Iba Toshiaki, Saitoh Daizoh, Wada Hideo, Asakura Hidesaku
Crit Care. 2014 Sep 15;18(5):497. doi: 10.1186/s13054-014-0497-x.
In a previous report, we demonstrated a favorable trend for supplementation with antithrombin (AT) concentrate at a dosage of 3,000 IU/day over 1,500 IU/day for the treatment of sepsis-associated disseminated intravascular coagulation (DIC) in patients with an AT activity of 70% or less. Since the survival difference did not reach statistical significance, we planned to examine the effects in a larger number of cases with severer disease.
We performed a non-randomized multi-institutional survey. In total, 307 septic DIC patients who had AT activity less than 40% and who had undergone AT substitution at a dose of either 1,500 IU/day or 3,000 IU/day for three consecutive days were analyzed. Of these, 259 patients received 1,500 IU/day (AT1500 group) and 48 patients received 3,000 IU/day (AT3000 group). The primary efficacy endpoints were recovery from DIC by day 7 and an all-cause mortality on day 28. Adverse bleeding events were also examined. A logistic regression analysis was conducted by using age, sex, body weight, initial AT activity, DIC score, platelet count, coadministration of heparin, recombinant thrombomodulin, suspected source of infection, surgery, and supplemented AT dose.
Supplementation significantly decreased the DIC score in the AT3000 group, leading to the superior resolution of DIC, compared with the results in the AT1500 group (66.7% versus 45.2%, P = 0.007). In addition, the AT3000 group exhibited a better survival than the AT1500 group (77.1% versus 56.4%, P = 0.010). Bleeding events were observed in 6.96% (severe bleeding: 3.04%) in the AT1500 group and 6.52% (severe bleeding, 4.35%) in the AT3000 group (P = 1.000; severe bleeding, P = 0.648). A logistic regression analysis revealed that the use of AT3000 (odds ratio (OR), 2.419; P = 0.025), a higher initial platelet count (OR, 1.054; P = 0.027), and patient age (OR, 0.977; P = 0.045) were significantly correlated with an improved survival.
The AT3000 group exhibited significantly improved rates of survival and recovery from DIC without an increased risk of bleeding, compared with the AT1500 group, among the patients with sepsis-associated DIC and an AT activity of less than 40%.
在之前的一份报告中,我们证明了对于抗凝血酶(AT)活性为70%或更低的脓毒症相关弥散性血管内凝血(DIC)患者,以3000 IU/天的剂量补充AT浓缩物优于1500 IU/天的剂量。由于生存差异未达到统计学显著性,我们计划在更多病情更严重的病例中研究其效果。
我们进行了一项非随机的多机构调查。总共分析了307例AT活性低于40%且连续三天接受1500 IU/天或3000 IU/天AT替代治疗的脓毒症DIC患者。其中,259例患者接受1500 IU/天(AT1500组),48例患者接受3000 IU/天(AT3000组)。主要疗效终点为第7天DIC恢复以及第28天全因死亡率。还检查了不良出血事件。通过使用年龄、性别、体重、初始AT活性、DIC评分、血小板计数、肝素、重组血栓调节蛋白的联合使用、疑似感染源、手术以及补充的AT剂量进行逻辑回归分析。
与AT1500组相比,AT3000组补充AT后DIC评分显著降低,DIC得到更好的缓解(66.7%对45.2%,P = 0.007)。此外,AT3000组的生存率高于AT1500组(77.1%对56.4%,P = 0.010)。AT1500组出血事件发生率为6.96%(严重出血:3.04%),AT3000组为6.52%(严重出血,4.35%)(P = 1.000;严重出血,P = 0.648)。逻辑回归分析显示,使用AT3000(比值比(OR),2.419;P = 0.025)、较高的初始血小板计数(OR = 1.054;P = 0.027)以及患者年龄(OR = 0.977;P = 0.045)与生存率提高显著相关。
在脓毒症相关DIC且AT活性低于40%的患者中,与AT1500组相比,AT3000组的生存率和DIC恢复率显著提高,且出血风险未增加。