Ultrasounds versus fluoroscopy guidance for axillary vein puncture for cardiac devices implantation : a multicenter randomized comparison

S. Bun, P. Taghji, P. Massoure, N. Roche, F. Squara, D. Scarlatti, P. Moceri, J. Deharo, E. Ferrari
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Abstract

Type of funding sources: None. Axillary vein (AV) puncture, an emerging route for cardiac implantable electronic devices (CIED), can be performed under ultrasounds (US) or fluoroscopic (Fluo) guidance. To compare US to fluroroscopy-guided AV puncture in a multicenter randomized controlled trial. Consecutive patients admitted for CIED (first implant or upgrade, including resynchronization therapy) intervention were prospectively randomized between US or Fluo guidance for AV puncture in the three participating centers. Access performances, radiation exposure and complications were compared in both groups. 102 patients were included (n = 51 patients per group). The two groups had similar characteristics concerning age (79.4 ± 10 years), and LVEF (47 ± 17%). 92 leads were implanted in both groups. AV catheterization was successful in 50/51 (98 %) in the US group versus 49/51 in the Fluo group (96 %, p = 0.56). AV access time and procedure time were not different between the two groups, respectively (156 ± 274 in the US group versus 137 ± 151 sec, p = 0.66; 54 ± 24 versus 61 ± 26 min; p = 0.13). Total fluoroscopy time (FT) and dose-area product were respectively lower in the US group, but without reaching significance: 197 ± 231 versus 247 ± 293 sec, p = 0.32; 0.39 ± 0.95 versus 0.75 ± 1.58 mGy.m², p = 0.14. FT for AV access was significantly higher in the Fluo group (51 ± 55 sec versus 0, p < 0.0001). There were two complications in each group during the 9 ± 6 months follow-up. Our study demonstrates that both US and fluoroscopy-guided AV catheterization for CIED are highly effective and safe techniques. Despite similar AV access time, compared to fluo guidance, US reduce time radiation exposure by 20 %.
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超声与透视引导下腋窝静脉穿刺心脏装置植入:一项多中心随机比较
资金来源类型:无。腋窝静脉穿刺(AV)是一种新兴的心脏植入式电子装置(CIED)穿刺途径,可以在超声(US)或透视(Fluo)引导下进行。在一项多中心随机对照试验中比较超声与透视引导下的房室穿刺。在三个参与中心,连续接受CIED(首次植入或升级,包括再同步治疗)干预的患者被前瞻性地随机分为US或Fluo引导的房室穿刺。比较两组患者的通路性能、辐射暴露及并发症。纳入102例患者(每组51例)。两组患者年龄(79.4±10岁)、LVEF(47±17%)相似。两组共植入导线92根。US组房室导管置入术成功率为50/51(98%),而Fluo组为49/51 (96%,p = 0.56)。两组间房室进入时间和手术时间无差异,US组分别为156±274秒和137±151秒,p = 0.66;54±24 vs 61±26分钟;P = 0.13)。美国组的总透视时间(FT)和剂量面积积分别较低,但没有达到显著性:197±231比247±293秒,p = 0.32;分别为0.39±0.95和0.75±1.58 mGy。M²,p = 0.14。Fluo组AV通路的FT显著高于对照组(51±55秒,p < 0.0001)。随访9±6个月,两组各发生2例并发症。我们的研究表明,超声和透视引导下的房室导管对CIED是非常有效和安全的技术。尽管AV接触时间相似,但与氟导引相比,美国减少了20%的时间辐射暴露。
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