Assessment of nutritional status in children with cystic fibrosis: conventional anthropometry and bioelectrical impedance analysis. A cross-sectional.

Slides:



Advertisements
Similar presentations
Calculating Body Mass Index Senior Health- Bauberger.
Advertisements

How to Calculate Your Body Mass Index (BMI)
Obes Facts 2014;7: DOI: / Fig. 1. Selection of the population studied.
Pattern of Growth in Children with Cerebral Palsy
Body Composition.
Answer the following questions:
Assessment of body composition using bioelectrical impedance analysis in Prader-Willi syndrome  Hsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, Chi-Yu.
Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
Weightproblems by teenagers
Cost of care and clinical condition in paediatric cystic fibrosis patients  Ulrich Baumann, Christiane Stocklossa, Wolfgang Greiner, Johann-Matthias Graf.
Adiponectin and body composition in cystic fibrosis
Zhumin Zhang, Suzanne M. Shoff, HuiChuan J. Lai 
Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation  Kris De Boeck, Anne Munck, Seth Walker, Albert Faro,
Development, validation, and implementation of a questionnaire assessing disease knowledge and understanding in adult cystic fibrosis patients  Karen.
Dysbiosis of bifidobacteria and Clostridium cluster XIVa in the cystic fibrosis fecal microbiota  Gwen Duytschaever, Geert Huys, Maarten Bekaert, Linda.
Increased body-mass index in patients with narcolepsy
How does heart rate recovery after sub-maximal exercise correlate with maximal exercise testing in children with CF?  Sarah P. Cohen, David M. Orenstein 
Melissa S. Putman, Joshua F
Measuring and improving respiratory outcomes in cystic fibrosis lung disease: Opportunities and challenges to therapy  Edith T. Zemanick, J. Kirk Harris,
Nadav Traeger, Qiuhu Shi, Allen J. Dozor  Journal of Cystic Fibrosis 
Measures of body habitus are associated with lung function in adults with cystic fibrosis: A population-based study  Doug L. Forrester, Alan J. Knox,
Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation  Kris De Boeck, Anne Munck, Seth Walker, Albert Faro,
Bioelectrical impedance in young patients with cystic fibrosis: Validation of a specific equation and clinical relevance  A.M. Charatsi, P. Dusser, R.
Laura Viviani, Baroukh M. Assael, Eitan Kerem 
Statistical limitations of percent ideal body weight as measure for nutritional failure in patients with cystic fibrosis  T.O. Hirche, H. Hirche, S. Jungblut,
Cirrhosis and other liver disease in cystic fibrosis
DATA ANALYSIS: STATISTICS AND GRAPHING
National Kidney Foundation  American Journal of Kidney Diseases 
An unusual cause of growth failure in cystic fibrosis: A salutary reminder of the interaction between glucocorticoids and cytochrome P450 inhibiting medication 
The applicability of urinary creatinine as a method of specimen normalization in the cystic fibrosis population  Brandie D. Wagner, Frank J. Accurso,
Supplemental Table 1: Differences in mean BMI-SDS between 2005 and 2015 – the obese lose weight while the overweight stabilize or even increase weight.
Advanced glycation end products are elevated in cystic fibrosis-related diabetes and correlate with worse lung function  William R. Hunt, Beth R. Helfman,
Grip strength is strongly associated with height, weight and gender in childhood: a cross sectional study of 2241 children and adolescents providing reference.
I Meyts, W Wuyts, M Proesmans, K De Boeck  Journal of Cystic Fibrosis 
Nutritional status is associated with health-related quality of life in children with cystic fibrosis aged 9–19years  Suzanne M. Shoff, Audrey Tluczek,
Treatment response of airway clearance assessed by single-breath washout in children with cystic fibrosis  Chiara Abbas, Florian Singer, Sophie Yammine,
Asians with cystic fibrosis in the UK have worse disease outcomes than clinic matched white homozygous ΔF508 controls  Jonathan McCormick, Simon A. Ogston,
UK Cystic Fibrosis Registry Annual Data Report 2017
A.H. Gifford  Journal of Cystic Fibrosis 
Agreement of bioelectric impedance analysis and dual-energy X-ray absorptiometry for body composition evaluation in adults with cystic fibrosis  S. Ziai,
Changes in weight and body mass index (BMI) associated with quality improvement. Changes in weight and body mass index (BMI) associated with quality improvement.
Association between practice patterns and body mass index percentile in infants and young children with cystic fibrosis  Raj Padman, Lloyd N. Werk, Gabriela.
Low sodium status in cystic fibrosis—as assessed by calculating fractional Na+ excretion—is associated with decreased growth parameters  Christiane Knepper,
E. Tschiedel, H. Grasemann, F. Ratjen  Journal of Cystic Fibrosis 
Different opinions of physicians on the importance of measures to prevent acquisition of Pseudomonas aeruginosa from the environment  Gratiana Steinkamp,
Depression and anxiety in adolescents and adults with cystic fibrosis in the UK: A cross- sectional study  Alistair J.A. Duff, Janice Abbott, Carolyn Cowperthwaite,
Sally H. Pattison, Geraint B. Rogers, Martin Crockard, J
Anjali Gupta, Judith A Noronha, Shobha, Meenakshi Garg 
Cytokine gene polymorphisms and severity of CF lung disease
Stenotrophomonas maltophilia in cystic fibrosis: Improved detection by the use of selective agar and evaluation of antimicrobial resistance  P. Goncalves-Vidigal,
D.Y.F. Mak, J. Sykes, A.L. Stephenson, L.C. Lands 
Novel concepts in evaluating antimicrobial therapy for bacterial lung infections in patients with cystic fibrosis  Geraint B. Rogers, Lucas R. Hoffman,
Danieli Barino Salinas, Patrick R
Aleksandar Dejanovic, PhD, Erin P. Harvey, MSc, Stuart M. McGill, PhD 
Nutritional decline in cystic fibrosis related diabetes: The effect of intensive nutritional intervention  H. White, K. Pollard, C. Etherington, I. Clifton,
Segregation of children with CF diagnosed via newborn screening and acquisition of Pseudomonas aeruginosa  Karen O. McKay, Peter J. Cooper, Peter P. van.
Trends in pathogens colonising the respiratory tract of adult patients with cystic fibrosis, 1985–2005  F.A. Millar, N.J. Simmonds, M.E. Hodson  Journal.
F. Vermeulen, P. Lebecque, K. De Boeck, T. Leal 
A new method of sweat testing: the CF Quantum®sweat test
Ruth H. Keogh, Sanja Stanojevic  Journal of Cystic Fibrosis 
Lung clearance index during hospital admission in school-age children with cystic fibrosis  Liam Welsh, Christopher Nesci, Haily Tran, Marisol Tomai,
D Peckham, A Watson, K Pollard, C Etherington, S.P Conway 
Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
DNase in stable cystic fibrosis infants: a pilot study
The effect of social deprivation on clinical outcomes and the use of treatments in the UK cystic fibrosis population: a longitudinal study  Dr David C.
Bigna M. Keller, Carmen Casaulta Aebischer, Richard Kraemer, Martin H
Michael W. Konstan, David J. Pasta, Jeffrey S. Wagener, Donald R
Population pharmacokinetics of tobramycin administered thrice daily and once daily in children and adults with cystic fibrosis  D.J. Touw, A.J. Knox,
Cystic fibrosis and pregnancy in the modern era: A case control study
Estimation of lean body mass in children
Presentation transcript:

Assessment of nutritional status in children with cystic fibrosis: conventional anthropometry and bioelectrical impedance analysis. A cross-sectional study in Dutch patients  Michael Groeneweg, Suzan Tan, Annemieke M Boot, Johan C de Jongste, Jan Bouquet, Maarten Sinaasappel  Journal of Cystic Fibrosis  Volume 1, Issue 4, Pages 276-280 (December 2002) DOI: 10.1016/S1569-1993(02)00099-1

Fig. 1 Mean Z-scores of total group of patients with CF (n=58). Mean Z-scores±CI. BMI, body mass index; W-H, weight-for-height; H-A, height-for-age; W-A, weight-for-age; SFS, lean body mass by skinfold sum; UAC, upper arm circumference and BIA, bioelectrical impedance analysis. Journal of Cystic Fibrosis 2002 1, 276-280DOI: (10.1016/S1569-1993(02)00099-1)

Fig. 2 Weight-for-height percentiles of boys (n=30) and girls (n=28) with CF. Weight-for-height curves for boys (left graph) and for girls (right graph). The middle line represents Z=0; the upper and lower line represent two times the S.D. Every single dot represents one patient. Journal of Cystic Fibrosis 2002 1, 276-280DOI: (10.1016/S1569-1993(02)00099-1)

Fig. 3 Height-for-age percentiles of boys (n=30) and girls (n=28) with CF. Height-for-age curves for boys (left graph) and for girls (right graph). The middle line represents Z=0; the upper and lower line represent two times the S.D. Every single dot represents one patient. Journal of Cystic Fibrosis 2002 1, 276-280DOI: (10.1016/S1569-1993(02)00099-1)