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Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis
BACKGROUND: This study aimed to assess the effect of hyperglycemia on all-cause mortality in pediatric patients with brain injury, based on currently available evidence. METHODS: We systematically searched the PubMed, Embase, and Cochrane Library databases with the keywords “hyperglycemia”, “brain i...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710234/ https://www.ncbi.nlm.nih.gov/pubmed/33235087 http://dx.doi.org/10.1097/MD.0000000000023307 |
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author | Chen, Shuyun Liu, Zhaohe |
author_facet | Chen, Shuyun Liu, Zhaohe |
author_sort | Chen, Shuyun |
collection | PubMed |
description | BACKGROUND: This study aimed to assess the effect of hyperglycemia on all-cause mortality in pediatric patients with brain injury, based on currently available evidence. METHODS: We systematically searched the PubMed, Embase, and Cochrane Library databases with the keywords “hyperglycemia”, “brain injury”, and “pediatrics”. The retrieved records were screened by title, abstract, and full-text to include original articles assessing the effects of hyperglycemia on pediatric brain injury. The extracted data were assessed by a fixed-effects model. The risk of bias in the eligible studies was evaluated with the Newcastle-Ottawa Scale. Publication bias was visually examined with a funnel plot. Begg and Egger tests, respectively, were used to identify small-study effects. Sensitivity analysis was performed to evaluate the robustness of the original effect size. RESULTS: Nine observational studies were identified from 1439 primary hits. A total of 970 pediatric patients, including 304 with hyperglycemia and brain injury, were included for meta-analysis. Hyperglycemia was strongly associated with a higher risk of all-cause mortality in pediatric patients (odds ratio = 11.60, 95% confidence interval [CI] 7.88–17.08; I(2) = 0%). The overall quality of eligible studies was low, but the funnel plot indicated no publication bias. CONCLUSIONS: Hyperglycemia is significantly associated with high all-cause mortality in pediatric patients with brain injury. However, the relationship should be confirmed by larger-scale observational studies and randomized controlled trials. |
format | Online Article Text |
id | pubmed-7710234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-77102342020-12-03 Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis Chen, Shuyun Liu, Zhaohe Medicine (Baltimore) 6200 BACKGROUND: This study aimed to assess the effect of hyperglycemia on all-cause mortality in pediatric patients with brain injury, based on currently available evidence. METHODS: We systematically searched the PubMed, Embase, and Cochrane Library databases with the keywords “hyperglycemia”, “brain injury”, and “pediatrics”. The retrieved records were screened by title, abstract, and full-text to include original articles assessing the effects of hyperglycemia on pediatric brain injury. The extracted data were assessed by a fixed-effects model. The risk of bias in the eligible studies was evaluated with the Newcastle-Ottawa Scale. Publication bias was visually examined with a funnel plot. Begg and Egger tests, respectively, were used to identify small-study effects. Sensitivity analysis was performed to evaluate the robustness of the original effect size. RESULTS: Nine observational studies were identified from 1439 primary hits. A total of 970 pediatric patients, including 304 with hyperglycemia and brain injury, were included for meta-analysis. Hyperglycemia was strongly associated with a higher risk of all-cause mortality in pediatric patients (odds ratio = 11.60, 95% confidence interval [CI] 7.88–17.08; I(2) = 0%). The overall quality of eligible studies was low, but the funnel plot indicated no publication bias. CONCLUSIONS: Hyperglycemia is significantly associated with high all-cause mortality in pediatric patients with brain injury. However, the relationship should be confirmed by larger-scale observational studies and randomized controlled trials. Lippincott Williams & Wilkins 2020-11-25 /pmc/articles/PMC7710234/ /pubmed/33235087 http://dx.doi.org/10.1097/MD.0000000000023307 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 6200 Chen, Shuyun Liu, Zhaohe Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis |
title | Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis |
title_full | Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis |
title_fullStr | Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis |
title_full_unstemmed | Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis |
title_short | Effect of hyperglycemia on all-cause mortality from pediatric brain injury: A systematic review and meta-analysis |
title_sort | effect of hyperglycemia on all-cause mortality from pediatric brain injury: a systematic review and meta-analysis |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710234/ https://www.ncbi.nlm.nih.gov/pubmed/33235087 http://dx.doi.org/10.1097/MD.0000000000023307 |
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