Cryopreserved vein allografts are used as alternative conduits for infrainguinal bypass but are prone to aneurysmal degeneration. A 60-year-old man presented with a pulsatile, tender right groin mass 2 years after thrombosis of a cryopreserved vein jump graft emanating from a prosthetic axillary to profunda bypass. Intraoperatively, the aneurysm was consistent with isolated dilatation of the hood of the thrombosed cryopreserved vein graft. This was excised and repaired with bovine pericardial patch angioplasty. The patient recovered with no recurrence for 2 years. Aneurysmal degeneration of the cryopreserved vein allograft can occur even after graft thrombosis.
Cryopreserved vein allografts are used as alternative conduits for infrainguinal bypass but are prone to aneurysmal degeneration. A 60-year-old man presented with a pulsatile, tender right groin mass 2 years after thrombosis of a cryopreserved vein jump graft emanating from a prosthetic axillary to profunda bypass. Intraoperatively, the aneurysm was consistent with isolated dilatation of the hood of the thrombosed cryopreserved vein graft. This was excised and repaired with bovine pericardial patch angioplasty. The patient recovered with no recurrence for 2 years. Aneurysmal degeneration of the cryopreserved vein allograft can occur even after graft thrombosis.
Autologous saphenous vein is the preferred conduit for infrainguinal lower extremity bypass. However, autologous veins are often unavailable. Alternative conduits such as cryopreserved cadaveric saphenous vein allografts, referred to as cryoveins in this paper, have been used in infected and contaminated fields. Cryovein durability is shown to be poor due to thrombosis and aneurysmal degeneration. Harris et al reported the late aneurysm formation rate between 5% and 33%. Management of aneurysmal cryovein bypasses can be challenging. The surgeon must weigh risk of hemorrhage from the aneurysm against risks of complications or thrombosis with surgical revision.This report describes a unique case of aneurysmal degeneration of the hood of a chronically thrombosed cryovein bypass that developed 2 years after major amputation. Consent for publication was obtained, and all identifying information has been omitted.
Case
A 60-year-old male smoker with complex vascular history and reconstructive surgeries for peripheral arterial disease presented with a pulsatile mass in his right groin causing pain and discomfort. He denied fever and chills. He previously had an ipsilateral below-the-knee amputation and was using a prosthesis to ambulate. Past medical history was significant for coronary artery disease, renal insufficiency, hypertension, and hyperlipidemia.His surgical history was complex. Having undergone an aortobifemoral bypass at an outside institution (Fig 1, A), he was first seen by our team 4 years later with bilateral femoral artery aneurysms concerning for infection (Fig 1, B). He underwent staged resection of the aneurysms and separate bilateral axillo-profunda femoral bypasses with polytetrafluoroethylene (PTFE) (Fig 1, C). He was kept on lifelong doxycycline. He subsequently underwent a cryovein jump graft from the hood of the extra-anatomical PTFE bypass to the posterior tibial artery for rest pain (Fig 1, D). After multiple reinterventions (5 endovascular, 4 open), the jump graft thrombosed and the patient underwent a right below-the-knee amputation with ligation of the distal aspect of the cryovein bypass, but the axillo-profunda prosthetic graft remained patent (Fig 1, E). He presented 2 years after thrombosis.
Fig 1
A, Patient had an aortobifemoral bypass due to aortic occlusion. B, Patient presented with bilateral femoral artery aneurysms. C, Aortobifemoral bypass was explanted and the patient received bilateral polytetrafluoroethylene (PTFE) axillo-profunda femoris artery bypass. D, Cryovein jump bypass (blue) was added from the hood of the distal end of the axillo-profunda bypass graft. E, Cryovein jump graft thrombosed and the patient received a below-the-knee amputation. F, Aneurysmal degeneration was found at the hood of the cryovein graft at its anastomosis on the profunda femoris artery.
A, Patient had an aortobifemoral bypass due to aortic occlusion. B, Patient presented with bilateral femoral artery aneurysms. C, Aortobifemoral bypass was explanted and the patient received bilateral polytetrafluoroethylene (PTFE) axillo-profunda femoris artery bypass. D, Cryovein jump bypass (blue) was added from the hood of the distal end of the axillo-profunda bypass graft. E, Cryovein jump graft thrombosed and the patient received a below-the-knee amputation. F, Aneurysmal degeneration was found at the hood of the cryovein graft at its anastomosis on the profunda femoris artery.Computed tomography angiography showed aneurysmal dilation of the distal axillofemoral bypass graft (Fig 2). There was concern for infection but no local or systemic signs of infection. He underwent surgical repair. A longitudinal incision was made in the proximal thigh, and the PTFE graft was circumferentially exposed for proximal control. The graft was well incorporated into soft tissue with no evidence of fluid or infection signs. The graft was accessed using a micropuncture system. On-table angiogram showed the aneurysm distal to the puncture site with no involvement of the distal anastomosis of the axillary to profunda artery and adequate outflow (Fig 3).
Fig 2
Axial cut of the computed tomography angiogram showing aneurysmal dilatation of the distal right axillofemoral prosthetic polytetrafluoroethylene (PTFE) bypass graft measuring 5.0 × 3.9 cm with extensive mural thrombus (yellow arrow).
Fig 3
Intraoperative angiogram before surgery with contrast filling the aneurysm sac (yellow arrow) 5 cm distal to the puncture site and no involvement of the anastomosis with the profunda artery (green arrow).
Axial cut of the computed tomography angiogram showing aneurysmal dilatation of the distal right axillofemoral prosthetic polytetrafluoroethylene (PTFE) bypass graft measuring 5.0 × 3.9 cm with extensive mural thrombus (yellow arrow).Intraoperative angiogram before surgery with contrast filling the aneurysm sac (yellow arrow) 5 cm distal to the puncture site and no involvement of the anastomosis with the profunda artery (green arrow).The aneurysm was found to be a full thickness dilation of the wall of the proximal anastomosis of the cryovein to the prosthetic graft without disruption of the suture line or the axillofemoral PTFE graft (Fig 1, F). It was dissected circumferentially and was well incorporated into the surrounding tissue with no evidence of fluid, purulence, or signs of active infection (Fig 4, A). The graft was clamped proximally, and the aneurysm was opened using electrocautery. After removing clots, the aneurysm was identified as a degenerated cryovein. A Pruitt balloon was used for distal control in the profunda to minimize redo dissection of the profunda artery and potential compromise of the outflow. Aneurysm tissue was removed by disconnecting the old suture line, which was intact. The distal graft was ligated with 2-0 silk ties. The aneurysmal wall of the cryovein was sent for cultures in addition to swabs from the surgical site (Fig 4, B).
Fig 4
Visualization of the aneurysm. A, Surgical view of the aneurysm of the cryovein bypass graft at its proximal anastomosis to the prosthetic axillo-profunda graft (yellow arrow). B, Graftotomy of the axillo-profunda bypass graft (green arrow) with a Pruitt balloon for distal control (yellow arrow).
Visualization of the aneurysm. A, Surgical view of the aneurysm of the cryovein bypass graft at its proximal anastomosis to the prosthetic axillo-profunda graft (yellow arrow). B, Graftotomy of the axillo-profunda bypass graft (green arrow) with a Pruitt balloon for distal control (yellow arrow).A bovine pericardial patch was used to close the defect in the PTFE graft. After hemostasis, a flat drain was placed, and the wound was closed. Prevena VAC was applied. He had an uneventful course and was discharged after 4 days. All intraoperative cultures were negative. Computed tomography angiography after 13 months showed no recurrence (Fig 5). He remains clinically stable and asymptomatic after 2 years.
Fig 5
Former aneurysm site no longer showing dilation (yellow arrow) in axial.
Former aneurysm site no longer showing dilation (yellow arrow) in axial.
Discussion
Infrainguinal bypass is an important revascularization option for patients with chronic limb-threatening ischemia. When autologous saphenous veins are unavailable, alternatives like prosthetic vascular grafts or cryoveins are considered. This paper reports a unique case of aneurysmal dilatation of a thrombosed cryovein bypass graft.Cryovein allografts have a 5-year patency rate of approximately 22%. Despite poor patency, cryoveins are the preferred conduit compared with prosthetics in infected fields due to a lower risk of reinfection. The incidence of infection in aortic reconstructions with autologous veins is 13% and with prosthetic grafts 10% to 15%. Meanwhile, one study found an infection rate in cryoveins of only 4% for aortic grafts.Nevertheless, cryoveins are thought to be antigenic and susceptible to immune attack on the walls, leading to early deterioration and degeneration. Some argue that thawing after cryopreservation causes trauma on the allograft leading to microfissures in the wall, leaving it vulnerable to disruption and aneurysm formation. Ziza et al reported an unofficial aneurysmal degeneration and rupture rate of 16% (N = 10) in infrainguinal bypass. Of these, four were due to infection. The association between infection and aneurysm formation is well documented, and thus infection was the first suspected culprit for this patient’s graft aneurysm, especially in the presence of a prosthetic graft. When the arterial wall is infected, it can lead to aneurysmal degeneration and rupture due to destabilization and inflammation from the pathogen.However, intraoperative cultures were negative and there has been no recurrence for 2 years. During the operation, additional cryovein was available for reconstruction if needed. As exploration revealed no gross signs of infection, we decided to use bovine pericardial patch to close the graftotomy in the axillo-profunda graft. This provided the fastest recovery for the patient who had numerous prior surgeries. He has been continued on suppressive oral antibiotics since prior operations. It is possible that there was a low-grade infection despite negative cultures, but we believe that is unlikely given the intraoperative findings.Aneurysms can form from repeated insults to vessel walls, one such force being turbulent flow that causes increased outward pressure on the wall. As his cryovein jump graft was anastomosed in an end-to-side configuration, associated with high levels of shear stress and strain at the hood of the anastomosis, turbulent flow combined with weakening of the wall of the cryovein could have contributed to wall degeneration.,Three papers have highlighted similar cases of aneurysmal degeneration or anastomotic changes in the absence of infection. Randon et al studied 108 cryovein allografts and found aneurysmal formation in 3, with 1 requiring excision. None had any infection. Hartranft et al reported a single case of anastomotic disruption in a group of 60 patients who underwent bypasses with cryopreserved saphenous vein allografts. O’Banion et al similarly found a single case of aneurysmal change in a cohort of 70 patients, but no cases of infection in the cryovein. Thus, it is feasible that the patient’s cryovein bypass lost vascular integrity through mechanical means rather than infection, highlighting a phenomenon in which occluded bypasses may still undergo mechanical stress after occlusion and amputation. His bypasses are continuing to be closely monitored.
Conclusions
This case report presents a patient with an unusual aneurysm emanating from the hood of a thrombosed cryovein bypass graft. The aneurysm was successfully treated with patch angioplasty and did not appear to be related to infection. Aneurysmal degeneration of a cryopreserved vein allograft can occur even after graft thrombosis.
Authors: Charles A Hartranft; Seth Noland; Aaron Kulwicki; Charles R Holden; Thomas Hartranft Journal: J Vasc Surg Date: 2014-07-03 Impact factor: 4.268
Authors: Vincent Ziza; Ludovic Canaud; Thomas Gandet; Nicolas Molinari; William Alonso; Robin Chastan; Pascal Branchereau; Eric Picard Journal: J Vasc Surg Date: 2015-07-02 Impact factor: 4.268
Authors: Michael P Harlander-Locke; Liv K Harmon; Peter F Lawrence; Gustavo S Oderich; Robert A McCready; Mark D Morasch; Robert J Feezor; Wei Zhou; Jean Bismuth; William C Pevec; Mateus P Correa; Jeffrey Jim; Joseph S Ladowski; Panagiotis Kougias; Paul G Bove; Catherine M Wittgen; John V White Journal: J Vasc Surg Date: 2013-11-14 Impact factor: 4.268