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首页> 外文期刊>Intensive care medicine >Antithrombin III in patients with severe sepsis. A randomized, placebo-controlled, double-blind multicenter trial plus a meta-analysis on all randomized, placebo-controlled, double-blind trials with antithrombin III in severe sepsis (see comments)
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Antithrombin III in patients with severe sepsis. A randomized, placebo-controlled, double-blind multicenter trial plus a meta-analysis on all randomized, placebo-controlled, double-blind trials with antithrombin III in severe sepsis (see comments)

机译:重度脓毒症患者的抗凝血酶III。一项随机,安慰剂对照,双盲,多中心试验以及对所有严重脓毒症中使用抗凝血酶III的随机,安慰剂对照,双盲试验进行荟萃分析(请参阅评论)

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OBJECTIVES: To evaluate the safety and potential efficacy of antithrombin III (AT III) in reducing mortality in patients with severe sepsis. DESIGN: Prospective, randomized, placebo-controlled, double-blind, phase II, multicenter, multinational clinical trial. SETTING: Seven academic medical center intensive care units (ICU) in Belgium, Denmark, the Netherlands, Norway and Sweden. PATIENTS: 42 patients with severe sepsis who received standard supportive care and antimicrobial therapy, in addition to the administration of AT III or placebo. INTERVENTIONS: Patients received either an intravenous loading dose of 3000 IU AT III followed by a maintenance dose of 1500 IU every 12 h for 5 days or equivalent amounts of placebo. MEASUREMENTS AND RESULTS: All patients were evaluated for safety and for 30-day all-cause mortality. CONCLUSIONS: The administration of AT III was safe and well-tolerated. It was followed by a 39 % reduction in 30-day all-cause mortality (NS). The reduction in mortality was accompanied by a considerably shorter stay in the ICU. Patients treated with AT III exhibited a better performance in overall severity of illness and organ failure scores (Acute Physiology and Chronic Health Evaluation II, multiple organ failure, organ system failure), which was noticeable soon after initiation of treatment. Patients treated with AT III demonstrated a better resolution of pre-existing organ failures and a lower incidence of new organ failures during the observation period. A meta-analysis comprising this and two other double-blind, placebo-controlled trials with AT III with a total of 122 patients suffering from severe sepsis confirms the positive trend. The results of the meta-analysis demonstrate a 22.9 % reduction in 30-day all-cause mortality in patients treated with AT III. Although still too small to be confirmative, the meta-analysis clearly points to the fact that a sufficiently powered phase III trial is warranted to prove whether AT III has a beneficial role in the treatment of severe sepsis.
机译:目的:评估抗凝血酶III(AT III)降低严重脓毒症患者死亡率的安全性和潜在疗效。设计:前瞻性,随机,安慰剂对照,双盲,II期,多中心,跨国临床试验。地点:比利时,丹麦,荷兰,挪威和瑞典的七个学术医疗中心重症监护室(ICU)。患者:42例严重脓毒症患者,除接受AT III或安慰剂治疗外,还接受了标准的支持治疗和抗菌治疗。干预措施:患者接受静脉内负荷剂量为3000 IU AT III,然后每12小时维持剂量1500 IU,持续5天或同等剂量的安慰剂。测量与结果:对所有患者的安全性和30天全因死亡率进行了评估。结论:AT III的给药安全且耐受性良好。随后,其30天全因死亡率(NS)降低了39%。死亡率的降低伴随着在ICU中的停留时间大大缩短。用AT III治疗的患者在总体疾病严重程度和器官衰竭评分(急性生理和慢性健康评估II,多器官衰竭,器官系统衰竭)方面表现更好,这在开始治疗后不久就很明显。在观察期间,接受AT III治疗的患者表现出更好的解决先前存在的器官衰竭的能力,并降低了新器官衰竭的发生率。一项荟萃分析,包括该研究以及另外两项针对AT III的双盲,安慰剂对照试验,总共有122名患有严重败血症的患者证实了这一积极趋势。荟萃分析的结果表明,接受AT III治疗的患者30天全因死亡率降低了22.9%。尽管仍太小而无法确定,但荟萃分析清楚地表明了这样一个事实,即有足够能力进行的III期临床试验有必要证明AT III在严重脓毒症的治疗中是否具有有益作用。

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