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Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital
Early identification of acute lung injury (ALI) in pediatric patients at risk of mortality is important for improving outcome. Assessment of soluble form of receptor for advanced glycation end products (sRAGE) as a valid biomarker for diagnosis of ALI among critically ill, pediatric patients in addi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882441/ https://www.ncbi.nlm.nih.gov/pubmed/29517700 http://dx.doi.org/10.1097/MD.0000000000009929 |
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author | Labib, John Rene Ibrahem, Sally Kamal Sleem, Hala Mohamed Ismail, Mohamed M. Abd El Fatah, Shaimaa A.M. Salem, Marwa Rashad Abdelaal, Amaal A. Al-hanafi, Hadeel |
author_facet | Labib, John Rene Ibrahem, Sally Kamal Sleem, Hala Mohamed Ismail, Mohamed M. Abd El Fatah, Shaimaa A.M. Salem, Marwa Rashad Abdelaal, Amaal A. Al-hanafi, Hadeel |
author_sort | Labib, John Rene |
collection | PubMed |
description | Early identification of acute lung injury (ALI) in pediatric patients at risk of mortality is important for improving outcome. Assessment of soluble form of receptor for advanced glycation end products (sRAGE) as a valid biomarker for diagnosis of ALI among critically ill, pediatric patients in addition to correlating levels of sRAGE and different outcomes of those patients. A Hospital-based case-control study was conducted in pediatric intensive care units (PICUs) at Cairo University Hospital, along a period of 6 months. Total of 68 pediatric patients following inclusion criteria were classified into: patients with ALI; with both ALI and sepsis; with sepsis and control patients. They were prospectively followed and their laboratory and immunological workup (at days 1 and 9) was done to measure serum sRAGE levels and detect (sRAGE) genotypes. The age of the included children ranged from 8 to 84 months. Plasma level of sRAGE was significantly higher in plasma from patients with ALI regardless of associated sepsis. Plasma sRAGE levels were positively correlated with lung injury score. When assessing sRAGE genotypes, TA and TT genotypes were significant in most of the ALI with and without sepsis patients. Monitoring levels of sRAGE and genotypes can significantly affect the survival of ALI children. |
format | Online Article Text |
id | pubmed-5882441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-58824412018-04-11 Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital Labib, John Rene Ibrahem, Sally Kamal Sleem, Hala Mohamed Ismail, Mohamed M. Abd El Fatah, Shaimaa A.M. Salem, Marwa Rashad Abdelaal, Amaal A. Al-hanafi, Hadeel Medicine (Baltimore) 6200 Early identification of acute lung injury (ALI) in pediatric patients at risk of mortality is important for improving outcome. Assessment of soluble form of receptor for advanced glycation end products (sRAGE) as a valid biomarker for diagnosis of ALI among critically ill, pediatric patients in addition to correlating levels of sRAGE and different outcomes of those patients. A Hospital-based case-control study was conducted in pediatric intensive care units (PICUs) at Cairo University Hospital, along a period of 6 months. Total of 68 pediatric patients following inclusion criteria were classified into: patients with ALI; with both ALI and sepsis; with sepsis and control patients. They were prospectively followed and their laboratory and immunological workup (at days 1 and 9) was done to measure serum sRAGE levels and detect (sRAGE) genotypes. The age of the included children ranged from 8 to 84 months. Plasma level of sRAGE was significantly higher in plasma from patients with ALI regardless of associated sepsis. Plasma sRAGE levels were positively correlated with lung injury score. When assessing sRAGE genotypes, TA and TT genotypes were significant in most of the ALI with and without sepsis patients. Monitoring levels of sRAGE and genotypes can significantly affect the survival of ALI children. Wolters Kluwer Health 2018-03-09 /pmc/articles/PMC5882441/ /pubmed/29517700 http://dx.doi.org/10.1097/MD.0000000000009929 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 6200 Labib, John Rene Ibrahem, Sally Kamal Sleem, Hala Mohamed Ismail, Mohamed M. Abd El Fatah, Shaimaa A.M. Salem, Marwa Rashad Abdelaal, Amaal A. Al-hanafi, Hadeel Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital |
title | Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital |
title_full | Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital |
title_fullStr | Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital |
title_full_unstemmed | Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital |
title_short | Diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital |
title_sort | diagnostic indicator of acute lung injury for pediatric critically ill patients at a tertiary pediatric hospital |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882441/ https://www.ncbi.nlm.nih.gov/pubmed/29517700 http://dx.doi.org/10.1097/MD.0000000000009929 |
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