Ultra-early tranexamic acid after subarachnoid haemorrhage (ULTRA): a randomised controlled trial

氨甲环酸 医学 临床终点 抗纤维溶解 随机对照试验 麻醉 优势比 蛛网膜下腔出血 改良兰金量表 临床试验 外科 动脉瘤 内科学 失血 缺血性中风 缺血
作者
René Post,Menno R. Germans,Maud A. Tjerkstra,Mervyn D. I. Vergouwen,Korné Jellema,Radboud W. Koot,Nyika D. Kruyt,Peter W. A. Willems,Jasper Wolfs,Frits C. de Beer,Hans Kieft,Dharmin Nanda,Bram van der Pol,Gerwin Roks,Frank de Beer,Patricia H.A. Halkes,Loes J.A. Reichman,Paul J.A.M. Brouwers,Renske M. van den Berg‐Vos,Vincent I.H. Kwa
出处
期刊:The Lancet [Elsevier BV]
卷期号:397 (10269): 112-118 被引量:188
标识
DOI:10.1016/s0140-6736(20)32518-6
摘要

In patients with aneurysmal subarachnoid haemorrhage, short-term antifibrinolytic therapy with tranexamic acid has been shown to reduce the risk of rebleeding. However, whether this treatment improves clinical outcome is unclear. We investigated whether ultra-early, short-term treatment with tranexamic acid improves clinical outcome at 6 months.In this multicentre prospective, randomised, controlled, open-label trial with masked outcome assessment, adult patients with spontaneous CT-proven subarachnoid haemorrhage in eight treatment centres and 16 referring hospitals in the Netherlands were randomly assigned to treatment with tranexamic acid in addition to care as usual (tranexamic acid group) or care as usual only (control group). Tranexamic acid was started immediately after diagnosis in the presenting hospital (1 g bolus, followed by continuous infusion of 1 g every 8 h, terminated immediately before aneurysm treatment, or 24 h after start of the medication, whichever came first). The primary endpoint was clinical outcome at 6 months, assessed by the modified Rankin Scale, dichotomised into a good (0-3) or poor (4-6) clinical outcome. Both primary and safety analyses were according to intention to treat. This trial is registered at ClinicalTrials.gov, NCT02684812.Between July 24, 2013, and July 29, 2019, we enrolled 955 patients; 480 patients were randomly assigned to tranexamic acid and 475 patients to the control group. In the intention-to-treat analysis, good clinical outcome was observed in 287 (60%) of 475 patients in the tranexamic acid group, and 300 (64%) of 470 patients in the control group (treatment centre adjusted odds ratio 0·86, 95% CI 0·66-1·12). Rebleeding after randomisation and before aneurysm treatment occurred in 49 (10%) patients in the tranexamic acid and in 66 (14%) patients in the control group (odds ratio 0·71, 95% CI 0·48-1·04). Other serious adverse events were comparable between groups.In patients with CT-proven subarachnoid haemorrhage, presumably caused by a ruptured aneurysm, ultra-early, short-term tranexamic acid treatment did not improve clinical outcome at 6 months, as measured by the modified Rankin Scale.Fonds NutsOhra.
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