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使用Perclose Proglide完全经皮入路进行主动脉疾病的血管内治疗。

Totally Percutaneous Access Using Perclose Proglide for Endovascular Treatment of Aortic Diseases.

作者信息

Saadi Eduardo Keller, Saadi Marina, Saadi Rodrigo, Tagliari Ana Paula, Mastella Bernardo

机构信息

Hospital de Clínicas de Porto Alegre (HCPA), Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil.

Universidade Luterana do Brasil (ULBRA), Canoas, RS, Brazil.

出版信息

Braz J Cardiovasc Surg. 2017 Jan-Feb;32(1):43-48. doi: 10.21470/1678-9741-2016-0065.

DOI:10.21470/1678-9741-2016-0065
PMID:28423129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5382908/
Abstract

OBJECTIVE

To evaluate our experience following the introduction of a percutaneous program for endovascular treatment of aortic diseases using Perclose Proglide® assessing efficacy, complications and identification of potential risk factors that could predict failure or major access site complications.

METHODS

A retrospective cohort study during a two-year period was performed. All the patients submitted to totally percutaneous endovascular repair (PEVAR) of aortic diseases and transcatheter aortic valve implantation since we started the total percutaneous approach with the preclosure technique from November 2013 to December 2015 were included in the study. The primary endpoint was major ipsilateral access complication, defined according to PEVAR trial.

RESULTS

In a cohort of 123 patients, immediate technical success was obtained in 121 (98.37%) patients, with only two (0.82%) cases in 242 vascular access sites that required intervention immediately after the procedure. Pairwise comparisons revealed increased major access complication among patients with >50% common femoral artery (CFA) calcification vs. none (P=0.004) and > 50% CFA calcification vs. < 50% CFA calcification (P=0.002). Small artery diameter (<6.5 mm) also increased major access complication compared to bigger diameters (> 6.5 mm) (P=0.027).

CONCLUSION

The preclosure technique with two Perclose Proglide® for PEVAR is safe and effective. Complications occur more often in patients with unfavorable access site anatomy and the success rate can be improved with proper patient selection.

摘要

目的

采用Perclose Proglide®评估经皮血管腔内治疗主动脉疾病方案的疗效、并发症,并识别可能预测失败或主要穿刺部位并发症的潜在风险因素,从而评估我们的经验。

方法

进行了一项为期两年的回顾性队列研究。自2013年11月至2015年12月我们开始采用预闭合技术的完全经皮方法以来,所有接受主动脉疾病完全经皮血管腔内修复术(PEVAR)和经导管主动脉瓣植入术的患者均纳入研究。主要终点是主要同侧穿刺并发症,根据PEVAR试验定义。

结果

在123例患者队列中,121例(98.37%)患者即刻获得技术成功,在242个血管穿刺部位中只有2例(0.82%)在术后需要立即干预。两两比较显示,股总动脉(CFA)钙化>50%的患者与无钙化患者相比主要穿刺并发症增加(P = 0.004),CFA钙化>50%的患者与CFA钙化<50%的患者相比主要穿刺并发症增加(P = 0.002)。与较大动脉直径(>6.5 mm)相比,小动脉直径(<6.5 mm)也增加了主要穿刺并发症(P = 0.027)。

结论

用于PEVAR的双Perclose Proglide®预闭合技术安全有效。在穿刺部位解剖结构不利的患者中并发症更常发生,通过适当的患者选择可以提高成功率。

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本文引用的文献

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Safety and utility of total percutaneous endovascular aortic repair with a single Perclose ProGlide closure device.使用单个Perclose ProGlide闭合装置进行全经皮血管腔内主动脉修复术的安全性和实用性。
J Vasc Surg. 2016 Mar;63(3):585-8. doi: 10.1016/j.jvs.2015.08.111. Epub 2015 Oct 23.
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A multicenter, randomized, controlled trial of totally percutaneous access versus open femoral exposure for endovascular aortic aneurysm repair (the PEVAR trial).多中心、随机、对照临床试验,评估经皮入路与开放股动脉入路在血管内主动脉瘤修复术中的应用(PEVAR 试验)。
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Femoral artery calcification as a determinant of success for percutaneous access for endovascular abdominal aortic aneurysm repair.股动脉钙化是经皮腔内腹主动脉瘤修复术成功的决定因素。
J Vasc Surg. 2013 Nov;58(5):1208-12. doi: 10.1016/j.jvs.2013.05.028. Epub 2013 Jul 2.
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Predictors of percutaneous access failure requiring open femoral surgical conversion during endovascular aortic aneurysm repair.血管内主动脉瘤修复期间经皮入路失败需要开放股动脉手术转换的预测因素。
J Vasc Surg. 2013 Nov;58(5):1213-9. doi: 10.1016/j.jvs.2013.04.065. Epub 2013 Jun 28.
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Efficacy and safety of the preclose technique following percutaneous aortic stent-graft implantation.经皮主动脉支架植入术后预闭技术的疗效和安全性。
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Vascular closure device failure: we are getting better but not there yet.血管闭合装置故障:我们正在取得进展,但尚未达到理想状态。
JACC Cardiovasc Interv. 2012 Aug;5(8):845-7. doi: 10.1016/j.jcin.2012.06.006.