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No effect of tranexamic acid on platelet function and thrombin generation (ETAPlaT) in postpartum haemorrhage: a randomised placebo-controlled trial

机译:氨甲环酸对产后出血的血小板功能和凝血酶生成(ETAPlaT)无影响:一项随机安慰剂对照试验

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摘要

>Background: Postpartum hemorrhage (PPH) is a leading cause of maternal mortality and morbidity. The WOMAN trial showed that tranexamic acid (TXA) reduces death due to bleeding in women with PPH. To determine whether TXA has pro-thrombotic effects in women with PPH, we measured endogenous thrombin potential (ETP), coagulation factors V, VIII, von Willebrand (vW), fibrinogen, D-Dimers and platelet function. >Methods: We conducted a sub-study within the WOMAN trial, an international randomized, parallel-group, double blind, placebo-controlled trial. Women with primary PPH were randomly allocated to receive 1 gram of tranexamic acid or matching placebo. Baseline blood samples were collected just prior to the first dose and a follow up sample was collected 30±15 minutes afterwards. We compared before and after changes in coagulation parameters between treatment groups using repeated measurement ANOVA. Change in ETP was the primary outcome. We did an intention-to-treat analysis using ANCOVA with adjustment for baseline and the time interval between the blood samples. >Findings: A total of 187 patients were randomized to receive TXA (n=93) or matching placebo (n=94). Six patients were excluded due to incomplete data. The reduction in ETP from baseline to follow up was 43.2 nM*min (95%CI, -16.6 to 103.1) in the TXA group and 4.6 nM*min (95%CI, -51.4 to 60.6) in the placebo group. The difference was not statistically significant (95%CI, -42.9 to 120). There were no significant effects of TXA treatment on any other parameters (ADPtest, TRAPtest, coagulation factors activity, fibrinogen levels, D-Dimer level). >Conclusion: We found no evidence that tranexamic acid treatment for PPH has substantial pro-coagulant effects. However, larger studies are needed to confirm or refute more modest effects. >Trial registration: (initially registered 10/12/2008, WOMAN-ETAPlat included on 28/10/2013) and (initially registered 31/03/2009, WOMAN-ETAPlat included on 28/10/2013).
机译:>背景:产后出血(PPH)是孕产妇死亡和发病的主要原因。 WOMAN试验显示,氨甲环酸(TXA)减少了PPH妇女因出血引起的死亡。为了确定TXA对PPH妇女是否具有促血栓形成作用,我们测量了内源性凝血酶电位(ETP),凝血因子V,VIII,血管性血友病(vW),纤维蛋白原,D-二聚体和血小板功能。 >方法:我们在WOMAN试验中进行了一项子研究,该试验是一项国际随机,平行分组,双盲,安慰剂对照试验。患有原发性PPH的女性被随机分配接受1克氨甲环酸或相匹配的安慰剂。在第一次给药之前收集基线血样,然后在30±15分钟后收集随访样本。我们使用重复测量方差分析比较了治疗组之间凝血参数变化前后的差异。 ETP的变化是主要结果。我们使用ANCOVA进行了意向性治疗分析,并调整了基线和血样之间的时间间隔。 >发现:总共187例患者被随机分配接受TXA(n = 93)或匹配的安慰剂(n = 94)。由于数据不完整,排除了六名患者。 TXA组从基线到随访的ETP降低为43.2 nM * min(95%CI,-16.6至103.1),安慰剂组为4.6nM * min(95%CI,-51.4至60.6)。差异无统计学意义(95%CI,-42.9至120)。 TXA治疗对任何其他参数(ADPtest,TRAPtest,凝血因子活性,纤维蛋白原水平,D-二聚体水平)均无显着影响。 >结论:我们没有发现证据表明氨甲环酸治疗PPH具有明显的促凝血作用。但是,需要更大的研究来确认或驳斥更为温和的影响。 >试用注册:(初始注册时间为2008年10月12日,WOMAN-ETAPlat包含于2013年10月28日)和(初始注册的时间为2009年3月31日,WOMAN-ETAPlat包含于2013年10月28日)。

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