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Ann Thorac Surg 2004;77:591-596
© 2004 The Society of Thoracic Surgeons
a Department of Cardiac Surgery, Naples, Italy
b Department of Cardiology, University "Federico II" of Naples, Naples, Italy
Accepted for publication June 25, 2003.
* Address reprint requests to Dr Iannelli, Via Santo Strato 8, 80121 Napoli, Italy.
e-mail: gabrieleiannelli{at}libero.it
| Abstract |
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METHODS: From March 2001 to July 2002, 15 of 22 patients with acute thoracic aortic syndromes were submitted to endovascular surgery: 3 patients (20%) for traumatic rupture, 4 patients (26.7%) for contained or free rupture of thoracic aortic aneurysm, and 8 patients (53.3%) for acute type B dissection evolving to rupture. Computed tomographic scan was diagnostic in all patients. The stent grafts were introduced through the femoral artery.
RESULTS: In the endovascular group there were no perioperative deaths or open conversions. The intraoperative angiography and computed tomographic scan performed on discharge showed no significant endoleaks and successful sealing of the aortic dissection. Average intensive care unit and hospital stay was 1.7 ± 0.8 and 5.9 ± 3.0 days. Follow-up ranged between 4 and 23 months and included clinical examinations and serial computed tomographic scan at 3, 6, and 12 months, and every 6 months thereafter. One 84-year-old patient with thoracic aortic aneurysm died of pneumonia 78 days after endovascular surgery. Only one type 1 endoleak was noted in the first patient with traumatic rupture, 3 months after the procedure.
CONCLUSIONS: Endovascular surgery is a safe technique, showing encouraging early and midterm results and allowing for prompt treatment of associated lesions in complex multitrauma patients.
| Introduction |
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Since the initial reports from Stanford [5], endovascular surgery to treat diseases of the thoracic aorta has been used with growing enthusiasm, encouraging many centers to investigate the feasibility of this approach [6]. After our initial experience with endovascular surgery for abdominal aortic aneurysm, in March 2001 we started an endovascular program only for emergency disorders of the thoracic aorta in high-risk patients.
The purpose of this study is to evaluate short-term and midterm results of endovascular surgery restricted to thoracic aortic emergencies.
| Material and methods |
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In the group with traumatic rupture, 2 patients showed hemothorax and 1 an increasing pseudoaneurysm with dysphonia caused by compression of the laryngeal nerve. In the group with acute type B dissection, all patients suffered from thoracic pain not responsive to morphine and antihypertensive therapy and from increasing false lumen diameter: antegrade in 7 patients and retrograde in 1. In the group with thoracic aortic aneurysm, 3 patients suffered from shock and one of them had a massive left hemothorax; the aneurismal diameter for all patients ranged from 7.5 cm to more than 9.0 cm.
The diameter of the selected stent graft exceeded the diameter of the aorta by a minimum of 10% for traumatic rupture to a maximum of 20% for aortic aneurysm and acute type B dissection. The excess diameter was required to increase the radial force of the device as a result of self-expansion of the endoprosthesis, thus allowing for improved sealing of the graft in the aorta. The criteria to assess anatomic suitability for device implantation were vascular access larger than 8 mm and an aortic arch angulated at less than 60 degrees.
Stent graft placement was performed in the catheterization laboratory or in the operating room. Patients received general anesthesia and mechanical ventilation. The surgical team included 2 cardiovascular surgeons, an interventional cardiologist, an anesthesiologist, a scrub nurse, and a standby bioengineer. The procedure began by introducing a 6F pigtail catheter (Cordis, Hamburg, Germany) through the radial artery for precise localization of the subclavian artery, intraprocedural aortography, and direct monitoring of invasive arterial pressure. Antibiotic prophylaxis with cefotaxime and heparin (5,000 U) was given intravenously. In all cases femoral access was achieved by surgical dissection of one of the femoral or iliac arteries chosen after contrast injection of the distal abdominal aorta to select the best side for access and the onset of the celiac axis (landing zone). In the 2 patients with previous aortobifemoral bypass, access was obtained through a prosthetic branch. A Keller-Tillerman introducer sheath (Cook Inc, Bloomington, IN) was inserted through the femoral or iliac artery over a 300-cm-long 0.035-inch Back-up Meier wire (Boston Scientific, Boston, MA). The delivery system was loaded onto the wire (through the sheath) to the level of the thoracic aorta. Hypotension (mean arterial pressure approximately 60 mm Hg) was induced by sodium nitroprusside just before the placement of the stent(s). Subsequent aortography confirmed the adequacy of treatment.
The endovascular criteria for a successful procedure are as follows: (1) absence of death or surgical conversion; (2) exclusion of aneurysm or transected tract; and (3) occlusion of thoracic tears. The persistence of a double lumen in the abdominal aorta was not considered as an indication of failure if the thoracic intimal tears were covered and there was no blood flow in the false lumen. To evaluate the presence of endoleaks, in accordance with the White classification [7], all patients underwent a spiral computed tomography before discharge and at 3, 6, and 12 months after treatment. The number of stent grafts implanted ranged from one to four: one graft in patients with traumatic rupture, 2.2 ± 1.0 grafts/patient in patients with aortic aneurysm and 2.7 ± 0.9 grafts/patient in patients with acute type B dissection. The "telescope technique" was used to cover the descending thoracic aorta with multiple stent grafts of increasing diameters, from the proximal to the distal aorta. The size and number of implanted stent grafts is illustrated in Table 2. The endovascular device used in our first patient with traumatic rupture was a Gore Excluder thoracic stent graft (WL Gore, Flagstaff, AZ), a self-expandable endoprosthesis with an inner polytetrafluoroethylene tube and outer nitinol exoskeleton wire support structure designed for the thoracic aorta. For all the other patients we used the endovascular Talent stent graft (Medtronic AVE, Santa Rosa, CA), a self-expandable endoprosthesis consisting of circumferential nitinol stent springs covered with a Dacron graft, compressed into a 22F to 25F Teflon delivery system.
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| Results |
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The average length of intensive care unit and hospital stay was 1.7 ± 0.8 and 5.9 ± 3.0 days, respectively.
The intraoperative angiography and computed tomographic scan on discharge showed no significant endoleaks in any of the patients, confirming successful sealing of dissected layers.
Midterm results
The follow-up ranged between 4 and 23 months (average 12.8 ± 5.8 months) and included a clinical examination and a serial computed tomographic scan at 3, 6, and 12 months, and every 6 months thereafter. Two patients with traumatic rupture of the aorta required orthopedic surgery (leg and arm fractures), performed in a trauma center 5 and 7 days after endovascular treatment. Both patients were discharged home 2 weeks after the complex multitrauma. Four older patients, who had a major comorbidity, were transferred to a rehabilitation center 7.1 ± 4.7 days after treatment. One of these, an 84-year-old with thoracic aortic aneurysm, died of septic shock from pneumonia 78 days after endovascular surgery.
Only one type 1 endoleak was noted 3 months after the endovascular procedure in the first patient treated for traumatic rupture by implantation of a Gore-Excluder. The patient refused surgical treatment and is still doing well, with no evidence of increasing endoleak at 23 months' follow-up.
| Comment |
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Postoperative complications include pulmonary failure requiring prolonged ventilation, myocardial infarction, renal failure, coagulopathy requiring massive blood transfusions, and neurologic complications such as paraplegia [3, 9]. This latter possibility is a catastrophic event, especially when occurring in younger patients with traumatic rupture of the aorta, as demonstrated by extensive meta-analysis resulting in 19.2% incidence of paraplegia [11]. Prolonged convalescence is also expected in these cases, along with increased costs for hospitalization [12, 13]. The surgical option must always take into consideration the complexity of the procedure and the unsatisfactory results often attained in emergency situations and with older patients [3, 9, 14]. Reluctance related to conventional surgery has encouraged many centers to consider alternative strategies involving less-invasive techniques [6, 1214].
Endovascular surgery is a promising therapy for disease of the descending aorta and has rapidly evolved as a valuable alternative to conventional surgery [5, 6, 1214]. More recently, an attempt was made to identify the ideal candidate for endovascular surgery by using a numerical score chart, in accordance with the clinical and anatomic criteria proposed by Alves and colleagues [15].
In our initial experience, with candidates not considered to be ideal according to the American Society of Anesthesiologists class distribution, we treated high-risk patients in emergency conditions with no resulting hospital mortality and only one late death in an elderly patient in whom the surgical risk was considered prohibitive (American Society of Anesthesiologists class 5).
Open conversion was not required, and no endoleaks were present in any of the 15 patients on discharge. At 3 months' follow-up the first patient in our serieswith a Gore-Excluder stent graft implanted for posttraumatic pseudoaneurysmshowed a significant type 1 endoleak, currently stable 23 months from treatment. This failure could be ascribed to our learning curve and to a progressive reduction of the device's radial force, considered essential for successful sealing.
In the other 2 patients with traumatic rupture of the aorta19 and 22 years oldthe result was more encouraging, requiring only a short hospital stay and early orthopedic treatment of the fractures, resulting in prompt recovery and absence of endoleaks, confirmed at the 14-month and 19-month follow-up.
No paraplegia occurred in our series, despite extensive covering of the entire descending aorta in 9 patients (60%) and of two thirds of the aorta in 3 patients (20%): the critical region between T9 and T12 was stented in all 12 patients. Although some authors [16] recommend evaluating the spinal cord supply, the preoperative angiography was never taken into consideration and no particular strategies were adopted. Anatomic occlusion of all intercostal arteries is not a prognostic discriminant for paraplegia, according to surgical reports on complete replacement of the descending aorta when safe clamping time (less than 30 minutes) was achieved [17].
One major vascular complication occurred in the 19-year-old woman because of the discrepancy between the diameter of the iliac artery and the size of the device. We highly recommend using a vascular access larger than 8 mm to avoid unfortunate complications during the introduction of the device and advise great care in the presence of an exceedingly angulated aortic arch (in excess of 60°) as this is dangerous to cross and increases the risk of dislocation of the device as a result of inadequate sealing. The rigidity of the stent graft might also cause difficulties as it would not sufficiently hug the aortic arch and might lead to an endoleak. The Talent endovascular graft used in our series improves proximal adherence, maneuverability, and conformation and is considered suitable for this procedure.
Endovascular stent graft surgery is a promising and less-invasive alternative to exclude aneurysms, transection, and dissection of the aorta from blood flow and makes it possible to treat patients considered otherwise unsuitable for conventional surgery. Although a long-term follow-up is mandatory to detect late failures related to the prosthetic device, we can conclude that endovascular surgery (1) is safer than conventional surgery for emergency or high-risk patients, (2) allows for prompt treatment of associated lesions in complex multitrauma patients in which heparinization and extracorporeal support are not indicated and delayed treatment may be life-threatening, and (3) may be considered as an hypothetical bridge to conventional surgery for younger patients, if some unforeseeable device failure should occur.
| References |
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