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The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome
BACKGROUND: The role of recombinant activated protein C (aPC) during sepsis is still controversial. It showed anti-inflammatory effect and improved the microvascular perfusion in experimental models of septic shock. The present study was aimed at testing the hypothesis that recombinant aPC therapy i...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848895/ https://www.ncbi.nlm.nih.gov/pubmed/24070065 http://dx.doi.org/10.1186/1471-2253-13-25 |
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author | Donati, Abele Damiani, Elisa Botticelli, Laura Adrario, Erica Lombrano, Maria Rita Domizi, Roberta Marini, Benedetto Van Teeffelen, Jurgen WGE Carletti, Paola Girardis, Massimo Pelaia, Paolo Ince, Can |
author_facet | Donati, Abele Damiani, Elisa Botticelli, Laura Adrario, Erica Lombrano, Maria Rita Domizi, Roberta Marini, Benedetto Van Teeffelen, Jurgen WGE Carletti, Paola Girardis, Massimo Pelaia, Paolo Ince, Can |
author_sort | Donati, Abele |
collection | PubMed |
description | BACKGROUND: The role of recombinant activated protein C (aPC) during sepsis is still controversial. It showed anti-inflammatory effect and improved the microvascular perfusion in experimental models of septic shock. The present study was aimed at testing the hypothesis that recombinant aPC therapy improves the microcirculation during severe sepsis. METHODS: Prospective observational study on patients admitted in a 12-beds intensive care unit of a university hospital from July 2010 to December 2011, with severe sepsis and at least two sepsis-induced organ failures occurring within 48 hours from the onset of sepsis, who received an infusion of aPC (24 mcg/kg/h for 96 hours) (aPC group). Patients with contraindications to aPC administration were also monitored (no-aPC group). At baseline (before starting aPC infusion, T0), after 24 hours (T1a), 48 hours (T1b), 72 hours (T1c) and 6 hours after the end of aPC infusion (T2), general clinical and hemodynamic parameters were collected and the sublingual microcirculation was evaluated with sidestream dark-field imaging. Total vessel density (TVD), perfused vessel density (PVD), De Backer score, microvascular flow index (MFIs), the proportion of perfused vessels (PPV) and the flow heterogeneity index (HI) were calculated for small vessels. The perfused boundary region (PBR) was measured as an index of glycocalyx damage. Variables were compared between time points and groups using non parametric or parametric statistical tests, as appropriate. RESULTS: In the 13 aPC patients mean arterial pressure (MAP), base excess, lactate, PaO2/FiO2 and the Sequential Organ Failure Assessment (SOFA) score significantly improved over time, while CI and ITBVI did not change. MFIs, TVD, PVD, PPV significantly increased over time and the HI decreased (p < 0.05 in all cases), while the PBR did not change. No-aPC patients (n = 9) did not show any change in the microcirculation over time. A positive correlation was found between MFIs and MAP. TVD, PVD and De Backer score negatively correlated with norepinephrine dose, and the SOFA score negatively correlated with MFIs, TVD and PVD. CONCLUSIONS: aPC significantly improves the microcirculation in patients with severe sepsis/septic shock. TRIAL REGISTRATION: NCT01806428 |
format | Online Article Text |
id | pubmed-3848895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38488952013-12-04 The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome Donati, Abele Damiani, Elisa Botticelli, Laura Adrario, Erica Lombrano, Maria Rita Domizi, Roberta Marini, Benedetto Van Teeffelen, Jurgen WGE Carletti, Paola Girardis, Massimo Pelaia, Paolo Ince, Can BMC Anesthesiol Research Article BACKGROUND: The role of recombinant activated protein C (aPC) during sepsis is still controversial. It showed anti-inflammatory effect and improved the microvascular perfusion in experimental models of septic shock. The present study was aimed at testing the hypothesis that recombinant aPC therapy improves the microcirculation during severe sepsis. METHODS: Prospective observational study on patients admitted in a 12-beds intensive care unit of a university hospital from July 2010 to December 2011, with severe sepsis and at least two sepsis-induced organ failures occurring within 48 hours from the onset of sepsis, who received an infusion of aPC (24 mcg/kg/h for 96 hours) (aPC group). Patients with contraindications to aPC administration were also monitored (no-aPC group). At baseline (before starting aPC infusion, T0), after 24 hours (T1a), 48 hours (T1b), 72 hours (T1c) and 6 hours after the end of aPC infusion (T2), general clinical and hemodynamic parameters were collected and the sublingual microcirculation was evaluated with sidestream dark-field imaging. Total vessel density (TVD), perfused vessel density (PVD), De Backer score, microvascular flow index (MFIs), the proportion of perfused vessels (PPV) and the flow heterogeneity index (HI) were calculated for small vessels. The perfused boundary region (PBR) was measured as an index of glycocalyx damage. Variables were compared between time points and groups using non parametric or parametric statistical tests, as appropriate. RESULTS: In the 13 aPC patients mean arterial pressure (MAP), base excess, lactate, PaO2/FiO2 and the Sequential Organ Failure Assessment (SOFA) score significantly improved over time, while CI and ITBVI did not change. MFIs, TVD, PVD, PPV significantly increased over time and the HI decreased (p < 0.05 in all cases), while the PBR did not change. No-aPC patients (n = 9) did not show any change in the microcirculation over time. A positive correlation was found between MFIs and MAP. TVD, PVD and De Backer score negatively correlated with norepinephrine dose, and the SOFA score negatively correlated with MFIs, TVD and PVD. CONCLUSIONS: aPC significantly improves the microcirculation in patients with severe sepsis/septic shock. TRIAL REGISTRATION: NCT01806428 BioMed Central 2013-09-26 /pmc/articles/PMC3848895/ /pubmed/24070065 http://dx.doi.org/10.1186/1471-2253-13-25 Text en Copyright © 2013 Donati 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 Donati, Abele Damiani, Elisa Botticelli, Laura Adrario, Erica Lombrano, Maria Rita Domizi, Roberta Marini, Benedetto Van Teeffelen, Jurgen WGE Carletti, Paola Girardis, Massimo Pelaia, Paolo Ince, Can The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome |
title | The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome |
title_full | The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome |
title_fullStr | The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome |
title_full_unstemmed | The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome |
title_short | The aPC treatment improves microcirculation in severe sepsis/septic shock syndrome |
title_sort | apc treatment improves microcirculation in severe sepsis/septic shock syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848895/ https://www.ncbi.nlm.nih.gov/pubmed/24070065 http://dx.doi.org/10.1186/1471-2253-13-25 |
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