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Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression

BACKGROUND: Intestinal failure (IF) is associated with significant morbidity and mortality, yet specific parameters that determine medium- and long-term outcomes remain ill defined. OBJECTIVE: The aim of this study was to determine the long-term outcomes in childhood IF and identify patient characte...

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Autores principales: Pierret, Aureliane Chantal Stania, Wilkinson, James Thomas, Zilbauer, Matthias, Mann, Jake Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669059/
https://www.ncbi.nlm.nih.gov/pubmed/31172170
http://dx.doi.org/10.1093/ajcn/nqz110
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author Pierret, Aureliane Chantal Stania
Wilkinson, James Thomas
Zilbauer, Matthias
Mann, Jake Peter
author_facet Pierret, Aureliane Chantal Stania
Wilkinson, James Thomas
Zilbauer, Matthias
Mann, Jake Peter
author_sort Pierret, Aureliane Chantal Stania
collection PubMed
description BACKGROUND: Intestinal failure (IF) is associated with significant morbidity and mortality, yet specific parameters that determine medium- and long-term outcomes remain ill defined. OBJECTIVE: The aim of this study was to determine the long-term outcomes in childhood IF and identify patient characteristics associated with clinical endpoints. DESIGN: MEDLINE and EMBASE were searched for cohorts of >10 pediatric-onset IF patients with >12 mo follow-up. Random-effects meta-analysis and meta-regression weighted by follow-up duration were used to calculate clinical outcome rates and patient factors associated with outcomes. Primary outcome was mortality rate; secondary outcomes included neurodevelopmental status, transplantation, IF-associated liver disease (IFALD), enteral autonomy, and sepsis. RESULTS: In total, 175 cohorts (9318 patients and 34,549 y follow-up) were included in the meta-analysis. Overall mortality was 5.2% per y (95% CI: 4.3, 6.0) and was associated with sepsis and IFALD on meta-regression. Mortality rate improved with time from 5.9% per y pre-2000 to 4.5% per y post-2005. Sepsis rate was also predictive of IFALD and liver failure. Enteral autonomy was associated with small bowel length but not presence of ileo-cecal valve. There was a relative lack of data on neurodevelopmental outcomes. CONCLUSIONS: Sepsis is the primary modifiable factor associated with mortality and liver failure, whereas enteral autonomy correlates with small-bowel length. No clear parameters have been identified that accurately predict neurodevelopmental outcomes, and hence further research is needed. Together, our findings are helpful for parental counseling and resource planning, and support targeting reduction in sepsis.
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spelling pubmed-66690592019-08-05 Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression Pierret, Aureliane Chantal Stania Wilkinson, James Thomas Zilbauer, Matthias Mann, Jake Peter Am J Clin Nutr Original Research Communications BACKGROUND: Intestinal failure (IF) is associated with significant morbidity and mortality, yet specific parameters that determine medium- and long-term outcomes remain ill defined. OBJECTIVE: The aim of this study was to determine the long-term outcomes in childhood IF and identify patient characteristics associated with clinical endpoints. DESIGN: MEDLINE and EMBASE were searched for cohorts of >10 pediatric-onset IF patients with >12 mo follow-up. Random-effects meta-analysis and meta-regression weighted by follow-up duration were used to calculate clinical outcome rates and patient factors associated with outcomes. Primary outcome was mortality rate; secondary outcomes included neurodevelopmental status, transplantation, IF-associated liver disease (IFALD), enteral autonomy, and sepsis. RESULTS: In total, 175 cohorts (9318 patients and 34,549 y follow-up) were included in the meta-analysis. Overall mortality was 5.2% per y (95% CI: 4.3, 6.0) and was associated with sepsis and IFALD on meta-regression. Mortality rate improved with time from 5.9% per y pre-2000 to 4.5% per y post-2005. Sepsis rate was also predictive of IFALD and liver failure. Enteral autonomy was associated with small bowel length but not presence of ileo-cecal valve. There was a relative lack of data on neurodevelopmental outcomes. CONCLUSIONS: Sepsis is the primary modifiable factor associated with mortality and liver failure, whereas enteral autonomy correlates with small-bowel length. No clear parameters have been identified that accurately predict neurodevelopmental outcomes, and hence further research is needed. Together, our findings are helpful for parental counseling and resource planning, and support targeting reduction in sepsis. Oxford University Press 2019-08 2019-06-07 /pmc/articles/PMC6669059/ /pubmed/31172170 http://dx.doi.org/10.1093/ajcn/nqz110 Text en Copyright © American Society for Nutrition 2019. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Communications
Pierret, Aureliane Chantal Stania
Wilkinson, James Thomas
Zilbauer, Matthias
Mann, Jake Peter
Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression
title Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression
title_full Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression
title_fullStr Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression
title_full_unstemmed Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression
title_short Clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression
title_sort clinical outcomes in pediatric intestinal failure: a meta-analysis and meta-regression
topic Original Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669059/
https://www.ncbi.nlm.nih.gov/pubmed/31172170
http://dx.doi.org/10.1093/ajcn/nqz110
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