AJCN Tufts Nutrition Symposium, Boston & Online Sept 2009
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American Journal of Clinical Nutrition, Vol. 88, No. 1, 161-166, July 2008
© 2008 American Society for Nutrition


ORIGINAL RESEARCH COMMUNICATION

Classification of malnutrition in cystic fibrosis: implications for evaluating and benchmarking clinical practice performance1,2,3

HuiChuan J Lai and Suzanne M Shoff

1 From the Department of Nutritional Sciences, University of Wisconsin College of Agriculture and Life Sciences, Madison, WI (HJL and SMS), and the Department of Pediatrics and Department of Biostatistics and Medical Informatics, University of Wisconsin School of Medicine and Public Health, Madison, WI (HJL)

Background: In 2005, the Cystic Fibrosis Foundation (CFF) revised the nutrition classification guidelines to eliminate the use of percentage of ideal body weight (%IBW) to define "nutritional failure"; the CFF also recommended that children with cystic fibrosis maintain a body mass index percentile (BMIp) ≥ 50th.

Objective: We assessed the effect of the 2005 CFF nutrition classification guidelines on evaluating the performance of nutritional care practices.

Design: Data from 14 702 children reported to the 2002 CFF Patient Registry were analyzed to compare malnutrition rates in 113 cystic fibrosis centers in the United States. Nutritional failure was defined according to the 2002 CFF criteria—ie, height < 5th percentile, %IBW < 90%, or BMIp < 10th. "Below BMI goal" was defined according to the 2005 CFF criterion, ie BMIp < 50th.

Results: Eliminating %IBW resulted in a 6% reduction (from 33% to 27%) in the nutritional failure rate in the United States. The use of BMIp < 50th led to the classification of 57% of children as below the BMI goal. Misclassification of nutritional failure according to %IBW ranged from 1% to 16% among 113 centers and was greater in the centers with a larger proportion of tall patients. After the elimination of %IBW, one-third of centers changed to a different tertile ranking for nutritional failure rates (kappa = 0.50, moderate-to-poor agreement). More than half the centers changed to a different tertile ranking, from nutritional failure to below BMI goal (kappa = 0.22, poor agreement).

Conclusion: Eliminating misclassification by %IBW and implementing the new BMI goal led to profound and unequal changes in malnutrition rates across cystic fibrosis centers.




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ICAN: Infant, Child, & Adolescent NutritionHome page
S. C. Casey
Cystic Fibrosis, Cystic Fibrosis--Related Diabetes, and Adolescence A Case Study
ICAN: Infant, Child, & Adolescent Nutrition, February 1, 2009; 1(1): 24 - 26.
[Abstract] [PDF]




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