Multi-modal characterization of the left atrium by a fully automated integration of pre-procedural cardiac imaging and electro-anatomical mapping.

Alignment Atrial fibrillation Imaging Integration Mapping Netherlands Trial Register NL7894 clinicaltrials.gov NCT04342312

Journal

International journal of cardiology. Heart & vasculature
ISSN: 2352-9067
Titre abrégé: Int J Cardiol Heart Vasc
Pays: Ireland
ID NLM: 101649525

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 05 07 2023
revised: 25 09 2023
accepted: 27 09 2023
medline: 19 10 2023
pubmed: 19 10 2023
entrez: 19 10 2023
Statut: epublish

Résumé

The combination of information obtained from pre-procedural cardiac imaging and electro-anatomical mapping (EAM) can potentially help to locate new ablation targets. In this study we developed and evaluated a fully automated technique to align left atrial (LA) anatomies obtained from CT- and MRI-scans with LA anatomies obtained from EAM. Twenty-one patients scheduled for a pulmonary vein (PV) isolation with a pre-procedural MRI were enrolled. Additionally, a recent computed tomography (CT) scan was available in 12 patients. LA anatomies were segmented from MRI-scans using ADAS-AF (Galgo Medical, Barcelona) and from the CT-scans using Slicer3D. MRI and CT anatomies were aligned with the EAM anatomy using an iterative closest plane-to-plane algorithm. Initially, the algorithm included the PVs, LA appendage and mitral valve anulus as they are the most distinctive landmarks. Subsequently, the algorithm was applied again, excluding these structures, with only three iterative steps to refine the alignment of the true LA surface. The result of the alignments was quantified by the Euclidian distance between the aligned anatomies after excluding PVs, LA appendage and mitral anulus. Our algorithm successfully aligned 20/21 MRI anatomies and 11/12 CT anatomies with the corresponding EAM anatomies. The average median residual distances were 1.9 ± 0.6 mm and 2.5 ± 0.8 mm for MRI and CT anatomies respectively. The average LA surface with a residual distance less than 5.00 mm was 89 ± 9% and 89 ± 10% for MRI and CT anatomies respectively. An iterative closest plane-to-plane algorithm is a reliable method to automatically align pre-procedural cardiac images with anatomies acquired during ablation procedures.

Sections du résumé

Background UNASSIGNED
The combination of information obtained from pre-procedural cardiac imaging and electro-anatomical mapping (EAM) can potentially help to locate new ablation targets. In this study we developed and evaluated a fully automated technique to align left atrial (LA) anatomies obtained from CT- and MRI-scans with LA anatomies obtained from EAM.
Methods UNASSIGNED
Twenty-one patients scheduled for a pulmonary vein (PV) isolation with a pre-procedural MRI were enrolled. Additionally, a recent computed tomography (CT) scan was available in 12 patients. LA anatomies were segmented from MRI-scans using ADAS-AF (Galgo Medical, Barcelona) and from the CT-scans using Slicer3D. MRI and CT anatomies were aligned with the EAM anatomy using an iterative closest plane-to-plane algorithm. Initially, the algorithm included the PVs, LA appendage and mitral valve anulus as they are the most distinctive landmarks. Subsequently, the algorithm was applied again, excluding these structures, with only three iterative steps to refine the alignment of the true LA surface. The result of the alignments was quantified by the Euclidian distance between the aligned anatomies after excluding PVs, LA appendage and mitral anulus.
Results UNASSIGNED
Our algorithm successfully aligned 20/21 MRI anatomies and 11/12 CT anatomies with the corresponding EAM anatomies. The average median residual distances were 1.9 ± 0.6 mm and 2.5 ± 0.8 mm for MRI and CT anatomies respectively. The average LA surface with a residual distance less than 5.00 mm was 89 ± 9% and 89 ± 10% for MRI and CT anatomies respectively.
Conclusion UNASSIGNED
An iterative closest plane-to-plane algorithm is a reliable method to automatically align pre-procedural cardiac images with anatomies acquired during ablation procedures.

Identifiants

pubmed: 37854978
doi: 10.1016/j.ijcha.2023.101276
pii: S2352-9067(23)00107-0
pmc: PMC10579959
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101276

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Références

Phys Med Biol. 2007 Oct 21;52(20):6323-37
pubmed: 17921587
Eur Heart J Cardiovasc Imaging. 2021 Dec 18;23(1):31-41
pubmed: 34747450
Front Physiol. 2020 Sep 16;11:1145
pubmed: 33041850
N Engl J Med. 2015 May 7;372(19):1812-22
pubmed: 25946280
Med Image Anal. 2019 Jul;55:65-75
pubmed: 31026761
Int J Med Robot. 2017 Dec;13(4):
pubmed: 28370919
J Am Coll Cardiol. 2017 Jan 24;69(3):303-321
pubmed: 28104073
Radiology. 2023 Jun;307(5):e222032
pubmed: 37278633
Nat Biomed Eng. 2019 Nov;3(11):870-879
pubmed: 31427780
PLoS Comput Biol. 2020 Sep 23;16(9):e1008086
pubmed: 32966275
JAMA. 2019 Apr 2;321(13):1261-1274
pubmed: 30874766
Europace. 2023 May 19;25(5):
pubmed: 37125968
J Cardiovasc Magn Reson. 2017 Aug 23;19(1):64
pubmed: 28835250
Magn Reson Imaging. 2012 Nov;30(9):1323-41
pubmed: 22770690
J Cardiovasc Electrophysiol. 2000 Aug;11(8):869-79
pubmed: 10969749
JAMA. 2022 Jun 21;327(23):2296-2305
pubmed: 35727277
J Am Coll Cardiol. 2012 Aug 14;60(7):628-36
pubmed: 22818076
JACC Clin Electrophysiol. 2018 Jan;4(1):59-68
pubmed: 29520376
J Cardiovasc Electrophysiol. 2008 Aug;19(8):821-7
pubmed: 18373607
Europace. 2021 Apr 6;23(4):565-574
pubmed: 33200213
J Interv Card Electrophysiol. 2012 Mar;33(2):161-9
pubmed: 22119854
Circulation. 2006 Jan 17;113(2):186-94
pubmed: 16401772
J Am Coll Cardiol. 2004 Jun 2;43(11):2044-53
pubmed: 15172410
JAMA. 2014 Feb 5;311(5):498-506
pubmed: 24496537
Invest Radiol. 2021 May 1;56(5):335-340
pubmed: 33273374
Front Cardiovasc Med. 2022 Jun 30;9:879139
pubmed: 35879962

Auteurs

Ben J M Hermans (BJM)

Department of Physiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands.

Geertruida P Bijvoet (GP)

Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Robert J Holtackers (RJ)

Department of Radiology and Nuclear Medicine, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Casper Mihl (C)

Department of Radiology and Nuclear Medicine, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Justin G L M Luermans (JGLM)

Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Bart Maesen (B)

Department of Cardiothoracic Surgery, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Kevin Vernooy (K)

Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Dominik Linz (D)

Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Sevasti-Maria Chaldoupi (SM)

Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Ulrich Schotten (U)

Department of Physiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands.
Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), Maastricht, the Netherlands.

Classifications MeSH