Abstract
Patients with tetralogy of Fallot, pulmonary atresia, and multiple aortopulmonary collateral arteries (Tet PA MAPCAs) have a wide spectrum of anatomy and disease severity. Management of these patients can be challenging and often require multiple high-risk surgical and interventional catheterization procedures. These interventions are made challenging by complex anatomy that require the proceduralist to mentally reconstruct three-dimensional anatomic relationships from two-dimensional images. Three-dimensional (3D) printing is an emerging medical technology that provides added benefits in the management of patients with Tet PA MAPCAs. When used in combination with current diagnostic modalities and procedures, 3D printing provides a precise approach to the management of these challenging, high-risk patients. Specifically, 3D printing enables detailed surgical and interventional planning prior to the procedure, which may improve procedural outcomes, decrease complications, and reduce procedure-related radiation dose and contrast load.
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References and Recommended Reading
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Jonas RA. Chapter 25: Tetralogy of Fallot with pulmonary atresia. Comprehensive Surgical Management of Congenital Heart Disease. 2004. pp 440–56.
Anwar S, Qureshi AM, Arruda J, Bolen MA. Pulmonary atresia with aortopulmonary and coronary artery collaterals. JACC Elsevier Inc. 2012;59:90.
Liao PK, Edwards WD, Julsrud PR, Puga FJ, Danielson GK, Feldt RH. Pulmonary blood supply in patients with pulmonary atresia and ventricular septal defect. JACC. 1985;6(6):1343–50. https://doi.org/10.1016/S0735-1097(85)80223-0.
Roche SL, Greenway SC, Reddington AN. Tetralogy of Fallot with pulmonary stenosis, pulmonary atresia, and absent pulmonary valve. Moss & Adams’ heart disease in infants, children, and adolescents, including the fetus and young adult. 2017. Chapter 41, 9th edn, pp 1–49.
Nelson JS, Bove EL, Hirsch-Romano JC. Tetralogy of Fallot. Pediatric and congenital cardiology, cardiac surgery and intensive care [Internet]. 3rd ed. London: Springer London; 2014. p. 1505–26. Available from: http://link.springer.com/10.1007/978-1-4471-4619-3_18
• Bauser-Heaton H, Borquez A, Han B, Ladd M, Asija R, Downey L, et al. Programmatic approach to management of tetralogy of Fallot with major aortopulmonary collateral arteries: A 15-year experience with 458 patients. Circ Cardiovasc Interv. 2017;10. A 15-year experience from a single institution on early complete unifocalization and repair with incorporation of all pulmonary vascular supply.
Asija R, Koth AM, Velasquez N, Chan FP, Perry SB, Hanley FL, et al. Postoperative outcomes of children with tetralogy of Fallot, pulmonary atresia, and major aortopulmonary collaterals undergoing reconstruction of occluded pulmonary artery branches. Ann Thorac Surg. 2016;101(6):2329–34. https://doi.org/10.1016/j.athoracsur.2015.12.049.
Loomba RS, Buelow MW, Woods RK. Complete repair of tetralogy of Fallot in the neonatal versus non-neonatal period: a meta-analysis. Pediatr Cardiol Springer US. 2017;38(5):893–901. https://doi.org/10.1007/s00246-017-1579-8.
Liava'a M, Brizard CP, Konstantinov IE, Robertson T, Cheung MM, Weintraub R, et al. Pulmonary atresia, ventricular septal defect, and major aortopulmonary collaterals: neonatal pulmonary artery rehabilitation without unifocalization. ATS Elsevier. 2012;93:185–91.
Watanabe N, Mainwaring RD, Reddy VM, Palmon M, Hanley FL. Early complete repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collaterals. Ann Thorac Surg. 2014;97(3):909–15–discussion 914–5. https://doi.org/10.1016/j.athoracsur.2013.10.115.
Fouilloux V, Bonello B, Kammache I, Fraisse A, Macé L, Kreitmann B. Management of patients with pulmonary atresia, ventricular septal defect, hypoplastic pulmonary arteries and major aorto-pulmonary collaterals: focus on the strategy of rehabilitation of the native pulmonary arteries. Arch Cardiovasc Dis. 2012;105(12):666–75. https://doi.org/10.1016/j.acvd.2012.08.003.
Tack P, Victor J, Gemmel P, Annemans L. 3D-printing techniques in a medical setting: a systematic literature review. BioMedical Engineering OnLine. BioMed Central; 2016; 1–21.
Byrne N, Velasco Forte M, Tandon A, Valverde I, Hussain T. A systematic review of image segmentation methodology, used in the additive manufacture of patient-specific 3D printed models of the cardiovascular system. JRSM Cardiovasc Dis. 2016;5:1–9.
• Vukicevic M, Mosadegh B, Min JK, Little SH. Cardiac 3D printing and its future directions. J Am Coll Cardiol Img. 2017;10(2):171–84. https://doi.org/10.1016/j.jcmg.2016.12.001. Review of cardiac 3D printing applications in structural heart disease.
Maragiannis D, Jackson MS, Igo SR, Schutt RC, Connell P, Grande-Allen J, et al. Replicating patient-specific severe aortic valve stenosis with functional 3D modeling. Circ Cardiovasc Imaging. 2015;8:e003626.
• Farooqi KM. In: Farooqi KM, editor. Rapid prototyping in cardiac disease. 1st ed. Cham: Springer International Publishing; 2017. Textbook on the applications of cardiac 3D printing, with focus on congenital heart disease.
Anwar S, Singh GK, Varughese J, Nguyen H, Billadello JJ, Sheybani EF, et al. 3D printing in complex congenital heart disease: across a spectrum of age, pathology, and imaging techniques. JACC: Cardiovasc Imaging. 2016.
Yoo S-J, Thabit O, Kim EK, Ide H, Yim D, Dragulescu A, et al. 3D printing in medicine of congenital heart diseases. 3D Printing in Medicine; 2016;2:1–12.
Meineri M, Hiansen JQ, Horlick EM. Structural and congenital heart disease interventions: the role of three-dimensional printing. Neth Heart J Bohn Stafleu van Loghum. 2017;25:1–11.
• Anwar S, Singh GH, Miller J, Sharma M, Manning P, Billadello JJ, et al. 3D printing is a transformative technology in congenital heart disease. JACC: Basic Transl Sci. In Press. State-of-the-art review of 3D printing in congenital heart disease.
Ngan EM, Rebeyka IM, Ross DB, Hirji M, Wolfaardt JF, Seelaus R, et al. The rapid prototyping of anatomic models in pulmonary atresia. J Thorac Cardiovasc Surg. 2006;132(2):264–9. https://doi.org/10.1016/j.jtcvs.2006.02.047.
Ryan JR, Moe TG, Richardson R, Frakes DH, Nigro JJ, Pophal S. A novel approach to neonatal management of tetralogy of Fallot, with pulmonary atresia, and multiple aortopulmonary collaterals. J Am Coll Cardiol Img. 2015;8(1):103–4. https://doi.org/10.1016/j.jcmg.2014.04.030.
Giannopoulos AA, Mitsouras D, Yoo S-J, Liu PP, Chatzizisis YS, Rybicki FJ. Applications of 3D printing in cardiovascular diseases. Nat Publ Group. 2016;13:701–18.
Olivieri LJ, Krieger A, Loke Y-H, Nath DS, Kim PCW, Sable CA. Three-dimensional printing of intracardiac defects from three-dimensional echocardiographic images: feasibility and relative accuracy. J Am Soc Echocardiogr. 2015;28(4):392–7. https://doi.org/10.1016/j.echo.2014.12.016.
Mashari A, Montealegre-Gallegos M, Knio Z, Yeh L, Jeganathan J, Matyal R, et al. Making three-dimensional echocardiography more tangible: a workflow for three-dimensional printing with echocardiographic data. Echo Res Pract. 2017;3:R57–64.
Muraru D, Veronesi F, Maddalozzo A, Dequal D, Frajhof L, Rabischoffsky A, et al. 3D printing of normal and pathologic tricuspid valves from transthoracic 3D echocardiography data sets. Eur Heart J Cardiovasc Imaging. 2016; jew215–7.
Meinel FG, Huda W, Schoepf UJ, Rao AG, Cho YJ, Baker GH, et al. Diagnostic accuracy of CT angiography in infants with tetralogy of Fallot with pulmonary atresia and major aortopulmonary collateral arteries. JCCT. 2013;7:367–75.
Jacobs CA, Lin AY. A new classification of three-dimensional printing technologies: systematic review of three-dimensional printing for patient-specific craniomaxillofacial surgery. Plast Reconstr Surg. 2017;139(5):1211–20. https://doi.org/10.1097/PRS.0000000000003232.
Zweifel DF, Simon C, Hoarau R, Pasche P, Broome M. Are virtual planning and guided surgery for head and neck reconstruction economically viable? J Oral Maxillofac Surg. 2015;73(1):170–5. https://doi.org/10.1016/j.joms.2014.07.038.
Acknowledgements
The authors wish to acknowledge Benjamin Johnson and Joseph Fullerton at 3D Systems—Healthcare as collaborators in the creation of the 3D models from Washington University School of Medicine. We also thank Dr. Geetika Khanna, Chief of Pediatric Radiology at Washington University School of Medicine for her expert consultation on some of the cases.
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Anwar, S., Rockefeller, T., Raptis, D.A. et al. 3D Printing Provides a Precise Approach in the Treatment of Tetralogy of Fallot, Pulmonary Atresia with Major Aortopulmonary Collateral Arteries. Curr Treat Options Cardio Med 20, 5 (2018). https://doi.org/10.1007/s11936-018-0594-2
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DOI: https://doi.org/10.1007/s11936-018-0594-2