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Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss

BACKGROUND: Prolonged or excessive blood loss is a common complication after cardiac surgery. Blood remnants and clots, remaining in the pericardial space in spite of chest tube drainage, induce high fibrinolytic activity that may contribute to bleeding complications. Continuous postoperative perica...

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Autores principales: Manshanden, Johan S.J., Gielen, Chantal L.I., de Borgie, Corianne A.J.M., Klautz, Robert J.M., de Mol, Bas A.J.M., Koolbergen, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587997/
https://www.ncbi.nlm.nih.gov/pubmed/26501121
http://dx.doi.org/10.1016/j.ebiom.2015.07.031
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author Manshanden, Johan S.J.
Gielen, Chantal L.I.
de Borgie, Corianne A.J.M.
Klautz, Robert J.M.
de Mol, Bas A.J.M.
Koolbergen, David R.
author_facet Manshanden, Johan S.J.
Gielen, Chantal L.I.
de Borgie, Corianne A.J.M.
Klautz, Robert J.M.
de Mol, Bas A.J.M.
Koolbergen, David R.
author_sort Manshanden, Johan S.J.
collection PubMed
description BACKGROUND: Prolonged or excessive blood loss is a common complication after cardiac surgery. Blood remnants and clots, remaining in the pericardial space in spite of chest tube drainage, induce high fibrinolytic activity that may contribute to bleeding complications. Continuous postoperative pericardial flushing (CPPF) with an irrigation solution may reduce blood loss by preventing the accumulation of clots. In this pilot study, the safety and feasibility of CPPF were evaluated and the effect on blood loss and other related complications was investigated. METHODS: Between November 2011 and April 2012 twenty-one adult patients undergoing surgery for congenital heart disease (CHD) received CPPF from sternal closure up to 12 h postoperative. With an inflow Redivac drain that was inserted through one of the chest tube incision holes, an irrigation solution (NaCl 0.9% at 38 °C) was delivered to the pericardial cavity using a volume controlled flushing system. Safety aspects, feasibility issues and complications were registered. The mean actual blood loss in the CPPF group was compared to the mean of a retrospective group (n = 126). RESULTS: CPPF was successfully completed in 20 (95.2%) patients, and no method related complications were observed. Feasibility was good in this experimental setting. Patients receiving CPPF showed a 30% (P = 0.038) decrease in mean actual blood loss 12 h postoperatively. CONCLUSIONS: CPPF after cardiac surgery was found to be safe and feasible in this experimental setting. The clinically relevant effect on blood loss needs to be confirmed in a randomized clinical trial.
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spelling pubmed-45879972015-10-23 Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss Manshanden, Johan S.J. Gielen, Chantal L.I. de Borgie, Corianne A.J.M. Klautz, Robert J.M. de Mol, Bas A.J.M. Koolbergen, David R. EBioMedicine Research Paper BACKGROUND: Prolonged or excessive blood loss is a common complication after cardiac surgery. Blood remnants and clots, remaining in the pericardial space in spite of chest tube drainage, induce high fibrinolytic activity that may contribute to bleeding complications. Continuous postoperative pericardial flushing (CPPF) with an irrigation solution may reduce blood loss by preventing the accumulation of clots. In this pilot study, the safety and feasibility of CPPF were evaluated and the effect on blood loss and other related complications was investigated. METHODS: Between November 2011 and April 2012 twenty-one adult patients undergoing surgery for congenital heart disease (CHD) received CPPF from sternal closure up to 12 h postoperative. With an inflow Redivac drain that was inserted through one of the chest tube incision holes, an irrigation solution (NaCl 0.9% at 38 °C) was delivered to the pericardial cavity using a volume controlled flushing system. Safety aspects, feasibility issues and complications were registered. The mean actual blood loss in the CPPF group was compared to the mean of a retrospective group (n = 126). RESULTS: CPPF was successfully completed in 20 (95.2%) patients, and no method related complications were observed. Feasibility was good in this experimental setting. Patients receiving CPPF showed a 30% (P = 0.038) decrease in mean actual blood loss 12 h postoperatively. CONCLUSIONS: CPPF after cardiac surgery was found to be safe and feasible in this experimental setting. The clinically relevant effect on blood loss needs to be confirmed in a randomized clinical trial. Elsevier 2015-07-31 /pmc/articles/PMC4587997/ /pubmed/26501121 http://dx.doi.org/10.1016/j.ebiom.2015.07.031 Text en © 2015 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Manshanden, Johan S.J.
Gielen, Chantal L.I.
de Borgie, Corianne A.J.M.
Klautz, Robert J.M.
de Mol, Bas A.J.M.
Koolbergen, David R.
Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss
title Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss
title_full Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss
title_fullStr Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss
title_full_unstemmed Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss
title_short Continuous Postoperative Pericardial Flushing: A Pilot Study on Safety, Feasibility, and Effect on Blood Loss
title_sort continuous postoperative pericardial flushing: a pilot study on safety, feasibility, and effect on blood loss
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587997/
https://www.ncbi.nlm.nih.gov/pubmed/26501121
http://dx.doi.org/10.1016/j.ebiom.2015.07.031
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