Savioli Monica, Cugno Massimo, Polli Federico, Taccone Paolo, Bellani Giacomo, Spanu Paolo, Pesenti Antonio, Iapichino Gaetano, Gattinoni Luciano
Dipartimento di Anestesia, UO di Anestesia e Rianimazione, Rianimazione Intensiva e Subintensiva e Terapia del Dolore, Fondazione IRCCS, Ospedale Maggiore Policlinico, Mangiagalli, Regina Elena di Milano, Milan, Italy.
Crit Care Med. 2009 Feb;37(2):424-31. doi: 10.1097/CCM.0b013e31819542da.
To investigate whether tight glycemic control, in patients with sepsis, may restore a normal fibrinolysis by lowering plasminogen activator inhibitor (PAI)-1 levels.
Prospective randomized clinical trial.
Three Italian university hospital intensive care units.
Ninety patients with severe sepsis/septic shock.
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).
Inflammation, coagulation, and fibrinolysis markers were assessed, along with Sepsis-related Organ Failure Assessment scores, >28 days.
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.
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.
研究脓毒症患者严格控制血糖是否可通过降低纤溶酶原激活物抑制剂(PAI)-1水平来恢复正常纤溶功能。
前瞻性随机临床试验。
三家意大利大学医院重症监护病房。
90例严重脓毒症/脓毒性休克患者。
患者被随机分为接受严格血糖控制组(治疗组,目标血糖80 - 110mg/dL)或传统血糖控制组(对照组,目标血糖180 - 200mg/dL)。
评估炎症、凝血和纤溶标志物,以及脓毒症相关器官功能衰竭评估评分,随访时间>28天。
在全部研究对象中,入组时,90例患者中有超过80例炎症和凝血被激活,而通过PAI-1活性和浓度评估,仅34例患者纤溶功能受损。炎症反应程度或凝血激活程度与预后无关。相反,研究开始时纤溶功能明确受抑制的34例患者的90天死亡率是纤溶功能正常的5例患者的两倍(44%对21%,p = 0.02)。随机分组后,在研究期间,治疗组每日平均血糖为112±23mg/dL,对照组为159±31mg/dL(p < 0.001),每日胰岛素总用量分别为57±59IU和36±44IU(p < 0.001)。治疗组可观察到纤溶功能有轻微但显著的增强,PAI-1活性(p < 0.001)、PAI-1浓度(p = 0.004)和纤溶酶 - 抗纤溶酶复合物(p < 0.001)的时间进程表明了这一点。用脓毒症相关器官功能衰竭评估评分评定的发病率在治疗组显著降低(p = 0.03)。
在严重脓毒症/脓毒性休克中,纤溶功能抑制似乎具有重要的发病机制作用。在此背景下,严格血糖控制似乎可随时间减轻纤溶功能损害和发病率。