Visualisation of coronary venous anatomy by computed tomography angiography prior to cardiac resynchronisation therapy implantation
- PMID: 30030750
- PMCID: PMC6115304
- DOI: 10.1007/s12471-018-1132-2
Visualisation of coronary venous anatomy by computed tomography angiography prior to cardiac resynchronisation therapy implantation
Abstract
Background: The purpose of this study was to illustrate the additive value of computed tomography angiography (CTA) for visualisation of the coronary venous anatomy prior to cardiac resynchronisation therapy (CRT) implantation.
Methods: Eighteen patients planned for CRT implantation were prospectively included. A specific CTA protocol designed for visualisation of the coronary veins was carried out on a third-generation dual-source CT platform. Coronary veins were semi-automatically segmented to construct a 3D model. CTA-derived coronary venous anatomy was compared with intra-procedural fluoroscopic angiography (FA) in right and left anterior oblique views.
Results: Coronary venous CTA was successfully performed in all 18 patients. CRT implantation and FA were performed in 15 patients. A total of 62 veins were visualised; the number of veins per patient was 3.8 (range: 2-5). Eighty-five per cent (53/62) of the veins were visualised on both CTA and FA, while 10% (6/62) were visualised on CTA only, and 5% (3/62) on FA only. Twenty-two veins were present on the lateral or inferolateral wall; of these, 95% (21/22) were visualised by CTA. A left-sided implantation was performed in 13 patients, while a right-sided implantation was performed in the remaining 2 patients because of a persistent left-sided superior vena cava with no left innominate vein on CTA.
Conclusion: Imaging of the coronary veins by CTA using a designated protocol is technically feasible and facilitates the CRT implantation approach, potentially improving the outcome.
Keywords: Cardiac resynchronisation therapy; Computed tomography angiography; Coronary veins; Fluoroscopic angiography.
Conflict of interest statement
Conflict of interest
U.C. Nguyên received a Kootstra Talent Fellowship research grant from Maastricht University and was additionally funded by a research grant from MS from the Dutch Heart Foundation (grant #2015T61). M.J.M. Cluitmans is supported by the Hein Wellens Fonds and is part-time employed by Philips. J.E. Wildberger received institutional grants from Agfa, Bayer, GE, Phillips, and Siemens and speaker fees from Bayer and Siemens. F.W. Prinzen received research grants from Medtronic, Abbott, LivaNova, Biosense Webster, MSD, and Biotronik. K. Vernooy received research grants from Medtronic and Abbott. J.G.L.M. Luermans, M. Strik, C.B. de Vos, B.L.J.H. Kietselaer and C. Mihl declare that they have no competing interests.
Ethical standards
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1975 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study.
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