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Associated Clinical and Laboratory Markers of Donor on Allograft Function After Heart Transplant
INTRODUCTION: Primary graft dysfunction is a major cause of mortality after heart transplantation. OBJECTIVE: To evaluate correlations between donor-related clinical/biochemical markers and the occurrence of primary graft dysfunction/clinical outcomes of recipients within 30 days of transplant. METH...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Sociedade Brasileira de Cirurgia Cardiovascular
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062732/ https://www.ncbi.nlm.nih.gov/pubmed/27556306 http://dx.doi.org/10.5935/1678-9741.20160025 |
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author | Braulio, Renato Sanches, Marcelo Dias Teixeira Junior, Antonio Lúcio Costa, Paulo Henrique Nogueira Moreira, Maria da Consolação Vieira Rocha, Monaliza Angela de Andrade, Silvio Amadeu Gelape, Cláudio Léo |
author_facet | Braulio, Renato Sanches, Marcelo Dias Teixeira Junior, Antonio Lúcio Costa, Paulo Henrique Nogueira Moreira, Maria da Consolação Vieira Rocha, Monaliza Angela de Andrade, Silvio Amadeu Gelape, Cláudio Léo |
author_sort | Braulio, Renato |
collection | PubMed |
description | INTRODUCTION: Primary graft dysfunction is a major cause of mortality after heart transplantation. OBJECTIVE: To evaluate correlations between donor-related clinical/biochemical markers and the occurrence of primary graft dysfunction/clinical outcomes of recipients within 30 days of transplant. METHODS: The prospective study involved 43 donor/recipient pairs. Data collected from donors included demographic and echocardiographic information, noradrenaline administration rates and concentrations of soluble tumor necrosis factor receptors (sTNFR1 and sTNFR2), interleukins (IL-6 and IL-10), monocyte chemoattractant protein-1, C-reactive protein and cardiac troponin I. Data collected from recipients included operating, cardiopulmonary bypass, intensive care unit and hospitalization times, inotrope administration and left/right ventricular function through echocardiography. RESULTS: Recipients who developed moderate/severe left ventricular dysfunction had received organs from significantly older donors (P =0.020). Recipients from donors who required moderate/high doses of noradrenaline (>0.23 µg/kg/min) around harvesting time exhibited lower post-transplant ventricular ejection fractions (P =0.002) and required longer CPB times (P =0.039). Significantly higher concentrations of sTNFR1 (P =0.014) and sTNFR2 (P =0.030) in donors were associated with reduced intensive care unit times (≤5 days) in recipients, while higher donor IL-6 (P =0.029) and IL-10 (P =0.037) levels were correlated with reduced hospitalization times (≤25 days) in recipients. Recipients who required moderate/high levels of noradrenaline for weaning off cardiopulmonary bypass were associated with lower donor concentrations of sTNFR2 (P =0.028) and IL-6 (P =0.001). CONCLUSION: High levels of sTNFR1, sTNFR2, IL-6 and IL-10 in donors were associated with enhanced evolution in recipients. Allografts from older donors, or from those treated with noradrenaline doses >0.23 µg/kg/min, were more frequently affected by primary graft dysfunction within 30 days of surgery. |
format | Online Article Text |
id | pubmed-5062732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Sociedade Brasileira de Cirurgia Cardiovascular |
record_format | MEDLINE/PubMed |
spelling | pubmed-50627322016-10-19 Associated Clinical and Laboratory Markers of Donor on Allograft Function After Heart Transplant Braulio, Renato Sanches, Marcelo Dias Teixeira Junior, Antonio Lúcio Costa, Paulo Henrique Nogueira Moreira, Maria da Consolação Vieira Rocha, Monaliza Angela de Andrade, Silvio Amadeu Gelape, Cláudio Léo Braz J Cardiovasc Surg Original Articles INTRODUCTION: Primary graft dysfunction is a major cause of mortality after heart transplantation. OBJECTIVE: To evaluate correlations between donor-related clinical/biochemical markers and the occurrence of primary graft dysfunction/clinical outcomes of recipients within 30 days of transplant. METHODS: The prospective study involved 43 donor/recipient pairs. Data collected from donors included demographic and echocardiographic information, noradrenaline administration rates and concentrations of soluble tumor necrosis factor receptors (sTNFR1 and sTNFR2), interleukins (IL-6 and IL-10), monocyte chemoattractant protein-1, C-reactive protein and cardiac troponin I. Data collected from recipients included operating, cardiopulmonary bypass, intensive care unit and hospitalization times, inotrope administration and left/right ventricular function through echocardiography. RESULTS: Recipients who developed moderate/severe left ventricular dysfunction had received organs from significantly older donors (P =0.020). Recipients from donors who required moderate/high doses of noradrenaline (>0.23 µg/kg/min) around harvesting time exhibited lower post-transplant ventricular ejection fractions (P =0.002) and required longer CPB times (P =0.039). Significantly higher concentrations of sTNFR1 (P =0.014) and sTNFR2 (P =0.030) in donors were associated with reduced intensive care unit times (≤5 days) in recipients, while higher donor IL-6 (P =0.029) and IL-10 (P =0.037) levels were correlated with reduced hospitalization times (≤25 days) in recipients. Recipients who required moderate/high levels of noradrenaline for weaning off cardiopulmonary bypass were associated with lower donor concentrations of sTNFR2 (P =0.028) and IL-6 (P =0.001). CONCLUSION: High levels of sTNFR1, sTNFR2, IL-6 and IL-10 in donors were associated with enhanced evolution in recipients. Allografts from older donors, or from those treated with noradrenaline doses >0.23 µg/kg/min, were more frequently affected by primary graft dysfunction within 30 days of surgery. Sociedade Brasileira de Cirurgia Cardiovascular 2016 /pmc/articles/PMC5062732/ /pubmed/27556306 http://dx.doi.org/10.5935/1678-9741.20160025 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Braulio, Renato Sanches, Marcelo Dias Teixeira Junior, Antonio Lúcio Costa, Paulo Henrique Nogueira Moreira, Maria da Consolação Vieira Rocha, Monaliza Angela de Andrade, Silvio Amadeu Gelape, Cláudio Léo Associated Clinical and Laboratory Markers of Donor on Allograft Function After Heart Transplant |
title | Associated Clinical and Laboratory Markers of Donor on Allograft
Function After Heart Transplant |
title_full | Associated Clinical and Laboratory Markers of Donor on Allograft
Function After Heart Transplant |
title_fullStr | Associated Clinical and Laboratory Markers of Donor on Allograft
Function After Heart Transplant |
title_full_unstemmed | Associated Clinical and Laboratory Markers of Donor on Allograft
Function After Heart Transplant |
title_short | Associated Clinical and Laboratory Markers of Donor on Allograft
Function After Heart Transplant |
title_sort | associated clinical and laboratory markers of donor on allograft
function after heart transplant |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062732/ https://www.ncbi.nlm.nih.gov/pubmed/27556306 http://dx.doi.org/10.5935/1678-9741.20160025 |
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