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Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections

BACKGROUND & AIMS: Bacterial infections in cirrhosis are associated with increased bleeding risk. To assess the factors responsible for bleeding tendency in patients with bacterial infections, we conducted a prospective study comparing all 3 aspects of hemostasis (platelets, coagulation, and fib...

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Autores principales: Zanetto, Alberto, Campello, Elena, Bulato, Cristiana, Gavasso, Sabrina, Saggiorato, Graziella, Shalaby, Sarah, Burra, Patrizia, Angeli, Paolo, Senzolo, Marco, Simioni, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131254/
https://www.ncbi.nlm.nih.gov/pubmed/35647501
http://dx.doi.org/10.1016/j.jhepr.2022.100493
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author Zanetto, Alberto
Campello, Elena
Bulato, Cristiana
Gavasso, Sabrina
Saggiorato, Graziella
Shalaby, Sarah
Burra, Patrizia
Angeli, Paolo
Senzolo, Marco
Simioni, Paolo
author_facet Zanetto, Alberto
Campello, Elena
Bulato, Cristiana
Gavasso, Sabrina
Saggiorato, Graziella
Shalaby, Sarah
Burra, Patrizia
Angeli, Paolo
Senzolo, Marco
Simioni, Paolo
author_sort Zanetto, Alberto
collection PubMed
description BACKGROUND & AIMS: Bacterial infections in cirrhosis are associated with increased bleeding risk. To assess the factors responsible for bleeding tendency in patients with bacterial infections, we conducted a prospective study comparing all 3 aspects of hemostasis (platelets, coagulation, and fibrinolysis) in hospitalized patients with decompensated cirrhosis with vs. without bacterial infections. METHODS: Primary hemostasis assessment included whole blood platelet aggregation and von Willebrand factor (VWF). Coagulation assessment included procoagulant factors (fibrinogen, factor II, V, VII, VIII, IX, X, XI, XII, XIII), natural anticoagulants (protein C, protein S, antithrombin) and thrombomodulin-modified thrombin generation test. Fibrinolysis assessment included fibrinolytic factors (plasminogen, t-PA, PAI-1, α2-AP, TAFIa/ai) and plasmin-antiplasmin complex (PAP). RESULTS: Eighty patients with decompensated cirrhosis were included (40 with and 40 without bacterial infections). Severity of cirrhosis and platelet count were comparable between groups. At baseline, patients with cirrhosis and bacterial infections had significantly lower whole blood platelet aggregation, without significant differences in VWF. Regarding coagulation, bacterial infections were associated with reduced procoagulant factors VII and XII, and a significant reduction of all natural anticoagulants. However, thrombomodulin-modified thrombin generation was comparable between the study groups. Finally, although mixed potentially hypo-fibrinolytic (lower plasminogen) and hyper-fibrinolytic (higher t-PA) changes were present in bacterial infections, a comparable level of PAP was detected in both groups. Upon resolution of infection (n = 29/40), platelet aggregation further deteriorated whereas coagulation and fibrinolysis factors returned to levels observed in patients without bacterial infections. CONCLUSION: In hospitalized patients with decompensated cirrhosis, bacterial infections are associated with reduced whole blood platelet aggregation and a significant decrease of all natural anticoagulants, which may unbalance hemostasis and potentially increase the risk of both bleeding and thrombosis. LAY SUMMARY: Bacterial infections are a common issue in hospitalized patients with decompensated cirrhosis (i.e. patients hospitalized due to severe complications of advanced chronic liver disease). Patients with decompensated cirrhosis who acquire infections may be at increased risk of bleeding complications following invasive procedures (that is a procedure in which the body is penetrated or entered, for instance by a needle or a tube). As bleeding complications in decompensated cirrhosis are associated with a high risk of further decompensation and death, there is an urgent need to understand the factors responsible for such increased bleeding tendency. Herein, we investigated the alterations of hemostasis (that is the physiological process responsible for clot formation and stability) in patients with decompensated cirrhosis and bacterial infections. We found that development of bacterial infections in these patients is associated with alterations of hemostasis (particularly of platelets and clotting cascade) that may increase the risk of both bleeding and thrombotic complications.
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spelling pubmed-91312542022-05-26 Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections Zanetto, Alberto Campello, Elena Bulato, Cristiana Gavasso, Sabrina Saggiorato, Graziella Shalaby, Sarah Burra, Patrizia Angeli, Paolo Senzolo, Marco Simioni, Paolo JHEP Rep Research Article BACKGROUND & AIMS: Bacterial infections in cirrhosis are associated with increased bleeding risk. To assess the factors responsible for bleeding tendency in patients with bacterial infections, we conducted a prospective study comparing all 3 aspects of hemostasis (platelets, coagulation, and fibrinolysis) in hospitalized patients with decompensated cirrhosis with vs. without bacterial infections. METHODS: Primary hemostasis assessment included whole blood platelet aggregation and von Willebrand factor (VWF). Coagulation assessment included procoagulant factors (fibrinogen, factor II, V, VII, VIII, IX, X, XI, XII, XIII), natural anticoagulants (protein C, protein S, antithrombin) and thrombomodulin-modified thrombin generation test. Fibrinolysis assessment included fibrinolytic factors (plasminogen, t-PA, PAI-1, α2-AP, TAFIa/ai) and plasmin-antiplasmin complex (PAP). RESULTS: Eighty patients with decompensated cirrhosis were included (40 with and 40 without bacterial infections). Severity of cirrhosis and platelet count were comparable between groups. At baseline, patients with cirrhosis and bacterial infections had significantly lower whole blood platelet aggregation, without significant differences in VWF. Regarding coagulation, bacterial infections were associated with reduced procoagulant factors VII and XII, and a significant reduction of all natural anticoagulants. However, thrombomodulin-modified thrombin generation was comparable between the study groups. Finally, although mixed potentially hypo-fibrinolytic (lower plasminogen) and hyper-fibrinolytic (higher t-PA) changes were present in bacterial infections, a comparable level of PAP was detected in both groups. Upon resolution of infection (n = 29/40), platelet aggregation further deteriorated whereas coagulation and fibrinolysis factors returned to levels observed in patients without bacterial infections. CONCLUSION: In hospitalized patients with decompensated cirrhosis, bacterial infections are associated with reduced whole blood platelet aggregation and a significant decrease of all natural anticoagulants, which may unbalance hemostasis and potentially increase the risk of both bleeding and thrombosis. LAY SUMMARY: Bacterial infections are a common issue in hospitalized patients with decompensated cirrhosis (i.e. patients hospitalized due to severe complications of advanced chronic liver disease). Patients with decompensated cirrhosis who acquire infections may be at increased risk of bleeding complications following invasive procedures (that is a procedure in which the body is penetrated or entered, for instance by a needle or a tube). As bleeding complications in decompensated cirrhosis are associated with a high risk of further decompensation and death, there is an urgent need to understand the factors responsible for such increased bleeding tendency. Herein, we investigated the alterations of hemostasis (that is the physiological process responsible for clot formation and stability) in patients with decompensated cirrhosis and bacterial infections. We found that development of bacterial infections in these patients is associated with alterations of hemostasis (particularly of platelets and clotting cascade) that may increase the risk of both bleeding and thrombotic complications. Elsevier 2022-04-20 /pmc/articles/PMC9131254/ /pubmed/35647501 http://dx.doi.org/10.1016/j.jhepr.2022.100493 Text en © 2022 The Author(s) https://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 Article
Zanetto, Alberto
Campello, Elena
Bulato, Cristiana
Gavasso, Sabrina
Saggiorato, Graziella
Shalaby, Sarah
Burra, Patrizia
Angeli, Paolo
Senzolo, Marco
Simioni, Paolo
Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections
title Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections
title_full Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections
title_fullStr Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections
title_full_unstemmed Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections
title_short Global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections
title_sort global hemostatic profiling in patients with decompensated cirrhosis and bacterial infections
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131254/
https://www.ncbi.nlm.nih.gov/pubmed/35647501
http://dx.doi.org/10.1016/j.jhepr.2022.100493
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