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Evaluation of custom-made Relay® stent-grafts for aortic arch landing zones 0 and I: experience from two high-volume aortic centres.
Dabravolskaite, Vaiva; Makaloski, Vladimir; Hakovirta, Harri; Kotelis, Drosos; Schoenhoff, Florian S; Lescan, Mario.
Afiliação
  • Dabravolskaite V; Department of Vascular Surgery, University Hospital of Bern, Bern, Switzerland.
  • Makaloski V; Department of Vascular Surgery, University Hospital of Turku, Turku, Finland.
  • Hakovirta H; Department of Vascular Surgery, Satakunnan keskussairaala, Pori, Finland.
  • Kotelis D; Department of Vascular Surgery, University Hospital of Bern, Bern, Switzerland.
  • Schoenhoff FS; Department of Vascular Surgery, University Hospital of Turku, Turku, Finland.
  • Lescan M; Department of Vascular Surgery, Satakunnan keskussairaala, Pori, Finland.
Eur J Cardiothorac Surg ; 66(1)2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38991832
ABSTRACT

OBJECTIVES:

To report experience with a Relay® stent-graft custom-made platform in treating different aortic arch pathology in 2 high-volume aortic centres.

METHODS:

A retrospective analysis of all patients treated between July 2016 and July 2023 with custom-made Relay® stent-graft (custom-made device). Underlying aortic arch pathology was an aneurysm, penetrating aortic ulcer, and dissection. Three custom-made device designs were used proximal scallop, fenestrations, and inner branches. The endpoints were technical success, perioperative stroke, death, and reintervention rate.

RESULTS:

Thirty-five patients (89% males) with a mean age of 70 ± 11 years were treated.Indication for treatment was penetrating aortic ulcer in 14 patients (40%), aneurysm in 11 patients (31%) and aortic dissection in 10 patients (29%). The technical success rate was 100%. Twenty-eight patients (80%) had proximal sealing in zone 0, and 7 (20%) had proximal sealing in zone 1. Nine patients (25.6%) had proximal scallops, 9 (25.6%) had 1 big fenestration and 17 (48.8%) had a branched device; 1 with single branch, 15 with double branches and 1 with triple branches. Thirty patients (86%) had previous or simultaneous left subclavian artery revascularization. No patient died during 30 days. Two patients (5.7%) had stroke postoperatively; both recovered without disabling deficits. The mean follow-up was 35 ± 26 months. Six patients (17.1%) died during follow-up. One patient required reinforcement of the bridging stent in the left common carotid artery and one additional vascular plugging of the left subclavian artery. Three patients received distal extension.

CONCLUSIONS:

The Relay® stent-graft custom-made platform showed a good performance in our study with a high technical success rate, low perioperative stroke and mortality, and low reintervention rates during the follow-up.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aorta Torácica / Desenho de Prótese / Prótese Vascular / Stents / Implante de Prótese Vascular Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Cardiothorac Surg Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aorta Torácica / Desenho de Prótese / Prótese Vascular / Stents / Implante de Prótese Vascular Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Cardiothorac Surg Ano de publicação: 2024 Tipo de documento: Article