Department of Cardiovascular Disease-Vascular and Endovascular Surgery and Angiology, Cittadella Hospital, Cittadella, Italy.
J Endovasc Ther. 2010 Aug;17(4):517-24. doi: 10.1583/09-3004.1.
To evaluate the reduction in type II endoleak risk after introducing a new prevention method, "thrombization" or clotting of the aneurysm sac, during endovascular aneurysm repair (EVAR) versus the standard EVAR technique.
From September 1999 to December 2008, 469 consecutive patients underwent EVAR for AAA at our institution. In 2003, the injection of fibrin glue with or without microcoils into the aneurysm sac was added to the EVAR treatment plan ("thrombization" technique). Patients who did not meet the inclusion criterion (at least 1-year follow-up imaging) were censored at the end of 2007, leaving 404 patients eligible for the study: 224 patients (210 men; mean age 71.9+/-8.5 years, range 25-88) undergoing EVAR alone from September 1999 to May 2003 (group 1) compared to 180 patients (161 men; mean age 72.6+/-8 years, range 46-89) who underwent EVAR + thrombization from June 2003 to December 2006 (group 2).
The 2 treatment groups were similar with regard to aneurysm morphology. No allergic or anaphylactic reactions were encountered related to the fibrin glue. Over median follow-up times of 72 months in group 1 and 26 months in group 2, there were 34 (15.2%) endoleaks in group 1 versus 4 (2.2%) in group 2 (p<0.0001). The incidence of type II endoleak was 0.25/100 person-months for group 1 versus 0.07/100 person-months for group 2. The preventive sac thrombization technique was significantly associated with a reduced risk of type II endoleak (HR 0.13, 95% CI 0.05 to 0.36; p<0.0001) regardless of the type of stent-graft fixation (infrarenal versus suprarenal).
The preventive method of intrasac "thrombization" using fibrin glue injection with or without the insertion of coils proves to be a simple, low cost, safe, and effective technique to significantly reduce the risk of type II endoleaks irrespective of the endograft used.
评估在血管内动脉瘤修复术(EVAR)中引入新的预防方法“血栓形成”或动脉瘤囊内凝块后,II 型内漏风险的降低情况,与标准 EVAR 技术相比。
1999 年 9 月至 2008 年 12 月,我院连续 469 例患者接受 EVAR 治疗AAA。2003 年,在 EVAR 治疗方案中加入纤维蛋白胶(或)微线圈注射到动脉瘤囊中(“血栓形成”技术)。未达到纳入标准(至少 1 年随访影像学)的患者于 2007 年底截止,404 例患者符合研究条件:1999 年 9 月至 2003 年 5 月期间接受单纯 EVAR 的 224 例患者(210 例男性;平均年龄 71.9+/-8.5 岁,范围 25-88)与 2003 年 6 月至 2006 年 12 月期间接受 EVAR+血栓形成术的 180 例患者(161 例男性;平均年龄 72.6+/-8 岁,范围 46-89)相比。
2 个治疗组在动脉瘤形态方面相似。未发生与纤维蛋白胶相关的过敏或过敏反应。在第 1 组中位随访时间为 72 个月,第 2 组为 26 个月的情况下,第 1 组有 34 例(15.2%)内漏,第 2 组有 4 例(2.2%)(p<0.0001)。第 1 组的 II 型内漏发生率为 0.25/100 人-月,第 2 组为 0.07/100 人-月。预防性囊内血栓形成技术与 II 型内漏风险降低显著相关(HR 0.13,95%CI 0.05 至 0.36;p<0.0001),与支架移植物固定类型(肾下型与肾上型)无关。
使用纤维蛋白胶注射(或)插入微线圈的腔内预防性“血栓形成”方法被证明是一种简单、低成本、安全且有效的技术,可显著降低 II 型内漏风险,与使用的移植物无关。