Hoffmann Johannes N, Mühlbayer Dieter, Jochum Marianne, Inthorn Dietrich
Department of Surgery, Klinikum Grosshadern, Munich, Germany.
Crit Care Med. 2004 Sep;32(9):1851-9. doi: 10.1097/01.ccm.0000139691.54108.1f.
Sepsis is frequently associated with coagulatory activation, which may contribute to deteriorated organ function. Antithrombin is one important endogenous coagulation inhibitor that is therapeutically applied during sepsis. This study investigates the effect of 14-day antithrombin application on coagulatory variables.
Prospective study.
Surgical intensive care unit of a university hospital.
Forty patients with severe sepsis.
Patients with severe sepsis were randomly assigned to receive either conventional intensive care treatment (n = 20, controls) or antithrombin substitution that aimed at a plasma antithrombin activity > or =120% during a long-term (14-day) study period (n = 20, antithrombin). To allow comparative analysis of laboratory variables over time, all patients who did not survive the 14-day-period (five controls and six antithrombin patients) were prospectively excluded from the final evaluation. Their data were included in an intent-to-treat analysis.
Antithrombin supplementation normalized global coagulation tests and increased prothrombin activity as well as fibrinogen concentration, reflecting less coagulation factor consumption (percent change from baseline in prothrombin activity, p <.01 vs. controls at days 9, 11-14 of antithrombin vs. controls [unpaired Student's t-test]; fibrinogen concentration, p <.01 vs. controls at days 10, 11, 13, and 14 of antithrombin). Simultaneously, antithrombin reduced contact system activation as indicated by increasing prekallikrein activities over time (% change, p <.01 vs. controls at days 6, 9-14) and increased protein C activities when compared with controls (% change, p <.01 vs. controls at days 10-14). Most changes occurred from day 7 to day 14 of antithrombin supplementation. Antithrombin did not influence C1 esterase inhibitor, plasminogen, alpha2 antiplasmin, or platelet counts (p >.01).
In this first study on long-term antithrombin therapy, antithrombin significantly reduced septic coagulatory response in patients with severe sepsis when given over 14 days.
脓毒症常伴有凝血激活,这可能导致器官功能恶化。抗凝血酶是一种重要的内源性凝血抑制剂,在脓毒症治疗中应用。本研究调查了14天应用抗凝血酶对凝血变量的影响。
前瞻性研究。
大学医院的外科重症监护病房。
40例严重脓毒症患者。
严重脓毒症患者被随机分配接受常规重症监护治疗(n = 20,对照组)或抗凝血酶替代治疗,在为期14天的研究期间,目标是使血浆抗凝血酶活性≥120%(n = 20,抗凝血酶组)。为了对实验室变量进行随时间的比较分析,所有未存活至14天的患者(5例对照组患者和6例抗凝血酶组患者)被前瞻性地排除在最终评估之外。他们的数据纳入意向性分析。
补充抗凝血酶使整体凝血试验正常化,并增加了凝血酶原活性以及纤维蛋白原浓度,反映出凝血因子消耗减少(凝血酶原活性相对于基线的百分比变化,抗凝血酶组在第9天、第11 - 14天与对照组相比,p <.01[非配对学生t检验];纤维蛋白原浓度,抗凝血酶组在第10天、第11天、第13天和第14天与对照组相比,p <.01)。同时,抗凝血酶减少了接触系统激活,这表现为随着时间的推移激肽释放酶原活性增加(百分比变化,抗凝血酶组在第6天、第9 - 14天与对照组相比,p <.01),并且与对照组相比,蛋白C活性增加(百分比变化,抗凝血酶组在第10 - 14天与对照组相比,p <.01)。大多数变化发生在补充抗凝血酶的第7天至第14天。抗凝血酶不影响C1酯酶抑制剂、纤溶酶原、α2抗纤溶酶或血小板计数(p >.01)。
在这项关于长期抗凝血酶治疗的首次研究中,给予严重脓毒症患者14天的抗凝血酶显著降低了脓毒症的凝血反应。