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Ann Thorac Surg 1996;61:241-244
© 1996 The Society of Thoracic Surgeons
Wessex Cardiothoracic Unit, Southampton General Hospital, Southampton, United Kingdom
Accepted for publication September 6, 1995.
| Abstract |
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| Introduction |
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If recurrent coarctation coexists with intracardiac defects that require surgical correction, then the problem for the surgeon becomes even greater. We describe 2 such cases in which median sternotomy and the institution of cardiopulmonary bypass were necessary to correct intracardiac defects. The recurrent coarctation was corrected by employing two similar methods of extraanatomic bypass completed entirely via a median sternotomy.
| Case Reports |
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-year-old boy presented with recurrent coarctation and subaortic stenosis. He had originally presented to another institution as a neonate with a type A interrupted aortic arch and a perimembranous ventricular septal defect that was corrected at 3 days of age by means of resection and end-to-end anastomosis via a median sternotomy. A residual coarctation was then repaired at 9 days of age with a subclavian flap angioplasty through a left thoracotomy. Further recurrent coarctation of the distal arch developed, which was treated with balloon dilation on four occasions. At presentation to our unit angiography and magnetic resonance imaging demonstrated severe stenosis of the distal arch extending into the proximal descending thoracic aorta (Fig 1
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-year-old boy originally presented as a neonate with a coarctation and multiple ventricular septal defects. The coarctation was repaired with a subclavian flap angioplasty and a pulmonary artery band applied at 10 days of age via a left thoracotomy. The ventricular septal defects were closed and the band was removed 16 months later. The child remained symptom-free, but follow-up investigation revealed severe mitral regurgitation and a hypoplastic aortic arch with a residual coarctation at the site of repair. The gradient across the coarctation was 30 mm Hg.
At operation the median sternotomy wound was reopened and the ascending aorta was found to be of good size at 15 mm diameter, tapering to 5 mm at the distal arch, with dense mediastinal adhesions. Cardiopulmonary bypass was established using bicaval cannulation, the heart was lifted, and the posterior pericardium was incised below the level of the inferior pulmonary veins to expose the descending thoracic aorta. A side-biting clamp was applied and a 12-mm zero-porosity woven Dacron conduit was anastomosed end-to-side using a 5-0 polypropyline suture. The conduit was then passed cranially through the oblique sinus and over the roof of the left atrium to lie beside the ascending aorta (Fig 4
). The aorta was then cross-clamped, cardioplegia given, and the left atrium opened. The mitral valve was found to be severely dysplastic such that repair was impossible, and a 23-mm CarboMedics (Austin, TX) mechanical prosthesis was inserted. The left atrium was closed and the proximal conduit was then anastomosed to the right-facing posterior side of the ascending aorta with the cross-clamp still applied. Cardiopulmonary bypass was discontinued with no residual gradient between ascending aorta and the femoral arteries. The patient went on to make a straightforward recovery, being discharged on the fifteenth postoperative day. Follow-up magnetic resonance imaging and Doppler studies showed normal flow in the conduit with no compression of the left atrium or of the conduit itself (Fig 5
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| Comment |
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The two most widely used forms of repair are a patch aortoplasty and a local extraanatomic bypass, both performed via a left thoracotomy [1, 2, 9]. Other well-reported techniques are resection with end-to-end anastomosis or interposition graft. Median sternotomy with cardiopulmonary bypass has been advocated, particularly when coexistent intracardiac abnormalities are present [1, 10, 11]. The use of cardiopulmonary bypass has the added attraction of avoiding the necessity to cross-clamp the aorta at normothermia with the concomitant risk of spinal cord ischemia, particularly if collateral circulation is not well developed [12].
More extensive extraanatomic conduits have occassionally been described. Jacob and associates [4] have reported a series of 10 ascending-descending aortic bypass grafts performed using a combined left thoracotomy (to perform the distal anastamosis) and median sternotomy where the proximal anastomosis is fashioned with a side-biting clamp on the left-facing side of the ascending aorta. A second technique is the ascending-distal abdominal aortic bypass graft described by Siderys and colleagues [13] and subsequently reported in another 4 cases [14, 15] using a single midline incision from suprasternal notch to below the umbilicus. The conduit is passed through a slit made in the center of the diaphragm and brought around the right side of the heart to be anastomosed to the right-facing side of the ascending aorta. This would clearly not be suitable in young children in view of consequent growth.
This article reports a technique in which the recurrent coarctation was successfully bypassed with an entirely intrathoracic conduit through a single incision. Only 4 comparable cases have been reported; these were in an article by Sweeney and associates [1] in which the patients had also required concomitant correction of intracardiac defects. However, in these cases the approach through the posterior wall of the left atrium was not described (patient 1), and in no case was the conduit brought through the oblique sinus (patients 1 and 2).
The pathway of the conduit is clearly shown in Figures 2 and 4![]()
. Each of these techniques provides a further option in management of such complex cases while avoiding the requirement for a second surgical incision or extension into the abdomen. The presence of dense fibrosis around the site of previous repair, a long coarcted segment, or poor collateral flow make local bypass procedures or resection difficult and hazardous. Cardiopulmonary bypass allows the heart to be lifted to expose the descending thoracic aorta and reduces the risk of spinal cord ischemia. If mediastinal adhesions prevent complete mobilization of the heart then the descending aorta can be exposed through the posterior wall of the left atrium. The disadvantage of the technique is that it does not provide good access to the descending aorta if there should be bleeding from the distal anastomosis. Fortunately, this did not prove to be a problem in either case, and the use of gelatin-resorcin-formol glue may contribute to decreasing the risk of bleeding.
| Footnotes |
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| References |
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