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Drug-Eluting Stent Shows Similar Patency Results as Prosthetic Bypass in Patients with Femoropopliteal Occlusion in a Randomized Trial




TekijätPatrick Björkman, Tommi Auvinen, Harri Hakovirta, Pekka Romsi, Johanna Turtiainen, Hannu Manninen, Maarit Venermo

KustantajaElsevier Inc.

Julkaisuvuosi2018

JournalAnnals of Vascular Surgery

Tietokannassa oleva lehden nimiAnnals of Vascular Surgery

Vuosikerta53

Aloitussivu165

Lopetussivu170

Sivujen määrä6

ISSN0890-5096

eISSN1615-5947

DOIhttps://doi.org/10.1016/j.avsg.2018.04.014


Tiivistelmä

Background: Claudication and critical limb threatening ischemia are significant causes of mortality in the elderly. The gold standard of superficial femoral artery (SFA) revascularization is thus far considered to be the femoropopliteal bypass. The aim of this study was to compare mid-term patency between drug-eluting stents (DESs) and prosthetic bypass grafts (BSX). Studies have reported comparable results for both the methods.

Methods: Forty-six patients with claudication or rest pain due to a 5–25 cm SFA occlusion were randomized between DES and BSX groups. The follow-up period was 24 months, and the primary outcome measure was overall patency. Secondary outcome measures were primary and primary assisted patency, change in ankle-brachial index (ABI), and amputation-free survival.

Results: Forty-one patients were eventually analyzed. Six-month secondary patency was 91% (DES) versus 83% (BSX) (P = 0.450). The corresponding numbers at 12 months in the DES and BSX groups were 74% and 80% (P = 0.750), respectively. At 24 months, the respective numbers were 56% and 71% (P = 0.830). There were no statistically significant differences in primary or assisted primary patency at 1, 6, or 12 months.

Conclusion: There were no demonstrable differences in patency rates or clinical outcomes such as ABI or major amputations between DES and BSX. Although underpowered, the results suggest noninferiority of the DES compared with prosthetic bypass surgery. Trial registration: The trial was preregistered at ClinicalTrials.org (NCT01450722).



Last updated on 2024-26-11 at 23:27