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Prosthetic Replacement of the Superior Vena Cava


 


   

1.

Which patients will be candidate for prosthetic replacement of the superior vena cava (SVC)?

SVC resection and revascularization is most commonly indicated for completely resecting mediastinal and, less frequently, bronchogenic tumors. While for mediastinal tumors of whatever histology, SVC resection and revascularization can be curative, th e indications for non-small cell bronchogenic tumors are rare since they depend on whether or not the SVC is invaded by the tumor itself or by superior mediastinal lymph nodes. In this last circumstance, prognosis is poor and surgery not justified.

SVC syndromes related to unresectable bronchogenic tumors should not be considered for SVC revascularization and internal jugular to right atrium or extra-anatomical by-pass(es) are not earned. Indications for palliative SVC procedures are exc eptional and might be evoked for slow-growing diseases, e.g. mediastinal primary or secondary fibrosis or SVC thrombosis of unknown etiology. Postoperative graft thrombosis is at risk and can have serious consequences in terms of pulmonary embolism. In this sense, the status of the cephalic venous collateral pathway plays a major role. Since the proximal anastomosis needs to be performed either at the origin of the SVC or at the level of one or both brachiocephalic veins, SVC revascularization can be made only if there is an excellent patency at the level of the cephalic venous bed. Moreover, the proximal veins should have normal walls.

Obstructed SVC usually present a rich collateral venous circulation which can be competitive and re duce the flow through the graft. Indications in this situation should be individually evaluated to avoid graft thrombosis.

Primary angiosarcomas or leiomyosarcomas of the SVC are rare, usually asymptomatic and along with congenital aneurysms are other indications.

Further indications include iatrogenic, blunt or penetrating injuries. Iatrogenic SVC thrombosis that may require prosthetic replacement may be caused by prolonged Swan-Ganz, endocardial pacing and central venous catheters . Thoracic blunt trauma or disinsertion of the brachiocephalic veins during sternotomy are other rare causes, as well as Behçet disease.

 

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2.

What types of materials are available for replacing the SVC?

The currently available materials for SVC reconstruction include spiral saphenous vein, free pericardial and polytetrafluoroethylene (PTFE) grafts. The major drawbacks of the first two are the requirement of an intraoperative time-consuming modeling and their potential compression induced by postoperative and radiation-induced fibrosis. Among the different vascular prostheses, PTFE graft is the only material remaining patent as a venous substitute because a neointima will growth on its internal wall. Its easy surgical manipulation over other autologous materials makes it the material of choice of SVC reconstruction.
 

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3.

Which are the preoperative investigations that each patient with suspected SVC invasion should have?

A preoperative work-up evaluating the extension of the primary disease should be performed routinely. All patients should have a superior vena cavography (simultaneous injection through both upper limbs) before operation to delineate the site and ex tension of the venous obstruction, presence of possible proximal thrombosis and to anticipate where the proximal graft anastomosis can be made. Echocardiography eliminates thrombosis extension into the right atrium and appreciates the patency of the jugular and axillary veins. Since a majority of patients with bronchogenic cancer may present with a clinically and radiologically silent SVC invasion, computer tomography (CT) of the thorax and pulmonary angiography are diagnostic; typically, t hese tumors arise from the ventral segment of the right upper lobe and invade the right mediastinal artery (angiography) and the posterior aspect of the SVC (contrast CT). Brain CT scan should always be performed to eliminate brain diseases which ma y increase brain edema during SVC clamping.
 

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4.

Which is the intraoperative monitoring?

Apart from the routine anesthetic procedures required for every major pulmonary resection procedure, pertinent to the SVC procedure are:
  
i. double-lumen tube to obtain one-lung ventilation;
ii. continuous arterial and venous pressure measurements to monitor the drop of the systemic pressure caused by the reduced venous return to the right heart during venous clamping;
iii. a cephalic vein catheter placed in the forearm or more proximally in the antecubital fossa or into the right internal jugular vein to monitor the venous pressure in the cephalic territory;
iv. foley catheter to monitor urine output;
v. electrocardiographic monitoring limb or chest limbs to monitor cardiac electrophysiological alterations during venous clamping, si nce the distal clamp may be too close to the sinus node. At least two venous lines should be placed in the lower limbs to achieve volume expansion during venous clamping.

Transient cyanotic faces during SVC clamping are reversible after venous declamping. Facies petechiae may develop but are usually transient and disappear after 1 to 2 weeks after the operation.

 

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5.

What kind of surgical approach should be used?

The usual approach include a right thoracotomy in the fifth intercostal space for bronchogenic tumors and a median sternotomy for tumors originating from the anterior compartment of the mediastinum, respectively. Median sternotomy allows a large expo sure of the entire anterior mediastinum, right atrium, both brachiocephalic veins and the SVC on their entire lengths and can be easily extended to the neck. The right thoracotomy has the best exposure of the right hilum, SVC and right atrium but ren ders dissection, control and revascularization of the left brachiocephalic vein demanding.
 

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6.

How prevent the hemodynamical effects of SVC clampage?

The effects of SVC clampage are different according to the degree of obstruction of the SVC. For patients whose SVC is completely obstructed or tightly stenosed, intraoperative venous clamping results in a negligible hemodynamical compromise since a functioning collateral venous network already exists and supplements the flow obstruction to the SVC. By contrast, when the intrathoracic or mediastinal disease does not obstruct the SVC, an even sharp venous clamping might induce an hemodynamicall y cascade of events including decreased cardiac inflow and outflow, increased venous pressure of the cephalic territory and alterations of the cerebral arterial-venous gradient leading to brain damage and intracranial bleeding.

For patients wi th SVC obstruction or tight SVC stenosis, venous clamping does not significantly modify cardiac output and cerebral circulation. Consequently, the duration of venous clamping is not a limiting factor and the operation can be carried out safely and routinely without taking into account the reconstructive SVC step. By contrast, for patients with nonobstructed SVC, venous clamping is associated with an hemodynamic compromise resulting in decreased cardiac output and increased venous pressure in the cephalic territory which may induce brain damage.

Several tools may mitigate this hemodynamic compromise in unobstructed SVC. i) Shunt procedures: intraluminal shunting of the blood from the brachiocephalic vein into the right atrium may re duce the hemodynamic consequences of venous clamping. However, whatever the type of shunt utilized, their major drawbacks are their potential thrombosis and that they fill the operative field making the performance of the distal anastomosis difficul t. ii) Pharmacological agents and fluid implementation: they should increase the venous blood return to the right atrium and maintain the physiological arterial-venous gradient in the cerebral territory. The first target is achieved by an adequate co mpensation of all blood losses by blood components and macromolecules. Since the cranial venous pressure may rise up to 40 mm Hg during venous clamping, maintenance of the cerebral arterial-venous gradient requires fluid administration (average 15- 20 mL/Kg) to normalize the cardiac output and eventually vasoconstrictive agents to increase the mean arterial pressure. iii) Shortening the venous clamping time. To reduce the venous clamping time (which can be prolonged up to 45 min), an accurat e surgical strategy should be defined. For right bronchogenic tumors with carinal or proximal pulmonary artery invasion, it is often easier to perform the vascular step first and then the airway procedure. During the latter, all attention should be d irected to avoid prosthesis bacterial contamination. For mediastinal tumors involving both upper lobes, operation should be made from the left to the right side. This permits a safe and immediate revascularization between the left brachiocephalic vei n and the right atrium; the right part of the excision is performed thereafter.

 

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7.

Which types of SVC reconstruction can be done?

Which types of SVC reconstruction can be done? When the circumference of the involved caval wall is less than 30%, a partial resection of the vein is possible. Its reconstruction can be made either directly with a running suture or indirectly with the interposition of a prosthetic or autologous pericardial or venous patch; closure up to 50% of the caval circumference can be made without hemodynamical imbalance. With larger involvements, prosthetic replacement of the SVC is necessary

Truncular replacement
It requires a tumor-free confluence of both brachiocephalic veins. This procedure, commonly associated to a right pneumonectomy, employs a straight not ringed PTFE graft (#18 or 20). After proximal (brachiocephalic veins confluence) and distal (cavoatrial junction) clampage, the invaded segment of the vein is completely excised. The proximal anastomosis between the SVC stump and the prosthesis is then performed first using a continuous 5-0 polypro pylene (Prolene, Ethicon, Inc., Somerville, NJ) suture started at the posterior aspect of the prosthesis in an in- to out-side fashion. After its completion, the distal anastomosis is then performed in the same way. Before tightening the stretches of the distal suture, the proximal clamp is released, the prosthesis is flashed with saline heparinized solution and deairation made. The distal clamp is then released and the knots tied. To avoid prosthesis kinking, the length of the graft should be adapted so that the distal anastomosis rests under tension.

Revascularization from the left brachiocephalic vein
This procedure, always performed through a median sternotomy, requires a ringed PTFE graft (#12 or 1 3). The ringed graft is imperative since after closure of the median sternotomy, the prosthesis may be too long, inducing thus its kinking. Minimal dissection of the left brachiocephalic vein is also mandatory to avoid its rotation above the proximal anastomosis. The distal anastomosis can be performed either on the right atrium or appendage or the inferior stump of the SVC.

Revascularization from the right brachiocephalic vein
Ringed grafts are preferr ed (# 12 or 14) to maintain their patency and to avoid their compression by the post-operative fibrosclerosis. The risks of kinking are minimal since the direction of the graft is almost vertical. The proximal anastomosis is not always easy to perform since the right brachiocephalic vein after its resection is often short; it has to be performed firstly. The distal anastomosis should be made on the SVC stump; this architecture results in the straightest and shortest graft. It is the revascularization of choice after resection of mediastinal tumors involving the origin of the SVC.

Revascularization of both brachiocephalic veins
Indications for revascularization of both brachiocephalic veins are extremely rare and confined only to those patients whose right or left-sided internal jugular vein is absent because of previous neck surgery (e.g. thyroid cancer surgery). In these rare situations, revascularization of a single brachiocephalic vein may result in an insufficient brain venous drainage. On the contrast, by revascularizing both brachiocephalic veins, the established venous circulation and hemodynamics is conserved. An Y-type graft should be avoided since it may result in thrombosis of the accessory limb of the Y-graft because the graft-to-graft anastomosis is thrombogenic (raw anastomotic surfaces); thus a separate distal implantation is preferable. The right graft should be anastomosed distally on the SVC stump (when possible) and the left one on the right atrium.

Apart from this indication, revascularization of both brachiocephalic veins decreases the blood flow through each graft and requires a more demanding technical procedure. For these reasons, SVC revascularization of the viable brachiocephalic vein with ligation of the contralateral brachiocephalic vein is preferred in almost all cases.

 

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8.

Are palliative SVC by-pass(es) justified?

Thrombosis of the SVC district is usually well tolerated and sensible to medical treatment, which succeeds in limiting thrombosis extension and the development of rich collateral venous network as in inferior vena cava thrombosis. The less tolerated SVC syndromes are those associating a SVC thrombosis to an extensive thrombosis into both brachiocephalic veins and even subclavian and jugular veins. In patients harboring such SVC syndromes, SVC revascularization carries out several technical problems, like the absence of excellent proximal venous bed and presence of a well-developed collateral venous circulation. Despite revascularization of the SVC might be performed using either jugular or axillary veins, this usually results in a low venous blood flow through the graft and long prosthesis (passing subcutaneously with major kinkings and thrombosis risks); even surgical created artero-venous fistulae aiming to increase the flow through the graft are unsuccessful. We therefore do not recommend palliative SVC revascularizations, the only exception being the full patency and normal wall of one brachiocephalic vein.
 

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9.

How anticoagulate the patient?