首页> 外文期刊>Critical care : >Reversal of Vitamin K Antagonist (VKA) effect in patients with severe bleeding: a French multicenter observational study (Optiplex) assessing the use of Prothrombin Complex Concentrate (PCC) in current clinical practice
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Reversal of Vitamin K Antagonist (VKA) effect in patients with severe bleeding: a French multicenter observational study (Optiplex) assessing the use of Prothrombin Complex Concentrate (PCC) in current clinical practice

机译:严重出血患者中维生素K拮抗剂(VKA)的作用逆转:一项法国多中心观察性研究(Optiplex)评估了凝血酶原复合物浓缩物(PCC)在当前临床实践中的使用

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IntroductionProthrombin Complex Concentrate (PCC) is a key treatment in the management of bleeding related to Vitamin K antagonists (VKA). This study aimed to evaluate prospectively PCC use in patients with VKA-related bleeding in view of the French guidelines published in 2008.MethodsAll consecutive patients with VKA-related bleeding treated with a 4-factor PCC (Octaplex?) were selected in 33 French hospitals. Collected data included demographics, site and severity of bleeding, modalities of PCC administration, International Normalized Ratio (INR) values before and after PCC administration, outcomes and survival rate 15 days after infusion.ResultsOf 825 patients who received PCC between August 2008 and December 2010, 646 had severe bleeding. The main haemorrhage sites were intracranial (43.7%) and abdominal (24.3%). Mean INR before PCC was 4.4 ± 1.9; INR was unavailable in 12.5% of patients. The proportions of patients who received a PCC dose according to guidelines were 15.8% in patients with initial INR 2-2.5, 41.5% in patients with INR 2.5-3, 40.8% in patients with INR 3-3.5, 26.9% in patients with INR > 3.5, and 63.5% of patients with unknown INR. Vitamin K was administered in 84.7% of patients. The infused dose of PCC did not vary with initial INR; the mean dose was 25.3 ± 9.8 IU/Kg. Rates of controlled bleeding and target INR achievement were similar, regardless of whether or not patients were receiving PCC doses as per the guidelines. No differences in INR after PCC treatment were observed, regardless of whether or not vitamin K was administered. INR was first monitored after a mean time frame of 4.5 ± 5.6 hours post PCC. The overall survival rate at 15 days after PCC infusion was 75.4% (65.1% in patients with intracranial haemorrhage). A better prognosis was observed in patients reaching the target INR.ConclusionsSevere bleeding related to VKA needs to be better managed, particularly regarding the PCC infused dose, INR monitoring and administration of vitamin K. A dose of 25 IU/kg PCC appears to be efficacious in achieving a target INR of 1.5. Further studies are required to assess whether adjusting PCC dose and/or better management of INR would improve outcomes.
机译:简介凝血酶原复合浓缩物(PCC)是治疗与维生素K拮抗剂(VKA)相关的出血的关键疗法。这项研究旨在根据2008年发布的法国指南对VKA相关性出血患者的PCC使用进行前瞻性评估。方法在33家法国医院中选择了所有接受4因子PCC(Octaplex?)治疗的VKA相关性出血患者。 。收集的数据包括人口统计学,出血部位和严重程度,PCC给药方式,PCC给药前后的国际标准化比率(INR)值,输注后15天的结局和生存率。结果2008年8月至2010年12月间825例接受PCC的患者646严重出血。主要出血部位为颅内(43.7%)和腹部(24.3%)。 PCC之前的平均INR为4.4±1.9; 12.5%的患者无法使用INR。最初接受INR 2-2.5的患者接受PCC剂量的比例为15.8%,INR 2.5-3的患者为41.5%,INR 3-3.5的患者为40.8%,INR 3-3.5的患者为26.9% > 3.5,有63.5%的INR未知患者。 84.7%的患者服用维生素K。 PCC的注入剂量不随初始INR而变化;平均剂量为25.3±9.8 IU / Kg。不管患者是否按照指南接受PCC剂量,控制出血率和目标INR达到率均相似。不论是否使用维生素K,在PCC治疗后均未观察到INR的差异。在PCC后平均时间4.5±5.6小时后,首先监测INR。 PCC输注后15天的总生存率为75.4%(颅内出血患者为65.1%)。达到目标INR的患者预后较好。结论与VKA相关的严重出血需要更好地处理,尤其是在PCC注入剂量,INR监测和维生素K给药方面。25IU / kg PCC剂量似乎有效以达到1.5的目标INR。需要进一步的研究来评估调整PCC剂量和/或更好地控制INR是否会改善预后。

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