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Living the heart in three dimensions: applications of 3D printing in CHD

Published online by Cambridge University Press:  14 June 2019

Mari Nieves Velasco Forte*
Affiliation:
Division of Imaging Sciences and Biomedical Engineering, King’s College, London, UK Cardiovascular Pathology Unit, Institute of Biomedicine of Seville, IBIS, Virgen del Rocio University Hospital/CSIC/University of Seville, Sevilla, Spain Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands
Tarique Hussain
Affiliation:
Department of Pediatrics, UT Southwestern Medical Center, 1935 Medical District Drive, Dallas, TX, USA
Arno Roest
Affiliation:
Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands
Gorka Gomez
Affiliation:
Cardiovascular Pathology Unit, Institute of Biomedicine of Seville, IBIS, Virgen del Rocio University Hospital/CSIC/University of Seville, Sevilla, Spain
Monique Jongbloed
Affiliation:
Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands
John Simpson
Affiliation:
Division of Imaging Sciences and Biomedical Engineering, King’s College, London, UK Department of Congenital Heart Disease, Evelina London Children’s Hospital, Guy’s and St Thomas’ NHS Foundation Trust, London, UK
Kuberan Pushparajah
Affiliation:
Division of Imaging Sciences and Biomedical Engineering, King’s College, London, UK Department of Congenital Heart Disease, Evelina London Children’s Hospital, Guy’s and St Thomas’ NHS Foundation Trust, London, UK
Nick Byrne
Affiliation:
Division of Imaging Sciences and Biomedical Engineering, King’s College, London, UK
Israel Valverde
Affiliation:
Division of Imaging Sciences and Biomedical Engineering, King’s College, London, UK Cardiovascular Pathology Unit, Institute of Biomedicine of Seville, IBIS, Virgen del Rocio University Hospital/CSIC/University of Seville, Sevilla, Spain Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands
*
Author for correspondence: Mari Nieves Velasco-Forte, School of Biomedical Engineering and Imaging Sciences, King’s College London, F04 Lambeth Wing, St Thomas’ Hospital, Westminster Bridge Rd, Lambeth, London SE1 7EH, UK. Tel: +44 7849 912341; E-mail: mnieves.velasco@kcl.ac.uk
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Abstract

Advances in biomedical engineering have led to three-dimensional (3D)-printed models being used for a broad range of different applications. Teaching medical personnel, communicating with patients and relatives, planning complex heart surgery, or designing new techniques for repair of CHD via cardiac catheterisation are now options available using patient-specific 3D-printed models. The management of CHD can be challenging owing to the wide spectrum of morphological conditions and the differences between patients. Direct visualisation and manipulation of the patients’ individual anatomy has opened new horizons in personalised treatment, providing the possibility of performing the whole procedure in vitro beforehand, thus anticipating complications and possible outcomes. In this review, we discuss the workflow to implement 3D printing in clinical practice, the imaging modalities used for anatomical segmentation, the applications of this emerging technique in patients with structural heart disease, and its limitations and future directions.

Information

Type
Review Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© Cambridge University Press 2019
Figure 0

Figure 1. Adapted from Velasco Forte et al. 3D balance steady-state precession acquired with image-based navigation for a patient with partial anomalous pulmonary venous connection. Sinus venosus defect in axial (a) and coronal (b) reformats. Pathway of anomalous pulmonary veins into the LA (white arrow) in coronal view (c). Ao = aorta; LA = left atrium; LPA = left pulmonary artery; LV = left ventricle; MPA = main pulmonary artery; RA = right atrium; RPA = right pulmonary artery; SVC = superior caval vein.

Figure 1

Figure 2. Steps of the segmentation process using an online open-access segmentation tool. (a) Image cropping. (b) Thresholding. (c) Manual editing of the anatomy. (d) 3D representation of the segmentation.

Figure 2

Figure 3. International study involving ten participating centers. Demographic, clinical and imaging data (CT and MRI) were collected by participating centres, de-identified and uploaded to a dedicated cloud server. Data was downloaded by a single centre (VRH) for consolidation, 3D printing and evaluation of 3D printing measurement accuracy. 3D printed models were sent by urgent delivery post to the referral centre for examination, communication with the medical team and parents of the patients and hands-on simulation of the surgery. Participating centres: Hospital Virgen del Rocio (Seville, Spain), Evelina Children’s Hospital (London, United Kingdom), Bristol Royal Hospital for Children (Bristol, United Kingdom), Leiden University Medical Centre (Leiden, The Netherlands), Montreal Children’s Hospital (Montreal, Canada), Fondazione Toscana Gabriele Monasterio (Massa, Italy), Hospital Sant Joan de Deu (Barcelona, Spain), Hospital de Cordoba (Cordoba, Spain), Hospital Regional de Malaga (Malaga, Spain), American University of Beirut (Beirut, Lebanon). Adapted from Valverde et al.34

Figure 3

Figure 4. 3D segmentation of the heart of a patient with partial anomalous pulmonary venous connection. The model was printed 1:1 scale, and 2 mm thickness was added using computer-aided design techniques. (a) Lateral view of the heart showing right upper pulmonary vein (RUPV, black arrow) draining into the superior caval vein (SVC). (b) Sagittal cut showing orifice of the drainage of the RUPV into the SVC (black arrow). (c) Axial reformat showing pathway of the RUPV (black arrow), draining into the SVC and continuing towards the left atrium (LA).

Figure 4

Figure 5. The flexible, translucent models were examined to confirm the expected relationship of the anomalous pulmonary veins (PVs) (arrows) to the superior caval vein (SVC) and left atrium (LA). Within the model, a balloon-mounted stent catheter was placed in the SVC to right atrium (RA) junction (blue catheter), while a dilator (red) was passed from the anomalous right upper PV to the left upper pulmonary vein (LUPV). The distance from the anomalous PV to the SVC–RA junction was measured using the three-dimensional (3D) model and the cross-sectional images described in the preceding text. This allowed calculation of the length of the stent to close the defect and redirect the flow of the partial anomalous pulmonary venous drainage towards the LA.

Figure 5

Figure 6. Adapted from Velasco et al. Patient-specific surface-rendered image (upper row) and respective 3D models (lower row) for the four patients included in the study.

Figure 6

Figure 7. Hypoplastic left heart syndrome (HLHS), spectrum of post-operative anatomies. (a, b, c) HLHS s/p hybrid procedure view: anterior, posterior, and lateral view, respectively. Note patent ductus arteriosus (PDA) with stent in situ (pink arrow). (d and e) S/p Norwood stage I, anterior and posterior view, respectively. Note Blalock–Taussig (BT) shunt (orange arrow) connecting to pulmonary branches (green arrow). (f, g, h) S/p Glenn procedure. (f) Anterior view, showing full anatomy. (g) Posterior view of Glenn configuration (superior caval vein (SVC) connected to right pulmonary artery (RPA)). (h) Posterior view of cardiac anatomy when removing Glenn connection. (i, j, k) S/p Fontan completion. (i) Anterior view of the cardiac anatomy. (j) Posterior view of the Fontan connection (SVC and inferior caval vein (IVC) to RPA). (k) Posterior view of cardiac anatomy when removing Fontan connection.

Figure 7

Figure 8. Tetralogy of Fallot (TOF). (a and b) Unrepaired TOF. Anterior and posterior view, respectively. Note severe RVOTO (right ventricular outflow tract obstruction, purple arrow). (c and d) TOF – absent pulmonary valve. Anterior and posterior view, respectively. Note dilatation of pulmonary branches and Blalock–Taussig (BT) shunt (yellow arrow) because of the severely narrow RVOT (purple arrow). (e, g, f) TOF – severe RVOTO. (e) Anterior view. (f) Posterior view. Note aberrant right subclavian artery (green arrow) and Major aortopulmonary collateral arteries (MAPCAs) (pink arrows). (g) Lateral view showing ventricular septal defect (VSD). (h, i, j) TOF – severe MPA dilatation post-repair with transannular patch. Posterior, lateral, and anterior view, respectively. Ao = aorta; IVC = inferior caval vein; LA = left atrium; LPA = left pulmonary artery; LV = left ventricle; MPA = main pulmonary artery; RA = right atrium; RPA = right pulmonary artery; RV = right ventricle; SVC = superior caval vein

Figure 8

Figure 9. Double-outlet right ventricle (DORV). (a, b, c) Atrioventricular septal defect (AVSD) and DORV. (a) Whole-heart anatomy. (b) Cuts performed in both ventricles to show internal morphology. (c) Lateral view after removal of ventricular cuts. Note AVSD (star) and aorta and main pulmonary artery (MPA) arising from the right ventricle (RV). (d and e) DORV – perimembranous ventricular septal defect (VSD). (d) Anterior view of whole-heart anatomy. Note cut performed in 3D model to show the internal structures and its relationships. (e) Anterior view after removing previous cut structures, showing aorta and MPA arising from the RV and VSD (star). (f, g, h) DORV – non-committed VSD. (f) Whole-heart anatomy. (g) Model has been cut in a coronal fashion to allow visualisation of internal structures, note aorta and MPA arising from RV and non-committed VSD (star). (h) Axial cut of the model showing VSD (star) at the level of the atrioventricular valves. (i, j, k) DORV – severe subpulmonary stenosis s/p bilateral Glenn. Each cardiac structure has been segmented in a different colour (light blue: MPA, navy blue: LA, pink: RA, green: ventricles, purple: aorta, turquoise: pulmonary arteries post bilateral Glenn). (i) Anterior view showing all cardiac structures, note VSD (star) and MPA (black arrow) posterior to aorta. (j) Right lateral view showing relationship of the great vessels and the severe subpulmonary stenosis (orange arrow). Note LA and RA have been removed. (k) Left lateral view showing all cardiac structures. Note severe RVOTO (orange arrow). Ao = aorta; IVC = inferior caval vein; LA = left atrium; LPA = left pulmonary artery; LV = left ventricle; RA = right atrium; RPA = right pulmonary artery; SVC = superior caval vein.