In-Stent Restenosis in Saphenous Vein Grafts (from the DIVA Trial)

  • Iosif Xenogiannis
  • , Bavana V. Rangan
  • , Lauren Uyeda
  • , Subhash Banerjee
  • , Robert Edson
  • , Deepak L. Bhatt
  • , Steven Goldman
  • , David R. Holmes
  • , Sunil V. Rao
  • , Kendrick Shunk
  • , Kreton Mavromatis
  • , Kodangudi Ramanathan
  • , Antony A. Bavry
  • , Edward O. McFalls
  • , Santiago Garcia
  • , Hoang Thai
  • , Barry F. Uretsky
  • , Faisal Latif
  • , Ehrin Armstrong
  • , Jose Ortiz
  • Hani Jneid, Jayson Liu, Kul Aggrawal, Todd A. Conner, Todd Wagner, Judit Karacsonyi, Beverly Ventura, Aaron Alsleben, Ying Lu, Mei Chiung Shih, Emmanouil S. Brilakis

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Saphenous vein grafts (SVGs) have high rates of in-stent restenosis (ISR). We compared the baseline clinical and angiographic characteristics of patients and lesions that did develop ISR with those who did not develop ISR during a median follow-up of 2.7 years in the DIVA study (NCT01121224). We also examined the ISR types using the Mehran classification. ISR developed in 119 out of the 575 DIVA patients (21%), with similar incidence among patients with drug-eluting stents and bare-metal stents (BMS) (21% vs 21%, p = 0.957). Patients in the ISR group were younger (67 ± 7 vs 69 ± 8 years, p = 0.04) and less likely to have heart failure (27% vs 38%, p = 0.03) and SVG lesions with Thrombolysis In Myocardial Infarction 3 flow before the intervention (77% vs 83%, p <0.01), but had a higher number of target SVG lesions (1.33 ± 0.64 vs 1.16 ± 0.42, p <0.01), more stents implanted in the target SVG lesions (1.52 ± 0.80 vs 1.31 ± 0.66, p <0.01), and longer total stent length (31.37 ± 22.11 vs 25.64 ± 17.42 mm, p = 0.01). The incidence of diffuse ISR was similar in patients who received drug-eluting-stents and BMS (57% vs 54%, p = 0.94), but BMS patients were more likely to develop occlusive restenosis (17% vs 33%, p = 0.05).

Original languageEnglish (US)
Pages (from-to)24-30
Number of pages7
JournalAmerican Journal of Cardiology
Volume162
DOIs
StatePublished - Jan 1 2022

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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