Selenium, systemic immune response syndrome, sepsis, and outcome in critically ill patients

被引:252
作者
Forceville, X
Vitoux, D
Gauzit, R
Combes, A
Lahilaire, P
Chappuis, P
机构
[1] Ctr Hosp Meaux, Dept Med & Surg Intens Care, F-77104 Meaux, France
[2] Hop Lariboisiere, Ctr Rech Claude Bernard, Serv Biochim & Biol Mol, F-75475 Paris, France
关键词
selenium; free radicals; glutathione peroxidase; systemic inflammatory response syndrome; sepsis; septic shock; cell hypoxia; organ failure; nosocomial pneumonia; hospital mortality;
D O I
10.1097/00003246-199809000-00021
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objectives: To confirm early, marked decrease in plasma selenium concentrations in patients admitted to a surgical and medical intensive care unit (ICU), and to study this decrease according to the presence or absence of systemic inflammatory response syndrome (SIRS), sepsis, or direct ischemia-reperfusion. Design: Prospective, observational study. Settings: Collaboration between the adult ICU of a 1,100-bed general hospital and a biochemical research laboratory of a university medical center. Patients: One hundred thirty-four consecutive surgical and medical ICU patients. Interventions: None. Measurements and Main Results: In the first 31 patients, plasma and urine selenium concentrations were measured by electrothermal atomic absorption spectrometry on admission and once weekly during their ICU stay. These values were compared first with severity scores, criteria for SIPS, sepsis, and organ system failure taken on admission, and then with nosocomial infection, organ system failure during ICU stay, and hospital mortality. An early, low mean plasma selenium concentration was observed in these patients compared with selenium laboratory reference values. Plasma selenium, measured on ICU admission, inversely correlated with Acute Physiology and Chronic Health Evaluation II or Simplified Acute Physiology I! scores. Patients with SIPS had lower selenium concentrations than those without SIPS. Mean urine selenium losses were normal in the first 31 patients. Plasma selenium concentration was low in all patients with severe sepsis and septic shock (range 0.20 to 0.72 mu mol/L) and in those patients with ischemia-reperfusion from aortic cross-clamping (range 0.34 to 0.68 mu mol/L). Despite recommended specific selenium supplementation, plasma selenium concentrations remained low for >2 wks in patients with SIPS. However, there was a slight increase in plasma selenium concentrations in surviving SIPS patients, whereas plasma selenium concentrations decreased in nonsurviving patients. The frequency of ventilator-associated pneumonia, organ system failure, and mortality was three times higher in patients with low plasma selenium concentration at the time of admission (selenium less than or equal to 0.70 mu mol/L) than for the other patients. Conclusions: In severely ill ICU patients with SIPS, we observed an early 40% decrease in plasma selenium concentrations, reaching values observed in deleterious nutritional selenium deficiency. This prolonged decrease in selenium concentrations could explain the three-fold increase in morbidity and mortality rates in these patients compared with other ICU patients. The efficacy of selenium treatment in SIPS patients with a high gravity index score or hypoperfusion needs further investigation. (Crit Care Med 1998; 26:1536-1544).
引用
收藏
页码:1536 / 1544
页数:9
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