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Transthoracic access for pulmonary artery stenting

Part of:Interventional Cardiology

Published online by Cambridge University Press:  04 December 2018

Thomas KrasemannOpen the ORCID record for Thomas Krasemann[Opens in a new window],
Ingrid van Beynum,
Pieter van de Woestijne and
Ad Bogers
Thomas Krasemann*
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, Sophia Kinderziekenhuis, Erasmus Medical Centre, Rotterdam, The Netherlands
Ingrid van Beynum
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, Sophia Kinderziekenhuis, Erasmus Medical Centre, Rotterdam, The Netherlands
Pieter van de Woestijne
Affiliation:
Department of Cardiothoracic Surgery, Erasmus Medical Centre, Rotterdam, The Netherlands
Ad Bogers
Affiliation:
Department of Cardiothoracic Surgery, Erasmus Medical Centre, Rotterdam, The Netherlands
*
Author for correspondence: T. Krasemann, MD(D), FRCP, Department of Pediatrics, Division of Cardiology, Sophia Kinderziekenhuis, Erasmus Medical Centre, Rotterdam, Wytemaweg 80, 3015CN Rotterdam, The Netherlands. Tel: +31-10-7032188; E-mail: t.krasemann@erasmusmc.nl
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Abstract

Pulmonary artery stenting may not be possible transcutaneously because of anatomic features. Although intraoperative stenting has been well described, we present a case in which stenting of the left pulmonary artery was performed transthoracically in a separate procedure. Unusual anatomic conditions may require a multi-disciplinary hybrid approach to achieve the desired results.

Keywords

Transthoracic accessstenting pulmonary arteryCHD

Information

Type
Brief Report
Information
Cardiology in the Young , Volume 29 , Issue 2 , February 2019, pp. 222 - 224
Copyright
© Cambridge University Press 2018 

Access for interventional treatment of native or treated CHD can be challenging. We report a complicated case in which rescuing of the left pulmonary artery was performed by stenting through a right thoracotomy and direct hilar access to the right pulmonary artery in a hybrid procedure.

Case report

A male infant with hypoplastic left heart underwent atrial septectomy and mitral commissurotomy on day 2 of life, followed by bilateral pulmonary artery banding and stenting of the arterial duct on days 8 and 10, respectively. The situation was converted to a Norwood/Sano palliation 2 months later. At the age of 5 months, the Sano-shunt was removed and a partial cavopulmonary anastomosis was created. This was not tolerated, and hence was taken down to a central aortopulmonary shunt. In addition, a re-coarctation needed stenting. He was discharged with saturations of ca. 80% in room air.

Four months later the child appeared progressively cyanosed with oxygen saturations of 70% measured transcutaneously. On CT the left pulmonary artery appeared narrow (Fig 1a). The CT scan was used for planning cardiac catheterisation, in particular, to plan necessary angulations of the X-ray tubes. Ballooning or stenting the left pulmonary artery was not successful from a femoral approach.

Figure 1

( a ) CT showing the central shunt, well-developed right pulmonary artery and hypoplastic left pulmonary artery (arrow). ( b ) Post-interventional CT confirming increased perfusion of the left pulmonary artery. Note that the proximal part is not covered by the stents.

Through a right thoracotomy the hilus of the right lung was carefully prepared, a purse string suture prepared, and through this an 8 F Terumo sheath inserted directly into the right pulmonary artery. As the child was kept in an oblique position during the intervention, X-ray tube angulations were adjusted accordingly, to achieve the best possible imaging of the pulmonary arteries. Angiography confirmed the severe stenosis of the left pulmonary artery and proximal right pulmonary artery that is left from the shunt (Fig 2a). After balloon interrogation with a Tyshak II 6×20 mm balloon; NuMed, Hopkinton, United States of America, three open cell stents with a diameter of 6 mm were introduced and positioned sequentially, beginning distally in the left pulmonary artery extending into the proximal right pulmonary artery, but not covering the shunt. The three stents were Cook Formula stents 6×12 mm and 6×20 mm, and a Bard Valeo stent 6×18 mm. Angiography showed a satisfactory result (Fig 2b). Because the sheath was introduced close to the shunt, the most proximal part of the right pulmonary artery could not be covered with a stent, as the balloon shoulder would have pushed the sheath out of the vessel. After stenting, the sheath was removed and the purse string suture closed.

Figure 2

Angiographic findings obtained through a 7 F sheath inserted into the left hilus through a left thoracotomy: ( a ) Pre-procedural small left pulmonary artery. ( b ) Final result after sequential stenting of the left pulmonary artery starting distally.

The child recovered clinically. Chest X-ray before discharge showed more vascular markings on the left side than pre-procedurally. A further CT angiogram confirmed good position of the stents and patent flow to the left pulmonary artery branches (Fig 1b).

A bidirectional Glenn was performed at the age of 14 months, after cardiac catheterisation was carried out to dilate the aortic stent and evaluate pulmonary vascular resistance, which was low with 2.3 Wood units/m2. Intraoperatively, the most proximal stent was removed and the remaining ones were longitudinally opened. The cavopulmonary anastomosis was extended with a pericardial patch into the left hilus. After the operation, the child needed prolonged respiratory and inotropic support due to a parainfluenza infection, but eventually recovered and was discharged with saturations of 75%. Five months later, he is doing well and is thriving.

Discussion

Stenting of pulmonary arteries in patients with CHD has been described in the early 1990s and is a part of clinical routine since then.Reference O’Laughlin, Perry, Lock and Mullins 1 Hybrid approaches to optimise the outcome of patients with complex CHD have been described, including intraoperative stenting of pulmonary arteries.Reference Bearl and Fleming 2 , Reference Ungerleider, Johnston, O’Laughlin, Jaggers and Gaskin 3 This is frequently done during operation of the underlying condition under direct sight.Reference Bokenkamp, Blom, De Wolf, Francois, Ottenkamp and Hazekamp 4

The usual transcutaneous approach was not possible in our patient owing to the position of the central aortopulmonary shunt. As a bidirectional Glenn was not tolerated earlier, we wanted to minimise the risk and stent the pulmonary arteries before further operations to allow the pulmonary vascular resistance to adapt. CT allowed detailed evaluation of the anatomical situation, and a hybrid approach to open the left pulmonary artery up to the hilus was planned and carried out. We found that this is the first report of transthoracic pulmonary artery stenting.

Conclusion

For unusual situations, multi-disciplinary hybrid approaches can be considered to achieve the desired results. In our case, transthoracic access for pulmonary artery stenting was chosen.

Acknowledgments

None.

Financial Support

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

Conflicts of Interest

None.

Footnotes

Cite this article: Krasemann T, van Beynum I, van de Woestijne P, Bogers Ad. (2018) Transthoracic access for pulmonary artery stenting. Cardiology in the Young page 222 of 224. doi: 10.1017/S1047951118001841

References

1. O’Laughlin, MP1, Perry, SB, Lock, JE, Mullins, CE. Use of endovascular stents in congenital heart disease. Circulation 1991; 83: 1923–1939.10.1161/01.CIR.83.6.1923Google Scholar
2. Bearl, DW, Fleming, GA. Utilizing hybrid techniques to maximize clinical outcomes in congenital heart disease. Curr Cardiol Rep 2017; 19: 72.Google Scholar
3. Ungerleider, RM1, Johnston, TA, O’Laughlin, MP, Jaggers, JJ, Gaskin, PR. Intraoperative stents to rehabilitate severely stenotic pulmonary vessels. Ann Thorac Surg 2001; 71: 476–481.Google Scholar
4. Bokenkamp, R, Blom, NA, De Wolf, D, Francois, K, Ottenkamp, J, Hazekamp, MG. Intraoperative stenting of pulmonary arteries. Eur J Cardiothorac Surg: Off J Eur Assoc Cardiothorac Surg 2005; 27: 544–547.Google Scholar
Figure 0

Figure 1(a) CT showing the central shunt, well-developed right pulmonary artery and hypoplastic left pulmonary artery (arrow). (b) Post-interventional CT confirming increased perfusion of the left pulmonary artery. Note that the proximal part is not covered by the stents.

Figure 1

Figure 2Angiographic findings obtained through a 7 F sheath inserted into the left hilus through a left thoracotomy: (a) Pre-procedural small left pulmonary artery. (b) Final result after sequential stenting of the left pulmonary artery starting distally.