BMJ Open (Jul 2021)

Identification of anatomic risk factors for acute coronary events by optical coherence tomography in patients with myocardial infarction and residual nonflow limiting lesions: rationale and design of the PECTUS-obs study

  • Peep Laanmets,
  • Martijn Meuwissen,
  • Niels van Royen,
  • Robert-Jan van Geuns,
  • Cyril Camaro,
  • Steven Teerenstra,
  • Saman Rasoul,
  • Erik Lipsic,
  • Rohit M Oemrawsingh,
  • Peter Damman,
  • Jan-Quinten Mol,
  • Anouar Belkacemi,
  • Rick HJA Volleberg,
  • Alexey V Protopopov,
  • Oleg V Krestyaninov,
  • Robert Dennert,
  • Jan-Peter van Kuijk,
  • Karin Arkenbout,
  • Dirk J van der Heijden,
  • Maarten AH van Leeuwen

DOI
https://doi.org/10.1136/bmjopen-2021-048994
Journal volume & issue
Vol. 11, no. 7

Abstract

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Introduction In patients with myocardial infarction, the decision to treat a nonculprit lesion is generally based on its physiological significance. However, deferral of revascularisation based on nonischaemic fractional flow reserve (FFR) values in these patients results in less favourable outcomes compared with patients with stable coronary artery disease, potentially caused by vulnerable nonculprit lesions. Intravascular optical coherence tomography (OCT) imaging allows for in vivo morphological assessment of plaque ‘vulnerability’ and might aid in the detection of FFR-negative lesions at high risk for recurrent events.Methods and analysis The PECTUS-obs study is an international multicentre prospective observational study that aims to relate OCT-derived vulnerable plaque characteristics of nonflow limiting, nonculprit lesions to clinical outcome in patients with myocardial infarction. A total of 438 patients presenting with myocardial infarction (ST-elevation myocardial infarction and non-ST-elevation myocardial infarction) will undergo OCT-imaging of any FFR-negative nonculprit lesion for detection of plaque vulnerability. The primary study endpoint is a composite of major adverse cardiovascular events (all-cause mortality, nonfatal myocardial infarction or unplanned revascularisation) at 2-year follow-up. Secondary endpoints will be the same composite at 1-year and 5-year follow-up, target vessel failure, target vessel revascularisation, target lesion failure and target lesion revascularisation.Ethics and dissemination This study has been approved by the Medical Ethics Committee of the region Arnhem-Nijmegen. The results of this study will be disseminated in a main paper and additional papers with subgroup analyses.Trial registration number NCT03857971.