Back to Search Start Over

Percutaneous Coronary Intervention of Native Coronary Artery versus Saphenous Vein Graft in Patients with Prior Coronary Artery Bypass Graft Surgery: Rationale and Design of the Multicenter, Randomized PROCTOR Trial.

Authors :
de Winter, Ruben W.
Walsh, Simon J.
Hanratty, Colm G.
Spratt, James C.
Sprengers, Ralf W.
Twisk, Jos W.R.
Vegting, Iris
Schumacher, Stefan P.
Bom, Michiel J.
Hoek, Roel
Verouden, Niels J.
Delewi, Ronak
Nap, Alexander
Knaapen, Paul
Twisk, Jos W
PROCTOR Trial Research Group
Source :
American Heart Journal; Mar2023, Vol. 257, p20-29, 10p
Publication Year :
2023

Abstract

<bold>Background: </bold>Patients with prior coronary artery bypass grafting (CABG) frequently require repeat percutaneous revascularization due to advanced age, progressive coronary artery disease and bypass graft failure. Percutaneous coronary intervention (PCI) of either the bypass graft or the native coronary artery may be performed. Randomized trials comparing native vessel PCI with bypass graft PCI are lacking and long-term outcomes have not been reported.<bold>Study Design: </bold>PROCTOR (NCT03805048) is a prospective, multicenter, randomized controlled trial, that will include 584 patients presenting with saphenous vein graft (SVG) failure and a clinical indication for revascularization, as determined by the local Heart Team. The trial is designed to compare the clinical and angiographic outcomes in patients randomly allocated in a 1:1 fashion to either a strategy of native vessel PCI or SVG PCI. The primary study endpoint is a 3-year composite of major adverse cardiac events (MACE: all-cause mortality, non-fatal target coronary territory myocardial infarction [MI], or clinically driven target coronary territory revascularization). At 3-years, after evaluation of the primary endpoint, follow-up invasive coronary angiography will be performed. Secondary endpoints comprise individual components of MACE at 1, 3 and 5 years follow-up, PCI-related MI, MI >48 hours after index PCI, target vessel failure, target lesion revascularization, renal failure requiring renal-replacement therapy, angiographic outcomes at 3-years and quality of life (delta Seattle Angina Questionnaire, Canadian Cardiovascular Society Grading Scale and Rose Dyspnea Scale).<bold>Conclusion: </bold>PROCTOR is the first randomized trial comparing an invasive strategy of native coronary artery PCI with SVG PCI in post-CABG patients presenting with SVG failure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00028703
Volume :
257
Database :
Supplemental Index
Journal :
American Heart Journal
Publication Type :
Academic Journal
Accession number :
161826421
Full Text :
https://doi.org/10.1016/j.ahj.2022.11.014