Department of Neurology, Shanghai 85th Hospital of PLA, Shanghai, China.
Department of Neurology, Oslo University Hospital, Oslo, Norway.
J Neurol Neurosurg Psychiatry. 2016 Dec;87(12):1330-1335. doi: 10.1136/jnnp-2016-313246. Epub 2016 May 13.
Antithrombotic agents increase risks of intracerebral haemorrhage (ICH) and associated adverse outcomes. We determined differential effects of early blood pressure (BP) lowering in patients with/without antithrombotic-associated ICH in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trials (INTERACT1 and 2).
Post hoc pooled analyses of the INTERACT studies-international, multicentre, prospective, open, blinded end point trials of patients with ICH (<6 h) and elevated systolic BP (SBP 150-180 mm Hg) randomly assigned to intensive (target SBP <140 mm Hg) or guideline-based (SBP <180 mm Hg) BP management. Associations of antithrombotic use and (1) death or dependency (modified Rankin scale scores 3-6) were analysed using logistic regression, and (2) of increased haematoma+intraventricular haemorrhage volume (IVH) with/without intraventricular haemorrhage (IVH) over 24 h were estimated in analyses of covariance.
In all, 3184 patients were included in these analyses. Antithrombotic-associated ICH (364 patients, 11%) was not associated with a significantly increased risk of death or dependency (OR 1.38, 95% CI 0.93 to 2.04). There was no heterogeneity in the BP-lowering treatment effect on death or dependency. Among 1309 patients who underwent follow-up CT after 24 h, absolute increase in haematoma±IVH volume was larger (5.2/5.0 mL) in those with compared to those without prior antithrombotics (2.2/0.9 mL; p=0.022/0.031). Intensive BP lowering reduced haematoma±IVH growth by 4.7/7.1 mL in patients on antithrombotics versus 1.3/1.4 mL in those without, although these differences did not reach statistical significance (p homogeneity=0.104/0.059).
In patients with ICH, prior antithrombotic therapy is associated with greater haematoma growth, which may be reduced by early intensive BP-lowering treatment.
NCT00226096, NCT00716079.
抗血栓药物会增加颅内出血(ICH)的风险和相关不良后果。我们在急性脑出血强化降压试验(INTERACT1 和 2)中确定了伴有和不伴有抗血栓相关 ICH 的患者早期降压的差异影响。
对 INTERACT 研究的事后汇总分析——一项国际、多中心、前瞻性、开放、盲终点试验,纳入发病 6 小时内的 ICH 患者和升高的收缩压(SBP 150-180mmHg),随机分配到强化治疗组(目标 SBP<140mmHg)或指南治疗组(SBP<180mmHg)。采用逻辑回归分析抗血栓药物使用与(1)死亡或依赖(改良 Rankin 量表评分 3-6)之间的关系,采用协方差分析估计血肿+脑室内出血(IVH)体积增加(24 小时内)与(2)伴有和不伴有 IVH 之间的关系。
共有 3184 名患者纳入这些分析。抗血栓相关 ICH(364 名患者,11%)与死亡或依赖风险的显著增加无关(OR 1.38,95%CI 0.93-2.04)。降压治疗对死亡或依赖的影响没有异质性。在 1309 名在 24 小时后进行了随访 CT 的患者中,与无抗凝治疗相比,有抗凝治疗的患者血肿+IVH 体积的绝对增加更大(5.2/5.0mL;p=0.022/0.031)。与无抗凝治疗相比,强化降压治疗使抗凝治疗患者的血肿+IVH 生长减少了 4.7/7.1mL,而无抗凝治疗患者的血肿+IVH 生长减少了 1.3/1.4mL,尽管这些差异没有达到统计学意义(p 同质性=0.104/0.059)。
在 ICH 患者中,先前的抗血栓治疗与更大的血肿增长相关,早期强化降压治疗可能会减少这种增长。
NCT00226096,NCT00716079。