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Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients
BACKGROUND: Transthoracic device closure of ventricular septal defect (VSD) is widely used in the clinic, especially in China. Changes in inflammatory marker levels after transthoracic device closure of VSD in pediatric patients have not been reported. METHODS: We retrospectively collected clinical...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454635/ https://www.ncbi.nlm.nih.gov/pubmed/30961628 http://dx.doi.org/10.1186/s13019-019-0900-4 |
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author | Huang, Jiang-Shan Chen, Qiang Chen, Liang-Wan Kuo, Yur-Ren Hong, Zhi-Nuan Cao, Hua |
author_facet | Huang, Jiang-Shan Chen, Qiang Chen, Liang-Wan Kuo, Yur-Ren Hong, Zhi-Nuan Cao, Hua |
author_sort | Huang, Jiang-Shan |
collection | PubMed |
description | BACKGROUND: Transthoracic device closure of ventricular septal defect (VSD) is widely used in the clinic, especially in China. Changes in inflammatory marker levels after transthoracic device closure of VSD in pediatric patients have not been reported. METHODS: We retrospectively collected clinical data for 85 pediatric patients in our hospital from September 2017 to January 2018. The patients were divided into two groups according to treatment (device group vs. surgical group). The clinical and experimental data from the two groups were statistically analyzed. RESULTS: Clinical outcomes were good in all patients without any fatal complications. Similar increasing trends in inflammatory markers (white blood cell (WBC) count, procalcitonin (PCT), C-reactive protein (CRP), and interleukin-6 (IL-6)) were found in the two groups, both of which showed noticeable systemic inflammatory responses. In addition, no significant difference in the postoperative levels of inflammatory markers was observed between these two groups. CONCLUSIONS: Although transthoracic device closure of VSD seems to be less traumatic and involves a quicker recovery, it also induces a systemic inflammatory response as measured by WBC count and PCT, CRP and IL-6 levels, and the altered trends in inflammatory markers were similar to those of conventional surgery under CPB. |
format | Online Article Text |
id | pubmed-6454635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64546352019-04-19 Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients Huang, Jiang-Shan Chen, Qiang Chen, Liang-Wan Kuo, Yur-Ren Hong, Zhi-Nuan Cao, Hua J Cardiothorac Surg Research Article BACKGROUND: Transthoracic device closure of ventricular septal defect (VSD) is widely used in the clinic, especially in China. Changes in inflammatory marker levels after transthoracic device closure of VSD in pediatric patients have not been reported. METHODS: We retrospectively collected clinical data for 85 pediatric patients in our hospital from September 2017 to January 2018. The patients were divided into two groups according to treatment (device group vs. surgical group). The clinical and experimental data from the two groups were statistically analyzed. RESULTS: Clinical outcomes were good in all patients without any fatal complications. Similar increasing trends in inflammatory markers (white blood cell (WBC) count, procalcitonin (PCT), C-reactive protein (CRP), and interleukin-6 (IL-6)) were found in the two groups, both of which showed noticeable systemic inflammatory responses. In addition, no significant difference in the postoperative levels of inflammatory markers was observed between these two groups. CONCLUSIONS: Although transthoracic device closure of VSD seems to be less traumatic and involves a quicker recovery, it also induces a systemic inflammatory response as measured by WBC count and PCT, CRP and IL-6 levels, and the altered trends in inflammatory markers were similar to those of conventional surgery under CPB. BioMed Central 2019-04-08 /pmc/articles/PMC6454635/ /pubmed/30961628 http://dx.doi.org/10.1186/s13019-019-0900-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Huang, Jiang-Shan Chen, Qiang Chen, Liang-Wan Kuo, Yur-Ren Hong, Zhi-Nuan Cao, Hua Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients |
title | Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients |
title_full | Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients |
title_fullStr | Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients |
title_full_unstemmed | Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients |
title_short | Changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients |
title_sort | changes in the levels of inflammatory markers after transthoracic device closure of ventricular septal defects in pediatric patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454635/ https://www.ncbi.nlm.nih.gov/pubmed/30961628 http://dx.doi.org/10.1186/s13019-019-0900-4 |
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