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Exposed Femoral Graft Following Multiple Arterial Reconstruction

51
History andProcedures
A 64-year-old male presented to outpatient clinic with exposed left femoral graft following a recent (3-week-old) crossover right femoral to left pop­liteal (8 mm INTERING® PTFE – W.L. Gore, Newark, DE) graft. Past medical history was sig­nicant for hypertension and nicotine abuse (60 pack years). Patient had undergone multiple arte­rial reconstructions in the past 15years. In 2002 the patient underwent bilateral iliac stenting: on the left common iliac stent (39mm × 7mm) and right common iliac stent (29 mm × 7 mm) Palmaz® GENESIS™ balloon expandable stents (Cardinal Health, Dublin OH). By 2003, the stenting had failed, and the patient underwent an aortobifemoral bypass graft using a 16 × 8mm knitted Dacron graft for symptomatic iliac artery occlusive disease. Proximal aortic anastomosis was performed end to end. In 2009, patient devel­oped thrombosis of the left limb of the graft requiring revision. In 2010, patient underwent right supercial femoral artery and popliteal angioplasty with stent placement. He presented in 2011 with a cold right foot and had developed thrombosis of the distal supercial femoral artery including the stent, and a right femoral-popliteal in situ bypass was performed. In 2015, patient underwent thrombectomy of the left limb of the aortobifemoral bypass graft extending to super­cial and deep femoral arteries after he presented with a painful numb left lower extremity. Patient
was seen again in June 2016 with a cold left leg and underwent left femoral to popliteal non­reversed great saphenous vein bypass secondary to supercial femoral artery thrombosis and a poor outow from branches of the deep femoral artery.
In August 2016 patient was seen as an outpa-
tient and was found to have supercial left groin wound dehiscence with small amount of serosan­guinous drainage. The seroma was drained; cul­tures were positive for Staphylococcus aureus, coagulase negative, and Streptococcus viridans. The following day the patient presented with bleeding from the left groin wound. He was noted to have a two-centimeter opening without exposed graft, with no active bleeding. However, there was surrounding induration. The patient was started on IV antibiotics Vancomycin and Zosyn, and a CTA was performed. The CTA demonstrated a patent aortobifemoral, bilateral femoral-popliteal bypasses, and left groin inam­matory changes with aneurysmal dilatation of the distal aortic limb graft without extravasation (Fig.51.1).
The patient was scheduled for a debridement
on the left groin with sartorius muscle ap on hospital day 4; however, on hospital day three, patient developed secondary hemorrhage in the left groin. He underwent emergent debridement of the skin and soft tissue and revision of the left femoral-popliteal bypass with takedown of the proximal anastomosis with a new anastomosis
© Springer Nature Switzerland AG 2020 S. S. Hans, Challenging Arterial Reconstructions, https://doi.org/10.1007/978-3-030-44135-7_51
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216
Fig. 51.1 Left unilateral limb of the aortobifemoral graft
infection with soft tissue thickening in the left groin, aneurysmal dilatation, and small amount of gas seen around the graft
51 Exposed Femoral Graft Following Multiple Arterial Reconstruction
extending into the proximal supercial femoral artery, with sartorius muscle ap and a wound vac therapy. At this time, cultures did not show any growth of microorganisms. On hospital day ten, patient was discharged with stable hemoglo­bin and hematocrit and continued negative pres­sure therapy and oral rifampin with IV Ancef for 6 weeks per recommendation of the infectious disease consultant.
Seven days later the patient presented again to the emergency department with active hemor­rhage from the left groin. He was hypotensive with acute blood loss, anemia, and stage III hem­orrhagic shock. He was taken to the operating room where bleeding was noted from the anasto­motic suture line of the distal left limb of the aor­tobifemoral bypass graft. The patient underwent removal of the left infected unilateral limb of the aortobifemoral bypass graft with suture ligation of the proximal graft and placement of wound vac. There were no Doppler arterial ows in the posterior tibial or the dorsalis pedis arteries. Cultures at this time grew vancomycin-resistant
Enterococcus faecalis (VRE) and Candida parapsilosis.
Following a performance of a left axillopopli­teal bypass 2 weeks later with an 8mm INTERING PTFE graft (W.L.Gore Inc., Newark, DE), patient regained posterior tibial Doppler signals. During his hospital stay, he was continued on intravenous
antibiotics. A repeat CTA was performed on post­operative day 9 showing a patent left axillopopli­teal bypass. He was discharged on post-operative day 14 with continued negative pressure therapy to his left groin, IV daptomycin, and PO Diucan for an additional 4 weeks. Patient was ambulating and continued to do well till his follow-up visit with palpable dorsalis pedis pulses.
On May 23, 2017, patient presented to the emergency room with cold pulseless left lower extremity. Doppler arterial study and CTA of the chest/abdomen showed occluded axillopopliteal bypass with no Doppler ow in the left foot. Patient underwent crossover femoral-popliteal (proximal) graft with 8 mm INTERING PTFE graft. A tunnel was made in the suprapubic space with 8mm tunneler.
Right limb of the well-incorporated Dacron graft and origin of the right femoral-popliteal in situ bypass were exposed, and popliteal artery just above the left knee joint was exposed and mobilized following transection of the medial head of the gastrocnemius. On the right-side crossover graft was sutured near the hood of the femoral-popliteal in situ bypass in an end-to-side fashion, and distal anastomosis to the popliteal artery was also performed in an end-to-side fash­ion (Fig. 51.2). Patient regained left dorsalis pedis pulse on the left foot. Patient presented to the clinic 3 weeks later with exposed PTFE graft in the left groin. Since sartorius muscle had already been used, patient underwent gracilis muscle ap with a split thickness skin graft and application of wound vac on June 13, 2017 (Fig. 51.3). Complete healing and coverage of the graft in the subsequent 3 weeks occurred (Fig. 51.4). Vascular lab study in May 2018 revealed an ankle brachial index of 0.85 on the right and 0.69 on the left. Patient was last seen in June 2019 with satisfactory healing and no clini­cal evidence of graft infection. Patient presented to the emergency room with the symptoms of acute lower limb ischemia secondary to throm­bosed cross-over right common femoral to left popliteal graft in March 2020. Following a failed thrombectomy, patient underwent left above knee amputation and will be tted with above knee prosthesis in April 2020.

Discussion

217
Fig. 51.3 Exposed PTFE graft and gracilis muscle ap
Fig. 51.2 CTA of the chest and abdomen showing patent
aorto-right femoral graft, ligated left limb of aortobifemo­ral graft. Patent right femoral-popliteal in situ bypass and left axillopopliteal bypass
Discussion
Aortic graft infections can be classied as (1A) early infection which is dened as manifesting less than 4 months from time of initial surgery. These infections tend to be of a higher grade with high virulence, or (1B) late infection is dened as greater than 4 months from time of initial surgery and is usually low grade with lower virulence. Graft infection occurs either by direct infection or by hematogenous seeding [14]. Although perioperative contamination is
Fig. 51.4 Satisfactory left groin healing
a frequent cause of infection, almost 50% of infections occur 25–70months following arte­rial reconstruction [57]. The most common
218
51 Exposed Femoral Graft Following Multiple Arterial Reconstruction
organisms are gram- positive organisms with Staphylococcus aureus predominating. Other common organisms are coagulase-negative staphylococci, streptococci, enterococci, and other gram-negative organisms (Pseudomonas, E. coli, Bacteroides).
The risk factors for aortic graft infection include but are not limited to prolonged operative time (greater than 4 hours), perioperative infec­tion at a different site, nasal carrier of staphylo­cocci, older age, female gender, critical limb ischemia, obesity, chronic obstructive pulmonary disease, hyperglycemia, malnutrition, end-stage renal disease, immunodeciency, an infected thrombus within an aortic aneurysm, inadequate choice/dosing/timing of perioperative antibiotics, breaks in sterile technique, tissue trauma, bacte­remia, and surgical site infections.
Multiple classication systems have been pre­sented to delineate type of aortic graft infection. Two most common classications used are by Szilagyi and Samson. According to Szilagyi’s classication, Grade (I) infection represents supercial infection with cellulitis involving the wound, Grade (II) deep infection involving sub­cutaneous tissue, and Grade (III) graft infections [8]. Samson classication Grade (I) infection limited to dermis, Grade (II) infection involving subcutaneous tissue, Grade (III) infection of the graft not involving the anastomosis, Grade (IV) infection involving the anastomosis but no bleed­ing or bacteremia present, and Grade (V) infec­tion involving anastomosis with bleeding and/or hemorrhage [6].
The main principle in treatment of aortic graft infection is debridement of surrounding infected tissue, excision of the graft, and secondary revas­cularization. Antibiotics play a key role in the treatment of these patients but are usually given for a time period of about 6 weeks. The gold stan­dard in the past for aortic graft infection was removal of the graft with an axillary-bifemoral bypass revascularization. The axillary-bifemoral bypass however is associated with a mortality of 25–40%, risk of aortic stump blowout (mortality 30%), graft thrombosis, poor long-term patency rates, and reinfection rates of 5–15%. In lieu of these outcomes, more recent literature has shown
that in situ reconstruction, debridement with or without muscle ap, is superior in terms of peri­operative mortality, limb amputations, and rein­fection rates [9]. The in situ revascularization can be performed with cryopreserved allograft, autol­ogous femoral-popliteal veins (deep veins), spiral vein grafts, rifampicin-soaked or silver-coated Dacron, or PTFE grafts. Nonetheless, extra­anatomical bypass grafts can by utilized in cases of inaccessible groin, hostile abdomens, and presence of severe comorbidities.
In patients with severe comorbidities, a more conservative approach with antibiotics, local debridement, muscle ap, and negative pressure therapy may be undertaken. In order to attempt to salvage the graft, it should be surrounding by healthy, non-infected viable tissue. In a retro­spective study by Ryu etal., the sartorius muscle ap provided coverage in the setting of soft tissue groin infections following a lower extremity revascularization [5]. In patients with nonavail­ability of sartorius muscle ap (as was in this patient), gracilis muscle ap is a suitable alterna­tive. Morasch etal. placed gracilis muscle ap in 18 patients with a failed graft in 2 patients at a mean follow-up of 40±10months. There was no recurrence of graft infection in their series [10]. Other muscle aps which can be used for cover­age of exposed grafts are the rectus femoris and tensor fascia lata. Anastomotic aneurysm of suture line hemorrhage, systemic sepsis, or aggressive bacterial infections (gram-negative infections) are contraindications to conservative management.
In patients with aortobifemoral graft, who present with a unilateral graft limb infection, a unilateral graft limb excision with revasculariza­tion or complete graft removal can be attempted. In a retrospective study, Crawford etal. demon­strated unilateral limb excision can be excised, provided infection is infrainguinal. In their study, 50% of the patients developed a subsequent infection in the main body or a contralateral limb at a median of 2 years after unilateral graft limb excision [2]. Factors predictive of contralateral limb or main body graft infection are culture pos­itive supra-inguinal graft infection and an origi­nal aortobifemoral graft placed for aortoiliac

References

219
occlusive disease. However, microbes cultured in supra-inguinal infections were unique from microbes causing recurrent graft infections in this study raising suspicion for a new infection in the contralateral limb.
In patients with an inaccessible groin (either secondary to infection or multiple previous inter­ventions), an in situ bypass or extra-anatomic bypass to the groin cannot be performed. Met et al. reported extra-anatomical bypass in 24 patients, specically axillopopliteal bypass for limb salvage in setting of inaccessible groin over an 11-year period [3]. Several case studies since the 1970s have shown 1-year patency of 58–77% with a limb salvage rate at 1 year of 65–86%. However, in a small study by Seeger etal., there was 100% graft thrombosis with 0% primary patency at 7 months [7]. Met etal. emphasized the overall disease condition along with technical surgical aspects may dictate the primary patency of the graft [3]. However there is limited data regarding 1-year patency rate of axillopopliteal bypass. In our patient, axillopopliteal bypass occluded 9 months following reconstruction, and patient subsequently underwent crossover femoral- popliteal bypass graft which has remained patent for the past 2 years and 3 months without any evidence of infection involving the main body of the right aortic limb. In most patients with infected limb with aortobifemoral graft, it is important to remove the entire graft. However, in this patient, the right limb was well incorporated and in the absence of any recurrence of infection. Keeping the main body and the right limb of the graft may occasionally be feasible.
reconstruction such as axillopopliteal or cross­femoral- popliteal bypasses can sometimes act more like a disease than a cure given their exceed­ingly high thrombosis rates. In most circum­stances, in-line, in situ, anatomic revascularization may be a better alternative, despite higher recur­rent infection rates, especially when prosthetic material is required. In order to achieve success with in situ reconstruction, bacterial isolates need to be minimally virulent in type, and new graft material must be sufciently covered by a well­perfused muscle ap. There are a number of suit­able options for muscle ap coverage of graft material in the groin region. Of those options, the gracilis muscle is best suited for this purpose as its blood supply is derived from branches of the deep femoral artery which generally remains pat­ent following any bypass reconstruction to the groin. Alternatives, including rectus muscle aps, which derive perfusion from the inferior epigas­tric artery and sartorius muscle with its super­cial femoral artery blood supply, have oftentimes lost their source of direct blood supply. In addi­tion, depending upon harvest techniques, the length of the gracilis muscle and the ability to mobilize it long distances on its pedicle make this tissue source the best option for covering large defects, even those that extend proximal to the inguinal ligament. Prosthetic graft infections are always vexing problems, and while virulent bac­terial isolates will generally mandate complete removal of all prosthetic, with careful technique, close follow-up and a bit of luck patients with less virulent infections can oftentimes get by, and limbs may be preserved, with partial excision and either extra anatomic or in situ revascularization.
Invited Commentary fromMark D.Morasch, MD, FACS, RPVI
This is obviously a very challenging case and very complex problem. The authors should be congratulated for their perseverance and persis­tence. I suspect that many vascular surgeons would have thrown their hands up at some point, ligated the conduit, removed the infected pros­thetic, and accepted amputation as an ultimate result. That said, long segment extra-anatomic
References
1. Calligaro KD, Veith FJ, Yuan JG, et al. Intra­abdominal aortic graft infection: complete or partial graft preservation in patients at very high risk. J Vasc Surg. 2003;38:1199–205.
2. Crawford JD, Landry GJ, Moneta GL, etal. Outcomes of unilateral graft limb excision for infected aorto­bifemoral graft limb. J Vasc Surg. 2016;63:407–13.
3. Met R, Hissink RJ, Van Reedt Dortland RWH, etal. Extra-anatomical reconstruction in the case of an inac-
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51 Exposed Femoral Graft Following Multiple Arterial Reconstruction
cessible groin: the axillo-popliteal bypass. Ann Vasc Surg. 2007;21:240–4.
4. O’Connor S, FRCP H, Andrew P, et al. A systemic review and meta-analysis of treatments for aortic graft infection. J Vasc Surg. 2006;44:38–45.
5. Ryu YD, Jung HJ, Ramaiah VG, et al. Infected groin (graft/patch): managed with sartorius muscle ap. Vasc Special Int. 2016;32(1):11–6.
6. Samson RH, et al. A modied classication and approach to the management of infections involv­ing peripheral arterial prosthetic grafts. J Vasc Surg. 1988;8(2):147–53.
7. Seeger JM, Pretus HA, Welborn BM, etal. Long-term outcome after treatment of aortic graft infection with
staged extra-anatomic bypass grafting and aortic graft removal. J Vasc Surg. 2000;32:451–61.
8. Szilagyi DE, Smith RF, Elliott JP, Vrandecic MP.Infection in arterial reconstruction with synthetic grafts. Am Surg. 1972;176:321–33.
9. Armstrong PA, Back MR, Bandyk DE, etal. Selective application of sartorius muscle aps and aggressive staged surgical debridement can inuence long term outcomes of complex prosthetic graft infection. J Vasc Surg. 2007;46(1):71–8.
10. Morasch MD, Sam AD, Kibbie MR, Dumaniau MJ.Early results with the use of gracilis muscle ap, coverage of infected groin wounds after vascular sur­gery. J Vasc Surg. 2004;39(6):1277–83.
Complications (Early andLate) ofAortofemoral Grafting
52
History andPhysical Examination
A 62-year-old male was seen in the outpatient clinic on January 2012 with symptoms of bilat­eral lower extremity claudication (hips and thighs) on walking 50 yards. He complained of erectile dysfunction. Medical comorbidities included hypertension, chronic obstructive pul­monary disease, and nicotine abuse (60 pack years). Bilateral femoral, popliteal, tibial, and dorsalis pedis pulses were absent. Non-invasive Doppler study revealed an ankle brachial index on the right was 0.52 and on the left 0.34. CTA showed infrarenal aortic occlusion with occlu­sion of both common iliac arteries and aneurys­mal hypogastric arteries (Fig.52.1).

Procedure

He underwent aorto-bifemoral graft (16×8mm knitted Dacron reconstruction) on January 29, 2012 for thrombosed aortic aneurysm (diameter
3.5cm). Thrombosis extended from 1 centimeter below the origin of the renal arteries. Post­operative course was complicated by respiratory failure secondary to pneumonia requiring venti­latory support for 3 days. He also noticed weak­ness of the right lower extremity with inability to
lift it against gravity. Following ICU stay, patient was transferred to regular medical/surgical oor. He was started on physical and occupational ther­apy. Patient had palpable pulses in both feet. Non-invasive Doppler arterial study in June 2013 showed ankle brachial index of 1.01 on the right and 1.02 on the left. For the rst 2 months follow­ing arterial reconstruction, he needed a right knee brace as the quadriceps muscle was weak but within 6 months regained normal motor function of the right lower extremity.
Patient did not come to follow-up for 5 years till July 2019 as he developed ischemic rest pain in the right foot with painful ulceration following sustaining trauma to the skin tendo Achilles (Fig.52.2). Non-invasive Doppler arterial study showed an ankle brachial index on the right 0.3 and on the left 0.5. In addition, bilateral masses were palpable in both groins. Duplex imaging of the groin showed a partially thrombosed anasto­motic aneurysm measuring 3.0cm in diameter on the right and 2.5 cm on the left. Aortogram in July 2019 showed patent aorto-bifemoral graft, right common femoral artery occlusion, and proximal and mid-segment right supercial fem­oral artery occlusion. There was reconstitution of popliteal artery on the right above the knee with runoff primarily with anterior tibial artery in the calf extending with continuation of the dorsalis
© Springer Nature Switzerland AG 2020 S. S. Hans, Challenging Arterial Reconstructions, https://doi.org/10.1007/978-3-030-44135-7_52
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52 Complications (Early andLate) ofAortofemoral Grafting
Fig. 52.1 CTA showing infrarenal aortic occlusion, bilateral common iliac, and hypogastric artery
artery as a long spatulated anastomosis was per­formed. Patient also underwent simultaneous right femoral-popliteal in situ bypass (Fig.52.4). In post-operative period, patient developed swell­ing of the lower extremity which subsided with elevation and use of elastic support below the knee.

Discussion

Aorto-bifemoral graft reconstruction in a patient
Fig. 52.2 Showing ischemic ulcer, right heel
pedis artery (Fig. 52.3). On August 8, 2019, patient underwent resection of the right femoral anastomotic aneurysm with removal of large amount of thrombus with interposition of a 5-cm­long 8-mm-diameter knitted Dacron graft sutured proximally to the previously placed Dacron graft. An end-to-end anastomosis to the deep femoral
was complicated by spinal cord ischemia with weakness of the muscles of the right thigh. This probably represents ischemia/infarction of the right lumbosacral root (Type III) as described in Chap. 10 [1]. This patient had aortic occlusion (thrombosis of a small diameter abdominal aortic aneurysm) and occlusion of both common iliac and aneurysmal hypogastric arteries. During aor­tic reconstruction, it is likely that patient had interruption of collateral circulation to the pelvic
Discussion
223
Fig. 52.3 Showing aortography with patent aorto-bifemoral graft, right supercial femoral artery occlusion
vasculature. This situation was unavoidable as distal segments of the hypogastric artery were not available for reconstruction of a separate bypass from limbs of the aortic graft. Fortunately, patient recovered from motor weakness and was ambulating without cane after 6 months of arte­rial reconstruction.
Femoral anastomotic aneurysms are described in Chap. 25. Femoral anastomotic aneurysms present as asymptomatic pulsatile masses about typically 5–10 years aortofemoral graft recon­struction. Local pressure symptoms (pain, femo­ral neuralgia) may be present. Thrombosis and rupture of the femoral anastomotic aneurysms are uncommon. In this patient, thrombosis of the right femoral anastomotic aneurysm with associated
right supercial artery occlusion resulted in criti­cal limb ischemia which was managed by revision of the right limb of the graft, removal of the anas­tomotic aneurysm, and anastomosis of the Dacron limb to the deep femoral artery. Patient also underwent simultaneous right femoral- popliteal in situ bypass resulting in restoration of arterial supply to the right lower extremity. Repair of fem­oral anastomotic aneurysm is indicated once the aneurysm reaches the size of 3cm or larger. The incidence of femoral anastomotic aneurysms is decreasing as fewer aorto-bifemoral grafts for iliac artery occlusive disease are being performed. This is the result of increasing use of percutane­ous interventions (iliac angioplasty and stenting) for aortoiliac artery occlusive disease.
224
52 Complications (Early andLate) ofAortofemoral Grafting
Fig. 52.4 Repair of thrombosed right femoral anastomotic aneurysm and right femoral-popliteal in situ bypass
Invited Commentary fromPeter K.Henke, MD
likely in this case), from internal iliac emboliza­tion, and could have been worsened with hypo-
tension. The incidence of paralysis with open Aortofemoral bypasses for aortoiliac disease have decreased markedly in frequency over the last 10–15 years given the advent of advanced endoluminal techniques [2]. In general, this approach is logical and is likely to reduce at least early morbidity and mortality and in general doesn’t burn a bridge for patients who may need an open procedure later. In the current case, open aortofemoral bypass (AFB) still remains the best option for an occluded abdominal aortic aneu­rysm with concomitant iliac disease. The patient had small internal aortic aneurysms, but these were patent and did not merit treatment.
The complication presented was an ischemic spinal episode with temporary paresis and is quite unusual [3]. Potential etiologies in this patient include sacrice of critical spinal collater­als with the infrarenal graft placement (most
AAA is less than 1%. Occasionally these are purely idiopathic and no denable cause can be found. Treatment is supportive as was done in this case, with reasonable recovery.
Anastomotic pseudoaneurysms after AFB are fairly common. These are particularly com­mon as these grafts age, after 5 or more years. Many are mild dilatations and don’t reach the size threshold of 2.5–3.0cm. There is little clear evidence for size to repair, but generally if they are associated with embolization or thrombosis, that is a clear indication for repair, regardless of size. Typically, repairs are performed using an interposition graft, as was described in the case, and hooded down the profunda. This is optimal and no good endovascular options exist. Secondly, if further revascularization is required, the patient can then have a bypass either off the