Hostname: page-component-848d4c4894-ttngx Total loading time: 0 Render date: 2024-06-03T04:13:55.834Z Has data issue: false hasContentIssue false

Catheter-based palliation for infants with tetralogy of Fallot

Published online by Cambridge University Press:  10 August 2020

Dasana Lingaswamy
Affiliation:
Department of Paediatric Cardiology, Amrita Institute of Medical Sciences, Kochi, India
Louisa Koepcke
Affiliation:
Paracelsus Medical School, Nuremberg, Germany
Mani Ram Krishna*
Affiliation:
Department of Paediatric Cardiology, Amrita Institute of Medical Sciences, Kochi, India
Brijesh P. Kottayil
Affiliation:
Department of Cardio-vascular and Thoracic Surgery, Amrita Institute of Medical Sciences, Kochi, India
Gopalraj S. Sunil
Affiliation:
Department of Cardio-vascular and Thoracic Surgery, Amrita Institute of Medical Sciences, Kochi, India
Katie Moynihan
Affiliation:
Department of Cardiology, Boston Children’s Hospital, Boston, MA, USA Department of Paediatrics, Harvard Medical School, Boston, MA, USA
Balaji Seshadri
Affiliation:
Department of Paediatrics (Cardiology), Oregon Health and Sciences University, Portland, OR, USA
Raman Krishna Kumar
Affiliation:
Department of Paediatric Cardiology, Amrita Institute of Medical Sciences, Kochi, India
*
Author for correspondence: Dr Mani Ram Krishna, Department of Paediatric Cardiology, Amrita Institute of Medical Sciences, AIMS, Ponekkara (P.O), Kochi 682041, India. Tel: +91 484 2853570. E-mail: mann_comp@hotmail.com

Abstract

Background:

The optimal management of symptomatic tetralogy of Fallot in neonates and younger infants with unfavourable anatomy is unclear and is further constrained by resource limitations in low and middle income countries.

Methods:

Retrospective medical record review of infants with tetralogy of Fallot undergoing corrective or palliative procedures between January 2016 and June 2019.

Results:

The study included 120 infants; of whom 83 underwent primary complete repair, four underwent surgical palliation, and 33 underwent catheter-based palliation, including balloon pulmonary valvuloplasty (n = 18), right ventricular outflow tract stenting (n = 14), and stenting of the patent arterial duct (n = 1). Infants undergoing catheter-based procedures were younger in age (median 32 days; inter-quartile range (IQR) 7–144 versus 210 days; IQR 158–250), with lower baseline saturation (65 ± 12% versus 87 ± 7%) and had smaller pulmonary artery z-scores compared to the complete repair cohort. Follow-up was available for 31/33 (94%) infants (median 7 months [IQR 4–11]) who underwent trans-catheter palliation; 12 underwent complete repair, 10 are well, awaiting repair, eight required further palliation (catheter: 6; surgical: 2), and one died post-discharge from non-cardiac causes.

Conclusion:

Catheter-based palliation is a safe and effective alternative in infants with tetralogy of Fallot who are at high risk for primary surgical repair.

Type
Original Article
Copyright
© The Author(s), 2020. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Lillehei, CW, Varco, RL, Cohen, M, et al. The first open heart corrections of tetralogy of Fallot: a 26–31 year follow-up of 106 patients. Ann Surg 1986; 204: 490502.CrossRefGoogle ScholarPubMed
Starnes, VA, Luciani, GB, Latter, DA, Griffin, ML. Current surgical management of tetralogy of Fallot. Ann Thorac Surg 1994; 58: 211215.CrossRefGoogle ScholarPubMed
Pigula, FA, Khalil, PN, Mayer, JE, del Nido, PJ, Jonas, RA. Repair of tetralogy of Fallot in neonates and young infants. Circulation 1999; 100 (19 Suppl): II157II161.CrossRefGoogle ScholarPubMed
Mouws, E, de Groot, NMS, van de Woestijne, PC, et al. Tetralogy of Fallot in the current era. Semin Thorac Cardiovasc Surg 2019; 31: 496504.CrossRefGoogle ScholarPubMed
Tamesberger, MI, Lechner, E, Mair, R, Hofer, A, Sames-Dolzer, E, Tulzer, G. Early primary repair of tetralogy of Fallot in neonates and infants less than four months of age. Ann Thorac Surg 2008; 86: 19281935.CrossRefGoogle ScholarPubMed
Ramakrishnan, KV, Zurakowski, D, Pastor, W, Jonas, RA, Sinha, P. Symptomatic tetralogy of Fallot in young infants: primary repair or shunt-pediatric health information system database analysis. World J Pediatr Congenit Heart Surg 2018; 9: 539545.CrossRefGoogle ScholarPubMed
Petrucci, O, O’Brien, SM, Jacobs, ML, Jacobs, JP, Manning, PB, Eghtesady, P. Risk factors for mortality and morbidity after the neonatal Blalock-Taussig shunt procedure. Ann Thorac Surg 2011; 92: 642651; discussion 51–52.CrossRefGoogle ScholarPubMed
Cavalcanti, PE, Sa, MP, Santos, CA, et al. Stratification of complexity in congenital heart surgery: comparative study of the Risk Adjustment for Congenital Heart Surgery (RACHS-1) method, Aristotle basic score and Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery (STS-EACTS) mortality score. Rev Bras Cir Cardiovasc 2015; 30: 148158.Google ScholarPubMed
Santoro, G, Gaio, G, Palladino, MT, et al. Transcatheter palliation of ‘complex’ tetralogy of Fallot. J Cardiovasc Med 2008; 9: 751752.CrossRefGoogle ScholarPubMed
Pettersen, MD, Du, W, Skeens, ME, Humes, RA. Regression equations for calculation of z scores of cardiac structures in a large cohort of healthy infants, children, and adolescents: an echocardiographic study. J Am Soc Echocardiogr 2008; 21: 922934.CrossRefGoogle Scholar
Kasturi, S, Balaji, S, Sudhakar, A, et al. Accuracy of a new echocardiographic index to predict need for trans-annular patch in tetralogy of Fallot. Pediatr Cardiol 2019; 40: 161167.CrossRefGoogle ScholarPubMed
Remadevi, KS, Vaidyanathan, B, Francis, E, Kannan, BR, Kumar, RK. Balloon pulmonary valvotomy as interim palliation for symptomatic young infants with tetralogy of Fallot. Ann Pediatr Cardiol 2008; 1: 27.Google ScholarPubMed
Stumper, O, Ramchandani, B, Noonan, P, et al. Stenting of the right ventricular outflow tract. Heart 2013; 99: 16031608.CrossRefGoogle ScholarPubMed
Mahesh, K, Kannan, BR, Vaidyanathan, B, Kamath, P, Anil, SR, Kumar, RK. Stenting the patent arterial duct to increase pulmonary blood flow. Indian Heart J 2005; 57: 704708.Google ScholarPubMed
Steiner, MB, Tang, X, Gossett, JM, et al. Alternative repair strategies for ductal-dependent tetralogy of Fallot and short-term postoperative outcomes, a multicenter analysis. Pediatr Cardiol 2015; 36: 177189.CrossRefGoogle ScholarPubMed
Wilder, TJ, Van Arsdell, GS, Benson, L, et al. Young infants with severe tetralogy of Fallot: early primary surgery versus transcatheter palliation. J Thorac Cardiovasc Surg 2017; 154: 16921700.e2.CrossRefGoogle ScholarPubMed
Loomba, RS, Buelow, MW, Woods, RK. Complete repair of tetralogy of Fallot in the neonatal versus non-neonatal period: a meta-analysis. Pediatr Cardiol 2017; 38: 893901.CrossRefGoogle ScholarPubMed
Hirsch, JC, Mosca, RS, Bove, EL. Complete repair of tetralogy of Fallot in the neonate: results in the modern era. Ann Surg 2000; 232: 508514.CrossRefGoogle ScholarPubMed
Savla, JJ, Faerber, JA, Huang, YV, et al. 2-Year outcomes after complete or staged procedure for tetralogy of Fallot in neonates. J Am Coll Cardiol 2019; 74: 15701579.CrossRefGoogle ScholarPubMed
Balaji, S, Kumar, RK. Partnership in healthcare: what can the west learn from the delivery of pediatric cardiac care in low- and middle-income countries. Ann Pediatr Cardiol 2015; 8: 13.Google ScholarPubMed
Kumar, RK. Congenital heart disease profile: four perspectives. Ann Pediatr Cardiol 2016; 9: 203204.CrossRefGoogle ScholarPubMed
Dorobantu, DM, Mahani, AS, Sharabiani, MTA, et al. Primary repair versus surgical and transcatheter palliation in infants with tetralogy of Fallot. Heart 2018; 104: 18641870.CrossRefGoogle ScholarPubMed