重组活化因子VII作为产后出血的二线治疗

S. Park, S. Yeom, S. Han, Y. Jo, H. Kim
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引用次数: 2

摘要

几十年来,严重或大量产后出血(PPH)一直是全世界孕产妇死亡的主要原因之一,并可导致严重的产科并发症。重组活化因子VII (rFVIIa)已成为治疗传统疗法难治性危及生命的PPH的金标准辅助止血剂,尽管它在PPH中的使用仍未获得许可。我们研究了rFVIIa对韩国PPH患者凝血功能、输血量、预后、严重程度变化的影响。方法回顾性分析2008年12月至2011年3月间使用rFVIIa治疗重度PPH的病例。我们比较了SOFA评分为8分或更高的患者到达急诊科时和24小时后的年龄、rfvia治疗、输血量和顺序器官衰竭评估(SOFA)评分。结果SOFA评分8分及以上的15名妇女参加了本研究,其中8名接受了rFVIIa治疗,7名未接受rFVIIa治疗。患者平均年龄31.7±7.5岁。给予或未给予rFVIIa的患者的初始和24小时后SOFA评分无统计学差异。在给予rFVIIa后,SOFA评分在首次出现和24小时后的变化显著降低(P = 0.016)。结论本分析旨在支持给予rFVIIa可降低危及生命的PPH患者的严重程度。对于没有有效标准治疗的严重PPH患者,需要迅速决定是否给予rFVIIa,以获得更有利的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage
Background Severe or massive postpartum hemorrhage (PPH) has remained a leading cause of maternal mortality for decades across the world and it results in critical obstetric complications. Recombinant activated factor VII (rFVIIa) has emerged as a gold standard adjunctive hemostatic agent for the treatment of life-threatening PPH refractory to conventional therapies although it remains off-licensed for use in PPH. We studied the effects of rFVIIa on coagulopathy, transfusion volume, prognosis, severity change in Korean PPH patients. Methods A retrospective review of medical records between December 2008 and March 2011 indicating use of rFVIIa in severe PPH was performed. We compared age, rFVIIa treatment, transfusion volume, and Sequential Organ Failure Assessment (SOFA) score at the time of arrival in the emergency department and after 24 hours for patients whose SOFA score was 8 points or higher. Results Fifteen women with SOFA score of 8 and above participated in this study and eight received rFVIIa administration whereas seven did not. Patients’ mean age was 31.7 ± 7.5 years. There was no statistically significant difference in initial and post-24 hours SOFA scores between patients administered rFVIIa or not. The change in SOFA score between initial presentation and after 24 hours was significantly reduced after rFVIIa administration (P = 0.016). Conclusions This analysis aimed to support that the administration of rFVIIa can reduce the severity of life-threatening PPH in patients. A rapid decision regarding the administration of rFVIIa is needed for a more favorable outcome in severe PPH patients for whom there is no effective standard treatment.
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