Pancreatic enzyme replacement therapy dosing and nutritional outcomes in children with cystic fibrosis

Journal of Pediatrics

Volumn 164, Issue 5, 2014, Pages

  Haupt, Mark E ^a   Kwasny, Mary J ^a   Schechter, Michael S ^b   McColley, Susanna A ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

^b VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

Author keywords

BMI; Body mass index; CF; CF Registry; CFF; CFF Patient Registry; Cystic Fibrosis; Cystic Fibrosis Foundation; FEV1 ; Forced expiratory volume in 1 second percent; Pancreatic enzyme replacement therapy; PERT

Indexed keywords

GROWTH HORMONE; PANCREAS ENZYME;

ADOLESCENT; ADULT; ARTICLE; BODY MASS; CHILD; CYSTIC FIBROSIS; DIABETES MELLITUS; DIET SUPPLEMENTATION; ENZYME REPLACEMENT; ETHNICITY; FEMALE; FORCED EXPIRATORY VOLUME; HUMAN; MAJOR CLINICAL STUDY; MALE; NUTRITIONAL ASSESSMENT; PANCREATIC ENZYME REPLACEMENT THERAPY; PRIORITY JOURNAL; PSEUDOMONAS AERUGINOSA; RACE; REGISTER; RETROSPECTIVE STUDY;

ADOLESCENT; BODY MASS INDEX; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; DRUG ADMINISTRATION SCHEDULE; ENZYME REPLACEMENT THERAPY; EXOCRINE PANCREATIC INSUFFICIENCY; FEMALE; HUMANS; LIPASE; MALE; MODELS, STATISTICAL; MULTIVARIATE ANALYSIS; NUTRITIONAL STATUS; REGISTRIES; RETROSPECTIVE STUDIES; TREATMENT OUTCOME; YOUNG ADULT;

EID: 84899106021     PISSN: 00223476     EISSN: 10976833     Source Type: Journal    
DOI: 10.1016/j.jpeds.2014.01.022     Document Type: Article

References (28)

1. Cystic Fibrosis Foundation Patient Registry: Annual Data Report 2010 2011 Cystic Fibrosis Foundation Bethesda, MD 1 32
2. B.S. Zemel, A.F. Jawad, S. Fitzsimmons, and V. Stallings 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 137 2000 374 380
3. P.B. Pencharz, and P.R. Durie Nutritional management of cystic fibrosis Ann Rev Nutr 13 1993 111 136
4. A.M. Dalzell, R.W. Shepherd, S.B. Dean, G.J. Cleghorn, T.L. Holt, and P.J. Francis Nutritional rehabilitation in cystic fibrosis: a 5-year follow-up study J Pediatr Gastroenterol Nutr 15 1992 141 145
5. E. Kerem, J. Reisman, M. Corey, G.J. Canny, and H. Levison Prediction of mortality in patients with cystic fibrosis N Engl J Med 326 1992 1187 1191
6. M. Corey, F.J. McLaughlin, M. Williams, and H. Levison A comparison of survival, growth and pulmonary function in patients with cystic fibrosis in Boston and Toronto J Clin Epidemiol 41 1988 588 591
7. R. Kraemer, A. Rudeberg, B. Hadorn, and E. Rossi Relative underweight in cystic fibrosis and its prognostic value Acta Paediatr Scand 67 1978 33 37
8. V.A. Stallings, L.J. Stark, K.A. Robinson, A.P. Feranchak, and H. Quinton 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 108 2008 832 839
9. R. Smyth, D. Ashby, U. O'Hea, E. Burros, P. Lewis, and D. van Velzen et al. Fibrosing colonopathy in cystic fibrosis: results of a case-control study Lancet 346 1995 1247 1251
10. S. FitzSimmons, G. Burkhart, D. Borowitz, R.J. Grand, T. Hammerstrom, and P. Drurie et al. High-dose pancreatic-enzyme supplements and fibrosing colonopathy in children with cystic fibrosis N Engl J Med 336 1997 1283 1289
11. K.J. Rothman, and C.E. Wenthworth III Mortality of cystic fibrosis patients being treated with tobramycin solution for inhalation Epidemiology 14 2003 55 59
12. C. Johnson, S.M. Butler, M.W. Konstan, W. Morgan, and M.E. Wohl Factors influencing outcomes in cystic fibrosis: a center based analysis Chest 123 2003 20 27
13. R. Padman, S.A. McColley, D.P. Miller, M.W. Konstan, W.J. Morgan, and M.S. Schechter et al. Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function Pediatrics 119 2007 e531 e537
14. P.J. Oades, A. Bush, P.S. Ong, and R.J. Brereton High-strength pancreatic enzyme supplements and large-bowel stricture in cystic fibrosis Lancet 343 1994 109
15. C.A. Campbell, J. Forrest, and C. Musgrove High-strength pancreatic enzyme supplements and large-bowel stricture in cystic fibrosis Lancet 343 1994 109 110
16. D. Borowitz, R. Grand, and P. Durie Use of pancreatic enzyme supplements for patients with cystic fibrosis in the context of fibrosing colonopathy: consensus committee J Pediatr 127 1995 681 684
17. D. Borowitz, R. Baker, and V. Stallings Consensus report on nutrition for pediatric patients with cystic fibrosis J Pediatr Gastroenterol Nutr 35 2002 246 259
18. S. Baker, D. Borowitz, L. Duffy, L. Fitzpatrick, J. Gyamfi, and R. Baker Pancreatic enzyme therapy and clinical outcomes in patients with cystic fibrosis J Pediatr 146 2005 189 193
19. M.S. Schechter, J. Wagener, M.W. Konstan, and W. Morgan Location and duration of treatment of cystic fibrosis respiratory exacerbations Am J Respir Crit Care Med 184 2011 278 author reply 279
20. M.S. Schechter Patient registry analyses: seize the data, but caveat lector J Pediatr 153 2008 733 735
21. S. Wen, and M. Kramer Uses of ecologic studies in the assessment of intended treatment effects J Clin Epidemiol 52 1999 7 12
22. J. Bosco, R. Silliman, S. Thwin, A. Geiger, D. Buist, and M. Prout et al. A most stubborn bias: no adjustment method fully resolves confounding by indication in observational studies J Clin Epidemiol 63 2010 64 74
23. R.D. Vandyke, G.L. McPhail, B. Huang, M.C. Fenchel, R.S. Amin, and A.C. Carle et al. Inhaled tobramycin effectively reduces FEV1 decline in cystic fibrosis. An instrumental variables analysis Ann Am Thorac Soc 10 2013 205 212
24. E.F. McKone, S.S. Emerson, K.L. Edwards, and M.L. Aitken Effect of genotype on phenotype and mortality in cystic fibrosis patients: a retrospective cohort study Lancet 363 2003 1671 1676
25. G.M. Bradley, K.A. Carson, A.R. Leonard, P.J. Mogayzel Jr., and M. Oliva-Hemker Nutritional outcomes following gastrostomy in children with cystic fibrosis Pediatr Pulmonol 47 2012 743 748
26. C. Best, A. Brearley, P. Gaillard, W. Regelmann, J. Billings, and J. Dunitz et al. A pre-post retrospective study of patients with cystic fibrosis and gastrostomy tubes J Pediatr Gastroenterol Nutr 53 2011 453 458
27. P. Farrell, M. Kosorok, M. Rock, A. Laxova, L. Zeng, and H. Lai et al. Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group Pediatrics 107 2001 1 13
28. E. Yen, H. Quinton, and D. Borowitz Better nutritional status in early childhood is associated with improved clinical outcomes and survival in patients with cystic fibrosis J Pediatr 162 2013 530 535