Intracerebral haemorrhage in patients taking different types of oral anticoagulants: a pooled individual patient data analysis from two national stroke registries.

IF 2.6 1区 医学
Bernhard M Siepen, Elisabeth Forfang, Mattia Branca, Boudewijn Drop, Madlaine Mueller, Martina B Goeldlin, Mira Katan, Patrik Michel, Carlo Cereda, Friedrich Medlin, Nils Peters, Susanne Renaud, Julien Niederhauser, Emmanuel Carrera, Timo Kahles, Georg Kägi, Manuel Bolognese, Stephan Salmen, Marie-Luise Mono, Alexandros A Polymeris, Susanne Wegener, Werner Z'Graggen, Johannes Kaesmacher, Michael Schaerer, Biljana Rodic, Espen Saxhaug Kristoffersen, Kristin T Larsen, Torgeir Bruun Wyller, Bastian Volbers, Thomas R Meinel, Marcel Arnold, Stefan T Engelter, Leo H Bonati, Urs Fischer, Ole Morten Rønning, David J Seiffge
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引用次数: 0

Abstract

Background: We investigated outcomes in patients with intracerebral haemorrhage (ICH) according to prior anticoagulation treatment with Vitamin K antagonists (VKAs), direct oral anticoagulants (DOACs) or no anticoagulation.

Methods: This is an individual patient data study combining two prospective national stroke registries from Switzerland and Norway (2013-2019). We included all consecutive patients with ICH from both registries. The main outcomes were favourable functional outcome (modified Rankin Scale 0-2) and mortality at 3 months.

Results: Among 11 349 patients with ICH (mean age 73.6 years; 47.6% women), 1491 (13.1%) were taking VKAs and 1205 (10.6%) DOACs (95.2% factor Xa inhibitors). The median percentage of patients on prior anticoagulation was 23.7 (IQR 22.6-25.1) with VKAs decreasing (from 18.3% to 7.6%) and DOACs increasing (from 3.0% to 18.0%) over time. Prior VKA therapy (n=209 (22.3%); adjusted ORs (aOR), 0.64; 95% CI, 0.49 to 0.84) and prior DOAC therapy (n=184 (25.7%); aOR, 0.64; 95% CI, 0.47 to 0.87) were independently associated with lower odds of favourable outcome compared with patients without anticoagulation (n=2037 (38.8%)). Prior VKA therapy (n=720 (49.4%); aOR, 1.71; 95% CI, 1.41 to 2.08) and prior DOAC therapy (n=460 (39.7%); aOR, 1.28; 95% CI, 1.02 to 1.60) were independently associated with higher odds of mortality compared with patients without anticoagulation (n=2512 (30.2%)).

Conclusions: The spectrum of anticoagulation-associated ICH changed over time. Compared with patients without prior anticoagulation, prior VKA treatment and prior DOAC treatment were independently associated with lower odds of favourable outcome and higher odds of mortality at 3 months. Specific reversal agents unavailable during the study period might improve outcomes of DOAC-associated ICH in the future.

服用不同类型口服抗凝剂患者的脑内出血:来自两个国家中风登记处的患者个体数据汇总分析。
背景:我们调查了脑内出血(ICH)患者的预后情况,根据患者之前是否接受过维生素 K 拮抗剂(VKA)、直接口服抗凝剂(DOAC)或无抗凝治疗而定:这是一项结合瑞士和挪威两个前瞻性国家卒中登记(2013-2019 年)的个体患者数据研究。我们纳入了两个登记处的所有连续 ICH 患者。主要结果为良好的功能预后(修正的兰金量表 0-2)和 3 个月的死亡率:在 11 349 名 ICH 患者(平均年龄 73.6 岁;47.6% 为女性)中,有 1491 人(13.1%)正在服用 VKAs,1205 人(10.6%)正在服用 DOAC(95.2% 为 Xa 因子抑制剂)。既往接受抗凝治疗的患者比例中位数为 23.7(IQR 22.6-25.1),随着时间的推移,VKA 的比例有所下降(从 18.3% 降至 7.6%),DOAC 的比例有所上升(从 3.0% 升至 18.0%)。与未接受抗凝治疗的患者(人数=2037(38.8%))相比,既往接受过 VKA 治疗(人数=209(22.3%);调整 ORs (aOR),0.64;95% CI,0.49 至 0.84)和既往接受过 DOAC 治疗(人数=184(25.7%);aOR,0.64;95% CI,0.47 至 0.87)的患者出现良好预后的几率较低。与未进行抗凝治疗的患者(n=2512 (30.2%))相比,既往接受过 VKA 治疗(n=720 (49.4%);aOR,1.71;95% CI,1.41 至 2.08)和既往接受过 DOAC 治疗(n=460 (39.7%);aOR,1.28;95% CI,1.02 至 1.60)的患者死亡率较高:结论:随着时间的推移,抗凝相关 ICH 的范围发生了变化。与未接受过抗凝治疗的患者相比,接受过 VKA 治疗和 DOAC 治疗的患者在 3 个月后出现良好预后的几率较低,而出现死亡的几率较高。在研究期间无法获得的特定逆转剂可能会改善未来 DOAC 相关 ICH 的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Investigative Medicine
Journal of Investigative Medicine MEDICINE, GENERAL & INTERNALMEDICINE, RESE-MEDICINE, RESEARCH & EXPERIMENTAL
自引率
0.00%
发文量
111
期刊介绍: Journal of Investigative Medicine (JIM) is the official publication of the American Federation for Medical Research. The journal is peer-reviewed and publishes high-quality original articles and reviews in the areas of basic, clinical, and translational medical research. JIM publishes on all topics and specialty areas that are critical to the conduct of the entire spectrum of biomedical research: from the translation of clinical observations at the bedside, to basic and animal research to clinical research and the implementation of innovative medical care.
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