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Dive into the research topics where Saber Davide Barbar is active.

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Featured researches published by Saber Davide Barbar.


Critical Care | 2009

Procalcitonin kinetics within the first days of sepsis: relationship with the appropriateness of antibiotic therapy and the outcome

Pierre Emmanuel Charles; Claire Tinel; Saber Davide Barbar; Serge Aho; Sébastien Prin; Jean Marc Doise; Nils Olivier Olsson; Bernard Blettery; Jean Pierre Quenot

IntroductionManagement of the early stage of sepsis is a critical issue. As part of it, infection control including appropriate antibiotic therapy administration should be prompt. However, microbiological findings, if any, are generally obtained late during the course of the disease. The potential interest of procalcitonin (PCT) as a way to assess the clinical efficacy of the empirical antibiotic therapy was addressed in the present study.MethodsAn observational cohort study including 180 patients with documented sepsis was conducted in our 15-bed medical intensive care unit (ICU). Procalcitonin measurement was obtained daily over a 4-day period following the onset of sepsis (day 1 (D1) to D4). The PCT time course was analyzed according to the appropriateness of the first-line empirical antibiotic therapy as well as according to the patient outcome.ResultsAppropriate first-line empirical antibiotic therapy (n = 135) was associated with a significantly greater decrease in PCT between D2 and D3 (ΔPCT D2–D3) (-3.9 (35.9) vs. +5.0 (29.7), respectively; P < 0.01). In addition, ΔPCT D2–D3 was found to be an independent predictor of first-line empirical antibiotic therapy appropriateness. In addition, a trend toward a greater rise in PCT between D1 and D2 was observed in patients with inappropriate antibiotics as compared with those with appropriate therapy (+5.2 (47.4) and +1.7 (35.0), respectively; P = 0.20). The D1 PCT level failed to predict outcome, but higher levels were measured in the nonsurvivors (n = 51) when compared with the survivors (n = 121) as early as D3 (40.8 (85.7) and 21.3 (41.0), respectively; P = 0.04). Moreover, PCT kinetics between D2 and D3 were also found to be significantly different, since a decrease ≥ 30% was expected in the survivors (log-rank test, P = 0.04), and was found to be an independent predictor of survival (odds ratio = 2.94; 95% confidence interval 1.22 to 7.09; P = 0.02).ConclusionsIn our study in an ICU, appropriateness of the empirical antibiotic therapy and the overall survival were associated with a greater decline in PCT between D2 and D3. Further studies are needed to assess the utility of the daily monitoring of PCT in addition to clinical evaluation during the early management of sepsis.


Critical Care | 2011

Mild-stretch mechanical ventilation upregulates toll-like receptor 2 and sensitizes the lung to bacterial lipopeptide

Pierre-Emmanuel Charles; Pierre Tissières; Saber Davide Barbar; Delphine Croisier; Julien Dufour; Irène Dunn-Siegrist; Pascal Chavanet; Jérôme Pugin

IntroductionMechanical ventilation (MV) could prime the lung toward an inflammatory response if exposed to another insult such as bacterial invasion. The underlying mechanisms are not so far clear. Toll-like receptors (TLRs) allow the host to recognize selectively bacterial pathogens and in turn to trigger an immune response. We therefore hypothesized that MV modulates TLR2 expression and in turn modifies responsiveness to agonists such as bacterial lipopeptide (BLP).MethodBoth in vitro and in vivo experiments were conducted. First, TLR2 expression and protein were measured in the A549 pulmonary epithelial cell line submitted to 8-hour cyclic stretch (20% elongation; 20/minute rate). After a 24-hour period of cyclic stretch, the inflammatory response of the A549 cells to the synthetic BLP, Pam3CSK4, was tested after 8 hours of exposure. In a second set of experiments, healthy anesthetized and paralyzed rabbits were submitted to 8-hour MV (tidal volume = 12 ml/kg, zero end-expiratory pressure; FIO2 = 50%; respiratory rate = 20/minute) before being sacrificed for TLR2 lung expression assessment. The lung inflammatory response to BLP was then tested in animals submitted to 24-hour MV before being sacrificed 8 hours after the tracheal instillation of Pam3CSK4.ResultsCyclic stretch of human pulmonary epithelial cell lines increased both TLR2 mRNA and protein expression. Cells submitted to cyclic stretch also increased IL-6 and IL-8 secretion in response to Pam3CSK4, a classical TLR2 ligand. A mild-stretch MV protocol induced a 60-fold increase of TLR2 mRNA expression in lung tissue when compared with spontaneously breathing controls. Moreover, the combination of MV and airway exposure to Pam3CSK4 acted synergistically in causing lung inflammation and injury.ConclusionsMild-stretch MV increases lung expression of TLR2 and sensitizes the lung to bacterial TLR2 ligands. This may account for the propensity of mechanically ventilated patients to develop acute lung injury in the context of airway bacterial colonization/infection.


Trials | 2014

Comparison of heparin to citrate as a catheter locking solution for non-tunneled central venous hemodialysis catheters in patients requiring renal replacement therapy for acute renal failure (VERROU-REA study): study protocol for a randomized controlled trial

Rémi Bruyère; Agnès Soudry-Faure; Gilles Capellier; Christine Binquet; Abdelouaid Nadji; Stephane Torner; Gilles Blasco; Maria Yannaraki; Saber Davide Barbar; Jean-Pierre Quenot

BackgroundThe incidence of acute kidney injury (AKI) is estimated at 10 to 20% in patients admitted to intensive care units (ICU) and often requires renal replacement therapy (RRT). ICU mortality in AKI patients can exceed 50%. Venous catheters are the preferred vascular access method for AKI patients requiring RRT, but carry a risk of catheter thrombosis or infection. Catheter lock solutions are commonly used to prevent such complications. Heparin and citrate locks are both widely used for tunneled, long-term catheters, but few studies have compared citrate versus heparin for patients with short-term, non-tunneled catheters. We aim to compare citrate 4% catheter lock solution versus heparin in terms of event-free survival of the first non-tunneled hemodialysis catheter inserted in ICU patients with AKI requiring RRT. Secondary objectives are the rate of fibrinolysis, incidence of catheter thrombosis and catheter-related infection per 1,000 catheter days, length of stay in ICU and in-hospital and 28-day mortality.Methods/DesignThe VERROU-REA study is a randomized, prospective, multicenter, double-blind, parallel-group, controlled superiority study carried out in the medical, surgical and nephrological ICUs of two large university hospitals in eastern France. A catheter lock solution composed of trisodium citrate at 4% will be compared to unfractionated heparin at a concentration of 5,000 IU/mL. All consecutive adult patients with AKI requiring extracorporeal RRT, and in whom a first non-tunneled catheter is to be inserted by the jugular or femoral approach, will be eligible. Catheters inserted by the subclavian approach, patients with acute liver failure, thrombopenia or contraindication to systemic anticoagulation will be excluded. Patients will be followed up daily in accordance with standard practices for RRT until death or discharge.DiscussionData is scarce regarding the use of non-tunneled catheters in the ICU setting in patients with AKI. This study will provide an evidence base for recommendations regarding the use of anticoagulant catheter locks for the prevention of dysfunction in non-tunneled hemodialysis catheters in patients with AKI in critical or intensive care.Trial registrationRegistered with Clinicaltrials.gov (registration number: NCT01962116) on 27 August 2013.


Trials | 2014

Impact on mortality of the timing of renal replacement therapy in patients with severe acute kidney injury in septic shock: the IDEAL-ICU study (initiation of dialysis early versus delayed in the intensive care unit): study protocol for a randomized controlled trial

Saber Davide Barbar; Christine Binquet; Mehran Monchi; Rémi Bruyère; Jean-Pierre Quenot


Intensive Care Medicine | 2012

Suffering among carers working in critical care can be reduced by an intensive communication strategy on end-of-life practices

Jean-Pierre Quenot; Jean-Philippe Rigaud; Sébastien Prin; Saber Davide Barbar; Arnaud Pavon; Mael Hamet; Nicolas Jacquiot; Bernard Blettery; Christian Hervé; Pierre Charles; Grégoire Moutel


Intensive Care Medicine | 2012

Impact of an intensive communication strategy on end-of-life practices in the intensive care unit

Jean-Pierre Quenot; Jean-Philippe Rigaud; Sébastien Prin; Saber Davide Barbar; Arnaud Pavon; Mael Hamet; Nicolas Jacquiot; Bernard Blettery; Christian Hervé; Pierre Charles; Grégoire Moutel


Intensive Care Medicine | 2010

Toll-like receptors: a link between mechanical ventilation, innate immunity and lung injury?

Pierre Emmanuel Charles; Saber Davide Barbar


Réanimation | 2015

Le choc septique de l’adulte en France : vingt ans de données épidémiologiques

Jean-Pierre Quenot; A. Pavon; I. Fournel; Saber Davide Barbar; R. Bruyère


Réanimation | 2016

Gestion de la durée de l’antibiothérapie selon les résultats des biomarqueurs

Jean-Pierre Quenot; A. Large; Auguste Dargent; P. Andreu; R. Bruyère; Saber Davide Barbar; Pierre-Emmanuel Charles


Réanimation | 2015

Critères d’initiation de l’épuration extrarénale en réanimation : peut-on se permettre d’attendre ?

Jean-Pierre Quenot; A. Large; R. Bruyère; Saber Davide Barbar

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Pierre Charles

Paris Descartes University

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Mael Hamet

University of Burgundy

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R. Bruyère

University of Burgundy

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Grégoire Moutel

Paris Descartes University

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