Venous Stents Placed for Postthrombotic Syndrome: The Role of Inflow Disease on Patency

Jay M Bakas1, Mark A F de Wolf2, Renate R van den Bos3

  • 1Department of Surgery, Erasmus University Medical Center, Rotterdam, The Netherlands.

Insights

Deep femoral vein (DFV) and femoral vein (FV) inflow disease significantly increases the risk of venous stent patency loss in patients with postthrombotic syndrome (PTS). This finding impacts treatment decisions and patient expectations for stent longevity.

Area of Science:

  • Vascular Surgery
  • Interventional Radiology
  • Venous Thromboembolism

Background:

  • Postthrombotic syndrome (PTS) can lead to chronic venous obstruction.
  • Venous stenting is a treatment option for severe PTS.
  • Factors influencing stent patency in PTS require further investigation.

Purpose of the Study:

  • To determine the impact of deep femoral vein (DFV) and/or femoral vein (FV) inflow disease on venous stent patency in PTS patients.
  • To identify specific inflow characteristics that predict stent failure.

Main Methods:

  • Retrospective analysis of 80 limbs with iliofemoral/iliocaval stents for PTS.
  • Classification of inflow disease as none, single-vessel, or double-vessel based on DFV/FV imaging.
  • Assessment of 1-year primary and secondary stent patency rates.
  • Statistical analysis using Kaplan-Meier and logistic regression.

Main Results:

  • One-year primary patency was significantly lower in limbs with inflow disease (57.7% single-vessel, 47.1% double-vessel) compared to those without (89.2%).
  • Inflow disease was a strong predictor of primary patency loss (univariate OR 7.17, multivariate OR 10.99 for FV disease).
  • No significant difference in secondary patency was observed.

Conclusions:

  • Inflow disease of the DFV/FV is a critical risk factor for early venous stent patency loss in PTS.
  • Pre-procedural assessment of inflow disease is crucial for patient counseling and managing expectations.
  • Further research may explore targeted inflow interventions to improve stent outcomes.
Abstract