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Ann Thorac Surg 1999;67:1986-1989
© 1999 The Society of Thoracic Surgeons
a Clinic for Cardiovascular Surgery, University Hospital, Zurich, Switzerland
Address reprint requests to Dr Vogt, Clinic for Cardiovascular Surgery, University Hospital, Ramistr 100, CH-8091 Zurich, Switzerland;
e-mail: paul.vogt{at}chi.usz.ch
Presented at the Aortic Surgery Symposium VI, April 30May 1, 1998, New York, NY.
| Abstract |
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Methods. Between January 1991 and December 1996, homografts were used in 18 patients (mean age, 61±12 years; range 4185) with thoracic (4/18; 22%) or abdominal (14/18; 78%) aortic graft infection. Sepsis was present in 14 patients (78%); 6 (33%) had various aortic fistulae. Total graft replacement using homografts was performed in 14 (78%), and partial graft replacement at the site of infection in 4 patients (22%).
Results. Hospital mortality was 11%. During the follow-up period of 22±15 months (range, 1265) there was 1 infection and 1 homograft-related late death after complete homograft replacement, and 1 percutaneous vascular stent placement after partial graft replacement. No other instances of reinfection, suture line rupture or anastomotic aneurysms were observed.
Conclusion. Total graft replacement with homografts provides an effective treatment for infected aortic grafts. Partial graft replacement at the site of infection is feasible and safe.
| Introduction |
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Recent findings with cryopreserved heart valve homografts in the treatment of acute infectious endocarditis [7] led us to use cryopreserved homografts for in situ replacement of infected aortic grafts. Their observed clinical resistance to bacterial infections [8] prompted us to limit the surgical procedure, performing only partial graft replacement when the vascular prosthetic infection involved only a small portion of the graft or was limited to the aortic graft anastomosis. This study presents our clinical experience with the treatment of infected aortic grafts, performing either total or partial graft replacement with cryopreserved homografts.
| Material and methods |
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Prosthetic vascular grafts of the thoracic aorta were affected in 4 patients (22%). One had infection of an ascending aortic graft previously implanted for an acute type A dissection, and the other had an infected composite graft after repair of annuloaortic ectasia. The other 2 patients had infection of a descending aortic graft: an aortobronchial fistula after aortoplasty with a Dacron patch for coarctation 23 years earlier, and an aortoesophageal fistula originating from the proximal anastomosis of a graft placed for chronic type B dissection 2 months earlier.
Abdominal aortic prosthetic grafts were infected in 14 patients (78%). Aortointestinal fistulae were found in 4: 2 patients had had inadvertent intestinal injury during the implantation of an aortobiiliac bifurcation graft years ago and were referred with huge abscesses; the other 2 patients had a proximal aneurysm of their aortobifemoral bifurcation graft rupturing into the retroperitoneal duodenum (Fig 1 ). One patient presented with persistent bleeding of the sinus tract of an ureterocutaneous fistula draining into the groin along the aortobifemoral prosthesis. Another patient had undergone 10 reoperations for infection of an aortobifemoral bifurcation prosthesis reaching from the infrarenal aorta to the distal part of the superficial femoral artery on both the right and left sides. Two patients were on dialysis because of end-stage diabetic nephropathy, having had renal transplantation, removal of a necrotic renal graft, aortoiliac reconstruction and placement of an extra-anatomic bypass graft with secondary infection; both were taking multiple combinations of several antibiotics, one for 6 months and the other for 2 years.
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Partial replacement of an infected aortic prosthesis was performed in 4 patients (22%), in whom only a limited infection of the aortic graft was found, involving only a small portion of the graft anastomosis itself. In the patient presenting with an aortoesophageal fistula originating from the proximal anastomosis of a descending thoracic aortic graft, only the proximal third of the descending aortic graft was replaced with a homograft, leaving the distal two-thirds of the aortic prosthesis in place. Distally, the homograft was anastomosed directly to the prosthetic graft, and the anastomosis was sealed with Gentamicin-impregnated fibrin glue. In the second patient, who presented with an aortoduodenal fistula due to the rupture of a proximal anastomotic aneurysm, only the enlarged proximal part of the bifurcation prosthesis containing the aortointestinal fistula was replaced with a descending aortic homograft (Fig 2 ). Again, the distal anastomosis between the homograft and the remaining bifurcation of the prosthesis was sealed with Gentamicin-impregnated fibrin glue, taking care not to expose the distal part of the bifurcation prosthesis when performing the anastomosis to the homograft. In the remaining 2 patients, extended groin infection was treated by replacing only the distal part of the corresponding leg of the aortobifemoral prosthesis, using a limited retroperitoneal approach.
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| Results |
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The mean duration of postoperative mechanical ventilation was 3 days (median 1, range 120), the mean intensive care stay was 3.6 days (median 2, range 242), whereas the mean hospital stay was 50±32 days (median 25, range 21150). The mean duration of postoperative antibiotic treatment was 43±13 days (median 42, range 2884). Reoperations were necessary in 3 patients: in 2 patients, an additional reconstructive procedure had to be performed for associated peripheral vascular occlusive disease. The third patient had a stabilization of an accidental hip fracture 6 weeks after homograft replacement of infrarenal bifurcation grafts, resulting in a total hospital stay of 150 days. All other hospital stays for more than 21 days were due to the need for prolonged intravenous antibiotic treatment. Delayed wound healing, necessitating secondary surgical wound closure, was observed in 3 patients (17%). No other instances of septic or homograft-related complications were observed, even in patients with partial graft replacement.
Late results
There were 2 late deaths (12.5%) during a follow-up of 22±15 months (range, 1265): an 85-year-old woman with an infrarenal bifurcation homograft died in another hospital from acute upper gastrointestinal tract bleeding. A homograft-duodenal fistula was found, and persistence of Candida albicans infection at the proximal infrarenal suture line was confirmed at autopsy. In this patient, who was treated early in our experience, antifungal treatment was discontinued after 6 weeks due to its severe side effects. The second late death was an 82-year-old man with an infrarenal bifurcation homograft whose prosthetic infection was caused by Aspergillus, Mycobacterium tuberculosis and Staphlyococcus aureus. He died 18 months later from a homograft-duodenal fistula without evidence of persistent infection.
There was 1 late reintervention in a patient who had partial replacement of the proximal third of an infected descending aortic prosthesis: 18 months after surgery, a mean pressure gradient of 42 mm Hg at the proximal anastomosis between the homograft and the vascular prosthesis was successfully reduced to 13 mm Hg by percutaneous placement of a stainless steel stent.
There were 2 late deaths which were neither infection nor homograft related: a 41-year-old man died 9 months postoperatively from severe diabetes-related complications, and a 59-year-old man died 29 months postoperatively from chronic renal failure years after failed renal transplantation.
Postoperative magnetic resonance imaging, computed tomographic, angiographic and transesophageal echocardiographic findings were normal in all surviving patients (Fig 3 ). No instances of reinfection, false aneurysm formation, homograft leakage, suture line rupture or homograft-related reoperations were observed, resulting in a disease-related cumulative survival of 70% at the end of the follow-up period.
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| Comment |
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Partial graft replacement may be a further step in this concept, and may be indicated when the vascular prosthetic infection is limited, involving only a small portion of the graft or the anastomosis itself, as demonstrated in our patients. This less invasive technique may simplify the operative procedure without increasing the risk of infection or homograft-related reoperations. The local application of antibiotic-impregnated fibrin sealant has reduced the reoperation rate for recurrent endocarditis with the use of a mechanical prosthesis [14]. We used aminoglycoside-impregnated fibrin sealant to cover the anastomosis between the vascular prosthesis and the homograft. Care was taken to limit the exposure of the remaining part of the prosthetic graft, and to seal its whole visible surface with antibiotic-impregnated fibrin glue. Our in vitro studies demonstrated that the local antibiotic concentration achieved by this technique was 30 to 200 times higher than the highest recommended aminoglycoside levels in the blood using standard intravenous treatment, eradicating even aminoglycoside-resistant staphylococci. Thus, antibiotic-impregnated fibrin sealant may prove a useful adjunct in the concept of partial replacement of infected aortic grafts.
We are aware that this retrospective study represents only a small series of patients. Larger clinical series and a longer follow-up will be necessary to document the feasibility and the safety of this less invasive approach to prosthetic aortic graft infection.
The long-term behavior of cryopreserved aortic homografts is unknown, although the low incidence of late homograft-related problems remains encouraging [9], and is superior to the long-term survival rates reported for conventional surgical treatment of major vascular infections [15, 16]. Programmed cryopreservation maintains the basic structure of collagen and elastic fibers [17], so that the mechanical properties of cryopreserved aortic homografts are not different from those of fresh human thoracic aortas [18], even though immunological rejection of cryopreserved allografts has been described [9, 19]. But we believe that cryopreserved aortic homografts will not behave like freshly implanted allografts, which seem to deteriorate uniformly [20]. Since the operative mortality in the surgical treatment of infected aortic grafts [13] is of major concern, and this can be decreased by the use of cryopreserved aortic homografts [810, 13], their use is justified even if they do progressively deteriorate: they can help eradicate the infection and allow later implantation of a prosthetic graft without the risk of recurrent infection. Positive experience with their use in the treatment of vascular infections combined with our results in patients with otherwise intractable aortic infections have convinced us that cryopreserved aortic homografts should be the conduits of choice in the management of infected aortic grafts.
| References |
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