Article

lock Open Access lock Peer-Reviewed

87

Views

CASE REPORT

Direct Anastomosis of Persistent Left Superior Vena Cava to Right Superior Vena Cava in a Pediatric Patient with Tetralogy of Fallot: an Alternative Technique

Mustafa YılmazI; Atakan AtalayI

DOI: 10.21470/1678-9741-2021-0096

ABSTRACT

The presence of persistent left superior vena cava to the left atrium connection without an innominate vein may give rise to technical challenges during intracardiac repair. In this report, the end-to-side anastomosis technique of the persistent left superior vena cava to the right superior vena cava is discussed in a patient with tetralogy of Fallot associated with persistent left superior vena cava draining directly into the left atrium. A successful end-to-side anastomosis between the persistent left superior vena cava and the right superior vena cava was performed and short-term anastomosis patency was documented via angiography.

ABBREVIATIONS AND ACRONYMS

CT = Computed tomography

L = Left

LP = Left posterior

PLSVC = Persistent left superior vena cava

R = Right

RA = Right anterior

SVC = Superior vena cava

INTRODUCTION

Persistent left superior vena cava (PLSVC) is the most common congenital thoracic venous system abnormality (0.3-0.5%). In congenital heart patients, the incidence increases approximately ten times and reaches 4.5%. PLSVC is observed in 20% of the patients with tetralogy of Fallot. This association can often be determined by preoperative examinations. However, occasionally, preoperative tests may be insufficient in the diagnosis of this association. The presence of PLSVC to the left atrium connection without an innominate vein may give rise to technical challenges during intracardiac repair when not determined prior to surgical intervention. In such situations, the surgeon should be aware of intra or extracardiac re-routing procedures to facilitate the intracardiac repair and eliminate the right-to-left shunt. In this case report, we will discuss the pros and cons of the end-to-side anastomosis technique of PLSVC to the right superior vena cava (SVC), which is an alternative extracardiac re-routing procedure, in a pediatric patient with tetralogy of Fallot who was admitted to the emergency department with a cyanotic spell attack.

Case Presentation

A 9-year-old girl was admitted to the emergency department with a deteriorated medical condition, agitation, and deep cyanosis. The patient’s oxygen saturation was 40%, and the diagnosis was confirmed as tetralogy of Fallot with severe infundibular and valvular stenosis via transthoracic echocardiography. Due to the patient’s advanced age, emergency cardiac catheterization was performed to evaluate additional abnormalities. No additional abnormalities were detected via cardiac catheterization.

The patient was urgently operated on to complete repair of the tetralogy of Fallot after obtaining written informed consent.

During the operation, PLSVC was detected, and there was no left innominate vein between the right and left SVC. The diameter of the PLSVC was equal to that of the right SVC, and it was coursing posterior to the left atrial appendage and in front of the left pulmonary artery. Considering the most common anatomy, we anticipated that the PLSVC would drain into the coronary sinus and planned to aspirate it through the coronary sinus during the operation.

Right atriotomy was performed after cardiopulmonary bypass and cardiac arrest. The coronary sinus was visualized in its normal localization and was of normal diameter. The right atrial septum was then incised, and the left atrium was inspected. The PLSVC was temporarily occluded. Inspection of the left atrium revealed that the roof of the coronary sinus was intact, and that the PLSVC was connected to the left atrium directly. Since the diameter of the PLSVC was about the same size as the right SVC, and the measured proximal pressure was 40 mmHg during temporary occlusion, a re-routing procedure for PLSVC became mandatory.

Due to the concern that the ischemic time would increase, we decided to divert the PLSVC drainage to the systemic venous system via an extracardiac route. Complete repair of the tetralogy of Fallot was performed with a transannular patch. Following cross-clamp removal, the PLSVC was transected from the left atrium, and all its proximal branches were ligated and divided under cardiopulmonary bypass support. Then the proximal part of the right SVC was dissected entirely free. The PLSVC was redirected to the right side over the anterosuperior aspect of the ascending aorta, and end-to-side anastomosis to the right SVC was performed. (Figure 1). No kinking or tension was observed on the suture line of the anastomosis.

Fig. 1 - Persistent left superior vena cava was carried over the ascending aorta and anastomosis was performed to the medial aspect of right superior vena cava. Black arrow=persistent left superior vena cava; yellow arrow=right superior vena cava; L=left; R=right

Computed tomography angiography and cardiac catheterization prior to discharge showed that the PLSVC and the anastomosis were patent, and there was no sign of stenosis or thrombosis (Figures 2 and 3). Postoperative recovery of the patient was uneventful, and the patient was discharged with warfarin anticoagulation on the postoperative 5th day without any complications.

Fig. 2 - Computed tomography angiographic image of the persistent left superior vena cava. Black arrow=patent persistent left superior vena cava and anastomosis; star=proximal part of clavicula (patient has pectus carinatum deformity); LP=left posterior; RA=right anterior

Fig. 3 - Postoperative cardiac catheterization. Yellow arrow=persistent left superior vena cava; red arrow=patent persistent left superior vena cava - right superior vena cava anastomosis; star=ligated stump of hemiazygos vein

After one month of discharge, the patient showed no symptoms of venous stasis. Currently, the patient is asymptomatic on the 6th postoperative month. Timeline of the case report has been presented in the Table 1.

Table 1 - Timeline of the case report.
Day 1 Admission to the emergency department
Symptom Deep cyanosis
Deteriorated medical condition
Diagnosis Echocardiography
· Tetralogy of Fallot with severe pulmonary stenosis
Cardiac catheterization
· No additional abnormality
Day 2 Cardiac operation Complete repair of Tetralogy of Fallot
End-to-side anastomosis of the persistent left SVC to right SVC
Day 6 Postoperative CT angiography and cardiac catheterization Anastomosis was patent
No sign of stenosis or thrombosis
Day 7 Discharge Discharged with warfarin anticoagulation
1st and 6th months after surgery The patient is asymptomatic and shows no signs of venous stasis

CT=computed tomography; SVC=superior vena cava

Table 1 - Timeline of the case report.

DISCUSSION

Systemic venous system abnormalities are generally benign anatomical structures that do not cause hemodynamic disturbances. However, sometimes these abnormalities can cause serious hemodynamic consequences on their own or in conjunction with additional congenital pathologies and may need to be corrected. Detection of these abnormalities prior to congenital heart surgery may provide the application of various surgical modifications during the operation.

PLSVC drains into the coronary sinus in 90% of all cases, and in only 8% of cases, the PLSVC is directly connected to the left atrium. The association of this situation with tetralogy of Fallot is much rarer. There are limited number of case reports describing this association in the literature[1].

In cases where PLSVC drains directly into the left atrium, multiple surgical options are available. Ligation of PLSVC[1], intra-atrial baffle formation[2], transection of PLSVC with left atrial tissue and implantation to the right atrium[3], end-to-side anastomosis of PLSVC to the left pulmonary artery[4], a graft interposition between PLSVC and the right atrium[5], forming an intra-atrial conduit with an inverted left atrial appendage flap[6], and performing end-to-side anastomosis to the right SVC under or over the aortic arch[7] are the surgical techniques reported in the literature[2-7]. Complex congenital pathologies are additionally detected in almost all cases where PLSVC is attached to the left atrium[1]. Therefore, it is necessary to evaluate each anatomical structure individually and to decide the most appropriate surgical technique to perform according to this anatomical structure.

In our patient, we preferred to perform an end-to-side direct anastomosis of the PLSVC to the right SVC for the following reasons:[1]the accurate diagnosis of the patient was confirmed during the cross-clamping period[2], and the possibility of performing the anastomosis after complete repair and during the rewarming period on the beating heart[3]. We had some concerns regarding the possible complications of intra-atrial baffle formation and extracardiac graft interposition techniques. In previous studies, it has been reported that the long-term patency of intra-atrial baffle formation is questionable due to the use of non-growing material and that it may become stenotic. Beside this, due to the lack of growth potential, extracardiac graft interposition is also not applicable for young children[1,4]. In addition, these grafts may be compressed between the sternum and the aorta.

In their cohort studies, van Son et al.[6], Ugaki et al.[8], and Cesnjevar et al.[9] showed that anatomic end-to-side anastomosis of PLSVC to the right SVC, anterior to the aortic arch, is a safe, feasible, and reproducible technique. Kawada et al.[3] and Reddy et al.[5] performed the anastomosis by redirecting the PLSVC under the aortic arc. Since PLSVC runs through the mediastinum more posteriorly than the right SVC, they suggested a more natural connection between the two SVCs could be achieved. The authors state that while performing this procedure, one must be sure that there is sufficient space between the main pulmonary artery and the aorta. Otherwise, the PLSVC may be compressed between these two structures.

Since the ascending aorta of the patient was dilated due to aortopathy (ascending aorta: 2.8 cm; Z-score: +3.79), we anticipated that the redirection of the PLSVC between the patient’s aorta and the main pulmonary artery, which was augmented transannularly, would also cause compression. As defined in the literature, the vena cava was extensively dissected free, and proximal branches were ligated and separated[2,6,10], thus, approximately 3.5-4 cm of the PLSVC length was obtained. The PLSVC was transected from the left atrium roof and redirected over the anterosuperior part of the ascending aorta. Anastomosis was comfortably performed to the medial wall of the right SVC. No kinking or tension was observed in the anastomosis.

The most significant disadvantage of this technique is the lack of knowledge concerning long-term vascular patency. In the literature, the longest follow-up period was 2.4 years[9]. Studies with a longer follow-up period and larger patient cohorts are required to prove the durability of PLSVC and patency of anastomosis.

CONCLUSION

In conclusion, there are multiple surgical options for patients with PLSVC draining directly into the left atrium. All these surgical techniques have their own shortcomings. Considering the sample cases in the literature, we believe that end-to-side direct anastomosis of the PLSVC to the right SVC might be a safe and applicable technique for pediatric patients with PLSVC draining into the left atrium.

REFERENCES


1. 1 Ramman TR, Dutta N, Chowdhuri KR, Agrawal S, Girotra S, Azad S, etal. Left superior vena cava draining into left atrium in tetralogy offallot-four cases of a rare association. World J Pediatr Congenit Heart Surg.2020;11(4):NP120-4. doi:10.1177/2150135117742625.

2. 2 Fuchigami T, Nishioka M, Akashige T, Nagata N. A surgicalintegration technique for right-sided and left-sided superior venae cavae. AnnThorac Surg. 2015;100(3):e63-5.doi:10.1016/j.athoracsur.2015.05.042. [MedLine]

3. 3 Kawada N, Yamagishi M, Morita K, Kanazawa T, Nakamura Y.Extracardiac rerouting of the persistent left superior vena cava in the leftisomerism heart. Jpn J Thorac Cardiovasc Surg. 2004;52(2):88-90.doi:10.1007/s11748-004-0092-1. [MedLine]

4. 4 Komai H, Naito Y, Fujiwara K. Operative technique for persistentleft superior vena cava draining into the left atrium. Ann Thorac Surg.1996;62(4):1188-90. doi:10.1016/0003-4975(96)00362-1. [MedLine]

5. 5 Reddy VM, McElhinney DB, Hanley FL. Correction of left superiorvena cava draining to the left atrium using extracardiac techniques. Ann ThoracSurg. 1997;63(6):1800-2. doi:10.1016/s0003-4975(97)83867-2. [MedLine]

6. 6 van Son JA, Hambsch J, Mohr FW. Repair of complex unroofedcoronary sinus by anastomosis of left to right superior vena cava. Ann ThoracSurg. 1998;65(1):280-1. doi:10.1016/s0003-4975(97)01267-8. [MedLine]

7. Vargas FJ. Reconstructive methods for anomalous systemic venous return: surgical management of persistent left superior vena cava. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2008:31-8. doi:10.1053/j.pcsu.2008.01.007.

8. Ugaki S, Kasahara S, Fujii Y, Sano S. Anatomical repair of a persistent left superior vena cava into the left atrium. Interact Cardiovasc Thorac Surg. 2010;11(2):199-201. doi:10.1510/ icvts.2009.230581.

9. Cesnjevar RA, Harig F, Dietz M, Alkassar M, Waellisch W, Rueffer A, et al. Growth of hypoplastic mitral valves in hypoplastic left heart complex and similar constellations after anatomical left superior vena cava correction. Eur J Cardiothorac Surg. 2021;59(1):236-43. doi:10.1093/ejcts/ezaa286.

10. Chihara S, Yasunaga H, Todo K. Anastomosis of left to right superior vena cava for repair of unroofed coronary sinus. Gen Thorac Cardiovasc Surg. 2012;60(4):244-6. doi:10.1007/ s11748-011-0815-z.

 

Authors’Roles & Responsibilities

MY= Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work, drafting the work or revising it critically for important intellectual content; agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved; final approval of the version to be published

AA= Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work, drafting the work or revising it critically for important intellectual content; agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved; final approval of the version to be published

Article receive on Sunday, February 14, 2021

Article accepted on Saturday, August 21, 2021

CCBY All scientific articles published at bjcvs.org are licensed under a Creative Commons license

Indexes

All rights reserved 2017 / © 2024 Brazilian Society of Cardiovascular Surgery DEVELOPMENT BY