Pulmonary outcome prediction for cystic fibrosis patients

Pediatric Pulmonology

Volumn 45, Issue 12, 2010, Pages 1153-1155

  Kraemer, Richard ^a   Thamrin, Cindy ^a  

^a UNIVERSITY OF BERN   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTIC FIBROSIS; DISEASE COURSE; DISEASE SEVERITY; FORCED EXPIRATORY VOLUME; HUMAN; LUNG FUNCTION; NOTE; PRIORITY JOURNAL; SCORING SYSTEM;

ADOLESCENT; CHILD; CYSTIC FIBROSIS; FORCED EXPIRATORY VOLUME; HUMANS; SEVERITY OF ILLNESS INDEX;

EID: 78649643623     PISSN: 87556863     EISSN: 10990496     Source Type: Journal    
DOI: 10.1002/ppul.21320     Document Type: Note

References (24)

1. Schluchter MD, Konstan MW, Davis PB,. Jointly modelling the relationship between survival and pulmonary function in cystic fibrosis patients. Stat Med 2002; 21: 1271-1287.
2. Shwachman H, Kulczycki LL,. Long-term study of one hundred five patients with cystic fibrosis; studies made over a five- to fourteen-year period. AMA J Dis Child 1958; 96: 6-15.
3. Koscik RE, Kosorok MR, Farrell PM, Collins J, Peters ME, Laxova A, Green CG, Zeng L, Rusakow LS, Hardie RC, Campbell PW, Gurney JW,. Wisconsin cystic fibrosis chest radiograph scoring system: validation and standardization for application to longitudinal studies. Pediatr Pulmonol 2000; 29: 457-467.
4. Weatherly MR, Palmer CG, Peters ME, Green CG, Fryback D, Langhough R, Farrell PM,. Wisconsin cystic fibrosis chest radiograph scoring system. Pediatrics 1993; 91: 488-495.
5. Taussig LM,. The score is. Pediatr Pulmonol 1994; 17: 279-280.
6. VanDevanter DR, Wagener JS, Pasta DJ, Elkin E, Jacobs JR, Morgan WJ, Konstan MW,. Pulmonary outcome prediction (POP) tools for cystic fibrosis patients. Pediatr Pulmonol 2010; 46 (in press).
7. Cole TJ, Green PJ,. Smoothing reference centile curves: the LMS method and penalized likelihood. Stat Med 1992; 11: 1305-1319.
8. Stanojevic S, Wade A, Stocks J, Hankinson J, Coates AL, Pan H, Rosenthal M, Corey M, Lebecque P, Cole TJ,. Reference ranges for spirometry across all ages: a new approach. Am J Respir Crit Care Med 2008; 177: 253-260.
9. Kerem E, Reisman J, Corey M, Canny GJ, Levison H,. Prediction of mortality in patients with cystic fibrosis. N Engl J Med 1992; 326: 1187-1191.
10. Milla CE, Warwick WJ,. Risk of death in cystic fibrosis patients with severely compromised lung function. Chest 1998; 113: 1230-1234.
11. Liou TG, Adler FR, Fitzsimmons SC, Cahill BC, Hibbs JR, Marshall BC,. Predictive 5-year survivorship model of cystic fibrosis. Am J Epidemiol 2001; 153: 345-352.
12. Mayer-Hamblett N, Rosenfeld M, Emerson J, Goss CH, Aitken ML,. Developing cystic fibrosis lung transplant referral criteria using predictors of 2-year mortality. Am J Respir Crit Care Med 2002; 166: 1550-1555.
13. Tiddens HA,. Detecting early structural lung damage in cystic fibrosis. Pediatr Pulmonol 2002; 34: 228-231.
14. Kraemer R, Blum A, Schibler A, Ammann RA, Gallati S,. Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis. Am J Respir Crit Care Med 2005; 171: 371-378.
15. Aurora P, Bush A, Gustafsson P, Oliver C, Wallis C, Price J, Stroobant J, Carr S, Stocks J,. Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis. Am J Respir Crit Care Med 2005; 171: 249-256.
16. Ranganathan SC, Stocks J, Dezateux C, Bush A, Wade A, Carr S, Castle R, Dinwiddie R, Hoo AF, Lum S, Price J, Stroobant J, Wallis C,. The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis. Am J Respir Crit Care Med 2004; 169: 928-933.
17. Gustafsson PM, Aurora P, Lindblad A,. Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis. Eur Respir J 2003; 22: 972-979.
18. Amin R, Subbarao P, Jabar A, Balkovec S, Jensen R, Kerrigan S, Gustafsson P, Ratjen F,. Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function. Thorax 2010; 65: 379-383.
19. Kraemer R, Meister B,. Fast real-time moment-ratio analysis of multibreath nitrogen washout in children. J Appl Physiol 1985; 59: 1137-1144.
20. Schibler A, Schneider M, Frey U, Kraemer R,. Moment ratio analysis of multiple breath nitrogen washout in infants with lung disease. Eur Respir J 2000; 15: 1094-1101.
21. Desmond KJ, Coates AL, Martin JG, Beaudry PH,. Trapped gas and airflow limitation in children with cystic fibrosis and asthma. Pediatr Pulmonol 1986; 2: 128-134.
22. Gustafsson PM, Kallman S, Ljungberg H, Lindblad A,. Method for assessment of volume of trapped gas in infants during multiple-breath inert gas washout. Pediatr Pulmonol 2003; 35: 42-49.
23. Kraemer R, Baldwin DN, Ammann RA, Frey U, Gallati S,. Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis. Respir Res 2006; 7: 138.
24. Kraemer R, Latzin P, Pramana I, Ballinari P, Gallati S, Frey U,. Long-term gas exchange characteristics as markers of deterioration in patients with cystic fibrosis. Respir Res 2009; 10: 106.