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Ann Thorac Surg 1999;67:1111-1116
© 1999 The Society of Thoracic Surgeons
a Department of Surgery, LDS Hospital, Salt Lake City, Utah, USA
Accepted for publication December 17, 1998.
Address reprint requests to Dr Donald Doty, 324 Tenth Ave, Salt Lake City, UT 84103
e-mail: ldddoty{at}ihc.com
| Abstract |
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Methods. Sixteen patients aged 17 to 68 years had operation for obstruction of the SVC with SVC syndrome caused by benign disease. Eleven patients had fibrosing mediastinitis with or without caseous necrosis, 4 had thrombosis caused by a catheter or a pacemaker electrode, and 1 had spontaneous thrombosis. All operations were performed using a composite spiral vein graft constructed from the patients own saphenous vein. Graft diameter ranged from 9.5 to 15.0 mm. Ten grafts were from the left innominate vein, and six grafts were from the right or left internal jugular vein. The grafts were placed to the right atrial appendage in all patients except 1. Follow-up extends from 1 month to 23 years 8 months (mean follow-up, 10.9 years).
Results. Fourteen of 16 grafts remain patent for up to 23 years, and all patients but 1 are free from SVC syndrome. One patient required revision of the graft for thrombosis 4 days after operation. Two grafts closed during the first year after operation: one because of recurrence of spontaneous venous thrombosis and the other because of aggressive fibrosing mediastinitis requiring operation for graft revision three times over a 12-year period prior to death.
Conclusions. These data demonstrate that a spiral vein bypass graft for treatment of the obstructed SVC relieves SVC syndrome and has excellent long-term patency.
| Introduction |
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Operative reconstruction of the SVC using a spiral vein bypass graft was first suggested by Chiu and associates [1] in 1974. Two years later, Doty and Baker [2] reported the use of a spiral vein bypass graft in a patient with granulomatous mediastinitis. Subsequently this operation has been used successfully for the treatment of SVC obstruction caused by benign disease and occasionally, obstruction resulting from malignant disease. Patients with type III SVC obstruction (nearly complete to complete obstruction of the SVC with reversal of azygos blood flow) benefit the most from the spiral vein bypass graft operation, particularly when there is cerebral or airway compromise [3].
Although malignancy is the cause of SVC obstruction in the majority of patients, benign etiologies are becoming increasingly more frequent in the immunosuppressed population. Mycobacterial, fungal, and opportunistic infections in these patients can be aggressive and invade the mediastinal structures [4]. Iatrogenic SVC obstruction is more commonly encountered with the increasing number of patients with transvenous pacemaker electrodes and central venous catheters for invasive monitoring, alimentation, and chemotherapy [5].
The purpose of this study is to report the long-term outcome after surgical intervention for SVC obstruction secondary to benign disease. This series of patients underwent SVC bypass with a spiral saphenous vein graft to relieve SVC obstruction with excellent late results in terms of conduit patency and relief of symptoms.
| Material and methods |
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Operative technique
The operation is performed through a median sternotomy or, more recently, through a minimal incision using a partial upper-half sternotomy (Fig 1). A simultaneous incision is made in the thigh over the course of the saphenous vein. The left innominate vein is mobilized to the junction of the left internal jugular vein and the left subclavian vein. When the innominate vein and the subclavian-jugular confluence are thrombosed, it is necessary to mobilize either the left or the right internal jugular vein as the outflow point from the upper venous compartment. In this situation, the midline incision can be extended to the left or the right and the strap muscles divided to provide unrestricted passageway for the bypass conduit. The largest jugular vein can also be exposed and mobilized through a secondary cervical incision. The two incisions are joined by a tunnel beneath the sternocleidomastoid muscle. Biopsy samples of abnormal tissues surrounding the SVC are obtained. Operative procedural data are summarized in Table 2.
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For example, if the innominate vein is 12 mm in diameter, the saphenous vein is 4 mm in diameter, and the distance to the right atrial appendage is 10 cm, then 30 cm of saphenous vein is required. Grafts employed in this series ranged from 9.5 to 15.0 mm in diameter. The required length of saphenous vein is removed, and the side branches are ligated. The vein is incised longitudinally through its entire length (Fig 2). A thoracostomy tube with the same diameter as the innominate or jugular vein is selected as a stent. The opened vein graft is flattened and wrapped around the stent in spiral fashion (Fig 3A), with the endothelial surface of the vein against the stent. Continuous stitches of 7-0 polypropylene suture are used to join the edges of the graft (Fig 3B), thereby forming a large conduit with the same internal diameter as the stent. There is no advantage to the use of a larger or smaller conduit. In theory, a smaller conduit could have some hemodynamic advantage by increasing flow velocity in the graft. Because the diameter of the graft is always smaller than that of the SVC, flow through the graft is always torrential because of the slightly increased venous pressure; consequently there is no need to reduce graft diameter to less than that of the inflow vein to prevent stasis in the graft.
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| Results |
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Three patients had graft closure within the first year after operation. One patient (patient no. 6) had thrombosis of the proximal innominate veingraft anastomosis 4 days after operation with recurrence of the face and neck swelling and other signs of SVC obstruction. Revision of the graft was performed, and the patient remains asymptomatic nearly 13 years later. Another patient (patient no. 7) had recurrence of symptoms 5 months after operation for spontaneous thrombosis of the SVC. She had not been given anticoagulants, and in retrospect, probably should have been treated with warfarin sodium after operation. Symptoms of SVC syndrome recurred, and graft closure was documented by computed tomographic scan. No further operative treatment was given.
The third patient (patient no. 4) experienced graft closure 1 year after the initial operation. This patient had aggressive fibrosing mediastinitis and retroperitonitis, which subsequently obliterated both internal jugular veins, the original bypass graft, three subsequent bypass grafts, and the inferior vena cava. Superior vena cava syndrome recurred promptly each time a bypass graft occluded. At a second operation in another institution, bilateral straight saphenous vein grafts were placed from the right and left external jugular veins to the right atrium. These grafts provided partial relief of symptoms for 8 years; then they also occluded. At this point, a 10-mm polytetrafluoroethylene graft was placed from the left internal jugular vein to the right atrial appendage. This graft occluded 3 years later, and a composite graft was constructed from the common iliac vein and inferior vena cava homograft tissue. This composite graft was placed from the left internal jugular vein near the angle of the mandible to the right atrium. The graft was enclosed in a 12-mm polytetrafluoroethylene graft. Four years after this operation, SVC syndrome recurred, and the patient died shortly thereafter.
Anticoagulation with warfarin was not used after operation in any patient. All of the patients received aspirin. Fifteen (94%) of the 16 patients have had resolution of symptoms of SVC obstruction. The patient with recurrence of symptoms had graft occlusion 5 months after operation described already. Another patient had complete resolution of symptoms for more than 11 years until the graft was divided during a coronary artery bypass operation at another institution. The graft was destroyed and replaced with a straight saphenous vein graft. This patient initially had some symptoms of venous obstruction but is now asymptomatic.
| Comment |
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Bypass of the SVC using autologous femoral vein was first reported by Klassen and associates [6] in 1951. The patients own femoral vein is generally of good caliber and length and can be removed easily. The diameter, however, cannot be adjusted to the dimensions of the inflow vein, and the length of femoral vein may not be sufficient for bypass grafts outside the thorax. The femoral vein is usually smaller than the internal jugular vein and, of course, substantially smaller than the SVC. There is also some concern that venous drainage from the leg after removal of the femoral vein can be impaired. Gladstone and coworkers [7] performed SVC bypass with autologous femoral vein in 5 patients with good relief symptoms; 2 patients experienced transient leg edema. Marshall and Kouchoukos [8] reported a case of recurrent SVC obstruction treated with an externally supported autologous femoral vein; the graft was patent on venography nearly 1 year after operation.
The construction of a composite vein graft from the patients own saphenous vein was first suggested by Benvenuto and colleagues [9], who created a "paneled" conduit from small sections of incised saphenous vein. This type of graft consists of parallel suture lines that run the length of the composite graft in contrast to a spiral vein bypass graft, which is also a composite vein graft but consists of a single suture line for the length of the conduit. At any point along the length of the graft, the foreign body of the suture contacts the bloodstream at only one point on the circumference of the graft. Our series of patients documents the excellent long-term patency of such grafts, with 87.5% (14/16) of spiral vein grafts patent at a mean of 10.9 years. The initial patient had potency of the spiral vein graft documented by venography nearly 24 years after operation. Gloviczki and associates [10] reported similar excellent results with spiral vein grafts in nonmalignant SVC obstruction; bifurcated spiral vein grafts, however, were subject to early occlusion of one graft limb. Concerns about thrombosis secondary to the long suture line in a spiral vein graft appear to be unfounded, as none of the patients in our series received anticoagulation.
Spiral vein bypass grafting is preferable to grafting with reversed saphenous vein, although there are reports of successful treatment of both benign and malignant SVC obstruction with single and double reversed saphenous vein grafts [11, 12]. The single patient in this series requiring double reversed saphenous vein grafting maintained patency in both grafts for 8 years, but relief of SVC syndrome was only partial during this period. Long-term patency after SVC bypass with polytetrafluoroethylene grafts has been disappointing. Gloviczki and coauthors [10] compared spiral vein bypass grafting with polytetrafluoroethylene grafting in benign SVC obstruction; the spiral vein grafts had superior patency. Nonsurgical interventions such as percutaneous transluminal angioplasty and stenting are currently inadequate to treat SVC obstruction compared with surgical treatment [13].
Although the current series of patients all had SVC obstruction resulting from benign disease, there may be a role for surgical intervention in malignancy. One of us (D.B.D.) [14] found that spiral vein bypass grafting provided excellent results for relief of SVC syndrome in 6 patients with malignant disease. No patient had recurrence of SVC obstruction, and 4 patients survived 1 year or more after operation. Smith and Brantigan [15] also reported the successful use of a spiral vein graft in a patient with adenocarcinoma of the lung; excellent palliation was achieved for the final 6 weeks of the patients life. Anderson and Li [16] used a spiral vein graft to reconstruct the SVC after segmental resection of a compressive sarcoma. This patient was free from symptoms of SVC obstruction 17 months after operation.
The spiral vein bypass graft has also been used for relief of SVC obstruction in the pediatric population, as reported by Brandt and associates [17]. In this case, the spiral vein graft was anastomosed to the left atrial appendage without cardiopulmonary bypass in a young child with SVC syndrome after intraatrial baffle construction. Fowl and colleagues [18] discussed successful use of spiral vein grafts in heavily contaminated locations. This indication may become more common with the increase in infectious diseases in the immunosuppressed population.
In summary, spiral vein bypass grafting for SVC obstruction, resulting from benign disease demonstrates excellent long-term results. Patients with nearly complete or complete obstruction will benefit from this operation, and about 90% of patients can be expected to have total resolution of symptoms relating to SVC syndrome. Most patients can be followed easily by the absence of clinical symptoms. Spiral vein bypass grafting could have an expanded role in the future treatment of SVC obstruction caused by malignant disease, in the pediatric patient, and in the immunosuppressed patient population.
| Footnotes |
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| References |
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