Literature DB >> 18614737

Classification of malnutrition in cystic fibrosis: implications for evaluating and benchmarking clinical practice performance.

HuiChuan J Lai1, Suzanne M Shoff.   

Abstract

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) > or = 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.

Entities:  

Mesh:

Year:  2008        PMID: 18614737      PMCID: PMC2527817          DOI: 10.1093/ajcn/88.1.161

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  27 in total

1.  Reliability of percentage ideal weight for height.

Authors:  V J Poustie; R M Watling; D Ashby; R L Smyth
Journal:  Arch Dis Child       Date:  2000-08       Impact factor: 3.791

Review 2.  Cystic fibrosis adult care: consensus conference report.

Authors:  James R Yankaskas; Bruce C Marshall; Beth Sufian; Richard H Simon; David Rodman
Journal:  Chest       Date:  2004-01       Impact factor: 9.410

Review 3.  Consensus report on nutrition for pediatric patients with cystic fibrosis.

Authors:  Drucy Borowitz; Robert D Baker; Virginia Stallings
Journal:  J Pediatr Gastroenterol Nutr       Date:  2002-09       Impact factor: 2.839

Review 4.  Nutrition in patients with cystic fibrosis: a European Consensus.

Authors:  M Sinaasappel; M Stern; J Littlewood; S Wolfe; G Steinkamp; Harry G M Heijerman; E Robberecht; G Döring
Journal:  J Cyst Fibros       Date:  2002-06       Impact factor: 5.482

5.  The presentation and use of height and weight data for comparing the nutritional status of groups of children under the age of 10 years.

Authors:  J C Waterlow; R Buzina; W Keller; J M Lane; M Z Nichaman; J M Tanner
Journal:  Bull World Health Organ       Date:  1977       Impact factor: 9.408

6.  The measurement of observer agreement for categorical data.

Authors:  J R Landis; G G Koch
Journal:  Biometrics       Date:  1977-03       Impact factor: 2.571

7.  2000 CDC Growth Charts for the United States: methods and development.

Authors:  Robert J Kuczmarski; Cynthia L Ogden; Shumei S Guo; Laurence M Grummer-Strawn; Katherine M Flegal; Zuguo Mei; Rong Wei; Lester R Curtin; Alex F Roche; Clifford L Johnson
Journal:  Vital Health Stat 11       Date:  2002-05

Review 8.  Association of nutritional status and pulmonary function in children with cystic fibrosis.

Authors:  Carlos E Milla
Journal:  Curr Opin Pulm Med       Date:  2004-11       Impact factor: 3.155

9.  Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis.

Authors:  Michael W Konstan; Steven M Butler; Mary Ellen B Wohl; Marcia Stoddard; Robert Matousek; Jeffrey S Wagener; Charles A Johnson; Wayne J Morgan
Journal:  J Pediatr       Date:  2003-06       Impact factor: 4.406

10.  Comparison of the use of body mass index percentiles and percentage of ideal body weight to screen for malnutrition in children with cystic fibrosis.

Authors:  Zhumin Zhang; HuiChuan J Lai
Journal:  Am J Clin Nutr       Date:  2004-10       Impact factor: 7.045

View more
  10 in total

1.  Nutritional status is associated with health-related quality of life in children with cystic fibrosis aged 9-19 years.

Authors:  Suzanne M Shoff; Audrey Tluczek; Anita Laxova; Philip M Farrell; HuiChuan J Lai
Journal:  J Cyst Fibros       Date:  2013-02-12       Impact factor: 5.482

2.  Incorporating genetic potential when evaluating stature in children with cystic fibrosis.

Authors:  Zhumin Zhang; Suzanne M Shoff; Huichuan J Lai
Journal:  J Cyst Fibros       Date:  2010-03       Impact factor: 5.482

3.  Pubertal height velocity and associations with prepubertal and adult heights in cystic fibrosis.

Authors:  Zhumin Zhang; Mary J Lindstrom; HuiChuan J Lai
Journal:  J Pediatr       Date:  2013-03-25       Impact factor: 4.406

4.  Early attained weight and length predict growth faltering better than velocity measures in infants with CF.

Authors:  Sonya L Heltshe; Drucy S Borowitz; Daniel H Leung; Bonnie Ramsey; Nicole Mayer-Hamblett
Journal:  J Cyst Fibros       Date:  2014-06-07       Impact factor: 5.482

5.  Refining the continuum of CFTR-associated disorders in the era of newborn screening.

Authors:  H Levy; M Nugent; K Schneck; D Stachiw-Hietpas; A Laxova; O Lakser; M Rock; M K Dahmer; J Biller; S Z Nasr; M Baker; S A McColley; P Simpson; P M Farrell
Journal:  Clin Genet       Date:  2016-01-20       Impact factor: 4.438

6.  Impact of MIF gene promoter polymorphism on F508del cystic fibrosis patients.

Authors:  Paola Melotti; Andrea Mafficini; Patrick Lebecque; Myriam Ortombina; Teresinha Leal; Emily Pintani; Xavier Pepermans; Claudio Sorio; Baroukh Maurice Assael
Journal:  PLoS One       Date:  2014-12-12       Impact factor: 3.240

7.  Multivariate joint modeling to identify markers of growth and lung function decline that predict cystic fibrosis pulmonary exacerbation onset.

Authors:  E R Andrinopoulou; J P Clancy; R D Szczesniak
Journal:  BMC Pulm Med       Date:  2020-05-19       Impact factor: 3.317

8.  Evaluation of Food Insecurity in Adults and Children With Cystic Fibrosis: Community Case Study.

Authors:  Perry S Brown; Dixie Durham; Rick D Tivis; Shannon Stamper; Cleary Waldren; Sarah E Toevs; Barbara Gordon; Tiffany A Robb
Journal:  Front Public Health       Date:  2018-11-26

9.  Novel therapeutic approaches for the management of cystic fibrosis.

Authors:  Ryan Jaques; Arslan Shakeel; Cameron Hoyle
Journal:  Multidiscip Respir Med       Date:  2020-11-26

10.  Nutritional status of adolescents with cystic fibrosis treated at a reference center in the southeast region of Brazil.

Authors:  Ieda Regina Lopes Del Ciampo; Luiz Antonio Del Ciampo; Regina Sawamura; Laiane Renolfi de Oliveira; Maria Inez Machado Fernandes
Journal:  Ital J Pediatr       Date:  2015-07-30       Impact factor: 2.638

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.