Temporal changes in coronary plaque as assessed by an artificial intelligence–based optical coherence tomography: from the first-in-human trial on DREAMS 3G scaffold

Author:

Garcia-Garcia Hector M1ORCID,Waksman Ron1,Melaku Gebremedhin D1,Garg Mohil1,Beyene Solomon1,Wlodarczak Adrian2ORCID,Kerai Ajay1,Levine Molly B1,van der Schaaf René J3,Torzewski Jan4,Ferdinande Bert5,Escaned Javier6ORCID,Iglesias Juan F7,Bennett Johan8ORCID,Toth Gabor G9ORCID,Joner Michael1011ORCID,Toelg Ralph12,Wiemer Marcus13,Olivecrona Göran14,Vermeersch Paul15ORCID,Haude Michael16

Affiliation:

1. Interventional Cardiology, MedStar Washington Hospital Center , 110 Irving Street NW, Suite 4B-1, Washington, DC 20010 , USA

2. Department of Cardiology, Miedziowe Centrum Zdrowia SA , Lubin , Poland

3. Department of Interventional Cardiology, OLVG , Amsterdam , The Netherlands

4. Cardiovascular Center Oberallgäu-Kempten , Kempten , Germany

5. Department of Cardiology, Ziekenhuis Oost Limburg (ZOL) , Genk , Belgium

6. Division of Cardiology, Hospital Clinico San Carlos IDISSC, Complutense University of Madrid , Madrid , Spain

7. Cardiology Division, University Hospital of Geneva , Geneva , Switzerland

8. Department of Cardiovascular Medicine, University Hospitals Leuven , Leuven , Belgium

9. Division Cardiology, Medical University Graz , Graz , Austria

10. Klinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München , München , Germany

11. Deutsches Zentrum für Herz- und Kreislauf-Forschung (DZHK) e.V. (German Center for Cardiovascular Research), Partner Site Munich Heart Alliance , Munich , Germany

12. Cardiology Department, Heart Center Segeberger Kliniken , Bad Segeberg , Germany

13. Department of Cardiology and Intensive Care, Johannes Wesling University Hospital, Ruhr University Bochum , Minden , Germany

14. Department of Cardiology, Skane University Hospital , Lund , Sweden

15. Interventional Cardiology, ZNA Middelheim , Antwerpen , Belgium

16. Medical Clinic I, Rheinland Klinikum Neuss GmbH, Lukaskrankenhaus , Neuss , Germany

Abstract

Abstract Aims The aim of the study is to assess the impact of the baseline plaque composition on the DREAMS 3G luminal late loss and to compare the serial plaque changes between baseline and 6 and 12 months (M) follow-up. Methods and results A total of 116 patients were enrolled in the BIOMAG-I trial. Patients were imaged with optical coherence tomography (OCT) pre- and post-DREAMS 3G implantation and at 6 and 12 M. OCTPlus software uses artificial intelligence to assess composition (i.e. lipid, calcium, and fibrous tissue) of the plaque. The differences between the OCT-derived minimum lumen area (MLA) post-percutaneous coronary intervention and 12 M were grouped into three terciles. Patients with larger MLA differences at 12 M (P = 0.0003) had significantly larger content of fibrous tissue at baseline. There was a reduction of 24.8% and 20.9% in lipid area, both P < 0.001, between the pre-DREAMS 3G OCT and the 6 and 12 M follow-up. Conversely, the fibrous tissue increased by 48.4% and 36.0% at 6 and 12 M follow-up, both P < 0.001. Conclusion The larger the fibrous tissue in the lesion at baseline, the larger the luminal loss seen at 6 and 12 M. Following the implantation of DREAMS 3G, favourable healing of the vessel coronary wall occurs as shown by a decrease in the lipid area and an increase in fibrous tissue.

Funder

Biotronik AG

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine

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