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Ann Thorac Surg 2004;77:707-708
© 2004 The Society of Thoracic Surgeons


Case report

Dissection in a pulmonary autograft

Edward H. Kincaid, MDa*, James D. Maloney, MDa, Sidney W. Lavender, II, PA-Ca, Neal D. Kon, MDa

a Department of Cardiothoracic Surgery, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA

Accepted for publication April 9, 2003.

* Address reprint requests to Dr Kincaid, Department of Cardiothoracic Surgery, Wake Forest University School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157, USA
e-mail: tkincaid{at}wfubmc.edu


    Abstract
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 Abstract
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 Comment
 References
 
We report the case of a type II aortic dissection involving the pulmonary autograft after a Ross procedure 6 years earlier. A dissection flap was present in both the native ascending aorta and right coronary sinus of the autograft. At reoperation, the valve was spared using a root remodeling technique.


    Introduction
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 Abstract
 Introduction
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 References
 
Dilation, and occasionally aneurysmal degeneration, of the pulmonary autograft are known to occur after the Ross procedure [1, 2]. In these cases, histopathological studies [3, 4] have demonstrated changes in the media of the vessel wall, a finding that should also predispose to dissection of the autograft root. To our knowledge, however, this complication has not been reported.

A 39-year-old man was admitted to our institution with chest and interscapular back pain. His history was significant for a bicuspid aortic valve and having undergone a Ross procedure in 1996 for severe aortic insufficiency. This operation was performed using a total root replacement technique. He was followed with annual echocardiograms that demonstrated good valvular function before a missed appointment in 2001. Echocardiography at the time of the current admission in 2002 revealed mild to moderate aortic insufficiency (AI), marked dilation of the ascending aorta to 5.5 cm, and mild pulmonary insufficiency with no gradient across the allograft pulmonic valve. In the operating room at the time of redo sternotomy, the ascending aorta was densely adherent to the underside of the sternum. For this reason, cardiopulmonary bypass (CPB) was initiated using femoral cannulation. After completion of the sternotomy, a significant amount of dense inflammatory tissue was appreciated around the ascending aorta and root. The patient was cooled to a core temperature of 20°C, and the circulation was arrested. Upon opening the aorta, there was an obvious flap in the ascending aorta that extended distally to the arch and proximally into the autograft at the level of the right coronary sinus (Fig 1). The right coronary artery was separated from the root by the dissection. There were intimal tears in both the native aorta and autograft. The left and noncoronary sinuses, along with the autograft leaflets, were normal in appearance. The repair was started by suturing a 24-mm knitted Dacron graft to the underside of the aortic arch. Cardiopulmonary bypass was reinstituted after an 11-minute period of circulatory arrest. Because the autograft was normal except for the right coronary sinus, only this portion of the root was removed. The ostium of the right coronary artery was mobilized on a button of normal aortic tissue that remained from the previous operation. A 24-mm Dacron tube graft was fashioned to have one sinus of Valsalva extending from the graft. This conduit was anastomosed to the sinotubular junction in the regions of the left and noncoronary sinuses, and the entire right sinus was replaced by suturing the Dacron sinus limb to the annulus. The right coronary ostium was then reimplanted into a separate opening in the Dacron sinus (Fig 2). Transesophageal echocardiography after termination of CPB revealed trace aortic insufficiency, and the patient's postoperative course was unremarkable. Histologic examination of the native aortic wall revealed focal myxoid degeneration. He remained asymptomatic in follow-up, and transthoracic echocardiography 4 months after discharge revealed mild aortic insufficiency, an aortic valve area of 3.3 cm2, and a mean gradient of 4 mm Hg.



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Fig 1. The ascending aorta and aortic root as viewed from the patient's left. A dissection flap (black arrow) is present in the native aorta and autograft root. The white arrow demonstrates the posterior aspect of the sinotubular junction.

 


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Fig 2. Modified root remodeling with Dacron graft replacement of the right coronary sinus (black arrow). The white arrow demonstrates the right coronary ostium.

 

    Comment
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 References
 
In 75% of patients with bicuspid aortic valves, one can detect histologic abnormalities, such as cystic medial necrosis and elastic fragmentation in the media of the aorta and pulmonary artery [3]. Whereas aortic dissection and aneurysm are known late complications of bicuspid aortic valve replacement [5], the association between the abnormal histology and late aortic degenerative pathology is purely theoretical. In a similar fashion, significant dilation of the autograft after the Ross procedure occurs in more than 50% of patients at 7 years [2]. Whereas one could reason that the combination of dilation and abnormal histology could predispose to dissection within the autograft root, this complication has not been reported. In this patient, the origin of the type II dissection was not clearly evident because intimal tears were located in both the native aorta and autograft root. Because of the known vascular tissue abnormalities present in patients with bicuspid aortic valves, strong consideration should be given to replacement of the grossly abnormal ascending aorta at the time of any aortic valvular operation. Additionally, strict surveillance should be recommended to follow the dimensions of remaining aortic and autograft tissue.

Repair of late pathology within the autograft using valve-sparing techniques has been described [6] and is feasible because the autograft leaflets usually remain pliable and potentially competent, even in the presence of degenerative changes in the sinuses or sinotubular junction. In this patient, a modified root remodeling technique was used because the tissue in two of the three sinuses appeared normal, and the annulus had remained fixed from the initial operation. Valve reimplantation could also have been performed, but would have required more extensive mobilization, an additional coronary reimplantation, and removal of unaffected root tissue.


    References
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 Abstract
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 Comment
 References
 

  1. Takkenberg J.J., Zondervan P.E., van Herwerden L.A. Progressive pulmonary autograft dilatation and failure after Ross procedure. Ann Thorac Surg 1999;67:551-553.[Abstract/Free Full Text]
  2. Simon-Kupilik N., Bialy J., Moidl R., et al. Dilatation of the autograft root after the Ross operation. Eur J Cardiothorac Surg 2002;21:470-473.[Abstract/Free Full Text]
  3. de Sa M., Moshkovitz Y., Butany J., David T.E. Histologic abnormalities of the ascending aorta and pulmonary trunk in patients with bicuspid aortic valve disease: clinical relevance to the Ross procedure. J Thorac Cardiovasc Surg 1999;118:588-596.[Abstract/Free Full Text]
  4. Bauer M., Pasic M., Meyer R., et al. Morphometric analysis of aortic media in patients with bicuspid and tricuspid aortic valve. Ann Thorac Surg 2002;74:58-62.[Abstract/Free Full Text]
  5. Russo C.F., Mazzetti S., Garatti A., et al. Aortic complications after bicuspid aortic valve replacement: long-term results. Ann Thorac Surg 2002;74(Suppl):1773-1776.
  6. Leyh R.G., Kofidis T., Fischer S., Kallenbach K., Harringer W., Haverich A. Aortic root reimplantation for successful repair of an insufficient pulmonary autograft valve after the Ross procedure. J Thorac Cardiovasc Surg 2002;124:1048-1049.[Free Full Text]



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This Article
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James D. Maloney
Neal D. Kon
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Right arrow Articles by Kincaid, E. H.
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Right arrow Valve disease


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