Optical coherence tomography (OCT)-angiography coregistration during stent implantation may be useful to avoid geographical mismatch and incomplete lesion coverage. Untreated lipid-rich plaque at stent edge is associated with subsequent stent edge restenosis. The present study sought to compare the frequency of untreated lipid-rich plaque at the stent edge between OCT-guided percutaneous coronary intervention (PCI) with and without OCT-angiography coregistration. We investigated 398 patients who underwent OCT-guided stent implantation (n = 198 in the coregistration group, and n = 200 in the no coregistration group). In OCT after PCI, untreated lipid-lich plaque was identified by the maximum lipid arc > 180˚ in the 5-mm stent edge segment. The PCI-targeted lesion characteristics and stent length were not different between the coregistration group and the no coregistration group. The frequency of untreated lipid-rich plaque in either proximal or distal stent edge segment was significantly lower in the coregistration group than in the no coregistration group (16% vs. 26%, P = 0.015). The frequency of stent-edge dissection (5% vs. 6%, P = 0.516) and untreated stenosis (2% vs. 3%, P = 0.724) was low and without significant differences between the two groups. In OCT-guided PCI, the use of OCT-angiography coregistration was associated with a reduced frequency of untreated lipid-rich plaque at stent edges. OCT-angiography coregistration has a positive impact on PCI results.
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Univ Melbourne, Cardiovasc Res Grp, Melbourne Med Sch, Melbourne, Vic, AustraliaUniv Melbourne, Cardiovasc Res Grp, Melbourne Med Sch, Melbourne, Vic, Australia
Hayat, Umair
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Thondapu, Vikas
Ul Haq, Muhammad Asrar
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Univ Melbourne, Cardiovasc Res Grp, Melbourne Med Sch, Melbourne, Vic, AustraliaUniv Melbourne, Cardiovasc Res Grp, Melbourne Med Sch, Melbourne, Vic, Australia
Ul Haq, Muhammad Asrar
Foin, Nicolas
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Natl Heart Ctr Singapore, Natl Heart Res Inst, Singapore, SingaporeUniv Melbourne, Cardiovasc Res Grp, Melbourne Med Sch, Melbourne, Vic, Australia
Foin, Nicolas
Jang, Ik-Kyung
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Harvard Univ, Massachusetts Gen Hosp, Boston, MA 02115 USAUniv Melbourne, Cardiovasc Res Grp, Melbourne Med Sch, Melbourne, Vic, Australia
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Royal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, EnglandRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Pighi, M.
Konstantinidis, N.
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Royal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, EnglandRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Konstantinidis, N.
Ghione, M.
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Royal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, EnglandRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Ghione, M.
Kilic, D.
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Royal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, EnglandRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Kilic, D.
Foin, N.
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Natl Heart Ctr Singapore, Singapore, SingaporeRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Foin, N.
Dall'Ara, G.
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Royal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, EnglandRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Dall'Ara, G.
Secco, G. G.
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Univ Piemonte Orientale, Maggiore della Carita Hosp, Novara, ItalyRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Secco, G. G.
Valente, S.
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Univ Florence, Intervent Cardiol Unit, Dept Heart & Vessels, AOU Careggi, Florence, ItalyRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England
Valente, S.
Di Mario, C.
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Royal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, EnglandRoyal Brompton & Harefield NHS Fdn Trust, NIHR Biomed Res Unit, London, England