The relationship between body growth and pulmonary function in children with cystic fibrosis

Acta Paediatrica, International Journal of Paediatrics

Volumn 103, Issue 2, 2014, Pages 162-167

  Woestenenk, Janna W ^a   Stellato, Rebecca K ^a   Terheggen Lagro, Suzanne W ^a   Van Der Ent, Cornelis K ^a   Houwen, Roderick H J ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Cystic fibrosis; Growth; Nutritional assessment; Respiratory function tests

Indexed keywords

ARTICLE; BODY GROWTH; BODY HEIGHT; BODY WEIGHT; CHILD; CHILD GROWTH; CHILDHOOD DISEASE; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; GROWTH DISORDER; HUMAN; LUNG FUNCTION; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; WEIGHT GAIN;

CYSTIC FIBROSIS; GROWTH; NUTRITIONAL ASSESSMENT; RESPIRATORY FUNCTION TESTS;

BODY HEIGHT; BODY WEIGHT; CHILD, PRESCHOOL; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; GROWTH; HUMANS; LUNG; MALE; RETROSPECTIVE STUDIES;

EID: 84892620965     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/apa.12462     Document Type: Article

References (21)

1. Borowitz D,. The interrelationship of nutrition and pulmonary function in patients with cystic fibrosis. Curr Opin Pulm Med 1996; 2: 457-61.
2. Zemel BS, Jawad AF, FitzSimmons S, Stallings VA,. Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry. J Pediatr 2000; 137: 374-80.
3. Konstan MW, Butler SM, Wohl ME, Stoddard M, Matousek R, Wagener JS, et al. Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis. J Pediatr 2003; 142: 624-30.
4. Peterson ML, Jacobs DR Jr, Milla CE,. Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis. Pediatrics 2003; 112: 588-92.
5. Steinkamp G, Wiedemann B,. Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project. Thorax 2002; 57: 596-601.
6. Assael BM, Casazza G, Iansa P, Volpi S, Milani S,. Growth and long-term lung function in cystic fibrosis: a longitudinal study of patients diagnosed by neonatal screening. Pediatr Pulmonol 2009; 44: 209-15.
7. Yen EH, Quinton H, Borowitz D,. Better nutritional status in early childhood is associated with improved clinical outcomes and survival in patients with cystic fibrosis. J Pediatr 2013; 162: 530-5.
8. Beker LT, Russek-Cohen E, Fink RJ,. Stature as a prognostic factor in cystic fibrosis survival. J Am Diet Assoc 2001; 101: 438-42.
9. Woestenenk JW, Hoekstra T, Hesseling C, van der Doef HP, van der Ent CK,. Comparison of height for age and height for bone age with and without adjustment for target height in pediatric patients with CF. J Cyst Fibros 2011; 10: 272-7.
10. Koopman M, Zanen P, Kruitwagen CL, van der Ent CK, Arets HG,. Reference values for paediatric pulmonary function testing: The Utrecht dataset. Respir Med 2011; 105: 15-23.
11. Castellani C, Cuppens H, Macek M Jr, Cassiman JJ, Kerem E, Durie P, et al. Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice. J Cyst Fibros 2008; 7: 179-96.
12. Fredriks AM, van BS, Burgmeijer RJ, Meulmeester JF, Beuker RJ, Brugman E, et al. Continuing positive secular growth change in The Netherlands 1955-1997. Pediatr Res 2000; 47: 316-23.
13. Talma H,. Groeidiagrammen 2010. Handleiding bij het meten en wegen van kinderen en het invullen van groeidiagrammen. 2010. TNO Kwaliteit van leven.
14. de Muinck Keizer-Schrama SM,. [Consensus 'diagnosis of short stature in children.' National Organization for Quality Assurance in Hospitals]. Ned Tijdschr Geneeskd 1998; 142: 2519-25.
15. Sinaasappel M, Stern M, Littlewood J, Wolfe S, Steinkamp G, Heijerman HG, et al. Nutrition in patients with cystic fibrosis: a European Consensus. J Cyst Fibros 2002; 1: 51-75.
16. Stallings VA, Stark LJ, Robinson KA, Feranchak AP, Quinton H,. Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review. J Am Diet Assoc 2008; 108: 832-9.
17. Dankert-Roelse JE, Merelle ME,. Review of outcomes of neonatal screening for cystic fibrosis versus non-screening in Europe. J Pediatr 2005; 147: S15-20.
18. Farrell PM, Lai HJ, Li Z, Kosorok MP, Laxova A, Green CG, et al. Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: enough is enough!. J Pediatr 2005; 147: S30-6.
19. Sims EJ, Clark A, McCormick J, Mehta G, Connett G, Mehta A,. Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy. Pediatrics 2007; 119: 19-28.
20. Farrell PM, Kosorok MR, Rock MJ, Laxova A, Zeng L, Lai HC, et al. Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group. Pediatrics 2001; 107: 1-13.
21. Rao L, Tiller C, Coates C, Kimmel R, Applegate KE, Granroth-Cook J, et al. Lung growth in infants and toddlers assessed by multi-slice computed tomography. Acad Radiol 2010; 17: 1128-35.