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Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series

In orally fed preterm infants, poor weight gain may be linked to low fecal pancreatic elastase-1 (FPE-1) activity, indicative of exocrine pancreatic insufficiency. The objective of this study was the retrospective assessment of the effect of exogenous digestive enzyme replacement by gavage in preter...

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Autores principales: Münch, Annette, Bührer, Christoph, Longardt, Ann Carolin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346403/
https://www.ncbi.nlm.nih.gov/pubmed/33839912
http://dx.doi.org/10.1007/s00431-021-04069-0
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author Münch, Annette
Bührer, Christoph
Longardt, Ann Carolin
author_facet Münch, Annette
Bührer, Christoph
Longardt, Ann Carolin
author_sort Münch, Annette
collection PubMed
description In orally fed preterm infants, poor weight gain may be linked to low fecal pancreatic elastase-1 (FPE-1) activity, indicative of exocrine pancreatic insufficiency. The objective of this study was the retrospective assessment of the effect of exogenous digestive enzyme replacement by gavage in preterm infants with growth failure and low FPE-1 (<200 μg/g). We analyzed weight gain relative to baseline and caloric intake during 14-day periods before and after institution of digestive enzyme replacement containing 6000 U lipase and 240 U protease kg(−1) d(−1). Among 46 of 132 preterm infants < 1250g birth weight surviving to at least 14 days in whom FPE-1 was determined, 38 infants had low FPE-1 (< 200 μg/g), and 33 infants received exogenous digestive enzyme replacement. Average daily weight gain significantly increased from 14.4 [range 2.6–22.4] g kg(−1) d(−1) to 17.4 [8.4–29.0] g kg(−1) d(−1) (P = 0.001), as did weight gain per kcal, from 0.08 [0.02–0.13] g kcal(−1) d(−1) to 0.11 [0.05–0.18] g kcal(−1) d(−1). Conclusion: In preterm infants with signs and symptoms of exocrine pancreatic insufficiency, exogenous digestive enzyme replacement is associated with improved growth. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-021-04069-0.
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spelling pubmed-83464032021-08-20 Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series Münch, Annette Bührer, Christoph Longardt, Ann Carolin Eur J Pediatr Original Article In orally fed preterm infants, poor weight gain may be linked to low fecal pancreatic elastase-1 (FPE-1) activity, indicative of exocrine pancreatic insufficiency. The objective of this study was the retrospective assessment of the effect of exogenous digestive enzyme replacement by gavage in preterm infants with growth failure and low FPE-1 (<200 μg/g). We analyzed weight gain relative to baseline and caloric intake during 14-day periods before and after institution of digestive enzyme replacement containing 6000 U lipase and 240 U protease kg(−1) d(−1). Among 46 of 132 preterm infants < 1250g birth weight surviving to at least 14 days in whom FPE-1 was determined, 38 infants had low FPE-1 (< 200 μg/g), and 33 infants received exogenous digestive enzyme replacement. Average daily weight gain significantly increased from 14.4 [range 2.6–22.4] g kg(−1) d(−1) to 17.4 [8.4–29.0] g kg(−1) d(−1) (P = 0.001), as did weight gain per kcal, from 0.08 [0.02–0.13] g kcal(−1) d(−1) to 0.11 [0.05–0.18] g kcal(−1) d(−1). Conclusion: In preterm infants with signs and symptoms of exocrine pancreatic insufficiency, exogenous digestive enzyme replacement is associated with improved growth. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-021-04069-0. Springer Berlin Heidelberg 2021-04-10 2021 /pmc/articles/PMC8346403/ /pubmed/33839912 http://dx.doi.org/10.1007/s00431-021-04069-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Münch, Annette
Bührer, Christoph
Longardt, Ann Carolin
Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series
title Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series
title_full Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series
title_fullStr Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series
title_full_unstemmed Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series
title_short Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series
title_sort digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a retrospective case series
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346403/
https://www.ncbi.nlm.nih.gov/pubmed/33839912
http://dx.doi.org/10.1007/s00431-021-04069-0
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