Tight glycemic control may favor fibrinolysis in patients with sepsis

被引:57
作者
Savioli, Monica [1 ]
Cugno, Massimo [2 ]
Polli, Federico [3 ]
Taccone, Paolo [1 ]
Bellani, Giacomo [4 ]
Spanu, Paolo [5 ]
Pesenti, Antonio [4 ]
Iapichino, Gaetano [3 ,5 ]
Gattinoni, Luciano [1 ,3 ]
机构
[1] Osped Maggiore Policlin, Fdn IRCCS, Dipartimento Anestesia, UO Anestesia & Rianimaz, Milan, Italy
[2] Univ Milan, Dept Internal Med, Milan, Italy
[3] Univ Milan, Ist Anestesiol & Rianimaz, Milan, Italy
[4] Univ Milano Bicocca, Azienda Osped San Gerardo Monza, Dipartimento Med Sperimentale, Dipartimento Med Perioperatoria & Terapia Intens, Milan, Italy
[5] Polo Univ Sao Paolo, Azienda Osped, UO Anestesia & Rianimaz, Milan, Italy
关键词
sepsis; shock; septic; fibrinolysis; plasminogen activator inhibitor 1; blood glucose; tight glucose control; TUMOR-NECROSIS-FACTOR; INTENSIVE INSULIN THERAPY; DISSEMINATED INTRAVASCULAR COAGULATION; PLACEBO-CONTROLLED TRIAL; RECEPTOR FUSION PROTEIN; PLASMINOGEN-ACTIVATOR; DOUBLE-BLIND; MONOCLONAL-ANTIBODY; SEPTIC SHOCK; FACTOR-ALPHA;
D O I
10.1097/CCM.0b013e31819542da
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Objective: To investigate whether tight glycemic control, in patients with sepsis, may restore a normal fibrinolysis by lowering plasminogen activator inhibitor (PAI)-1 levels. Design: Prospective randomized clinical trial. Setting: Three Italian university hospital intensive care units. Patients: Ninety patients with severe sepsis/septic shock. Interventions: Patients were randomized to receive either tight glycemic control (treatment group, target glycemia, 80-110 mg/ dL) or conventional glycemic control (control group, target glycemia, 180-200 mg/dL). Measurements: Inflammation, coagulation, and fibrinolysis markers were assessed, along with Sepsis-related Organ Failure Assessment scores, >28 days. Main Results. In the whole population, at enrolment, inflammation and coagulation were activated in >80 of 90 patients, whereas fibrinolysis, as assessed by PAI-1 activity and concentration, was impaired in only 34 patients. The extent of the inflammatory reaction or of the coagulation activation was unrelated to outcome. In contrast, 90-day mortality rate of the 34 patients in whom fibrinolysis was definitely inhibited at study entry was twice that of the 56 patients in whom fibrinolysis was intact (44% vs. 21%, p = 0.02). After randomization, during the study, daily glycemia averaged 112 +/- 23 mg/dL in the treatment group and 159 +/- 31 mg/dL in controls (p < 0.001), with total daily administered insulin 57 +/- 59 IU and 36 +/- 44 IU, respectively (p < 0.001). A small, but significant, enhancement of fibrinolysis could be observed in the treatment group, as indicated by the time course of PAI-1 activity (p < 0.001), PAI-1 concentration (p = 0.004), and plasmin-antiplasmin complexes (p < 0.001). Morbidity, rated with the Sepsis-related Organ Failure Assessment score, became significantly lower (p = 0.03) in the treatment group. Conclusions: Fibrinolysis inhibition, in severe sepsis/septic shock, seems to have a relevant pathogenetic role. In this context, tight glycemic control seems to reduce, with time, the fibrinolytic impairment and morbidity. (Crit Care Med 2009; 37:424-431)
引用
收藏
页码:424 / 431
页数:8
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