Literature DB >> 24560182

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

Mark E Haupt1, Mary J Kwasny2, Michael S Schechter3, Susanna A McColley4.   

Abstract

OBJECTIVES: To utilize the Cystic Fibrosis Foundation Patient Registry to evaluate whether pancreatic enzyme dose is associated with better nutritional status as measured by average body mass index (BMI) percentile. STUDY
DESIGN: A retrospective analysis of the Cystic Fibrosis Foundation Patient Registry from 2005-2008 was performed. The final analysis included 42 561 patient visits from 14 482 patients 2-20 years of age taking pancreatic enzyme replacement therapy from 179 programs. Cystic fibrosis care programs were assigned to quartiles based on adjusted mean patient BMI percentiles. Differences in median lipase dose between programs in the highest and lowest BMI quartiles were examined using a mixed effects model that adjusted for individual patient BMI, age, race, ethnicity, forced expiratory volume in 1 second percent, acid-blocker use, presence of Pseudomonas aeruginosa, nutritional supplement use, growth hormone use, and diagnosis of cystic fibrosis-related diabetes.
RESULTS: A significant difference in median enzyme dose existed between the highest and lowest BMI quartiles. Multivariable analysis demonstrated the effect persisted after adjustment for covariates. Highest quartile programs had a median enzyme dose of 1755 lipase units/kg/meal compared with 1628 lipase units/kg/meal for lowest quartile programs.
CONCLUSION: Patients attending US cystic fibrosis programs achieving highest nutritional outcomes, measured by mean BMI percentile, have higher enzyme dosing than those attending programs at lower performance levels. Further randomized clinical trials are necessary to determine the role of enzyme dose in improving nutritional outcomes.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24560182     DOI: 10.1016/j.jpeds.2014.01.022

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  12 in total

1.  Pancreatic Enzyme Replacement Therapy Use in Infants With Cystic Fibrosis Diagnosed by Newborn Screening.

Authors:  Daniel Gelfond; Sonya L Heltshe; Michelle Skalland; James E Heubi; Margaret Kloster; Daniel H Leung; Bonnie W Ramsey; Drucy Borowitz
Journal:  J Pediatr Gastroenterol Nutr       Date:  2018-04       Impact factor: 2.839

2.  Malabsorption blood test: Assessing fat absorption in patients with cystic fibrosis and pancreatic insufficiency.

Authors:  Maria R Mascarenhas; John Mondick; Jeffrey S Barrett; Martha Wilson; Virginia A Stallings; Joan I Schall
Journal:  J Clin Pharmacol       Date:  2015-03-23       Impact factor: 3.126

Review 3.  Personalized medicine in CF: from modulator development to therapy for cystic fibrosis patients with rare CFTR mutations.

Authors:  Misak Harutyunyan; Yunjie Huang; Kyu-Shik Mun; Fanmuyi Yang; Kavisha Arora; Anjaparavanda P Naren
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-12-14       Impact factor: 5.464

4.  Early Life Growth Trajectories in Cystic Fibrosis are Associated with Pulmonary Function at Age 6 Years.

Authors:  Don B Sanders; Aliza Fink; Nicole Mayer-Hamblett; Michael S Schechter; Gregory S Sawicki; Margaret Rosenfeld; Patrick A Flume; Wayne J Morgan
Journal:  J Pediatr       Date:  2015-09-02       Impact factor: 4.406

5.  Innovative approach for self-management and social welfare of children with cystic fibrosis in Europe: development, validation and implementation of an mHealth tool (MyCyFAPP).

Authors:  Joaquim Calvo-Lerma; Celia P Martinez-Jimenez; Juan-Pablo Lázaro-Ramos; Ana Andrés; Paula Crespo-Escobar; Erlend Stav; Cornelia Schauber; Lucia Pannese; Jessie M Hulst; Lucrecia Suárez; Carla Colombo; Celeste Barreto; Kris de Boeck; Carmen Ribes-Koninckx
Journal:  BMJ Open       Date:  2017-03-16       Impact factor: 2.692

6.  A quality improvement program to improve nutritional status of children with Cystic Fibrosis aged 2-12 years old over a 3 year period at CF center Roscoff, Brittany.

Authors:  Krista Revert; Laurence Audran; Jocelyne Pengam; Pascal Lesne; Dominique Pougheon Bertrand
Journal:  Orphanet J Rare Dis       Date:  2018-02-08       Impact factor: 4.123

7.  Relationship of Initial Pancreatic Enzyme Replacement Therapy Dose With Weight Gain in Infants With Cystic Fibrosis.

Authors:  Michael S Schechter; Suzanne Michel; Shufang Liu; B Woun Seo; Mudra Kapoor; Rupal Khurmi; Mark Haupt
Journal:  J Pediatr Gastroenterol Nutr       Date:  2018-10       Impact factor: 2.839

8.  Glucose tolerance in Canadian and French cystic fibrosis adult patients.

Authors:  Quitterie Reynaud; Valérie Boudreau; Sandrine Touzet; Katherine Desjardins; Stéphanie Poupon Bourdy; Emilie Blond; Yves Berthiaume; Rémi Rabasa-Lhoret; Isabelle Durieu
Journal:  Sci Rep       Date:  2019-03-18       Impact factor: 4.379

9.  Evaluation of a five-year predicted survival model for cystic fibrosis in later time periods.

Authors:  Theodore G Liou; Christiana Kartsonaki; Ruth H Keogh; Frederick R Adler
Journal:  Sci Rep       Date:  2020-04-20       Impact factor: 4.379

Review 10.  Timing of pancreatic enzyme replacement therapy (PERT) in cystic fibrosis.

Authors:  Christabella Ng; Giles Major; Alan R Smyth
Journal:  Cochrane Database Syst Rev       Date:  2021-08-02
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