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1000 Titel
  • Clinical outcomes of a balloon-expandable stent for symptomatic obstructions of the subclavian or innominate arteries
1000 Autor/in
  1. Fumagalli, Riccardo Mario |
  2. Schürch, Kerstin |
  3. Grigorean, Alexandru |
  4. Holy, Erik W. |
  5. Münger, Mario |
  6. Pleming, William |
  7. Kucher, Nils |
  8. Barco, Stefano |
1000 Erscheinungsjahr 2023
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2023-10-03
1000 Erschienen in
1000 Quellenangabe
  • 52(6):409-415
1000 Copyrightjahr
  • 2023
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1024/0301-1526/a001092 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:p> Summary: 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<jats:sup>®</jats:sup> (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. </jats:p>
1000 Sacherschließung
lokal Female [MeSH]
lokal Stents [MeSH]
lokal upper extremity
lokal Aged [MeSH]
lokal Humans [MeSH]
lokal Treatment Outcome [MeSH]
lokal Brachiocephalic Trunk/diagnostic imaging [MeSH]
lokal Angioplasty
lokal Angioplasty, Balloon/adverse effects [MeSH]
lokal peripheral arterial disease
lokal Original communication
lokal Male [MeSH]
lokal Vascular Patency [MeSH]
lokal Peripheral Arterial Disease/diagnostic imaging [MeSH]
lokal Peripheral Arterial Disease/therapy [MeSH]
lokal cohort study
lokal stent
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-6794-1986|https://orcid.org/0009-0005-5846-2763|https://frl.publisso.de/adhoc/uri/R3JpZ29yZWFuLCBBbGV4YW5kcnU=|https://frl.publisso.de/adhoc/uri/SG9seSwgRXJpayBXLg==|https://frl.publisso.de/adhoc/uri/TcO8bmdlciwgTWFyaW8=|https://orcid.org/0000-0001-9262-7588|https://frl.publisso.de/adhoc/uri/S3VjaGVyLCBOaWxz|https://frl.publisso.de/adhoc/uri/QmFyY28sIFN0ZWZhbm8=
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1000 Erstellt am 2024-05-14T11:48:07.345+0200
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