Intravascular Ultrasound Assessment of In-Stent Restenosis in Saphenous Vein Grafts. Academic Article uri icon

Overview

abstract

  • Outcomes after percutaneous coronary interventions (PCI) in saphenous vein grafts (SVG) are inferior compared with native coronary arteries, but the mechanisms of SVG in-stent restenosis (ISR) have not been well-described. Thus, we aimed to evaluate the patterns of SVG ISR using intravascular ultrasound (IVUS) in 54 SVG ISR lesions. Stent underexpansion was defined as minimum stent area (MSA) <5 mm2. The time from stent implantation to presentation with ISR (9 BMS, 18 first-generation DES, and 27 second-generation DES) was 3.7 ± 3.0 years. IVUS-defined ISR patterns were categorized as mechanical (33%) or biological (67%). Mechanical patterns comprised 10 cases of stent underexpansion (MSA = 4.2 ± 0.9 mm2), 6 stent fractures or deformations, and 2 uncovered aorto-anastomotic lesions. Biological patterns comprised 19 cases of neoatherosclerosis, 13 excessive neointimal hyperplasia (NIH, 65 ± 11%), and 4 thrombi. Compared with biological patterns of ISR, mechanical patterns were more frequently located at the SVG anastomosis (72% vs 39%, p = 0.04) and at the SVG hinge motion site (55% vs 21%, p = 0.02). Although patients with mechanical patterns of ISR presented earlier than those with biological patterns (2.3 vs 4.4 years, p = 0.009), 61% of them were diagnosed >1 year after stent implantation. In conclusion, SVG ISR is dominated by biological patterns including neoatherosclerosis. Mechanical patterns of SVG ISR are associated with earlier presentation and location at graft anastomosis or hinge motion site.

publication date

  • January 4, 2019

Research

keywords

  • Coronary Occlusion
  • Coronary Restenosis
  • Coronary Vessels
  • Graft Occlusion, Vascular
  • Percutaneous Coronary Intervention
  • Saphenous Vein
  • Ultrasonography, Interventional

Identity

Scopus Document Identifier

  • 85059803293

Digital Object Identifier (DOI)

  • 10.1016/j.amjcard.2018.12.030

PubMed ID

  • 30642605

Additional Document Info

volume

  • 123

issue

  • 7