Rivaroxaban and Aspirin in Drug-Coated Balloon Angioplasty for Femoropopliteal In-Stent Restenosis: A Retrospective

Zhihong Wang1, Lei Sheng1, Hongbin Gu1

  • 1Department of Vascular Surgery, The Ninth Medical Center of the Chinese People's Liberation Army General Hospital, Beijing, China.

PubMed

Insights

Rivaroxaban and aspirin effectively treat femoropopliteal artery in-stent restenosis after drug-coated balloon intervention, reducing recurrence and improving vascular patency safely compared to dual antiplatelet therapy.

Area of Science:

  • Vascular Surgery
  • Interventional Cardiology
  • Pharmacology

Background:

  • Femoropopliteal artery in-stent restenosis (ISR) after drug-coated balloon (DCB) treatment can lead to target lesion restenosis.
  • Optimizing antithrombotic therapy post-DCB intervention is crucial for managing ISR.

Purpose of the Study:

  • To evaluate the efficacy and safety of rivaroxaban combined with aspirin (RA Group) versus dual antiplatelet therapy (DAPT) for ISR following DCB intervention.
  • To compare clinical outcomes and vascular patency rates between the two treatment groups.

Main Methods:

  • A consecutive cohort of 92 patients with femoropopliteal ISR post-DCB intervention were analyzed.
  • Patients were divided into an RA group (rivaroxaban + aspirin) and a DAPT group.
  • Outcomes were compared over a 12-month follow-up period.

Main Results:

  • The RA group demonstrated significantly lower rates of ISR recurrence and clinically driven target lesion revascularization compared to the DAPT group (P < 0.05).
  • Vascular patency rates were higher in the RA group at both 6 and 12 months post-intervention (P < 0.05).
  • No major adverse events (death, MI, stroke, amputation, major bleeding) were observed; only minor bleeding occurred in 5 patients.

Conclusions:

  • Rivaroxaban combined with aspirin offers a safe and effective alternative to DAPT for managing femoropopliteal ISR after DCB intervention.
  • This regimen improves key follow-up outcomes, including reduced restenosis and enhanced vascular patency.
Abstract

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