首页> 外文期刊>European journal of vascular and endovascular surgery: the official journal of the European Society for Vascular Surgery >Catheter-directed foam sclerotherapy of great saphenous veins in combination with pre-treatment reduction of the diameter employing the principals of perivenous tumescent local anesthesia
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Catheter-directed foam sclerotherapy of great saphenous veins in combination with pre-treatment reduction of the diameter employing the principals of perivenous tumescent local anesthesia

机译:大隐静脉的导管定向泡沫硬化疗法结合使用静脉肿胀局部麻醉的原则减小直径的预处理

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摘要

Objectives The aim of this study was to evaluate occlusion rates of great saphenous veins (GSV) with a diameter between 5-10 mm that received a pre-treatment size reduction via perivenous tumescent application (TA) followed by catheter-directed foam sclerotherapy (CDFS). Methods A prospective blinded randomized clinical trial comparing the occlusion rates of GSV at 1-, 6-, and 12-month follow-up. Fifty patients were included and randomized into two groups. CDFS was performed accessing the GSV at knee level and applying 8 mL of 2% polidocanol-foam (EasyFoam) while the catheter was withdrawn. Strictly perivenous TA was performed in group 1 before applying the sclerosant agent. Occlusion rates and clinical scores were assessed by blinded examiners. Results After 12 months in group 1 full occlusion was achieved in 73.9%, partial occlusion in 8.7%, and 17.4% were classified as treatment failure. In group 2, 75% of the targeted GSV were fully occluded, 20% were partially occluded, and 5% were diagnosed as treatment failure. Both groups showed a significant reduction of the vein diameter. Patient's tolerance and satisfaction with the treatment was high in both groups. Conclusion No benefit could be found using additional TA to reduce the vein diameter before the treatment.
机译:目的这项研究的目的是评估直径为5-10 mm的大隐静脉(GSV)的闭塞率,该隐静脉通过静脉肿胀应用(TA)进行了治疗前尺寸缩小,然后进行了导管定向泡沫硬化疗法(CDFS) )。方法:一项前瞻性盲法随机临床试验,比较了GSV在1、6和12个月随访中的闭塞率。纳入50例患者,随机分为两组。抽出导管时,在膝盖处进入GSV并用8 mL 2%的多多酚醇泡沫(EasyFoam)进行CDFS。在应用硬化剂之前,在第1组进行严格的静脉TA。闭塞率和临床评分由盲人检查员评估。结果第1组12个月后,完全闭塞率为73.9%,部分闭塞率为8.7%,而17.4%被归类为治疗失败。在第2组中,目标GSV的75%被完全阻塞,20%被部分阻塞,5%被诊断为治疗失败。两组均显示静脉直径显着减小。两组患者对治疗的耐受性和满意度均很高。结论在治疗前使用额外的TA来减小静脉直径没有发现任何益处。

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