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Ann Thorac Surg 1996;61:1146-1152
© 1996 The Society of Thoracic Surgeons


Original Article: Cardiovascular

Using Aortic Allograft Material to Treat Mycotic Aneurysms of the Thoracic Aorta

Christoph Knosalla, MD, Yuguo Weng, MD, A. Charles Yankah, MDPhD, Joseph Hofmeister, MD, Roland Hetzer, MDPhD

Department of Cardiothoracic and Vascular Surgery, German Heart Institute Berlin, Berlin, Germany

Accepted for publication October 20, 1995.


    Abstract
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
Background. Although mycotic aneurysms are rare in this age of antibiotics, they nevertheless represent life-threatening lesions of the aortic wall because of their high incidence of rupture and significantly high rate of recurrence.

Methods. Between March 1988 and August 1994, cryopreserved allograft material was used to treat 8 patients (mean age, 62.5 years; range, 47 to 80 years) with mycotic aneurysms of the thoracic aorta at our institution. Two patients had emergency operations; the other operations in 6 patients were elective. The aneurysms were located at the previous cannulation site of the aorta (n = 1) or at the donor/recipient aortic anastomosis (n = 1) in the patients who had heart transplantation, in the ascending aorta in 3 patients with aortic valve endocarditis, in the aortic arch in 2, and in the descending aorta in 1. The operative technique consisted of excision of the mycotic aneurysm followed by allograft patch reconstruction in 5 patients, an allograft composite graft replacement of the ascending aorta in 2 patients with endocarditis, and combined aortic allograft root replacement and allograft patch reconstruction of the ascending aorta in 1 patient.

Results. The underlying infections of the aorta were treated successfully in 6 patients. One heart transplant recipient had reoperation because of recurrent mycotic aneurysm after allograft patch reconstruction at the donor/recipient anastomosis. There was one early death involving a patient with Salmonellasp sepsis.

Conclusions. The use of aortic allograft material for repairing mycotic aortic aneurysms is a promising and effective operative concept for managing thoracic aortic infections.


    Introduction
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
For editorial comment, see page 1053.

Replacement of the aorta with allograft material was introduced for clinical use in the early years of vascular surgery [13]. Although the clinical results were encouraging, several disadvantages were recognized, such as difficulties with procurement and preservation of human allografts or secondary dilation and calcification caused by allograft degeneration, as observed in a large number of patients. Since the early 1960s, aortic replacement with prosthetic material became the treatment of choice for diseases of the aortic wall. Nevertheless, cur-

For editorial comment, see page 1053.

rent operative procedures involving the use of prosthetic material for treating aortic infections, as reviewed by Robinson and Johansen [4], carry substantial early and late mortality rates as a result of recurrent infection. After achieving excellent long-term results with allograft replacement in managing active endocarditis [5], we decided to use allograft material to repair mycotic aortic aneurysms.


    Material and Methods
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
Between March 1988 and September 1994, 8 patients were evaluated and underwent operative repair of mycotic aortic aneurysms at the German Heart Institute Berlin. Patients with aortic annulus abscess but without mycotic aortic aneurysm were not included in the study. There were 6 men and 2 women, ranging in age from 47 to 80 years (mean age, 62.5 years). Two patients underwent operations under emergency conditions, whereas the remainder were scheduled for elective operations.

Five patients had previously undergone cardiac operations (Table 1Go): 2 were heart transplant recipients, 1 of whom had experienced mediastinitis 2 weeks after transplantation; and 3 had had prosthetic valve endocarditis. One of them had undergone aortic valve replacement three times because of recurrent prosthetic valve infection. In the last operation, valve replacement was combined with in situ prosthetic graft replacement for a mycotic aneurysm of the ascending aorta. Another patient who had undergone aortic valve replacement, including composite replacement of the ascending aorta, at another institution presented with endocarditis of the aortic valve associated with a mycotic aneurysm of the ascending aorta. One patient had been treated with cortisone and methotrexate for several years for chronic polyarthritis (see Table 1Go). Diabetes mellitus was found in 2 patients. One patient exhibited no predisposing conditions.


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Table 1. . Characteristics of Patients With Mycotic Aortic Aneurysms Treated With Allograft Material, German Heart Institute Berlin, March 1989 to September 1994
 
In the patients who had heart transplantation, the aneurysm was located at the previous cannulation site or at the donor/recipient anastomosis. In 3 patients with aortic valve endocarditis, the location was the ascending aorta (in 1 of them at the cannulation site of the previous operation); in 2 patients, the aneurysm was found in the aortic arch; and in 1 patient, it was in the descending aorta (Table 2Go).


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Table 2. . Localization, Operations, and Reoperations for Mycotic Aortic Aneurysms
 
Staphylococcus aureus was the causative organism in 3 patients; S aureus and Pseudomonas aeruginosa were causative in 1 (Table 3Go). Streptococcus faecalis, Salmonella sp, and pneumococci were each found in 1 patient. Mycobacterium avium and Candida albicans were found in a heart transplant recipient.


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Table 3. . Pathogens and Causes of Death (Early and Late) With Mycotic Aortic Aneurysm, German Heart Institute Berlin
 
Graft preparation included sterile procurement and storage at 4°C in a preservation fluid with antibiotics according to the method of Yankah and Hetzer [6]. After 24 hours of storage, the allografts were placed in fresh antibiotic medium supplemented with 10% dimethyl sulfoxide (Fisher Scientific Co, Pittsburgh, PA). The grafts were then cryopreserved with a computer-controlled rate freezer that lowered the temperature 1°C per minute down to a temperature of -40°C. The specimens were then placed in the vapor phase of a liquid nitrogen freezer.

Operations were performed through a median sternotomy in 7 patients. A thoracoabdominal approach was preferred in the case involving mycotic aneurysm of the descending aorta. If the aneurysm was located in the ascending or descending aorta, the operation was performed with cardiopulmonary bypass and moderate hypothermia. Patients with aneurysms in the aortic arch were given deep hypothermia of 15°C with a reduced flow of 0.5 L/min. Cardiopulmonary bypass through femoral cannulation was applied in 4 patients. In the other patients, cardiopulmonary bypass was instituted through cannulation of the ascending aorta and right atrial drainage.

Resection of the aneurysm and reconstruction that maintained continuity of the aorta were possible using an aortic allograft patch (Figs 1Go–3) in 3 patients (see Table 2Go). Two patients with aortic valve endocarditis were treated with an allograft as a composite graft (Figs 4Go–6), 1 additionally with combined aortic valve replacement with allograft and allograft patch reconstruction of the ascending aorta (Figs 7, 8GoGo). Aortic arch replacement with allograft material (Fig 9Go) was performed in the 2 patients whose aneurysms were located in the aortic arch (Fig 10Go).



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Fig 1. . Allograft patch reconstruction of a mycotic aortic aneurysm at the previous cannulation site in a heart transplant recipient (patient 1). (LCA = left coronary artery; RCA = right coronary artery.)

 


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Fig 4. . Infected aortic valve and ascending aorta composite graft, paravalvular leaks, dehiscence of subaortic curtain, and mitral valve jet lesion in patient 3. (LCA = left coronary artery; RCA = right coronary artery.)

 


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Fig 7. . Prosthetic valve endocarditis and infected ascending aortic prosthetic graft in patient 2. (LCA = left coronary artery; RCA = right coronary artery.)

 


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Fig 8. . Allograft aortic root replacement and subtotal ascending aortic allograft patch replacement in patient 2. (LCA = left coronary artery; RCA = right coronary artery.)

 


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Fig 9. . Partial aortic arch replacement with allograft in patients 6 and 7. (LCA = left coronary artery; RCA = right coronary artery.)

 


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Fig 10. . Computed tomographic scan of a saccular mycotic aneurysm in the aortic arch in patient 6.

 
All patients were treated with appropriate parenteral antibiotics for 6 weeks. All were continuously followed up until death or until completion of the study. The mean follow-up was 13 months (range, 5 days to 3 years 4 months).


    Results
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
Underlying infection of the aorta was treated successfully in 6 patients. In 1 case in which a heart transplant recipient underwent allograft patch reconstruction involving resection of the mycotic aortic aneurysm at the donor/recipient anastomosis, recurrent aneurysm made it necessary to replace the ascending aorta with an aortic allograft conduit (Fig 11Go). The patient died of Candida sepsis 8 days after the last intervention. There was one early death involving a 70-year-old woman with Salmonella sp sepsis. Autopsy findings of both patients indicated that the aortic repair was intact, with no evidence of infection.



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Fig 11. . Allograft ascending aorta replacement in patient 5. (LCA = left coronary artery; RCA = right coronary artery.)

 
Late death occurred in 2 patients of causes unrelated to their mycotic aortic aneurysms (2 months and 31 months after operation). At the time of death, they exhibited no signs of infection. In the other patients, we have never seen calcification of the allograft material during follow-up (Fig 12Go).



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Fig 12. . Chest roentgenogram in patient 1, 2 years after allograft patch reconstruction, looks normal and exhibits no signs of calcification.

 

    Comment
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
More than a century has passed since Sir William Osler, in the historic Gulstonian Lecture given at the Royal College of Physicians in London in 1885, reported a case of ``malignant endocarditis'' in which he introduced the term mycotic aneurysm, described as resulting from septic emboli in bacterial endocarditis [7]. Increasing understanding of its pathogenesis led to the proposal that mycotic aneurysms be classified on the basis of preexisting arterial status and the sources of infection [8]. In this study, only mycotic aneurysms occurring in the previously normal or arteriosclerotic aorta are discussed. Infected preexisting arteriosclerotic aneurysms and recently infected arterial prostheses were excluded from the study.

Mycotic aortic aneurysms are rare, yet potentially life-threatening, lesions of the aortic wall. Kaufman and associates [9] reported mortality rates of 80% for such aneurysms (100% if the aneurysm was caused by S aureus and Escherichia coli). In cases involving S aureus infections, we observed a mortality rate of 25%. In recent years, there have been reports of patients being successfully treated by in situ reconstruction of mycotic aneurysms of the aorta using prosthetic material in selected cases [4, 10], particularly in those with minimally virulent infections and negative blood or perigraft cultures [11].

Pasic and co-workers [12] reported six in situ reconstructions of the thoracic aorta performed during a 21-year period at the University Hospital Zurich. Repeat operations were performed in 2 patients, in 1 to repair an acute rupture 1 cm distal to the previous repair of an aneurysm in the ascending aorta. Operative treatment in all of the patients involved in situ placement of the grafts after evacuation of clots and local debridement. No recurrent ruptures were observed at our institution when allograft material was used to treat mycotic aortic aneurysms. There was one early death in a patient with Salmonellasp sepsis who underwent operation for repair of an acute rupture of a mycotic aneurysm of the aortic arch. In a heart transplant recipient with a mycotic aneurysm at the donor/recipient anastomosis, the ascending aorta was ultimately replaced with an aortic allograft as a composite graft.

Kieffer and associates [13] reported the results of in situ fresh allograft replacement of infected infrarenal aortic prosthetic grafts in 43 patients. The mortality rate was 12% and the rate of recurrence was 2.3%. Moreover, there were no early or late amputations in the entire series, an outcome that was not reported for any of the conventional methods.

In this study, 3 cases of mycotic aortic aneurysms resulted from septic embolization from endocarditis. With the introduction of modern antibiotic therapy, the prevalence of endocarditis has decreased and the spectrum of causative organisms for mycotic aneurysm has changed markedly. As reported in various studies, the most common pathogens today are staphylococci, streptococci, and Salmonella sp [14, 15]. The microbiologic findings of this study are similar to those in the medical literature. We found that in 2 patients, mycotic aortic aneurysms developed at the cannulation site from a previous operation, which had been afflicted by mediastinitis. As reported previously, infections of the aortic wall may occur at potentially weakened areas, such as suture lines or cannulation sites, where intimal and endothelial ischemia or insult may have occurred [16].

Although it has been shown that immunosuppressive treatment may increase arterial allograft patency and prevent aneurysmal degeneration [17, 18], this was not considered feasible under the infective conditions of mycotic aneurysms. However, unlike in other studies, all of the allografts in this study were matched for blood type [19].

Although antibiotic therapy may control the symptoms of sepsis associated with mycotic aortic aneurysm, it does not heal the lesion or prevent rupture [9, 20]. The required duration of antibiotic therapy remains a matter of opinion. Most authors advocate 4 to 6 weeks [21]. For cases involving repair of mycotic aneurysms with prosthetic material, Chan and colleagues [21] recommended permanent antibiotic therapy, as late recurrent infections have been reported [22].

It was believed that using any prosthetic material to treat mycotic aortic aneurysms of the thoracic aorta, in which extraanatomic reconstruction was not possible, would present a high risk of recurrent infection. The use of allograft material may reduce the rate of late postoperative infections and improve survival [19]. In this study, only 1 patient exhibited recurrent infection.

However, as shown in patient 1, allograft patch plasty can be performed on well-circumscribed mycotic aneurysms to repair the defect in the aortic wall. Complete debridement of all necrotic tissue and patch closure of the cavity to viable tissue without tension are essential features for preventing reinfection and recurrent aneurysm formation [23]. For cases involving greater inflammatory involvement of the aortic wall, we recommend replacing the affected part of the aorta with allograft material. If it is necessary to use a composite graft because of prosthetic valve infection or aortic annulus abscess, an allograft composite graft should be used. A prosthetic graft may be used as a patch or conduit if no homologous material is available [12].

In conclusion, the use of aortic allograft material to replace mycotic aortic aneurysms is a promising and effective concept, capable of bringing thoracic aortic infections into complete remission.



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Fig 2. . Allograft patch reconstruction of a mycotic aortic aneurysm at the site of the anastomosis of a heart transplant recipient (patient 5). After resection of the tissue of both rims, a direct anastomosis of the posterior aspect of the aorta was created, and a wedge-shaped allograft patch plasty was performed using allograft material. (LCA = left coronary artery; RCA = right coronary artery.)

 


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Fig 3. . Allograft patch reconstruction of the descending aorta in patient 8.

 


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Fig 5. . Allograft aortic root and ascending aortic replacement, reconstruction of subaortic curtain with allograft mitral leaflet, and closure of jet lesion in patient 3. (LCA = left coronary artery; RCA = right coronary artery.)

 


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Fig 6. . Allograft aortic root and ascending aortic replacement in a case of prosthetic valve infection and a mycotic aneurysm at the previous cannulation site (patient 4). (LCA = left coronary artery; RCA = right coronary artery.)

 

    Footnotes
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
Address reprint requests to Dr Knosalla, Department of Cardiothoracic and Vascular Surgery, German Heart Institute Berlin, Augustenburger Platz 1, D-13353 Berlin, Germany.


    References
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 

  1. Dubost C, Allary M, Oeconomos N. Resection of an aneurysm of the abdominal aorta: re-establishment of the continuity by a preserved human arterial graft, with results after five months. Arch Surg 1952;64:405–8.
  2. Gross RE, Hurwitt ES, Bill AH, et al. Preliminary observations of the use of human arterial grafts in the treatment of certain cardiovascular defects. N Engl J Med 1948;239:578–9.[Medline]
  3. Oudot J, Beaconsfield P. Thrombosis of the bifurcation treated by resection and homograft replacement. Arch Surg 1953;66:365–74.
  4. Robinson JA, Johansen K. Aortic sepsis: is there a role for in situ reconstruction? J Vasc Surg 1991;13:677–84.[Medline]
  5. Knosalla C, Siniawski H, Weng Y, Yankah AC, Hetzer R. Diagnosis and surgical treatment of active infective aortic valve endocarditis with associated periannular abscess. Cardiovasc Surg 1995;3(Suppl 1):14.
  6. Yankah AC, Hetzer R. Procurement and viability of cardiac valve allografts. In: Yankah AC, Hetzer R, Miller DC, Ross DN, Sommerville J, Yacoub MH. Cardiac valve allografts 1962–1987. New York: Springer, 1988:23–6.
  7. Osler W. The Gulstonian lectures on malignant endocarditis. Br Med J 1885;1:467–70.[Free Full Text]
  8. Patel S, Johnston KW. Classification and management of mycotic aneurysms. Surg Gynecol Obstet 1977;144:691–4.[Medline]
  9. Kaufman SL, White RI, Harrington DP, Barth KH, Siegelman SS. Protean manifestations of mycotic aneurysms. AJR 1978;131:1019–25.[Abstract]
  10. Ralph-Edwards A, David TE, Bos J. Infective endocarditis in patients who had replacement of the aortic root. Ann Thorac Surg 1994;58:429–33.[Abstract]
  11. Jacobs MJHM, Reul GJ, Gregoric I, Cooley DA. In-situ replacement and extra-anatomic bypass for the treatment of infected abdominal aortic grafts. Eur J Vasc Surg 1991;5:83–6.[Medline]
  12. Pasic M, Carrel T, von Segesser L, Turina M. In situ repair of mycotic aneurysm of the ascending aorta. J Thorac Cardiovasc Surg 1993;105:321–6.[Abstract]
  13. Kieffer E, Bahnini A, Koskas F, Ruotolo C, LeBlevec D, Plissonnier D. In situ allograft replacement of infected infrarenal aortic prosthetic grafts: results in forty-three patients. J Vasc Surg 1993;17:349–56.[Medline]
  14. Bennett D. Primary mycotic aneurysms of the aorta-report of case and review of the literature. Arch Surg 1967;94: 758–65.[Abstract/Free Full Text]
  15. Jarrett F, Darling C, Mundth ED, Austen G. Experience with infected aneurysm of the abdominal aorta. Arch Surg 1975;110:1281–6.[Abstract/Free Full Text]
  16. Knosalla C, Weng Y, Warnecke H, et al. Mycotic aortic aneurysm after orthotopic heart transplantation-report of three cases and review of the literature. J Heart Transplant (in press).
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  19. Donaldson RM, Ross DM. Homograft aortic root replacement for complicated prosthetic valve endocarditis. Circulation 1984;70(Suppl 1):178–81.
  20. Mundth ED, Darling RC, Alvarado RH, Buckley MJ, Linton RR, Austen WG. Surgical management of mycotic aneurysms and the complications of vascular reconstructive surgery. Am J Surg 1969;117:460–70.[Medline]
  21. Chan FY, Crawford ES, Coselli JS, Safi HJ, Williams TW Jr. In situ prosthetic graft replacement for mycotic aneurysm of the aorta. Ann Thorac Surg 1989;47:193–203.[Abstract]
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