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Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy

The use of opioid analgesics to control pain after median sternotomy in cardiac surgical patients is worldwide accepted and established. However, opioids have a wide range of possible side effects, concerning prolonged extubation time, gastrointestinal tract dyskinesia and urinary tract disorders mo...

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Autores principales: Koukis, Ioannis, Argiriou, Mihalis, Dimakopoulou, Antonia, Panagiotakopoulos, Victor, Theakos, Nikolaos, Charitos, Christos
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2259353/
https://www.ncbi.nlm.nih.gov/pubmed/18221527
http://dx.doi.org/10.1186/1749-8090-3-2
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author Koukis, Ioannis
Argiriou, Mihalis
Dimakopoulou, Antonia
Panagiotakopoulos, Victor
Theakos, Nikolaos
Charitos, Christos
author_facet Koukis, Ioannis
Argiriou, Mihalis
Dimakopoulou, Antonia
Panagiotakopoulos, Victor
Theakos, Nikolaos
Charitos, Christos
author_sort Koukis, Ioannis
collection PubMed
description The use of opioid analgesics to control pain after median sternotomy in cardiac surgical patients is worldwide accepted and established. However, opioids have a wide range of possible side effects, concerning prolonged extubation time, gastrointestinal tract dyskinesia and urinary tract disorders mostly retention. All these may lead to a prolonged ICU stay or overall hospitalization time increase. To determine whether a continuous subcutaneous regional anesthetic infusion delivered directly to the sternotomy site would result in decreased levels of postoperative pain and opioid requirements in cardiac surgical patients undergoing median sternotomy. The continuous subcutaneous infusion (OnQ Painbuster system) was applied in 37 patients. 3 patients were exempted due to prolonged ICU stay. 29 patients underwent CABG, 5 had AVR, 1 MVR and modified Maze, 1 patient had a 3-valve repair due to endocarditis and another one had reconstruction of the left ventricle. Requirements of opioid analgesics were recorded for 96 hours after operation. Pain was assessed using the visual analog scale and the total postoperative hospital length of stay was also measured. The postoperative pain was significantly diminished (0 – 3 at VAS). The mean postoperative length of stay was 5,8 days, rather improved compared to the average stay of 6,7 days. Continuous subcutaneous infusion of ropivacaine directly at the median sternotomy significantly diminishes postoperative pain and the need for opioid analgesic use. Moreover, it seems to reduce overall postoperative length of stay for all cardiac surgical patients.
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spelling pubmed-22593532008-03-04 Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy Koukis, Ioannis Argiriou, Mihalis Dimakopoulou, Antonia Panagiotakopoulos, Victor Theakos, Nikolaos Charitos, Christos J Cardiothorac Surg Study Protocol The use of opioid analgesics to control pain after median sternotomy in cardiac surgical patients is worldwide accepted and established. However, opioids have a wide range of possible side effects, concerning prolonged extubation time, gastrointestinal tract dyskinesia and urinary tract disorders mostly retention. All these may lead to a prolonged ICU stay or overall hospitalization time increase. To determine whether a continuous subcutaneous regional anesthetic infusion delivered directly to the sternotomy site would result in decreased levels of postoperative pain and opioid requirements in cardiac surgical patients undergoing median sternotomy. The continuous subcutaneous infusion (OnQ Painbuster system) was applied in 37 patients. 3 patients were exempted due to prolonged ICU stay. 29 patients underwent CABG, 5 had AVR, 1 MVR and modified Maze, 1 patient had a 3-valve repair due to endocarditis and another one had reconstruction of the left ventricle. Requirements of opioid analgesics were recorded for 96 hours after operation. Pain was assessed using the visual analog scale and the total postoperative hospital length of stay was also measured. The postoperative pain was significantly diminished (0 – 3 at VAS). The mean postoperative length of stay was 5,8 days, rather improved compared to the average stay of 6,7 days. Continuous subcutaneous infusion of ropivacaine directly at the median sternotomy significantly diminishes postoperative pain and the need for opioid analgesic use. Moreover, it seems to reduce overall postoperative length of stay for all cardiac surgical patients. BioMed Central 2008-01-25 /pmc/articles/PMC2259353/ /pubmed/18221527 http://dx.doi.org/10.1186/1749-8090-3-2 Text en Copyright © 2008 Koukis 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 Study Protocol
Koukis, Ioannis
Argiriou, Mihalis
Dimakopoulou, Antonia
Panagiotakopoulos, Victor
Theakos, Nikolaos
Charitos, Christos
Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy
title Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy
title_full Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy
title_fullStr Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy
title_full_unstemmed Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy
title_short Use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy
title_sort use of continuous subcutaneous anesthetic infusion in cardiac surgical patients after median sternotomy
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2259353/
https://www.ncbi.nlm.nih.gov/pubmed/18221527
http://dx.doi.org/10.1186/1749-8090-3-2
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