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Ann Thorac Surg 2005;80:1117-1120
© 2005 The Society of Thoracic Surgeons
Departments of Cardiothoracic Surgery and Interventional Radiology, University of Vienna Medical School, Vienna, Austria
Accepted for publication February 18, 2004.
* Address reprint requests to Dr Czerny, Waehringer Guertel 18-20, Vi-enna, Austria A-1090 (Email: bypass{at}eunet.at).
| Abstract |
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| Introduction |
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In August 2003, a 57-year-old man was submitted to our department presenting with chest pain and beginning hemodynamic instability. The contrast enhanced computed tomographic scan revealed a contained rupture of a distal descending aortic aneurysm with a maximum diameter of 10.0 cm with contrast medium effusion into the right pleural cavity as well as into the posterior mediastinum. An endovascular approach was deemed feasible. Subsequently the patient was taken into the interventional radiologists suite.
After achievement of general anesthesia, as well as exposure of the right common femoral artery, a 5 French pigtail catheter was advanced through the right brachial artery into the aortic arch to reconfirm characterization of the morphology and extent of the aneurysm as well as serial angiography. After systemic heparinization with 5,000 IU, the delivery system was advanced under fluoroscopic guidance until the tip reached the middle portion of the descending thoracic aorta. Afterward, two Talent stent-grafts (Medtronic, Santa Rosa, CA) with a maximum diameter of 42 mm and 46 mm each, and a length of 13 cm were inserted into the distal descending thoracic aorta. At completion angiography, no endoleak could be observed. The patient was discharged from the hospital 4 days after stent-graft placement.
After 1 month postoperatively, the patient was readmitted to the hospital with chest pain as well as swallowing disorders. In addition, infectious factors were elevated (the C-reactive protein was 17.5 mg/dL and the leukocyte count was 16.5 g/L). The patients body temperature was 38.5°C. A computed tomographic scan revealed regular perfusion of the stent-graft with no signs of endoleaks. However, a fistula between the distal esophagus and the excluded aneurysm sac was observed (Fig 1).
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| Comment |
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Aortoesophageal fistulas synchronously complicating ruptured descending thoracic aneurysms are a known severe complication making already sophisticated conventional surgical procedures even more demanding [8]. However, metachronous fistulas are rarely seen. The mechanism of fistula development in our patient remains speculative. Pressure erosion of the aneurysm sac could have been a mechanism. Chronic inflammation due to the resorption of the posterior mediastinal hematoma may have represented another potential mechanism leading to fistula development.
With regard to treatment of aortoesophageal fistulas, a variety of surgical approaches is now available. Esophagectomy together with cervical esophagostomy and feeding gastrostomy are commonly applied due to the nonreconstructability of esophageal lesions. Most authors recommend prosthetic replacement of the diseased aortic segment with biological coverage of the alloplastic material with vital tissue such as omentum [8]. However, little is known with regard to treatment of infected thoracic endovascular stent-grafts. Due to the subsequent broadening of the invasiveness of the procedure, we decided to leave the stent-grafts in place. Thromboexclusion with ascending to abdominal aortic bypass would have represented an alternative. Parietal thrombus material was partially removed, and the remaining aneurysm sac was irrigated with beta-isodonic solution and sealed with vancomycin. We decided not to fully remove the parietal thrombus due to the potentially resulting instability of the overlapping stent-grafts. Little is known about the behavior of overlapping stent-grafts when oblique stability is lost by opening the aneurysmal sac and removing stability supporting tissue.
Another point of vital importance is maintenance of antibiotic therapy in these patients. Microbiologic cultures revealed a multi-sensitive staphylococcus aureus within the aneurysm sac. Therefore a chronic therapy with ciprofloxacin was initiated. With regard to duration of antibiotic therapy no guidelines are available. However we decided to leave the patient on maintenance therapy for at least 1 year.
After a period of 3 months, continuity was reinstalled with a retrosternally guided, pedicled isoperistaltic transverse colonic conduit. We chose an extra-anatomic conduction to avoid reopening of the right hemithorax. Alternatively a cervical esophagogastrostomy could have been performed. However a pedicled colonic conduit represents the more physiologic solution for an otherwise healthy individual.
In summary, management of an aortoesophageal fistula after endovascular stent-graft placement without removing the stent-grafts is feasible. This approach may extend therapeutic options when dealing with this rarely observed and complex entity.
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