Faculty of Medicine, Prof. I.G.N.G Ngoerah General Hospital, Universitas Udayana, Denpasar, Bali, Indonesia.
Department of Neurology, Faculty of Medicine, Prof. I.G.N.G Ngoerah General Hospital, Universitas Udayana, Denpasar, Bali, Indonesia.
J Neurol. 2024 May;271(5):2274-2284. doi: 10.1007/s00415-024-12235-1. Epub 2024 Feb 24.
Brain arteriovenous malformations (bAVMs) carry a risk of hemorrhage. We aim to identify factors associated with subsequent hemorrhages.
Systematic searches were conducted across the ScienceDirect, Medline, and Cochrane databases. Assessed risk factors included bAVM size, bAVM volume, hemorrhage and seizure presentations, presence of deep venous drainage, deep-seated bAVMs, associated aneurysms, and Spetzler-Martin grade. Subgroup analyses were conducted on prior treatments, hemorrhage presentation, AVM size, and type of management.
The meta-analysis included 8 cohort studies and 2 trials, with 4,240 participants. Initial hemorrhage presentation (HR 2.41; 95% CI 1.94-2.98; p < 0.001), any deep venous drainage (HR 1.52; 95% CI 1.09-2.13; p = 0.01), and associated aneurysms (HR 1.78; 95% CI 1.41-2.23; p < 0.001) increased secondary hemorrhage risk. Conversely, higher Spetzler-Martin grades (HR 0.77; 95% CI 0.68-0.87; p < 0.001) and larger malformation volumes (HR 0.87; 95% CI 0.76-0.99; p = 0.04) reduced risk. Subgroups showed any deep venous drainage in patients without prior treatment (HR 1.64; 95% CI 1.25-2.15; p < 0.001), bAVM > 3 cm (HR 1.79; 95% CI 1.15-2.78; p = 0.01), and multimodal interventions (HR 1.69; 95% CI 1.12-2.53; p = 0.01) increased risk. The reverse effect was found for patients initially presented without hemorrhage (HR 0.79; 95% CI 0.67-0.93; p = 0.01). Deep bAVM was a risk factor in > 3 cm cases (HR 2.72; 95% CI 1.61-4.59; p < 0.001) and multimodal management (HR 2.77; 95% CI 1.66-4.56; p < 0.001). Kaplan-Meier analysis revealed increased hemorrhage risk for initial hemorrhage presentation, while cumulative survival was higher in intervened patients over 72 months.
Significant risk factors for bAVMs hemorrhage include initial hemorrhage, any deep venous drainage, and associated aneurysms. Deep venous drainage involvement is a risk factor in cases without prior treatment, those with bAVM > 3 cm, and cases managed with multimodal interventions. Deep bAVM involvement also emerges as a risk factor in cases > 3 cm and those managed with multimodal approaches.
脑动静脉畸形(bAVM)有出血风险。我们旨在确定与后续出血相关的因素。
在 ScienceDirect、Medline 和 Cochrane 数据库中进行了系统搜索。评估的危险因素包括 bAVM 大小、bAVM 体积、出血和癫痫发作表现、存在深部静脉引流、深部 bAVM、伴发的动脉瘤和 Spetzler-Martin 分级。亚组分析针对既往治疗、出血表现、AVM 大小和管理类型进行。
荟萃分析包括 8 项队列研究和 2 项试验,涉及 4240 名参与者。初始出血表现(HR 2.41;95%CI 1.94-2.98;p<0.001)、任何深部静脉引流(HR 1.52;95%CI 1.09-2.13;p=0.01)和伴发的动脉瘤(HR 1.78;95%CI 1.41-2.23;p<0.001)增加了二次出血风险。相反,较高的 Spetzler-Martin 分级(HR 0.77;95%CI 0.68-0.87;p<0.001)和较大的畸形体积(HR 0.87;95%CI 0.76-0.99;p=0.04)降低了风险。亚组显示,无既往治疗的患者中存在任何深部静脉引流(HR 1.64;95%CI 1.25-2.15;p<0.001)、AVM>3cm(HR 1.79;95%CI 1.15-2.78;p=0.01)和多模态干预(HR 1.69;95%CI 1.12-2.53;p=0.01)增加了风险。对于最初无出血表现的患者,情况则相反(HR 0.79;95%CI 0.67-0.93;p=0.01)。深部 AVM 是>3cm 病例的危险因素(HR 2.72;95%CI 1.61-4.59;p<0.001)和多模态管理(HR 2.77;95%CI 1.66-4.56;p<0.001)的危险因素。Kaplan-Meier 分析显示,初始出血表现的出血风险增加,而干预 72 个月后,接受治疗的患者的累积生存率更高。
bAVM 出血的显著危险因素包括初始出血、任何深部静脉引流和伴发的动脉瘤。深部静脉引流参与是无既往治疗、AVM>3cm 和多模态干预治疗患者的危险因素。深部 AVM 参与也是>3cm 病例和多模态治疗病例的危险因素。