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INTRODUCTION: Sepsis, responsible for 2% of ail hospital admissions in one year, has a 30% mortality rate in Intensive Care Units (ICU). Several scores are used to evaluate critical patients and their prognosis. The SOFA score helps to establish the importance of organic dysfonctions and is based on six criteria. One of these criteria is the bilirubin level. During a sepsis, a pathologie level of bi lirubin is associated with a higher risk of death. However the overall evaluation of the liver fonction is important for the prognosis. The main purpose of this study is to determine which enzyme or metabolic product is correlated to a higher risk of death during a septic shock. METHOD: We conducted a prospective study including 100 adult patients hospitalised in the ICU of Saint-Luc Hospital from 20 11 to 2013. Among them, 50 patients presented a severe sepsis or a septic shock. We measured the levels of bilirubin, lactate, INR, glycemia and hepatic enzymes during their hospitalisation period in the ICU. This group was compared to 30 patients who underwent a hepatic transplant, and to 20 patients who had a cardiac surgery and a subsequent vasopressor treatment. The same biologie parameters were measured for those two groups. RESULTS AND DISCUSSION: On average the hospital isation period in ICU of patients with severe sepsis and septic shock lasted for 8, 3 days, with a mortality rate of 30%. Patients who underwent a liver transplant stayed in ICU for 5, 2 days and the mortality after the surgery was 10%.The bilirubin level of patients who died due to sepsis (5,21 mg/dl) is similar to the bilirubin of patients who left the ICU after the liver transplant (5,39 mg/dl). Among septic patients there is a significant difference between the bilirubin levels of patients who died (5,21 mg/dl) compared to those who survived (1,05 mg/dl). On the other hand, among the patients who had a liver transplant, the bilirubin levels were similar in patients who died (5,37 mg/dl) and patients who survived (5,39 mg/dl). We concluded that the bilirubin is not a good prognostic factor after a liver transplant. The death of septic patients occurs with a lactate level 2, 6 times higher than for those who recover (respectively 5, 92 and 2, 27 mmol/l). The same conclusion can be done for the liver transplants, where the lactate level is 2, 68 mmol/l among the recovery group and 9,82 mmol/l for the patients who
Shock, Septic
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Hepatic Insufficiency
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Sepsis
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Shock, Septic --- Coronary Circulation --- physiopathology --- drug effects
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Drotrecongin alpha activated, marketed under the name of Xigris®, is a drug for the treatment of the septic shock in the adult presenting with at least two organ failures. This drug was put on the market under exceptional circumstances, therefore it is discussed every year. Indeed, when the drug was put on the market, only one study had shown the effectiveness of Xigris®. Thereafter, many studies have failed to show efficacy in other patient groups. On the other hand, it was shown that Xigris® could involve serious adverse drug effects such as hemorrhage. This serious undesirable effect weighs much in the benefit/risk balance of Xigris®. The different studies published helped to clearly define the patients in which the drug should be used (for example …). The question remains open: Is it necessary to continue to use this drug for the treatment of the severe sepsis knowing that it has a big risk of undesirable effect and that there is no existing alternative for the moment? Studies are still ongoing and further results will be available in 2011 La drotrecogin alpha active, commercialisée sous le nom de Xigris®, est un médicament indiqué dans le traitement du choc septique chez l’adulte présentant au moins deux défaillances d’organes. Ce médicament a été mis sur le marché avec circonstance exceptionnelle, ce qui signifie que sa balance risques-bénéfices doit être rediscutée chaque année. En effet, lors de l’obtention de son AMM (autorisation de mise sur le marché), seule une étude avait démontré l’efficacité du Xigris®. Depuis, les études réalisées n’ont pu démontrer une efficacité supérieure à celle déjà annoncée. Par contre, il a été montré que le Xigris® pouvait entraîner des risques de saignements sérieux. Cet effet indésirable sérieux pèse lourdement dans la balance bénéfice/risque du Xigris®. Les différentes études ont permis de préciser les conditions d’utilisations strictes de cette molécule (à savoir …). En terme de pharmacovigilance la question est donc ouverte : faut il continuer à utiliser ce médicament pour le traitement du sepsis sévère sachant qu’il a un risque important d’effet indésirables et qu’il n’existe aucune alternative pour le moment ? Des études sont toujours en cours et les premiers résultats seront publiés pour le deuxième quadrimestre 2011
Sepsis --- Drug Toxicity --- Shock, Septic --- Adult --- drotrecogin alfa activated
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Acute Disease --- Shock, Septic --- Kallikreins --- Aprotinin --- enzymology --- analysis --- blood
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