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使用液体栓塞剂的脑动静脉畸形的血管内治疗:一项前瞻性、多中心研究(BRAVO)的结果。

Endovascular treatment of brain arteriovenous malformations using a liquid embolic agent: results of a prospective, multicentre study (BRAVO).

机构信息

Department of Radiology, Hôpital Maison-Blanche, Reims, France,

出版信息

Eur Radiol. 2013 Oct;23(10):2838-45. doi: 10.1007/s00330-013-2870-6. Epub 2013 May 8.

Abstract

OBJECTIVES

To evaluate the safety and efficacy of a new liquid embolic agent in brain arteriovenous malformation (bAVMs) embolisation.

METHODS

A prospective, multicentre series was conducted at 11 interventional centres in Europe to evaluate embolisation of bAVMs with the new liquid embolic agent. Technical conditions, complications, clinical outcome and anatomical results were independently analysed.

RESULTS

From December 2005 to December 2008, 117 patients (72 male; 45 female, aged 18-75 years) were included. Clinical presentation was mostly haemorrhage (34.2 %) and seizures (28.2 %). Most AVMs were located in the brain hemispheres (85.5 %). AVMs were <3 cm in 52.1 % of patients and ≥ 3 cm in 47.9 %. Morbidity was observed in 6/117 patients (5.1 %), related to haemorrhagic events in 2 cases and non-haemorrhagic complications in 4 cases. Five patients (4.3 %) died in relation to the treatment (bleeding in 4 patients and extensive venous thrombosis in 1). Complete occlusion of the AVM by embolisation alone was obtained in 23.5 % of patients. Complementary treatment was performed in 82.3 % of patients with partial AVM occlusion, mostly radiosurgery.

CONCLUSIONS

In this prospective, multicentre, European, observational series, the new liquid embolic agent proved to be suitable for BAVM embolisation, with acceptable morbidity and mortality and good efficacy.

KEY POINTS

• Numerous interventional techniques have been used to embolise brain arteriovenous malformations (AVMs). • This prospective multicentre study demonstrates the suitability of a liquid embolic agent. • The safety of treatment using Onyx is acceptable. • Such embolisation leads to complete AVM occlusion in 23.5 % of patients.

摘要

目的

评估一种新型液体栓塞剂在脑动静脉畸形(bAVM)栓塞中的安全性和疗效。

方法

在欧洲的 11 个介入中心进行了一项前瞻性、多中心系列研究,以评估新型液体栓塞剂在治疗 bAVM 中的效果。技术条件、并发症、临床结果和解剖学结果均进行了独立分析。

结果

2005 年 12 月至 2008 年 12 月,共纳入 117 例患者(72 例男性,45 例女性,年龄 18-75 岁)。临床表现主要为出血(34.2%)和癫痫发作(28.2%)。大多数 AVM 位于大脑半球(85.5%)。52.1%的患者 AVM 直径<3cm,47.9%的患者 AVM 直径≥3cm。117 例患者中出现并发症 6 例(5.1%),其中 2 例与出血事件相关,4 例与非出血性并发症相关。5 例(4.3%)患者与治疗相关死亡(4 例患者出血,1 例患者广泛静脉血栓形成)。单纯栓塞可使 23.5%的 AVM 完全闭塞。82.3%部分闭塞 AVM 的患者接受了补充治疗,主要为放射外科治疗。

结论

在这项前瞻性、多中心、欧洲观察性系列研究中,新型液体栓塞剂被证明适合于 bAVM 栓塞,具有可接受的发病率和死亡率及良好的疗效。

关键点

  1. 已经有许多介入技术用于栓塞脑动静脉畸形(AVM)。

  2. 这项前瞻性多中心研究证明了一种液体栓塞剂的适用性。

  3. 使用 Onyx 治疗的安全性是可以接受的。

  4. 这种栓塞可以使 23.5%的患者 AVM 完全闭塞。

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