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首页> 外文期刊>VASA: Zeitschrift fuer Gefarsskrankheiten. Journal for vascular diseases >Haemostasis for 568 large femoral artery access sites-outcomes and predictors of success [Blutstillung nach 568 arterienoperationen - ergebnisse und erfolgspr?diktoren]
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Haemostasis for 568 large femoral artery access sites-outcomes and predictors of success [Blutstillung nach 568 arterienoperationen - ergebnisse und erfolgspr?diktoren]

机译:568股大动脉入路止血-结果和成功的预测因素[568动脉手术后的止血-结果和成功的预测因素]

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Background: The introduction of stent grafts for thoracic and abdominal aorta (T/EVAR) has raised the demand for percutaneous closure devices for larger femoral arterial access sites. The aim of our study was to evaluate the success and complication rate of completely percutaneous T/EVAR with Prostar XL? and surgical haemostasis over a 50- month period. Patients and methods: Between December 16th 2005 and February 17th 2010 T/EVAR was performed in 306 patients with 568 arterial access sites with diameters of 12 to 24 Fr. The exclusion criteria for percutaneous haemostasis were a calcif ed anterior wall at the puncture site and/or a stenotic common femoral artery, seen on computed tomographic angiography. Results: Surgical haemostasis was performed in 184 (32.4%, o-T/EVAR group) while percutaneous haemostasis was attempted at 384 sites (67.6%, p-T// EVAR group). Most of the procedures were elective; five of twelve emergency patients had percutaneous haemostasis that was successful in all. Percutaneous haemostasis failed at 23 sites. No data about follow-up was recorded for 54 sites (9,5%). The technical success rate of percutaneous haemostasis was 93.6% (338/361 sites). A larger size of the access site resulted in significantly more complications of haemostasis in both groups (p-T/EVAR group p = 0.019; o-T/EVAR group p = 0.003). p-T/EVAR caused more mild complications compared to o-T/EVAR (p = 0.03). No deaths as consequence of failed haemostasis were recorded. Conclusions: Complete percutaneous T/EVAR is technically feasible and safe in a majority of patients. Good patient selection based on adequate pre-procedural imaging and technical expertise of the operators are key to success. Surgical back-up is strongly recommended to assist in those patients in whom p-T/EVAR fails.
机译:背景:用于胸主动脉和腹主动脉的支架移植物(T / EVAR)的引入增加了对较大股动脉进入部位的经皮闭合装置的需求。我们研究的目的是评估Prostar XL完全经皮T / EVAR的成功率和并发症发生率。并在50个月内止血。患者和方法:在2005年12月16日至2010年2月17日之间,对306个直径568至12 Fr的568个动脉通路部位的患者进行了T / EVAR。经皮断层血管造影术所见的经皮止血的排除标准是穿刺部位的钙化前壁和/或狭窄的股总动脉。结果:184例(32.4%,o-T / EVAR组)进行了手术止血,而384个部位(67.6%,p-T // EVAR组)尝试了经皮止血。大多数程序是选修的。十二名急诊患者中有五名经皮止血,全部成功。经皮止血在23个部位失败。没有关于54个部位(9,5%)的随访数据。经皮止血的技术成功率为93.6%(338/361个位点)。较大的进入部位导致两组止血并发症明显增加(p-T / EVAR组p = 0.019; o-T / EVAR组p = 0.003)。与o-T / EVAR相比,p-T / EVAR引起的并发症更为轻微(p = 0.03)。没有记录止血失败引起的死亡。结论:对大多数患者而言,完全经皮T / EVAR在技术上是可行的且安全。基于足够的术前术前影像和操作员的技术专长来进行良好的患者选择是成功的关键。强烈建议进行手术支持以帮助p-T / EVAR失败的患者。

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