Yogendrakumar Vignan, Demchuk Andrew M, Aviv Richard I, Rodriguez-Luna David, Molina Carlos A, Blas Yolanda S, Dzialowski Imanuel, Kobayashi Adam, Boulanger Jean-Martin, Lum Cheemun, Gubitz Gord, Padma Vasantha, Roy Jayanta, Kase Carlos S, Bhatia Rohit, Hill Michael D, Dowlatshahi Dar
Department of Medicine (Neurology), Ottawa Hospital Research Institute and University of Ottawa, Ottawa, Canada.
Calgary Stroke Program, Department of Clinical Neurosciences, Department of Radiology, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Eur Stroke J. 2017 Sep;2(3):257-263. doi: 10.1177/2396987317715836. Epub 2017 Jun 15.
The role of intracerebral haemorrhage location in haematoma expansion remains unclear. Our objective was to assess the effect of lobar versus non-lobar haemorrhage on haematoma expansion and clinical outcome.
We analysed data from the prospective PREDICT study where patients with intracerebral haemorrhage presenting to hospital under 6 h of symptom onset received baseline computed tomography (CT), CT angiogram, 24 h follow-up CT, and 90-day mRS. Intracerebral haemorrhage location was categorised as lobar versus non-lobar, and primary outcomes were significant haematoma expansion (>6 ml) and poor clinical outcome (mRS > 3). Multivariable regression was used to adjust for relevant covariates. The primary analysis population was divided by spot sign status and the effect of haemorrhage location was compared to haematoma expansion in exploratory post hoc analysis.
Among 302 patients meeting the inclusion criteria, lobar haemorrhage was associated with increased haematoma expansion >6 ml (p = 0.003), poor clinical outcome (p = 0.011) and mortality (p = 0.017). When adjusted for covariates, lobar haemorrhage independently predicted significant haematoma expansion (aOR 2.2 (95% CI: 1.1-4.3), p = 0.021) and poor clinical outcome (aOR 2.6 (95% CI: 1.2-5.6), p = 0.019). Post hoc analysis showed that patients who were spot sign negative had a higher degree of haematoma expansion with baseline lobar haemorrhage (lobar 26% versus deep 11%; p = 0.01). No significant associations were observed in spot-positive patients (lobar 52% versus deep 47%; p = 0.69).
Haematoma expansion is more likely to occur with lobar intracerebral haemorrhage and haemorrhage location is associated with poor clinical outcome. As expansion is a promising therapeutic target, hemorrhage location may be helpful for prognostication and as a selection tool in future ICH clinical trials.
脑内出血部位在血肿扩大中所起的作用仍不明确。我们的目的是评估脑叶出血与非脑叶出血对血肿扩大及临床结局的影响。
我们分析了前瞻性PREDICT研究的数据,该研究中症状发作6小时内入院的脑内出血患者接受了基线计算机断层扫描(CT)、CT血管造影、24小时随访CT以及90天改良Rankin量表(mRS)评估。脑内出血部位分为脑叶性和非脑叶性,主要结局为显著血肿扩大(>6毫升)和不良临床结局(mRS>3)。采用多变量回归对相关协变量进行校正。主要分析人群按斑点征状态进行划分,并在探索性事后分析中比较出血部位对血肿扩大的影响。
在302例符合纳入标准的患者中,脑叶出血与>6毫升的血肿扩大增加相关(p = 0.003)、不良临床结局(p = 0.011)及死亡率(p = 0.017)相关。校正协变量后,脑叶出血独立预测显著血肿扩大(校正比值比2.2(95%可信区间:1.1 - 4.3),p = 0.021)和不良临床结局(校正比值比2.6(95%可信区间:1.2 - 5.6),p = 0.019)。事后分析显示,斑点征阴性的患者基线脑叶出血时血肿扩大程度更高(脑叶26% 对深部11%;p = 0.01)。在斑点征阳性的患者中未观察到显著关联(脑叶52% 对深部47%;p = 0.69)。
脑叶性脑内出血更易发生血肿扩大,且出血部位与不良临床结局相关。由于血肿扩大是一个有前景的治疗靶点,出血部位可能有助于预后评估,并作为未来脑出血临床试验的选择工具。