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J Thorac Cardiovasc Surg 2007;134:839-843
© 2007 The American Association for Thoracic Surgery
Editorial |
a Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Tex
b Cardiovascular Surgery Service of the Texas Heart Institute at St. Lukes Episcopal Hospital, Houston, Tex.
Received for publication May 1, 2007; accepted for publication May 14, 2007. * Address for reprints: Scott A. LeMaire, MD, Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, One Baylor Plaza, BCM 390, Houston, TX 77030. (Email: slemaire{at}bcm.edu).
Infections involving ascending aortic grafts are extremely difficult to eradicate and are frequently lethal. Successfully treating this complication is always challenging and is especially problematic when the infection extends into adjacent prosthetic material in the aortic root—as in patients with composite valve grafts (CVGs)—or in the aortic arch. Although antibiotics are a critical component of treatment, they are rarely effective as the sole form of therapy. Among the many patients described in reports of ascending aortic graft infection, only a handful have been successfully treated with antibiotics alone.1-4
We1
previously reported that of 7 patients with infected ascending/arch grafts in whom nonoperative treatment was attempted, medical treatment ultimately failed in 3 (43%), necessitating operation. In 1995, Gott and associates4
reported that of 7 patients treated nonoperatively for CVG endocarditis, only 2 (29%) survived. These authors later reported using antibiotics alone to successfully treat 5 patients with Marfan syndrome who had early CVG endocarditis, but the authors emphasized that this treatment approach is not sufficient in patients with severe prosthetic infections.3
In their brief communication in this issue, Akowuah and colleagues5
describe treating 2 patients with antibiotics alone; both patients died. The dismal results of nonoperative management justify aggressive surgical treatment of infected ascending aortic grafts.
The cornerstone surgical strategy for treating patients with infected peripheral vascular grafts is graft removal and extra-anatomic bypass. Although technically possible,6
extra-anatomic bypass is not suitable for managing ascending aortic graft infections; therefore, the surgical options involve either salvaging the existing graft or replacing it in situ. In either case, the need to leave prosthetic material in an infected surgical field makes it difficult to eradicate the infection. In 1984, Hargrove and Edmunds7
introduced guidelines to address this problem, emphasizing the need for prompt and thorough surgical debridement, antiseptic irrigation, and appropriate antibiotic therapy. Notably, these early recommendations—which were based on the authors pioneering experience with only 4 patients—remain the central guiding principles for treating patients with infected thoracic aortic grafts today.5
Beyond these well-established principles of debridement and antimicrobial treatment, the options for dealing with an infected ascending aortic graft are characterized by the two main areas of controversy: whether to remove the infected graft and, if it is removed, what to replace it with. Although evidence-based practice guidelines are becoming available for many issues cardiothoracic surgeons face,8
it is unlikely that such guidelines will ever be established for managing this challenging problem. The literature on surgical treatment of ascending aortic graft infection fails to provide even the lowest level of evidence (level C, consensus expert opinion) on which to base a concrete recommendation. Although plenty of expert opinion is available, consensus is clearly lacking. The accumulated expert opinion, however, comprises a valuable armamentarium that surgeons can use when planning treatment for their patients. In their report, Akowuah and colleagues5
illustrate the value of using individualized treatment strategies in different clinical situations; this provides a welcome opportunity to review the available options.
Graft Removal and Replacement With a Synthetic Graft
Infected ascending aortic grafts have often been replaced with new synthetic grafts, especially during the era before bioprosthetic alternatives became commercially available. In cases in which the extent of replacement has been relatively limited, outcomes have generally been very good. In 1990, we1
reported using new Dacron tube grafts or patches to treat postoperative aortic infections in 10 patients; there were no early deaths, 1 late death, and no cases of recurrent infection. Along with other groups that have used synthetic grafts to replace infected ascending aortic grafts, we have emphasized the value of thorough debridement and other measures to reduce the chance of recurrent infection, including postoperative mediastinal irrigation with an antibacterial solution and coverage of the graft with viable tissue pedicles.7,9-11
Completely removing infected prosthetic material and replacing it with a new graft is particularly challenging when the infection involves a CVG. Combining root rereplacement with aggressive debridement in an inflamed and necrotic field often results in prolonged operations with substantial blood loss. Given the technical challenges of this procedure and the poor condition of many of these patients, it is not surprising that these operations have been associated with poor outcomes. In our cumulative experience, 5 of the 11 patients with infections who had new CVGs placed died within 30 days (46%).1,12
Other groups have reported similarly disappointing results when new CVGs were used to replace infected CVGs.4,13
A few groups, however, have achieved very satisfying results using this approach to treat CVG infection. Ralph-Edwards, David, and Bos14
reported excellent early survival (10/11, 91%) in patients in whom CVGs were used to replace infected grafts. This series was noteworthy for the authors use of extensive debridement that often required reconstruction of the left ventricular outflow tract with glutaraldehyde-fixed bovine pericardium and lengthening of the coronary arteries with saphenous vein or synthetic grafts. However, in a subsequent report,15
the authors noted a 25% incidence of recurrent prosthetic valve endocarditis in their series; this group currently uses homograft roots whenever available. Hagl and colleagues16
have also reported excellent early survival in 23 patients treated with aggressive debridement and replacement with new CVGs; moreover, all but 1 patient in the series remained free of recurrent endocarditis during follow-up. Because of these results, the Mount Sinai group continues to use CVGs in this setting, except in patients with contraindications to anticoagulation, who are better served by having the infected CVG replaced with a homograft.
Graft Removal and Replacement With a Tissue Graft
Several groups currently favor replacing infected ascending aortic prostheses with cryopreserved aortic homografts.2,3,17-19
Although homografts are not impervious to endocarditis,19-21
they appear to be more resistant to infection than synthetic grafts, perhaps because homografts allow better antibiotic penetration and inherently attract immune cells.17
Retrospective data have suggested that, compared with using synthetic grafts, using cryopreserved homografts for treating vascular infections is associated with improved outcomes, including better elimination of infection, fewer postoperative complications, and longer disease-related survival.22
The malleability of the homograft tissue is considered a technical advantage because it enables the graft to conform to a widely debrided annulus.18
In situ replacement of contaminated or infected grafts in the aortic root, ascending aorta, and transverse aortic arch has been associated with encouraging early and midterm results; although available reports only describe small groups of patients, these patients collective early survival exceeds 90%.2,3,15,18,23-25
One commonly cited disadvantage of using homografts is their predisposition to progressive deterioration and ultimate need for rereplacement.16,19
Another limitation is the relatively low tensile strength of the homograft tissue; because of this, it is extremely important to avoid anastomotic tension caused by using an inappropriately short graft. Unfortunately, in many cases, a single homograft will not reach the distal ascending aorta or transverse arch.18
Gaps between the distal end of the homograft and the native aorta can be bridged with a segment of synthetic graft, but this essentially defeats one of the purposes of selecting a tissue graft in the first place. Extensive aortic replacement can be accomplished by using total arch homografts, but these are rarely available.23
To address this problem, Lytle and colleagues18
have described using 2 standard aortic root homografts to perform hemiarch replacement; reversing the distal homograft after its valve has been removed allows the larger proximal end to be used for the arch anastomosis.
Although tissue replacement of infected CVGs has traditionally required the use of homografts, porcine xenograft roots have emerged as another option for replacing the infected root. Akowuah and colleagues5
successfully treated 1 of their patients by using a xenograft root. These grafts have the advantage of on-the-shelf availability and have been particularly useful in areas of the world where homografts are difficult or impossible to obtain.26,27
Compared with homografts, xenografts appear to be less susceptible to progressive degeneration. Mohammadi and colleagues28
recently described outstanding freedom from structural valve deterioration in a large series of patients who received porcine xenografts. Valve dysfunction developed in only 1 of 133 patients who had porcine xenograft root implantations. This problem was due to a leaflet tear and required reoperation 12 years after the initial implantation. Porcine xenograft endocarditis is also rare28
; although these grafts have a synthetic sewing cuff, their treatment with glutaraldehyde may confer resistance to infection.
Porcine xenografts, however, are even shorter than most homograft roots; therefore, an additional segment of graft is generally required to bridge the gap between the distal end of the xenograft and the patients aorta. As described above, this can be accomplished with a segment of synthetic graft or the tubular portion of a homograft. Additionally, stentless xenograft roots are not recommended for use in cases that require extensive annular debridement; the irregular base for the proximal suture line can cause significant distortion of the valve and produce regurgitation.16
Regardless of the type of conduit used, removing and replacing an infected ascending aortic graft is a major undertaking that carries substantial risk of morbidity and mortality. The alternative surgical approach that Akowuah and colleagues5
highlight—extensive mediastinal debridement and irrigation—has been used successfully by many groups (Table 1).
1,2,7,12,13,29-35
All of their reports include patients with ascending aortic grafts, many of whom also received an arch graft, CVG, or separate aortic valve prosthesis. These patients collective early survival is 91%. Nearly all of the reports include follow-up of at least 2 years, and most specifically document the absence of recurrent graft infection after the definitive procedure.
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Several factors have been discussed in the context of selecting patients who are likely to benefit from graft-sparing procedures. This approach is particularly well-suited for patients with poor physiologic reserve, who are unlikely to tolerate graft removal.32
Akowuah and colleagues5
reserved this approach for patients with grafts contaminated from adjacent sternal wound infections; although graft-sparing operations seem ideal for this type of patient, we and other groups have applied this approach without using sternal wound infection as a criterion.1,13,35
The severity of graft involvement is another aspect to consider. In a case reported by Hargrove and Edmunds,7
the decision not to remove the graft was based largely on the fact that the "suture lines were completely covered with healthy autogenous tissue." Although intact grafts with unexposed suture lines are desirable, we and other authors have used this approach in selected patients with contaminated anastomoses, including those with anastomotic leaks, pseudoaneurysms, and aortocutaneous fistulas.1,2,12,29,34
In most cases, the culprit anastomotic defects were treated by primary repair. Kawachi and colleagues34
used Dacron patches to repair suture line dehiscence at the distal anastomosis. We1
have avoided leaving the graft in place in patients with antibiotic-resistant infections (indicted by persistent positive blood cultures), severe graft deformity, prosthetic valve vegetations, or adjacent diseased aortic segments that needed replacement (because of severe aortic valve regurgitation, large aneurysm, or aortocardiac fistula, for example).
Strategies to Prevent Recurrent Infection
Irrespective of how the infected graft is specifically dealt with, several strategies are commonly used to prevent recurrent infection. Irrigation with antiseptic solutions—principally povidone–iodine or antibiotics—is a ubiquitous component of treatment, although the mode of delivery has varied. At a minimum, the aortic graft and surrounding mediastinal tissues are thoroughly irrigated during the operation. Mediastinal catheters are commonly placed to enable postoperative irrigation.32
Finally, if the sternum is left open after the debridement procedure, the mediastinum can be packed with sponges soaked in povidone–iodine.13
When povidone–iodine is used for postoperative irrigation, care is taken to avoid iodine toxicity and resulting hepatic dysfunction. Precautions include using dilute solutions (eg, 1% povidone–iodine) for irrigation while monitoring daily serum iodine concentrations (normal range, 4 to 8 mg/dL) and liver enzyme levels.13,32,33
Other methods of delivering local antibiotics may also be useful. Some authors have used gentamicin-impregnated fibrin glue to seal anastomoses and fill dead space.24,34
When using synthetic grafts for replacement, we routinely soak gelatin-sealed Dacron grafts in rifampin before implantation; although this practice has not been adequately studied in the setting of thoracic aortic reconstructions, encouraging results have been reported in the peripheral vascular surgery literature.36,37
The development of effective, commercially available antibiotic-bonded grafts would be useful for these cases.
It may also be helpful to avoid using suture and reinforcement materials that are likely to harbor bacteria. When working in a contaminated field, we favor using monofilament suture instead of braided suture. We also avoid synthetic materials when buttressing anastomoses and cannulation sites; pledgets and reinforcing strips can be made from excess homograft tissue, autologous pericardium, or glutaraldehyde-treated bovine pericardium instead of Teflon felt.22
Most reports describe using viable tissue to obliterate dead space and provide vascularized coverage of the graft. Occasionally, this can be accomplished by mobilizing local tissues, such as the thymus and pericardial fat pads.1
More commonly, coverage is achieved with a pedicled omental or muscle flap. Omentum is particularly popular because, in patients who have not had previous abdominal surgery, omentum can be easily accessed by extending the sternotomy incision into the abdomen for a short distance.7,9,11-13,25,29,30,32,33
The blood supply to the omentum is preserved by basing the pedicle on the right gastroepiploic artery. In addition to filling dead space, the vascularized omental pedicle improves oxygen supply to the region, enhances immunologic response, increases antibiotic delivery, and absorbs wound secretions that can serve as substrates for bacterial growth.9,29,32
Muscle flaps used in patients with ascending aortic graft infection have included pectoralis major, rectus abdominis, latissimus dorsi, and serratus anterior.1,7,13,31,33,35
Occasionally, a combination of flaps is necessary to achieve adequate coverage. The aortic graft can be covered with a vascularized flap during the original debridement/graft replacement procedure or in a delayed manner after a period of closed mediastinal irrigation or open wound care.
The final aspect of preventing recurrent graft infection is administering systemic antibiotics. In most cases, a period of intravenous antibiotic administration is followed by long-term oral antibiotic therapy. Choices regarding the length of antibiotic treatment remain arbitrary, and the efficacy of long-term antibiotics remains unproven.7
Approaches to antibiotic treatment have ranged from a 7-day course of intravenous antibiotics without subsequent oral therapy34
to lifelong antibiotic treatment.1,7,33
Although we continue to advocate lifelong suppressive antibiotic therapy—especially in patients with residual synthetic graft material—there is admittedly no evidence supporting this practice.12
It certainly seems reasonable to limit the length of antibiotic treatment in patients whose infected grafts have been replaced with homografts. In many reported cases, the approach to antibiotic treatment was individualized according to multiple clinical factors, including severity of infection, comorbid conditions, the specific pathogens involved, and the postoperative course. Hagl and colleagues16
recommend a strategy that is based on operative findings: if surgical cultures are positive, patients would receive at least 6 weeks of antibiotic therapy; if the cultures are negative but organisms are seen on Gram stain, patients would receive at least 4 weeks of antibiotic treatment; and if cultures and Gram stain are negative, antibiotic treatment would be continued for only 2 weeks.
Because of the dire consequences of thoracic aortic graft infection, we maintain an aggressive approach to prophylaxis in all patients undergoing thoracic aortic repairs, despite the absence of supportive evidence. Specifically, we routinely apply topical cephalosporin or vancomycin powder to the graft and continue intravenous antibiotics postoperatively until all chest drains and central venous lines are removed. It is important to recognize that the threat of aortic graft infection persists long after hospital discharge. One unusual aspect of Akowuah and colleagues series5
is the short interval between the initial operation and the graft infection (range 6-30 days). Many other series have demonstrated that the risk of aortic graft infection continues for years after the initial operation.1,2,7,12,14,16
We believe that this risk justifies an aggressive approach to antibiotic prophylaxis whenever patients with aortic grafts require invasive procedures that produce bacteremia, such as bronchoscopy, colonoscopy, and dental procedures, regardless of the length of time since the graft was implanted; we favor periprocedural intravenous broad-spectrum antibiotics over oral antibiotic prophylaxis in these patients. Experimental models are desperately needed to improve strategies for short- and long-term prevention of thoracic aortic graft infection.38
It is notable how little evidence is available to guide surgeons in treating patients with ascending aortic graft infection. There are, however, many established options for managing the infected graft, all of which have their place within the surgical armamentarium. In situ replacement can be effective but is often associated with substantial morbidity and mortality, especially in patients with infected CVGs. In many cases, existing grafts can be salvaged through a regimen of aggressive debridement, irrigation, and coverage with healthy tissue. Ultimately, the treatment strategy should be selected on the basis of relevant clinical factors and tailored specifically to the individual patient.
| See related article on page 1051.
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Acknowledgments
We thank Stephen N. Palmer, PhD, ELS, for providing editorial assistance.
Footnotes
1 Joseph Coselli, MD, reports consulting fees from Vascutek Terumo and Edwards LifeSciences and grant support from St Jude Medical and Cook, Inc. ![]()
References
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S. Sato, Y. Nitta, Y. Saiki, S. Kawamoto, A. Iguchi, M. Kaku, Y. Tabata, and K. Tabayashi Enhanced Perigraft Angiogenesis Prevents Prosthetic Graft Infection Ann. Thorac. Surg., October 1, 2008; 86(4): 1278 - 1284. [Abstract] [Full Text] [PDF] |
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