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Editor's Choice - Two Year Results of the Randomised DISCOVER Trial Comparing Covered Versus Bare Metal Stents in the Common Iliac Artery.
Bekken, Joost A; Vroegindeweij, Dammis; Vos, Jan Albert; de Vries, Jean-Paul P M; Lardenoije, Jan Willem H P; Petri, Bart-Jeroen; Pierie, Maurice E N; van Weel, Vincent; Teijink, Joep A W; Fioole, Bram.
Afiliação
  • Bekken JA; Department of Vascular Surgery, Maasstad Hospital, Rotterdam, the Netherlands. Electronic address: joostbekken@hotmail.com.
  • Vroegindeweij D; Department of Interventional Radiology, Maasstad Hospital, Rotterdam, the Netherlands.
  • Vos JA; Department of Interventional Radiology, St. Antonius Hospital, Nieuwegein, the Netherlands.
  • de Vries JPM; Department of Surgery, Division of Vascular Surgery, University Medical Centre, Groningen, the Netherlands; Department of Vascular Surgery, St. Antonius Hospital, Nieuwegein, the Netherlands.
  • Lardenoije JWHP; Department of Vascular Surgery, Rijnstate Hospital, Arnhem, the Netherlands.
  • Petri BJ; Department of Vascular Surgery, University Medical Centre Utrecht, Utrecht, the Netherlands.
  • Pierie MEN; Department of Vascular Surgery, Isala Clinics, Zwolle, the Netherlands.
  • van Weel V; Department of Vascular Surgery, Meander Medical Centre, Amersfoort, the Netherlands.
  • Teijink JAW; Department of Vascular Surgery, Catharina Hospital, Eindhoven, the Netherlands.
  • Fioole B; Department of Vascular Surgery, Maasstad Hospital, Rotterdam, the Netherlands.
Eur J Vasc Endovasc Surg ; 65(3): 359-368, 2023 Mar.
Article em En | MEDLINE | ID: mdl-36336284
ABSTRACT

OBJECTIVE:

It has been suggested that covered stents (CS) may lower restenosis rates compared with bare metal stents (BMS) after endovascular treatment of the common iliac artery. This trial aimed to provide additional evidence on the efficacy of CS vs. BMS in the common iliac artery.

METHODS:

This multicentre, randomised, single blind controlled superiority trial compared balloon expandable CS and balloon expandable BMS for advanced atherosclerotic lesions in the common iliac artery; this was defined as a stenosis > 3 cm in length or occlusion. The primary end point was freedom from binary restenosis after two years of follow up. The study was conducted according to the principles of the Declaration of Helsinki (version October 2008) and registered with the Dutch Trial register (NTR3381).

RESULTS:

One hundred and seventy-four limbs were included between 2012 and 2019 with 87 limbs in each group. Six patients crossed over from the BMS group to the CS group but were analysed according to an intention to treat principle. Freedom from binary restenosis after two years of follow up was 84.7% (95% CI 76.7 - 92.7%) in the BMS group and 89.1% (95% CI 82.4 - 95.8%) in the CS group (p = .40). Freedom from occlusion was 95.0% (95% CI 90.3 - 95.7%) in the BMS group and 96.4% (95% CI 92.5 - 100%) in the CS group (p = .66). Freedom from target lesion revascularisation was 91.1% (95% CI 84.8 - 97.3%) and 95.2% (95% CI 90.7 -99.7%), respectively (p = .31). Technical success, complications, haemodynamic success, and clinical success were also comparable between both groups. Per-protocol analysis did not affect the outcomes of the study.

CONCLUSION:

No difference was found between balloon expandable CS and BMS for treating advanced atherosclerotic lesions of the common iliac artery.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Revista: Eur J Vasc Endovasc Surg Assunto da revista: ANGIOLOGIA Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Revista: Eur J Vasc Endovasc Surg Assunto da revista: ANGIOLOGIA Ano de publicação: 2023 Tipo de documento: Article