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Showing papers by "Jacques Duranteau published in 2005"


Journal ArticleDOI
TL;DR: In trauma patients and in septic shock patients, norepinephrine clearance is negatively related to SAPS II, and group, gender, and BW did not influence CL or V.
Abstract: Background There is considerable variability in the inter-patient response to norepinephrine. Pharmacokinetic studies of dopamine infusion in volunteers and in patients have also shown large variability. The purpose of this study was to define the pharmacokinetics of norepinephrine in septic shock and trauma patients. Methods After Ethical Committee approval and written informed family consent, 12 patients with septic shock and 11 trauma patients requiring norepinephrine infusion were studied. Norepinephrine dose was increased in three successive steps of 0.1 mg kg−1 min−1 at 15-min intervals (20% maximum allowed increase in arterial pressure). Arterial blood was sampled before and at 0.5, 13, and 15 min after each infusion rate change and 30 s, 1, 2, 5, 10, and 15 min after return to baseline dosing. Norepinephrine was assayed by HPLC. The pharmacokinetics were modelled using NONMEM (one-compartment model). The effects of group, body weight (BW), gender and SAPS II (Simplified Acute Physiology Score II) [Le Gall JR, Lemeshow S, Saulnier F. A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. J Am Med Assoc 1993; 270: 2957–63] patients score on clearance (CL) and volume of distribution (V) were tested. Results Group, gender, and BW did not influence CL or V. CL was negatively related to SAPS II. CL and T1/2 varied from 3 litre min−1 and 2 min, respectively, when SAPS II=20 to 0.9 litre min−1 and 6.8 min when SAPS II=60. Conclusion In trauma patients and in septic shock patients, norepinephrine clearance is negatively related to SAPS II.

86 citations


Journal ArticleDOI
TL;DR: In endothelial cells submitted to hypoxia and glucose depletion followed by reoxygenation with glucose, the pathway implicated in mitochondrial complex III ROS production is ceramide dependent and is decreased by the antiapoptotic protein Bcl-2.
Abstract: In endothelium, reoxygenation after hypoxia (H/R) has been shown to induce production of reactive oxygen species (ROS) by complex III of the mitochondrial respiratory chain. The purpose of the pres...

55 citations


Journal ArticleDOI
TL;DR: The current use of recombinant activated factor VII (rFVIIa; NovoSeven®) in trauma patients is described and emphasis is placed on current uses as defined by key studies, efficacy data, and safety data.
Abstract: In this article we describe the current use of recombinant activated factor VII (rFVIIa; NovoSeven®) in trauma patients. Emphasis is placed on current uses as defined by key studies, efficacy data, and safety data. Most published studies in trauma patients are retrospective case studies and reports, although an international, double-blind, randomized, controlled, phase II study has been conducted that reported on the efficacy of rFVIIa in reducing the amount of blood products transfused in blunt trauma patients. That study demonstrated the efficacy and safety profile of this hemostatic agent as compared with placebo as adjunctive therapy in the management of severe bleeding associated with trauma. Further prospective, randomized, and placebo-controlled clinical trials will yield more information on the role of rFVIIa in the management of traumatic bleeding.

39 citations


Journal ArticleDOI
TL;DR: Serum from trauma patients with hemorrhagic shock induces reactive oxygen species formation in naive endothelial cells which is correlated to shock severity which is strongly correlated positively to Simplified Acute Physiology Score II and lactatemia and negatively to [HCO3−].
Abstract: Objective Shock induces oxidative stress by ischemia-reperfusion phenomenon. Endothelial cells are involved in the inflammatory response and oxidative stress responsible for microcirculation impairment and organ failure. We examined the potential of serum from patients to induce in vitro reactive oxygen species production by cultured human umbilical vein endothelial cells (HUVECs).

32 citations