Department of Clinical Neurosciences, Johns Hopkins Medical Institutions, Baltimore, MD 21231, USA.
Stroke. 2012 Jun;43(6):1666-8. doi: 10.1161/STROKEAHA.112.650523. Epub 2012 Apr 3.
The Clot Lysis: Evaluating Accelerated Resolution of IVH (CLEAR IVH) program is assessing the efficacy of intraventricular recombinant tissue-type plasminogen activator (rtPA) for spontaneous intraventricular hemorrhage (IVH). This subanalysis assesses the effect of dose of rtPA by region on clearance of IVH.
Sixty-four patients within 12 to 24 hours of spontaneous IVH were randomized to placebo or 0.3 mg, 1 mg, or 3 mg of rtPA twice daily through an extraventricular drain. Twelve subregions of the ventricles were scored from 0 to 4. Effect of dose on IVH clearance to 50% of baseline score was compared by survival analysis for all regions combined and by subregion. Models including ventricular region, dose, and baseline score were compared by Cox proportional hazards.
IVH score reduced faster across all regions with increasing rtPA dose (clearance to 50%: log-rank P<0.0001; placebo-11.43 days, 95% CI, 5.68-17.18; 0.3 mg-3.19 days, 1.00-5.38; 1 mg-3.54 days, 0.45-6.64; 3 mg-2.59 days, 1.72-3.46). In the combined models, dose and baseline score were independently associated with reduction in IVH score, which was quickest in the midline ventricles, then the anterior half of the lateral ventricles and slowest in the posterior half of the lateral ventricles (clearance to 50%: P<0.0001; rtPA dose: hazard ratio, 1.47, 1.30-1.67; midline versus anterolateral hazard ratio, 1.71, 1.08-2.71; midline versus posterolateral hazard ratio, 4.05, 2.46-6.65; baseline score hazard ratio, 0.96, 0.91-1.01) with a significant interaction between dose and ventricular region (P=0.005).
rtPA accelerates resolution of IVH. This effect is dose-dependent, is greatest in the midline ventricles, and least in the posterolateral ventricles.
血栓溶解:评估脑出血加速清除(CLEAR IVH)项目正在评估脑室内重组组织型纤溶酶原激活剂(rtPA)治疗自发性脑室内出血(IVH)的疗效。这项亚分析评估了脑室内 rtPA 剂量对 IVH 清除的影响。
64 例自发性 IVH 患者在发病后 12 至 24 小时内随机接受安慰剂或每日两次通过脑室外引流给予 0.3mg、1mg 或 3mg rtPA。将脑室的 12 个亚区评分 0 至 4 分。通过生存分析比较所有区域联合和亚区的剂量对 IVH 清除至基线评分 50%的影响。包括脑室区域、剂量和基线评分的模型通过 Cox 比例风险进行比较。
随着 rtPA 剂量的增加,所有区域的 IVH 评分下降速度更快(清除至 50%:对数秩 P<0.0001;安慰剂组为 11.43 天,95%CI 为 5.68-17.18;0.3mg 组为 3.19 天,1.00-5.38;1mg 组为 3.54 天,0.45-6.64;3mg 组为 2.59 天,1.72-3.46)。在联合模型中,剂量和基线评分与 IVH 评分的降低独立相关,中线脑室最快,然后是侧脑室前半部分最慢,侧脑室后半部分最慢(清除至 50%:P<0.0001;rtPA 剂量:风险比 1.47,1.30-1.67;中线与前外侧风险比 1.71,1.08-2.71;中线与后外侧风险比 4.05,2.46-6.65;基线评分风险比 0.96,0.91-1.01),剂量和脑室区域之间存在显著的交互作用(P=0.005)。
rtPA 加速了 IVH 的清除。这种作用是剂量依赖性的,在中线脑室最大,在后侧脑室最小。