Hostname: page-component-745bb68f8f-v2bm5 Total loading time: 0 Render date: 2025-02-11T14:57:47.514Z Has data issue: false hasContentIssue false
  • English
  • Français

Transcatheter closure of post-procedural right ventricular pseudoaneurysms in a neonate with pulmonary atresia

Part of: Advanced Imaging

Published online by Cambridge University Press:  09 February 2021

Sheng-Ling Jan Open the ORCID record for Sheng-Ling Jan [Opens in a new window] ,
Chen-Hao Wu  and
Ming-Chih Lin
Sheng-Ling Jan*
Affiliation:
Department of Pediatrics, Children’s Medical Center, Taichung Veterans General Hospital, Taichung; School of Medicine, National Yang-Ming University, Taipei; and School of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
Chen-Hao Wu
Affiliation:
Department of Radiology, Taichung Veterans General Hospital, Taichung, Taiwan
Ming-Chih Lin
Affiliation:
Department of Pediatrics, Children’s Medical Center, Taichung Veterans General Hospital, Taichung; School of Medicine, National Yang-Ming University, Taipei; and School of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
*
Author for correspondence: Sheng-Ling Jan, MD, PhD, Department of Pediatrics, Children’s Medical Center, Taichung Veterans General Hospital, 1650 Taiwan Boulevard Sect. 4, Taichung 40705, Taiwan. Tel.: + 886-4-23741259; Fax: + 886-4-23741359. E-mail: sljan@vghtc.gov.tw
Rights & Permissions [Opens in a new window]

Abstract

Post-procedural right ventricular pseudoaneurysm is a rare but life-threatening complication of interventional catheterisation. We describe a 3-day-old newborn who underwent transcatheter intervention for pulmonary atresia with a complication of right ventricular pseudoaneurysms, and transcatheter embolisation of the pseudoaneurysms was performed at 3-week-old. It is the first described case that receives transcatheter closure of right ventricular pseudoaneurysms in a newborn with a favourable outcome.

Keywords

Congenital heart diseasedevice closurepseudoaneurysmpulmonary atresia
Type
Brief Report
Information
Cardiology in the Young , Volume 31 , Issue 6 , June 2021 , pp. 1051 - 1053
Check for updates
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Perforation of the atretic pulmonary valve with balloon dilation is a standard initial therapy in selected patients with pulmonary atresia with intact ventricular septum. Reference Alwi, Geetha and Bilkis1–Reference Chubb, Pesonen and Sivasubramanian7 The incidence of inadvertent right ventricular outflow tract perforation, sepsis or multi-organ failure, and mortality was between 4 and 15%. Reference Bakhru, Marathe and Saxena5–Reference Marasini, Gorrieri and Tuo8 A post-procedural right ventricular pseudoaneurysm is an extremely rare complication, requiring urgent management due to its potentially life-threatening nature. Transcatheter intervention for the treatment of a right ventricular pseudoaneurysm is reported much less frequently. Reference Herbert, Ikemba and Nugent9,Reference Alkhouli, Waits, Chaturvedi and Ling10

Case report

We describe a 3-day-old male newborn with 38 weeks of gestation and birth weight of 2.63 kg who underwent transcatheter intervention for pulmonary atresia with intact ventricular septum. The procedure was aborted due to right ventricular perforation with cardiac tamponade. Two weeks later, two large pseudoaneurysms (7 × 11 and 8 × 12 mm) arising from the right ventricular anterior wall were detected by echocardiography (Fig 1a). Cardiac CT and right ventricular angiography revealed three aneurysm sacs (6 × 8, 9 × 16, and 11 × 17 mm), one at the anterior region of the right ventricular outflow tract and two others arising from the anterior right ventricular free wall (Fig 2a–d). The two large false aneurysms appeared to connect to the right ventricle with a narrow neck that measured 3.8 mm in diameter and 4.9 mm in length. Because of the rapid growth of the two large pseudoaneurysms, which had a high risk of rupture, and surgical operation was not feasible because of the anterior location and concern for rupture with opening the sternum, transcatheter approach for embolisation of the pseudoaneurysms was performed at 3-week-old (body weight of 2.97 kg). A 4Fr delivery catheter (Amplatzer TorqVue LP catheter, Abbott Medical, Minnesota, United States of America) was advanced over the 0.018” Terumo guidewire into the right ventricle. This was technically challenging and successfully achieved delivery of the catheter across the narrow neck into the aneurysm. Once the sheath was in position, the guidewire was removed and the device was inserted promptly. A 5/4 Amplatzer Duct Occluder II Additional Sizes (Abbott Park, Illinois, United States of America) was selected for closure of the two large pseudoaneurysms (Fig 2e and f), as the 5 mm waist diameter and 4 mm length matched the dimension of the neck of the pseudoaneurysm and the smaller disc diameter was suitable for a small right ventricular chamber. With the left disc of the device deployed in the aneurysm, the long sheath was retracted to the right ventricle, the right disc was deployed, and then the device was released. Then, perforation of the atretic pulmonary valve was approached using a combined coronary guidewire and a microcatheter followed by sequential balloon pulmonary valvuloplasty (Fig 2g and h). There were no post-catheterisation complications. A repeat echocardiogram revealed the closure device was in a good position, and progressive thrombosis of embolised pseudoaneurysms (Fig 1b), as well as another smaller pseudoaneurysm, resolved spontaneously after right ventricular decompression. He was discharged after a 2-month hospitalisation.

Figure 1. Transthoracic echocardiograms. ( a ) Two large pseudoaneurysms with forward flow at colour Doppler in the short-axis view. ( b ) Two large pseudoaneurysms were embolised using a closure device (arrow) and were completely thrombosed. ADO-II AS = Amplatzer Duct Occluder II Additional Sizes; LV = left ventricle; Ps = pseudoaneurysms; RV = right ventricle.

Figure 2. Images of CT and interventional catheterisation. ( a–d ) Cardiac CT and right ventriculography showed three false aneurysm sacs (arrow heads). The two large aneurysms appeared as one lesion with two lobes (white arrows). ( e and f ) RVG showed an ADO-II AS (black arrows) that was placed in the narrow neck with a good position, and aneurysms regressed totally 8 months later. ( g ) Perforation of the atretic valve by the coronary guidewire. ( h ) A 6 mm Tyshak II Balloon was used for pulmonary valvuloplasty. ADO-II AS = Amplatzer Duct Occluder II Additional Sizes; AO = aorta; PA = pulmonary artery; RA = right atrium; RV = right ventricle.

Discussion

Pulmonary atresia with intact ventricular septum is a complex CHD with significant morphological variability, and transcatheter pulmonary valvotomy and sequential balloon dilatation have become established as the procedure of first choice. Reference Alwi, Geetha and Bilkis1 Although successful perforation of the atretic valve can be achieved in 80–89% of patients, this method is technically challenging and associated with severe complications, including right ventricular outflow tract perforation, stroke, sepsis, multi-organ failure, and mortality. Reference Alwi, Budi, Mood, Leong and Samion3,Reference Bakhru, Marathe and Saxena5,Reference Patil, Saxena and Gupta6 Peri-procedural complications leading to death were observed in about 10% of cases. Reference Bakhru, Marathe and Saxena5–Reference Marasini, Gorrieri and Tuo8 A major cause of early mortality is cardiac tamponade due to right ventricular outflow tract tear. Immediate pericardial drainage and surgical repair of cardiac rupture could be life-saving procedures for patients with cardiac tamponade; however, about half of the patients complicated with this complication died. Reference Bakhru, Marathe and Saxena5–Reference Marasini, Gorrieri and Tuo8 Amongst the post-procedural complications, RV pseudoaneurysm is a rare complication. A suitable approach for treating right ventricular pseudoaneurysm is surgery. For right ventricular pseudoaneurysm with the anterior location and concern for aneurysm rupture with catastrophic bleeding during opening the sternum, but our patient was too small, and therefore surgical operation was not deemed feasible. Cases of successful percutaneous closure of right ventricular pseudoaneurysm have been reported in the literature, but they are rare in childhood, and this treatment may be considered in patients who are poor candidates for surgery. Reference Herbert, Ikemba and Nugent9,Reference Alkhouli, Waits, Chaturvedi and Ling10 Because of the high risk of rupture due to rapid growth of the large false aneurysms with high right ventricular pressure, in this case, interventional catheterisation for embolisation of the pseudoaneurysms was required.

The Amplatzer Duct Occluder II is a self-expanding occlusion device with a central waist plug and retention discs deployed on both ends. This low-profile device is implanted forward from a 4Fr delivery catheter, and is feasible in right ventricular pseudoaneurysm patients weighing less than 5 kg. Despite the small size of the patient and challenging catheter course, the intervention was tolerated by minimising the time for delivery of the catheter into position in the false aneurysm. Safety and device stability was demonstrated over 1 year of follow-up in this patient.

Conclusion

Perforation of the atretic pulmonary valve in selected patients with pulmonary atresia with intact ventricular septum is effective, but right ventricular perforation is a severe complication that frequently leads to a fatal outcome. Post-procedural right ventricular pseudoaneurysm is relatively rare but life-threatening complication in patients with pulmonary atresia with intact ventricular septum who underwent interventional catheterisation. The results of the present case demonstrate that transcatheter intervention for embolisation of a right ventricular pseudoaneurysm can be a safe and effective treatment, even in a relatively small patient.

Acknowledgements

No acknowledgement was received for this study.

Financial support

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

Conflict of interest

None.

Ethical statement

This article does not contain any studies with human participants performed by any of the authors.

References

Alwi, M, Geetha, K, Bilkis, AA, et al. Pulmonary atresia with intact ventricular septum percutaneous radiofrequency-assisted valvotomy and balloon dilation versus surgical valvotomy and Blalock Taussig shunt. J Am Coll Cardiol 2000; 35: 468–476.10.1016/S0735-1097(99)00549-5CrossRefGoogle ScholarPubMed
Gibbs, JL, Blackburn, ME, Uzun, O, Dickinson, DF, Parsons, JM, Chatrath, RR. Laser valvotomy with balloon valvoplasty for pulmonary atresia with intact ventricular septum: five years’ experience. Heart 1997; 77: 225–228.10.1136/hrt.77.3.225CrossRefGoogle ScholarPubMed
Alwi, M, Budi, RR, Mood, MC, Leong, MC, Samion, H. Pulmonary atresia with intact septum: the use of Conquest Pro coronary guidewire for perforation of atretic valve and subsequent interventions. Cardiol Young 2013; 23: 197–202.10.1017/S1047951112000595CrossRefGoogle ScholarPubMed
Lamers, L, Garn, B, Ellsworth, E, Graziano, JN. Decreased incidence of right-ventricular outflow tract complications using a retrograde snare technique for radiofrequency pulmonary valve perforation. Pediatr Cardiol 2012; 33: 1275–1280.10.1007/s00246-012-0295-7CrossRefGoogle ScholarPubMed
Bakhru, S, Marathe, S, Saxena, M, et al. Transcatheter pulmonary valve perforation using chronic total occlusion wire in pulmonary atresia with intact ventricular septum. Ann Pediatr Cardiol 2017; 10: 5–10.Google ScholarPubMed
Patil, NC, Saxena, A, Gupta, SK, et al. Perforating the atretic pulmonary valve with CTO hardware: technical aspects. Catheter Cardiovasc Interv 2016; 88: E145–E150.10.1002/ccd.25760CrossRefGoogle ScholarPubMed
Chubb, H, Pesonen, E, Sivasubramanian, S, et al. Long-term outcome following catheter valvotomy for pulmonary atresia with intact ventricular septum. J Am Coll Cardiol 2012; 59: 1468–1476.10.1016/j.jacc.2012.01.022CrossRefGoogle ScholarPubMed
Marasini, M, Gorrieri, PF, Tuo, G, et al. Long-term results of catheter-based treatment of pulmonary atresia and intact ventricular septum. Heart 2009; 95: 1520–1524.10.1136/hrt.2009.169078CrossRefGoogle ScholarPubMed
Herbert, C, Ikemba, C, Nugent, A. Device closure of a pseudoaneurysm of the right ventricular outflow tract in an infant with right ventricle-to-pulmonary artery homograft. Catheter Cardiovasc Interv 2014; 83: 587–590.10.1002/ccd.24990CrossRefGoogle Scholar
Alkhouli, M, Waits, B, Chaturvedi, A, Ling, FS. Percutaneous closure of right ventricular pseudoaneurysm. JACC Cardiovasc Interv 2015; 8: e147–e148.10.1016/j.jcin.2015.04.019CrossRefGoogle ScholarPubMed
Figure 0

Figure 1. Transthoracic echocardiograms. (a) Two large pseudoaneurysms with forward flow at colour Doppler in the short-axis view. (b) Two large pseudoaneurysms were embolised using a closure device (arrow) and were completely thrombosed. ADO-II AS = Amplatzer Duct Occluder II Additional Sizes; LV = left ventricle; Ps = pseudoaneurysms; RV = right ventricle.

Figure 1

Figure 2. Images of CT and interventional catheterisation. (a–d) Cardiac CT and right ventriculography showed three false aneurysm sacs (arrow heads). The two large aneurysms appeared as one lesion with two lobes (white arrows). (e and f) RVG showed an ADO-II AS (black arrows) that was placed in the narrow neck with a good position, and aneurysms regressed totally 8 months later. (g) Perforation of the atretic valve by the coronary guidewire. (h) A 6 mm Tyshak II Balloon was used for pulmonary valvuloplasty. ADO-II AS = Amplatzer Duct Occluder II Additional Sizes; AO = aorta; PA = pulmonary artery; RA = right atrium; RV = right ventricle.