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Improving nutritional status in a pediatric cystic fibrosis center
dc.contributor.authorRamírez, Ixsyen_US
dc.contributor.authorFilbrun, Amyen_US
dc.contributor.authorHasan, Awsen_US
dc.contributor.authorKidwell, Kelley M.en_US
dc.contributor.authorNasr, Samya Z.en_US
dc.date.accessioned2015-06-01T18:51:56Z
dc.date.available2016-07-05T17:27:58Zen
dc.date.issued2015-06en_US
dc.identifier.citationRamírez, Ixsy ; Filbrun, Amy; Hasan, Aws; Kidwell, Kelley M.; Nasr, Samya Z. (2015). "Improving nutritional status in a pediatric cystic fibrosis center." Pediatric Pulmonology 50(6): 544-551.en_US
dc.identifier.issn8755-6863en_US
dc.identifier.issn1099-0496en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/111789
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherquality improvementen_US
dc.subject.othernutritionen_US
dc.subject.otherteam approachen_US
dc.subject.othercystic Fibrosisen_US
dc.subject.otherpediatricen_US
dc.subject.otherbody mass index (BMI)en_US
dc.titleImproving nutritional status in a pediatric cystic fibrosis centeren_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/111789/1/ppul23128.pdf
dc.identifier.doi10.1002/ppul.23128en_US
dc.identifier.sourcePediatric Pulmonologyen_US
dc.identifier.citedreferencePowers SW, Jones JS, Ferguson KS, Piazza‐Waggoner C, Daines C, Acton JD. Randomized clinical trial of behavior and nutrition treatment to improve energy intake and growth in toddlers and preschoolers with Cystic Fibrosis. Pediatrics 2005; 116: 1442 – 1450.en_US
dc.identifier.citedreferenceCystic Fibrosis Foundation. Cystic Fibrosis Foundation Patient Registry: 2011 Annual Data Report. Bethesda, MD, Cystic Fibrosis Foundation. 2012.en_US
dc.identifier.citedreferenceKerem E, Reisman J, Corey M, Canny GJ, Levison H. Prediction of mortality in patients with Cystic Fibrosis. NE J Med 1992; 326: 1187 – 1191.en_US
dc.identifier.citedreferenceMilla CE. Nutrition and lung disease in Cystic Fibrosis. Clin Chest Med 2007; 28: 319 – 330.en_US
dc.identifier.citedreferenceStark LJ, Opipari‐Arrigan L, Quittner AL, Bean J, Powers SW. The effects of an intensive behavior and nutrition intervention compared to standard of care on weight outcome in CF. Pediatr Pulmonol 2011; 46: 31 – 35.en_US
dc.identifier.citedreferenceStallings 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 – 839.en_US
dc.identifier.citedreferenceGaskin KJ, Exocrine pancreatic function. In: Walker WA,Goulet O,Kleinman RE,Sherman PM,Schneider BL,Sanderson IR. editors. Pediatric gastrointestinal disease. Hamilton, ON, Canada: B.C Decker; 2004. pp 1607–1623.en_US
dc.identifier.citedreferenceOnenstein DM. Cystic Fibrosis. In: Rudolph CD, Rudolph AM, Hostetter MK, Lister G, Seigel NJ. editors. Rudolph's Pediatrics. New York: McGraw Hill; 2002. pp 1969–1980.en_US
dc.identifier.citedreferenceNasr S, Drury Z. Appetite stimulants use in Cystic Fibrosis. Pediatr Pulmonol 2008; 43: 209 – 219.en_US
dc.identifier.citedreferenceWhite H, Pollard K, Etheringtion C, Clifton I, Morton AM, Owen D, Conway SP, Peckham DG. Nutritional decline in cystic fibrosis related diabetes: The effect of intensive nutritional intervention. Journal of Cystic Fibrosis 2009; 8: 179 – 185.en_US
dc.identifier.citedreferenceOpipari‐Arrigan L, Powers Scott W, Quittner AL, Stark LJ. Mealtime problems predict outcome in clinical trial to improve nutrition in children with CF. Pediatr Pulmonol 2010; 45: 78 – 82.en_US
dc.identifier.citedreferenceWatson H, Bilton D, Truby H. A randomized controlled trial of a new behavioral home‐Based nutrition education program, “Eat Well with CF,” in adults with Cystic Fibrosis. J Am Diet Assoc 2008; 108: 847 – 852.en_US
dc.identifier.citedreferenceMunck A. Nutritional considerations in patients with Cystic Fibrosis. Expert Rev Resp Med 2010; 4: 47 – 56.en_US
dc.identifier.citedreferenceBorowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with Cystic Fibrosis. J Pediatr Gastroenterol Nutr 2002; 35: 246 – 259.en_US
dc.identifier.citedreferenceSchall JI, Bentley T, Stallings V. Meal patterns, dietary fat intake and pancreatic enzyme use in preadolescent children with Cystic Fibrosis. J Pediatr Gastroenterol Nutr 2006; 43: 651 – 659.en_US
dc.identifier.citedreferenceMatel JL, Milla CE. Nutrition in Cystic Fibrosis. Semin Respir Crit Care Med 2009; 30: 579 – 586.en_US
dc.identifier.citedreferenceLeonard A, Davis E, Rosenstein BJ, Zeitlin PL, Paranjape SM, Peeler D, Maynard C, Mogayzel PJ. Description of a standardized nutrition classification plan and its relation to nutritional outcomes in children with Cystic Fibrosis. J Pediatr Psychol 2010; 35: 6 – 13.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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