: 574-581.
31. Rosenfeld M, Emerson J, Accurso F, et al. Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis. Pediatr Pulmonol 1999; 28: 321-328.
32. Belessis Y, Dixon B, Hawkins G, et al. Early cystic fibrosis lung disease detected by bronchoalveolar lavage and lung clearance index. Am J Respir Crit Care Med 2012; 185: 862-873.
33. Owens CM, Aurora P, Stanojevic S, et al. Lung clearance index and HRCT are complementary markers of lung abnormalities in young children with CF. Thorax 2011; 66: 481-488.
34. Aurora P, Gustafsson P, Bush A, et al. Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis. Thorax 2004; 59: 1068-1073.
35. Lum S, Gustafsson P, Ljungberg H, et al. Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests. Thorax 2007; 62: 341-347.
36. Eichinger M, Optazaite DE, Kopp-Schneider A, et al. Morphologic and functional scoring of cystic fibrosis lung disease using MRI. Eur J Radiol 2012; 81: 1321-1329.