Henry M, Amor M, Henry I, Klonaris C, Chati Z, Masson I, Kownator S, Luizy F, Hugel M
UCCI, Polyclinique, Essey-les-Nancy, France.
J Endovasc Surg. 1999 Nov;6(4):321-31. doi: 10.1177/152660289900600405.
To study the feasibility and safety of carotid angioplasty and stenting using a new cerebral protection device that temporarily occludes the distal internal carotid artery (ICA).
Forty-eight high-risk patients (39 men, mean age 69.1 +/- 8 years, range 54 to 86) with 53 ICA stenoses underwent percutaneous angioplasty and stenting via the femoral approach under cerebral protection afforded by a 0.014-inch GuardWire balloon occlusion device. Mean stenosis was 82.1% +/- 9.65% (range 70 to 96) and mean lesion length was 16.0 +/- 7.5 mm (range 6 to 50). Thirty-three (62%) lesions were calcified, and 38 (72%) were ulcerated. Thirty-two (60%) of the lesions were asymptomatic. With the occlusion balloon inflated in the distal ICA, the lesion was dilated and stented. The area was cleaned by aspiration and flushed via an aspiration catheter advanced over the wire. Blood samples were collected from the external carotid artery (ECA) and analyzed to measure the size and number of particles collected. Computed tomography and neurological examinations were performed the day after the procedure.
Immediate technical success was achieved in all patients with the implantation of 38 Palmaz stents, 8 Expander stents, and 11 Wallstents. Carotid occlusion was well tolerated in all patients but 1 who had multiple, severe carotid lesions and poor collateralization. Mean cerebral flow occlusion time was 346 +/- 153 seconds during predilation and 303 +/- 143 seconds during stent placement. Total mean flow occlusion time was 542 +/- 243 seconds. One immediate neurological complication (transient amaurosis) occurred in a patient who had an anastomosis between the external carotid (EC) and ICA territories. Debris was removed in all patients with a mean 0.8-mm diameter catheter.
Cerebral protection with the GuardWire device is easy, safe, and effective in protecting the brain from cerebral embolism. Larger studies are warranted.
研究使用一种可暂时阻断颈内动脉(ICA)远端的新型脑保护装置进行颈动脉血管成形术和支架置入术的可行性和安全性。
48例高危患者(39例男性,平均年龄69.1±8岁,范围54至86岁),共53处ICA狭窄,在0.014英寸GuardWire球囊阻断装置提供的脑保护下,经股动脉途径接受经皮血管成形术和支架置入术。平均狭窄率为82.1%±9.65%(范围70至96),平均病变长度为16.0±7.5毫米(范围6至50)。33处(62%)病变钙化,38处(72%)有溃疡形成。32处(60%)病变无症状。在ICA远端球囊阻断的情况下,对病变进行扩张并置入支架。通过抽吸清洁该区域,并经沿导丝推进的抽吸导管冲洗。从颈外动脉(ECA)采集血样并进行分析,以测量所收集颗粒的大小和数量。术后第二天进行计算机断层扫描和神经学检查。
所有患者均即刻获得技术成功,共植入38枚Palmaz支架、8枚Expander支架和11枚Wallstent支架。除1例有多处严重颈动脉病变且侧支循环不良的患者外,所有患者对颈动脉阻断均耐受良好。预扩张期间平均脑血流阻断时间为346±153秒,支架置入期间为303±143秒。总平均血流阻断时间为542±243秒。1例颈外动脉(EC)与ICA区域之间存在吻合的患者发生了1例即刻神经并发症(短暂性黑矇)。所有患者均使用平均直径0.8毫米的导管清除了碎屑。
使用GuardWire装置进行脑保护在保护大脑免受脑栓塞方面简便、安全且有效。有必要进行更大规模的研究。