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Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation

INTRODUCTION: The aim of the study was to assess the diagnostic accuracy of procalcitonin (PCT) as a marker for complications and as a prognostic factor for mortality after liver transplantation. MATERIAL AND METHODS: Liver transplant patients between January 2007 and April 2011 were prospectively i...

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Autores principales: Perrakis, Aristotelis, Stirkat, Falk, Croner, Roland S., Vassos, Nikolaos, Raptis, Dimitrios, Yedibela, Süleyman, Hohenberger, Werner, Müller, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848368/
https://www.ncbi.nlm.nih.gov/pubmed/27186183
http://dx.doi.org/10.5114/aoms.2016.59264
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author Perrakis, Aristotelis
Stirkat, Falk
Croner, Roland S.
Vassos, Nikolaos
Raptis, Dimitrios
Yedibela, Süleyman
Hohenberger, Werner
Müller, Volker
author_facet Perrakis, Aristotelis
Stirkat, Falk
Croner, Roland S.
Vassos, Nikolaos
Raptis, Dimitrios
Yedibela, Süleyman
Hohenberger, Werner
Müller, Volker
author_sort Perrakis, Aristotelis
collection PubMed
description INTRODUCTION: The aim of the study was to assess the diagnostic accuracy of procalcitonin (PCT) as a marker for complications and as a prognostic factor for mortality after liver transplantation. MATERIAL AND METHODS: Liver transplant patients between January 2007 and April 2011 were prospectively included in the study. Procalcitonin serum concentration was recorded before, 6 h after reperfusion and then daily. Postoperative clinical course was prospectively analyzed from admission to discharge. Main surgical data such as operating procedure, type of reperfusion, operating and ischemic times, high urgency (HU) status and MELD score at the time of transplantation were also recorded. RESULTS: Sixteen patients with initial PCT > 5 ng/ml suffered ≥ 1 complication (p = 0.03). However, there was no association between the level of the 1(st) peak PCT and the further postoperative course or the occurrence of complications. Patients in whom a 2(nd) PCT peak occurred had a significantly higher risk for a complicated course, for a complicated sepsis course and for mortality (p < 0.0001). Warm ischemic time over 58 min, operating time over 389 min and HU status were significant independent factors for a complicated postoperative course (p < 0.001, p < 0.001 and p = 0.03 respectively). CONCLUSIONS: Based on our results, we believe that PCT course and the occurrence of a 2(nd) peak seem to possess important diagnostic and prognostic power in the post-transplant setting after liver transplantation.
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spelling pubmed-48483682016-05-16 Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation Perrakis, Aristotelis Stirkat, Falk Croner, Roland S. Vassos, Nikolaos Raptis, Dimitrios Yedibela, Süleyman Hohenberger, Werner Müller, Volker Arch Med Sci Clinical Research INTRODUCTION: The aim of the study was to assess the diagnostic accuracy of procalcitonin (PCT) as a marker for complications and as a prognostic factor for mortality after liver transplantation. MATERIAL AND METHODS: Liver transplant patients between January 2007 and April 2011 were prospectively included in the study. Procalcitonin serum concentration was recorded before, 6 h after reperfusion and then daily. Postoperative clinical course was prospectively analyzed from admission to discharge. Main surgical data such as operating procedure, type of reperfusion, operating and ischemic times, high urgency (HU) status and MELD score at the time of transplantation were also recorded. RESULTS: Sixteen patients with initial PCT > 5 ng/ml suffered ≥ 1 complication (p = 0.03). However, there was no association between the level of the 1(st) peak PCT and the further postoperative course or the occurrence of complications. Patients in whom a 2(nd) PCT peak occurred had a significantly higher risk for a complicated course, for a complicated sepsis course and for mortality (p < 0.0001). Warm ischemic time over 58 min, operating time over 389 min and HU status were significant independent factors for a complicated postoperative course (p < 0.001, p < 0.001 and p = 0.03 respectively). CONCLUSIONS: Based on our results, we believe that PCT course and the occurrence of a 2(nd) peak seem to possess important diagnostic and prognostic power in the post-transplant setting after liver transplantation. Termedia Publishing House 2016-04-12 2016-04-01 /pmc/articles/PMC4848368/ /pubmed/27186183 http://dx.doi.org/10.5114/aoms.2016.59264 Text en Copyright © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Perrakis, Aristotelis
Stirkat, Falk
Croner, Roland S.
Vassos, Nikolaos
Raptis, Dimitrios
Yedibela, Süleyman
Hohenberger, Werner
Müller, Volker
Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation
title Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation
title_full Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation
title_fullStr Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation
title_full_unstemmed Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation
title_short Prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation
title_sort prognostic and diagnostic value of procalcitonin in the post-transplant setting after liver transplantation
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848368/
https://www.ncbi.nlm.nih.gov/pubmed/27186183
http://dx.doi.org/10.5114/aoms.2016.59264
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