KeizmanETajman YardenSMishaliD. The bilateral bidirectional Glenn operation as a risk factor prior to Fontan completion in complex congenital heart disease patients. World J Pediatr Congenit Heart Surg. 2019;10(2):174–181.
2.
OnoMKasnar-SamprecJHagerA. Clinical outcome following total cavopulmonary connection: a 20-year single-centre experience. Eur J Cardiothorac Surg. 2016;50(4):632–641.
3.
NakanoTKadoHTatewakiH. Results of extracardiac conduit total cavopulmonary connection in 500 patients. Eur J Cardiothorac Surg. 2015;48(6):825–832.
4.
AlsoufiBMcCrackenCSchlosserB. Outcomes of multistage palliation of infants with functional single ventricle and heterotaxy syndrome. J Thorac Cardiovasc Surg. 2016;151(5):1369–1377.
5.
CaoFZouMMaL. Improving outcomes of patients with heterotaxy and functional single ventricle: a 10 year follow-up of 70 cases in a single institution. Zhonghua Wai Ke Za Zhi. 2018;56(5):379–385.
6.
NakhlehNFrancisRGieseRA. High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy. Circulation. 2012;125(18):2232–2242.
7.
SwisherMJonasRTianXLeeESLoCWLeatherburyL. Increased postoperative and respiratory complications in patients with congenital heart disease associated with heterotaxy. J Thorac Cardiovasc Surg. 2011;141(3):637–644.
8.
d’UdekemYIyengarAGalatiJ. Redefining expectations of long-term survival after the Fontan procedure. Circulation. 2014;130(suppl 1):S32–S38.
9.
NewburgerJWSleeperLAGaynorJW. Transplant-free survival and interventions at 6 years in the SVR trial. Circulation. 2018;137(21):2246–2253.
10.
OhyeRGSleeperLAMahonyL. Comparison of shunt types in the Norwood procedure for single-ventricle lesions. N Engl J Med. 2010;362(21):1980–1992.
11.
PundiKNJohnsonJNDearaniJA. 40-year follow-up after the Fontan operation: long-term outcomes of 1,052 patients. J Am Coll Cardiol, 2015;66(15):1700–1710.