Clinical outcomes of a balloon-expandable stent for symptomatic obstructions of the subclavian or innominate arteries.

IF 2.1 4区 医学 Q3 PERIPHERAL VASCULAR DISEASE Vasa-european Journal of Vascular Medicine Pub Date : 2023-11-01 Epub Date: 2023-10-03 DOI:10.1024/0301-1526/a001092
Riccardo M Fumagalli, Kerstin Schürch, Alexandru Grigorean, Erik W Holy, Mario Münger, William Pleming, Nils Kucher, Stefano Barco
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Abstract

Background: Upper-extremity peripheral arterial disease (PAD) may present with a broad spectrum of signs and symptoms. If an endovascular treatment is planned, percutaneous angioplasty and stent placement may lead to a better patency compared to percutaneous angioplasty alone. We assessed the characteristics and clinical course of patients with upper-extremity PAD who received angioplasty and a balloon-expandable stent. Patients and methods: We analyzed data from consecutive patients treated with angioplasty and placement of a balloon-expandable BeSmooth Peripheral Stent System® (Bentley, Germany) at the Angiology Department (University Hospital Zurich) between 2018 and 2022. The primary outcome was re-intervention at the target lesion within 6 months from index angioplasty and during available follow-up. The study was approved by the local ethical commission. Results: A total of 27 patients were treated. The median age was 70 (Q1-Q3: 60-74) years and 59% were men. The subclavian artery (74%) represented the most frequently treated target lesion, followed by the innominate artery (26%). The mean improvement in blood pressure in the treated arm was 21 (95%CI 7 to 35) mmHg at 24 hours and 29 (95%CI 15 to 43) mmHg at 6 months. At 6 months, 2 (8%) patients required a target lesion re-intervention. During the remaining follow-up period up to 24 months, one of these two patients required additional intervention and a total of 3 (11%) patients died due to sepsis, cancer, and unknown causes, respectively. Conclusions: Percutaneous catheter-based treatment with a balloon-expandable stent for symptomatic upper extremity PAD appeared to be effective and safe.

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球囊扩张支架治疗锁骨下动脉或无名动脉症状性阻塞的临床结果。
背景:上肢外周动脉疾病(PAD)可能表现出广泛的体征和症状。如果计划进行血管内治疗,与单独的经皮血管成形术相比,经皮血管成型术和支架置入可能会带来更好的通畅性。我们评估了接受血管成形术和球囊扩张支架治疗的上肢PAD患者的特征和临床病程。患者和方法:我们分析了2018年至2022年间在血管科(苏黎世大学医院)接受血管成形术和放置球囊扩张BeSmooth外周支架系统®(德国本特利)的连续患者的数据。主要结果是在指数血管成形术后6个月内和随访期间对目标病变进行再次干预。这项研究得到了当地伦理委员会的批准。结果:共有27例患者接受了治疗。中位年龄为70岁(Q1-Q3:60-74),59%为男性。锁骨下动脉(74%)是最常治疗的靶病变,其次是无名动脉(26%)。治疗组24小时血压平均改善21(95%CI 7至35)mmHg,6个月血压平均改善29(95%CI 15至43)mmHg。6个月时,2名(8%)患者需要靶病变再干预。在长达24个月的剩余随访期内,这两名患者中有一名需要额外干预,共有3名(11%)患者分别死于败血症、癌症和未知原因。结论:经皮导管球囊扩张支架治疗症状性上肢PAD是有效和安全的。
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来源期刊
CiteScore
3.90
自引率
11.10%
发文量
61
审稿时长
1 months
期刊介绍: Vasa is the European journal of vascular medicine. It is the official organ of the German, Swiss, and Slovenian Societies of Angiology. The journal publishes original research articles, case reports and reviews on vascular biology, epidemiology, prevention, diagnosis, medical treatment and interventions for diseases of the arterial circulation, in the field of phlebology and lymphology including the microcirculation, except the cardiac circulation. Vasa combines basic science with clinical medicine making it relevant to all physicians interested in the whole vascular field.
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