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Journal of Cystic Fibrosis
Volume 9, Issue 2
, Pages 75-83
, March 2010
An overview of international literature from cystic fibrosis registries: 2. Neonatal screening and nutrition/growth
References
- An overview of international literature from cystic fibrosis registries. 1. Mortality and survival studies in cystic fibrosis. J Cyst Fibr. 2009;8:229–237
- . Potential impact of newborn screening for cystic fibrosis on child survival: a sistematic review and analysis. J Pediatr. 2006;149:362–366
- . Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr. 2002;35:246–259
- . Role of nutrition in lung development before and after birth. In: Harding R, Pinkerton KE, Plopper CG editor. The lung, development, aging and the environment. London: Elsevier Academic Press; 2004;p. 253–266
- . Prediction of lung function in the inadequately nourished. Arch Dis Child. 1998;79:18–21
- . Early diagnosis of cystic fibrosis in the newborn period and risk of Pseudomonas aeruginosa acquisisition in the first 10
years of life:a registry-based longitudinal study. Pediatrics. 2001;107:274–279 - . The impact of early cystic fibrosis diagnosis on pulmonary function in children. J Pediatr. 2002;141:804–810
- . Demographics of the UK cystic fibrosis population: implications for neonatal screening. Eur J Hum Genet. 2002;10:583–590
- . Association between initial disease presentation, lung disease outcomes, and survival in patients with cystic fibrosis. Am J Epidemiol. 2004;159:537–546
- . The survival advantage of patients with cystic fibrosis diagnosed through neonatal screening: evidence from the United States Cystic Fibrosis Foundation Registry Data. J Pediatr. 2005;147:S57–63
- . Steering Committee of the UK Cystic Fibrosis Database. Neonatal screening for cystic fibrosis is beneficial even in the context of modern treatment. J Pediatr. 2005;147:S42–46
- . Complication associated with symptomatic diagnosis in infants with cystic fibrosis. J Pediatr. 2005;147:S37–41
- . Newborn screening for cystic fibrosis is associated with reduced treatment intensity. J Pediatr. 2005;147:306–311
- Economic implications of newborn screening for cystic fibrosis: reduced therapy may offset screening costs. Lancet. 2007;369:1187–1195
- . Cystic fibrosis diagnosed after 2
months of age leads to worse outcomes and requires more therapy. Pediatrics. 2007;119:19–28 - . The meaning of “early” diagnosis in a new era of cystic fibrosis care. Pediatrics. 2007;119:156–157
- . Studies in cystic fibrosis: report of 130 patients diagnosed under 3
months of age over a 20-year period. Pediatrics. 1970;46:335–343 - . A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol. 1988;41:583–591
- Growth status in children with cystic fibrosis based on the National Cystic Fibrosis Patient Registry data: evaluation of various criteria used to identify malnutrition. J Pediatr. 1998;132:478–485
- . Comparison of the use of body mass index percentiles and percentage of ideal body weight to screen for malnutrition in children with cystic fibrosis. Am J Clin Nutr. 2004;80:982–991
- . Comparison of growth status patients with cystic fibrosis between the United States and Canada. Am J Clin Nutr. 1999;69:531–538
- Young adults with cystic fibrosis are shorter than healthy peers because their parents are also short. Eur J Pediatr. 2005;164:781–782
- . 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;137:374–380
- Risk of persistent growth impairment after alternate-day prednisone treatment in children with cystic fibrosis. N Engl J Med. 2000;342:851–859
- . Cystic Fibrosis Foundation Prednisone Trial Group. A multicenter study of alternate-day prednisone therapy in patients with cystic fibrosis. J Pediatr. 1995;126:515–523
- . Nutritional status of patients with cystic fibrosis with meconium ileus: a comparison with patients meconium ileus and diagnosed early through neonatal screening. Pediatrics. 2000;105:53–61
- . The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States. Am J Respir Crit Care Med. 2001;163:1331–1337
- . Stature as a prognostic factor in cystic fibrosis survival. J Am Diet Assoc. 2001;101:438–442
- . 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
- For the Investigators and Coordinators of the ESCF. Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis. J Pediatr. 2003;142:624–630
- . Overweight and obesity in ΔF508 homozygous cystic fibrosis. J Pediatr. 2005;147:402–404
- . Evaluation of body mass index percentiles for assessment of malnutrition in children with cystic fibrosis. Eur J Clin Nutr. 2007;61:759–768
- . Clinical Practice Guidelines on Growth and Nutrition Subcommittee; Ad Hoc Working Group. 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;108:832–839
- . Cystic fibrosis mortality and survival in the UK: 1947–2003. Eur Respir J. 2007;29:522–526
- . Cystic fibrosis in Asians. Arch Dis Child. 1993;68:120–122
- Clinical outcome of cystic fibrosis presenting with or without meconium ileus: a matched cohort study. J Pediatr Surg. 2006;41:1556–1560
PII: S1569-1993(09)00149-0
doi: 10.1016/j.jcf.2009.11.002
© 2009 European Cystic Fibrosis Society. Published by Elsevier Inc All rights reserved.
Next »
Journal of Cystic Fibrosis
Volume 9, Issue 2
, Pages 75-83
, March 2010
