Nuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.
PLoS One. 2010 Sep 2;5(9):e12492. doi: 10.1371/journal.pone.0012492.
Flow diversion is a new approach to the endovascular treatment of intracranial aneurysms which uses a high density mesh stent to induce sac thrombosis. These devices have been designed for the treatment of complex shaped and large size aneurysms. So far published safety and efficacy data on this approach is sparse.
Over 8 months, standardized clinical and angiographic data were collected on 70 patients treated with a flow diverter device (SILK flow diverter (SFD)) in 18 centres worldwide. Treatment and early follow up details were audited centrally. SFDs were deployed alone in 57 (81%) or with endosaccular coils in 10 (14%) aneurysms, which included: 44 (63%) saccular, 26 (37%) fusiform shapes and 18 (26%) small, 37 (53%) large, 15 (21%) giant sizes. Treatment outcome data up to 30 days were reported for all patients, with clinical (50 patients) and imaging (49 patients) follow up (median 119 days) data available.
Difficulties in SFD deployment were reported in 15 (21%) and parent artery thrombosis in 8 (11%) procedures. Procedural complications caused stroke in 1 and serious extracranial bleeding in 3 patients; 2 of whom developed fatal pneumonias. Delayed worsening of symptoms occurred in 5 patients (3 transient, 1 permanent neurological deficit, and 1 death) and fatal aneurysm bleeding in 1 patient. Overall permanent morbidity rates were 2 (4%) and mortality 4 (8%). Statistical analysis revealed no significant association between complications and variables related to treated aneurysm morphology or rupture status.
This series is the largest reporting outcome of the new treatment approach and provides data for future study design. Procedural difficulties in SFD deployment were frequent and anti-thrombosis prophylaxis appears to reduce the resulting clinical sequelae, but at the cost of morbidity due to extracranial bleeding. Delayed morbidity appears to be a consequence of the new approach and warrants care in selecting patients for treatment and future larger studies.
血流导向装置是一种新的治疗颅内动脉瘤的血管内治疗方法,它使用高密度网支架诱导囊血栓形成。这些装置是为治疗复杂形状和大尺寸动脉瘤而设计的。到目前为止,关于这种方法的安全性和疗效数据还很少。
在 8 个月的时间里,在全球 18 个中心收集了 70 例使用血流导向装置(丝滑血流导向装置(SFD))治疗的患者的标准化临床和血管造影数据。治疗和早期随访细节在中心进行审核。SFD 单独用于 57 例(81%)或与腔内线圈联合用于 10 例(14%)动脉瘤,其中包括:44 例(63%)囊状,26 例(37%)梭形,18 例(26%)小,37 例(53%)大,15 例(21%)巨大。所有患者均报告了 30 天内的治疗结果,50 例患者有临床随访,49 例患者有影像学随访(中位随访时间为 119 天)。
15 例(21%)患者出现 SFD 放置困难,8 例(11%)患者出现母动脉血栓形成。手术并发症导致 1 例中风和 3 例严重的颅外出血;其中 2 例发展为致命性肺炎。5 例患者出现症状延迟恶化(3 例为短暂性,1 例为永久性神经功能缺损,1 例死亡),1 例患者发生致命性动脉瘤出血。总的永久性发病率为 2(4%),死亡率为 4(8%)。统计分析显示,并发症与治疗后动脉瘤形态或破裂状态相关的变量之间无显著相关性。
本系列是对新治疗方法的最大结果报告,为未来的研究设计提供了数据。SFD 放置困难频繁,抗血栓形成预防似乎减少了由此产生的临床后果,但代价是颅外出血导致的发病率增加。迟发性发病率似乎是新方法的结果,需要在选择患者进行治疗和未来更大的研究时加以注意。