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Fontan operation for tricuspid atresia with absent pulmonary valve: a case series

Part of: Surgery

Published online by Cambridge University Press:  09 September 2021

Moyu Hasegawa Open the ORCID record for Moyu Hasegawa [Opens in a new window] ,
Shigemitsu Iwai  and
Yosuke Kugo
Moyu Hasegawa*
Affiliation:
Department of Cardiovascular Surgery, Osaka Women’s and Children’s Hospital, Izumi, Osaka, Japan
Shigemitsu Iwai
Affiliation:
Department of Cardiovascular Surgery, Osaka Women’s and Children’s Hospital, Izumi, Osaka, Japan
Yosuke Kugo
Affiliation:
Department of Cardiovascular Surgery, Osaka Women’s and Children’s Hospital, Izumi, Osaka, Japan
*
Author for correspondence: M. Hasegawa, MD, Department of Cardiovascular Surgery, Osaka Women’s and Children’s Hospital, 840 Murodocho, Izumi, Osaka594-1101, Japan. Tel: +81-725-561220; Fax: +81-725-565682. E-mail: [email protected]
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Abstract

Combined tricuspid atresia and absent pulmonary valve with dysplasia of the right ventricular myocardium is a very rare congenital heart anomaly with a poor prognosis. We present three cases of this rare disease that reached the Fontan operation without prior surgical intervention of the right ventricle or pulmonary artery; no right ventriclar dilation was detected. All patients had uneventful post-operative courses.

Keywords

Fontan operationtricuspid atresiaabsent pulmonary valve
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 5 , May 2022 , pp. 813 - 814
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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
© The Author(s), 2021. Published by Cambridge University Press

Combined tricuspid atresia and absent pulmonary valve, together with an intact ventricular septum and right ventricular dysplasia, is extremely rare. Surgical management, especially intervention for the non-functional right ventricle and pulmonary artery, has been discussed. In previous reports, right ventriclar exclusion and pulmonary artery division or banding were performed concomitantly with the Fontan operation Reference Szwast, Tian and McCann1,Reference Takahara, Manabe, Mori, Kuroda and Kitagawa2 . Conversely, we avoid intervention because this could cause right ventriclar hypertension and dilation, resulting in left ventricular outflow tract obstruction. We present three cases underwent the Fontan operation with good outcome.

Case report

We present three cases of combined tricuspid atresia and absent pulmonary valve detected on fetal echocardiography. All cases underwent right-modified Blalock–Taussig shunt, bidirectional Glenn procedure, and Fontan operation. The right ventricular end-diastolic volume index was measured through cardiac catheterisation. Table 1 summarises the details of the cases. In Case 1, a right ventricular aneurysm was diagnosed during the first echocardiography. The series of right ventriculograms in Case 2 are shown in Figure 1. In all cases, no coronary-to-right ventriclar fistulas were detected. Regarding the Fontan operation, an 18-mm polytetrafluoroethylene graft was used. Aspirin was administered as an anticoagulant. The follow-up periods for the three cases were 10, 8, and 3 years after the Fontan operation. In Case 1 and 2, the latest cardiac catheterizations showed no right ventricular dilation (Table 1) . Until now, no left ventricular outflow tract obstruction was noted nor were thromboembolic events.

Figure 1. Right ventriculogram of Case 2 during cardiac catheterisation before bidirectional Glenn procedure (a), before Fontan operation (b), and 1 year after the Fontan operation (c). Superior vena cava angiogram after the Fontan operation (d). PA, pulmonary artery; RV, right ventricle; SVC, superior vena cava.

Table 1. Details of the cases

PA = pulmonary artery; RVEDVI = right ventricle end-diastolic volume index.

Discussion

Cases of tricuspid atresia and absent pulmonary valve with an intact ventricular septum and right ventricular dysplasia are extremely rare. Reference Szwast, Tian and McCann1 Only a few cases undergo Fontan operation because of the rarity of the disease and the poor prognosis. Reference Szwast, Tian and McCann1

Characteristically, the right ventriclar myocardium, similar to that in Uhl’s disease, gradually increases in size gradually and affects the left ventricle. Reference Takahara, Manabe, Mori, Kuroda and Kitagawa2 Another morphological feature is asymmetrical ventricular septal hypertrophy, which could also lead to left ventricular outflow tract obstruction. Furthermore, pulsatile flow from the right ventricle to the pulmonary artery causes unnatural backward flow in systemic veins, which is a limitation for Fontan circulation. Reference Klimes, Abdul-Khaliq and Ovroutski3 Thus, surgical interventions for right ventricle and pulmonary artery remain controversial.

In our practice, they are not manipulated because right ventriclar dilation may cause right ventricular hypertension. The inflow to the right ventricle, such as from the Thebesian veins, could contribute to the increased pressure. The presence of significant coronary-to-right ventriclar fistulas would have further increased the inflow. We believed that right ventricular hypertension would have exacerbated right ventricular hypertrophy, and pressure needs to be reduced by opening the tricuspid valve or retaining pulmonary artery forward flow. This is a completely different approach to those mentioned in previous reports. To date, the volume of the right ventricle has not increased to such a point so as to cause left ventricular outflow tract obstruction. Regarding the flow in the systemic veins after the Fontan operation, cardiac catheterisation detected no significant pulse flow in the superior or inferior vena cava pressure line. This indicates that the pulmonary artery forward flow does not affect Fontan circulation.

It is difficult to apply this strategy to all cases. From our experience, we believe that this approach is suitable for cases in which right ventricular end-diastolic volume index is less than 30 mL/m2. We will continue to monitor for right ventriclar dilation, left ventriclar function, and the overall condition of these patients.

Acknowledgements

The authors thank Editage (www.editage.jp) for English language editing.

Financial support

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Conflicts of interest

None.

Ethical standards

This article does not contain any studies with human participants.

Informed consent

All participants provided informed consent.

References

Szwast, A, Tian, Z, McCann, M, et al. Anatomic variability and outcome in prenatally diagnosed absent pulmonary valve syndrome. Ann Thorac Surg 2014; 98: 152–158. DOI 10.1016/j.athoracsur.2014.03.002.CrossRefGoogle ScholarPubMed
Takahara, Y, Manabe, T, Mori, K, Kuroda, Y, Kitagawa, T. A case of Fontan-type operation for membranous tricuspid atresia with dysplasia of the right ventricular myocardium, and absence of the pulmonary valve. Pediatr Cardiol Card Surg 2002; 18: 388–393.Google Scholar
Klimes, K, Abdul-Khaliq, H, Ovroutski, S, et al. Pulmonary and caval blood flow patterns in patients with intracardiac and extracardiac Fontan: magnetic resonance study. Clin Res Cardiol 2007; 96: 160–167. DOI 10.1007/s00392-007-0470-z.CrossRefGoogle ScholarPubMed
Figure 0

Figure 1. Right ventriculogram of Case 2 during cardiac catheterisation before bidirectional Glenn procedure (a), before Fontan operation (b), and 1 year after the Fontan operation (c). Superior vena cava angiogram after the Fontan operation (d). PA, pulmonary artery; RV, right ventricle; SVC, superior vena cava.

Figure 1

Table 1. Details of the cases