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Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study
BACKGROUND: Delayed sternal closure (DSC) after cardiac surgery is a therapeutic option in the treatment of the severely impaired heart in pediatric cardiac surgery. The results with the technique of DSC over a 4-year period are examined with regard to mortality and morbidity. METHODS: We retrospect...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514162/ https://www.ncbi.nlm.nih.gov/pubmed/23031425 http://dx.doi.org/10.1186/1749-8090-7-102 |
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author | Özker, Emre Saritaş, Bülent Vuran, Can Yörüker, Uygar Ulugöl, Halim Türköz, Riza |
author_facet | Özker, Emre Saritaş, Bülent Vuran, Can Yörüker, Uygar Ulugöl, Halim Türköz, Riza |
author_sort | Özker, Emre |
collection | PubMed |
description | BACKGROUND: Delayed sternal closure (DSC) after cardiac surgery is a therapeutic option in the treatment of the severely impaired heart in pediatric cardiac surgery. The results with the technique of DSC over a 4-year period are examined with regard to mortality and morbidity. METHODS: We retrospectively reviewed records of 38 patients who had undergone DSC among 1100 congenital cardiac operations. Indication of DSC, time to sternal closure, pre and post closure cardiopulmonary and metabolic status, mortality, rate of wound and bloodstream infections were recorded. RESULTS: The mean sternal closure time was 2.9 days. The mortality rate was 34.2% (n = 13). Twenty (52.6%) patients required prolonged antibiotic use due to postoperative infection. There was gram negative microorganism predominance. There were 4 (10.5%) patients with postoperative mediastinitis. Postoperative infection rate statistically increased with cardiopulmonary bypass time (CPBT), sternal closure time (SCT) and intensive care unit (ICU) stay time (p = 0.039;p = 0.01;p = 0.012). On the other hand, the mortality rate significantly increased with increased cross clamp time (CCT), SCT, and extracorporeal membrane oxygenation (ECMO) use (p = 0.017; p = 0.026; p = 0.03). Single ventricular physiology was found to be risk factor for mortality in delayed sternal closure (p < 0.007). CONCLUSIONS: Elective DSC does not reduce the morbidity. The prolonged sternal closure time is associated with increased rate of postoperative infection rate; therefore early closure is strongly advocated. |
format | Online Article Text |
id | pubmed-3514162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35141622012-12-05 Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study Özker, Emre Saritaş, Bülent Vuran, Can Yörüker, Uygar Ulugöl, Halim Türköz, Riza J Cardiothorac Surg Research Article BACKGROUND: Delayed sternal closure (DSC) after cardiac surgery is a therapeutic option in the treatment of the severely impaired heart in pediatric cardiac surgery. The results with the technique of DSC over a 4-year period are examined with regard to mortality and morbidity. METHODS: We retrospectively reviewed records of 38 patients who had undergone DSC among 1100 congenital cardiac operations. Indication of DSC, time to sternal closure, pre and post closure cardiopulmonary and metabolic status, mortality, rate of wound and bloodstream infections were recorded. RESULTS: The mean sternal closure time was 2.9 days. The mortality rate was 34.2% (n = 13). Twenty (52.6%) patients required prolonged antibiotic use due to postoperative infection. There was gram negative microorganism predominance. There were 4 (10.5%) patients with postoperative mediastinitis. Postoperative infection rate statistically increased with cardiopulmonary bypass time (CPBT), sternal closure time (SCT) and intensive care unit (ICU) stay time (p = 0.039;p = 0.01;p = 0.012). On the other hand, the mortality rate significantly increased with increased cross clamp time (CCT), SCT, and extracorporeal membrane oxygenation (ECMO) use (p = 0.017; p = 0.026; p = 0.03). Single ventricular physiology was found to be risk factor for mortality in delayed sternal closure (p < 0.007). CONCLUSIONS: Elective DSC does not reduce the morbidity. The prolonged sternal closure time is associated with increased rate of postoperative infection rate; therefore early closure is strongly advocated. BioMed Central 2012-10-02 /pmc/articles/PMC3514162/ /pubmed/23031425 http://dx.doi.org/10.1186/1749-8090-7-102 Text en Copyright ©2012 Özker et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Özker, Emre Saritaş, Bülent Vuran, Can Yörüker, Uygar Ulugöl, Halim Türköz, Riza Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study |
title | Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study |
title_full | Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study |
title_fullStr | Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study |
title_full_unstemmed | Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study |
title_short | Delayed Sternal Closure After Pediatric Cardiac Operations; Single Center Experience: a Retrospective Study |
title_sort | delayed sternal closure after pediatric cardiac operations; single center experience: a retrospective study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514162/ https://www.ncbi.nlm.nih.gov/pubmed/23031425 http://dx.doi.org/10.1186/1749-8090-7-102 |
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