Suppr超能文献

抑制纤维蛋白溶解需要何种浓度的氨甲环酸?一项药效学研究的系统评价

What concentration of tranexamic acid is needed to inhibit fibrinolysis? A systematic review of pharmacodynamics studies.

作者信息

Picetti Roberto, Shakur-Still Haleema, Medcalf Robert L, Standing Joseph F, Roberts Ian

机构信息

Clinical Trials Unit, London School of Hygiene and Tropical Medicine, London, UK.

Australian Centre for Blood Diseases, Central Clinical School, Monash University, Melbourne, Victoria, Australia.

出版信息

Blood Coagul Fibrinolysis. 2019 Jan;30(1):1-10. doi: 10.1097/MBC.0000000000000789.

Abstract

: Intravenous tranexamic acid (TXA) reduces death because of bleeding in patients with trauma and postpartum haemorrhage. However, in some settings intravenous injection is not feasible. To find different routes of administration, we first need to determine the minimal concentration of TXA in the blood that is required to inhibit fibrinolysis.We conducted a systematic review of in-vitro and in-vivo pharmacodynamics studies. We searched MEDLINE, EMBASE, OviSP, and ISI Web of Science from database inception to November 2017 for all in-vitro (including simulated clotting models) or in-vivo studies reporting the relationship between the TXA concentration in blood or plasma and any reliable measure of fibrinolysis.We found 21 studies of which 20 were in vitro and one was in vivo. Most in-vitro studies stimulated fibrinolysis with tissue plasminogen activator and measured fibrinolysis using viscoelastic, optical density, or immunological assays. TXA concentrations between 10 and 15 mg/l resulted in substantial inhibition of fibrinolysis, although concentrations between 5 and 10 mg/l were partly inhibitory.TXA concentrations of 10-15 mg/l may be suitable targets for pharmacokinetic studies, although TXA concentrations above 5 mg/l may also be effective.

摘要

静脉注射氨甲环酸(TXA)可降低创伤患者和产后出血患者因出血导致的死亡风险。然而,在某些情况下,静脉注射并不可行。为了找到不同的给药途径,我们首先需要确定抑制纤维蛋白溶解所需的血液中TXA的最低浓度。我们对体外和体内药效学研究进行了系统评价。我们检索了MEDLINE、EMBASE、OviSP和ISI Web of Science数据库,从建库至2017年11月,查找所有报告血液或血浆中TXA浓度与任何可靠的纤维蛋白溶解指标之间关系的体外研究(包括模拟凝血模型)或体内研究。我们共找到21项研究,其中20项为体外研究,1项为体内研究。大多数体外研究使用组织型纤溶酶原激活剂刺激纤维蛋白溶解,并使用粘弹性、光密度或免疫测定法测量纤维蛋白溶解。10至15毫克/升的TXA浓度可显著抑制纤维蛋白溶解,尽管5至10毫克/升的浓度也有部分抑制作用。10至15毫克/升的TXA浓度可能是药代动力学研究的合适靶点,尽管高于5毫克/升的TXA浓度也可能有效。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验