eMedicine Specialties > Radiology > Vascular/Interventional

Deep Venous Thrombosis, Lower Extremity: Follow-up

Author: Eric K Hoffer, MD, Director, Vascular and Interventional Radiology, Associate Professor of Radiology, Section of Angiography and Interventional Radiology, Dartmouth-Hitchcock Medical Center
Coauthor(s): John J Borsa, MD, Consulting Staff, Department of Radiology, St Joseph Medical Center
Contributor Information and Disclosures

Updated: Apr 10, 2009

Intervention

Image-guided therapy

Percutaneous transcatheter treatment of patients with DVT consists of thrombus removal with CDT, mechanical thrombectomy, angioplasty, and/or stenting of venous obstructions. Patients may or may not be given PE prophylaxis by means of filter placement in the IVC. The lack of data from multicenter prospective randomized trial data regarding the safety and efficacy of these therapies complicated the decision to intervene and the choice of intervention. Problems in the existing literature are variability in patient selection and the lack of standard definitions of short- or long-term efficacy and complications. A consensus regarding indications exists, though it is based on mid-level evidence from nonrandomized controlled trials.

Goals of endovascular therapy include reducing the severity and duration of lower-extremity symptoms, preventing PE, diminishing the risk of recurrent venous thrombosis, and preventing PTS. When an invasive procedure is considered, the benefit must be weighed against the added risk compared with standard anticoagulant therapy. If it is to be performed, the intervention must improve the results of current medical therapy. The risk of PE is 2%, the risk of recurrent DVT is 4%, and the risk of major bleeding is 5%. Most difficult to discern, the risk of PTS is 45% at 2 years.

Asymptomatic DVT is not considered an indication for endovascular intervention at this time. The incidence of PTS at 5 years after asymptomatic calf or proximal DVT is low at 5%.57 The absence of symptoms may reflect the lack of the obstructive effect that is proposed to initiate the insufficiency. Although the incidence of PTS may not warrant treatment, some reports suggest that treatment of asymptomatic DVT may be necessary to prevent most cases of PE that are diagnosed at autopsy. Asymptomatic proximal DVT had a mortality risk of 13.7% versus 2% in patients without DVT.

Catheter-directed thrombolysis

Indications

Indications for intervention include the relatively rare phlegmasia or symptomatic IVC thrombosis that responds poorly to anticoagulation alone, or symptomatic iliofemoral or femoropopliteal DVT in patients with a low risk of bleeding. In the last groups, the goal is to reduce the high risk of PTS or to achieve symptomatic relief in conjunction with angioplasty or stent placement.

Phlegmasia cerulea dolens is an indication for emergency CDT in patients with moderate or low bleeding risks. This recommendation is based on reports of limb salvage without the high rates of limb amputation and death when alternative therapies are used.58 In patients with a high risk for hemorrhagic complications, surgical thrombectomy remains an effective option, though it often results in incomplete thrombus removal, recurrent DVT, and an increased incidence of systemic complications.

Acute or subacute IVC thrombosis that causes at least moderate pelvic congestion, limb symptoms, or compromised visceral venous drainage warrants CDT. Involvement of the suprarenal cava, renal veins, and/or hepatic veins may precipitate acute renal or hepatic failure. Thrombus that involves the upper IVC may make it impossible to place an IVC filter for PE prophylaxis.

Subacute and chronic iliofemoral DVT is accompanied by moderate-to-severe pelvic or limb symptoms with a low bleeding risk. Because of recanalization of the iliac vein is unlikely, iliofemoral DVT often produces valvular reflux. This combination of outflow obstruction and reflux is associated with the most symptomatic forms of PTS. In this situation, patients have venous damage, and the alternative is venous bypass. In these instances, CDT is seldom expected to completely clear the vein, but it is often used to remove any acute component of thrombus and to uncover chronic stenoses or underlying anatomic abnormality as an adjunct to angioplasty or stent placement. Compared with systemic thrombolysis, CDT improves the preservation of valve competence (44% vs 13%).

The indication for CDT in the relatively common event of acute iliofemoral or femoropopliteal DVT is somewhat controversial. CDT may be superior to anticoagulation with regard to decreasing the incidence of recurrent DVT and PTS. However, the evidence is not conclusive. CDT improves thrombus clearance compared with systemic thrombolysis. Few DVT resolve after heparin therapy, but systemic thrombolysis improves the rate to 30%, and CDT removes e80% of thrombi.59 Reports of CDT for the management of acute DVT between 1994 and 2004 described anatomic and clinical success rates of 76-100%. The incidence of major hemorrhagic complications was 0-24%.

A prospective registry of 287 patients treated with a mean 53-hour urokinase (uPA) infusion showed anatomic success in 83%. About 34% of patients received adjunctive stent placement for underlying lesions. Complications of major bleeding and rethrombosis were observed in 11% and 25% of patients, respectively, at 30-day follow-up.60,61

A randomized trial in which surgical thrombectomy with anticoagulation was compared with anticoagulation alone demonstrated the early clearance of thrombus to reduce PTS. At 10-year follow-up of the surgical versus anticoagulation cohorts, the rate of lower-extremity swelling was 18% and 71%, respectively, whereas the incidence of ulceration was 8% and 18%, respectively. Any clinical advantage for rapid clearance with CDT (similar to surgical thrombectomy) relies on a demonstration that outcomes reflect a similar reduction in the incidence of PTS, and furthermore, on a determination of whether that reduction justifies the increased incidence of major bleeding (11% vs 3% with anticoagulation).62,63

Three studies demonstrated improved long-term venous function after CDT versus anticoagulation alone. Two showed a decrease in reflux or symptoms from 41-70% to 11-22%. In a retrospective case-control study, quality-of-life scores (including stigmata, health distress, physical function, and symptoms) were improved at 22-month follow-up after CDT with anticoagulation versus anticoagulation alone.64

The transcatheter approach facilitates the diagnosis of predisposing anatomic lesions or anomalies. In patients with iliofemoral DVT, CDT was successful for recanalization in 92-100% of patients, and it revealed an underlying lesion in 50-66%. Treatment of these stenoses with angioplasty and stent placement reestablished unobstructed flow and achieved a prompt clinical response. Studies with 2-year follow-up documented a 5-11% incidence of valvular incompetence.

Technique

Access to the popliteal vein is usually obtained with ultrasonographic guidance, though the common femoral, tibial, or internal jugular veins are also used. When thrombolysis is planned, use of ultrasonography and a micropuncture 21-gauge needle are recommended to minimize bleeding risk. Diagnostic venography is used to identify the extent of DVT, and fluoroscopic guidance is the most accurate and straightforward means of placing infusion catheters or devices. A sheath is placed, and a multiple–side-hole catheter or wire is used to deliver the drug and maximize exposure of the lytic to the surface area of the thrombus.

Plasminogen activators include streptokinase, u-PA, tissue-type plasminogen activator (tPA), tenecteplase (TNK), and recombinant tPA (r-tPA). The US Food and Drug Administration (FDA) has approved only streptokinase for systemic thrombolytic therapy of DVT. However, this agent is not currently recommended because of high rates of allergic reaction and bleeding complications and because of the availability of lower-risk agents. uPA was used extensively in the 1980s and 1990s, but it was temporarily taken off the market, and tPA and r-tPA subsequently became the agents of choice. In a retrospective analysis of CDT for DVT, no significant differences were observed between uPA, tPA, and r-tPA with regard to success rate (>97%) or major complications (3-8%).

Recommended continuous dosages for CDT of unilateral leg DVT are tPA 0.5-1.0 mg/h, r-tPA 0.25-0.75 U/h, or TNK 0.25-0.5 mg/h. Other administration options include an initial lacing dose, which entails an initial bolus given throughout the target thrombus, and a front-loaded dose, which is a high concentration given for the first few hours. No advantage has been demonstrated for either approach.

Most practitioners use concomitant heparinization. Full heparinization was commonly used in conjunction with uPA, whereas the current trend has been to administer subtherapeutic heparin with tPA. LMWH has not been studied in this setting. In the coronary literature, enoxaparin improved outcomes (death and myocardial infarction reduced from 12 to 9.9%), but it significantly increased bleeding complications (from 1.4% to 2.1%).

During thrombolysis, patients remain on bed rest with frequent monitoring of vital signs, and puncture sites. Pericatheter oozing, enlarging hematoma, or evidence of GI-GU bleeding warrant immediate attention. Additional punctures, particularly arterial or intramuscular punctures, should be avoided. A separate IV access facilitates blood sampling to be performed at 6-hour intervals to monitor the patient's hematocrit, platelet count, activated partial thromboplastin time (aPTT, if concomitant heparinization is used), and possibly fibrinogen values. Monitoring fibrinogen levels is controversial, though levels 4.4 µmol/L ( <150 mg/dL) might indicate a clinically significant systemic effect.

Contraindications are the same as those for thrombolysis in general. Absolute contraindications include active internal bleeding or DIC, a cerebrovascular event, trauma, or neurosurgery within 3 months. Relative contraindications include major surgery within 10 days, obstetric delivery, major trauma, organ biopsy, intracranial or spinal cord tumor, uncontrolled hypertension, major GI hemorrhage (within 3 mo), serious allergic reaction to a thrombolytic agent, known right-to-left cardiac or pulmonary shunt or left-heart thrombus, and an infected venous thrombus.

Percutaneous mechanical thrombectomy devices

Percutaneous mechanical thrombectomy devices are a popular adjunct to CDT. Although these devices may not completely remove thrombus, they are effective for debulking and for minimizing the dose and time required for infusing a thrombolytic. In patients at high risk for hemorrhagic complications of thrombolysis, mechanical thrombectomy may obviate infusion. Such devices are most commonly used to initially restore antegrade flow (in cases of limb threat) or to manage a resistant thrombus identified during thrombolysis.

The most basic mechanical method for thrombectomy is thromboaspiration, or the aspiration of thrombus through a sheath. Balloon maceration of the thrombus may be done to facilitate the procedure. The most technically advanced devices, approved primarily for interventions requiring hemodialysis access, may be divided by mechanism into categories of recirculation and fragmentation. Recirculation devices engage thrombus and destroy it by continuously mixing it by creating a hydrodynamic vortex.

Fragmentation devices leave macroscopic particulate effluent and include devices that chop, brush, or cut the clot. With these devices, concomitant lytic infusion and possible IVC filter placement are necessary to ensure PE prophylaxis. With recirculation devices, only the Trellis-8 Peripheral Infusion System (Bacchus Vascular, Inc., Santa Clara, CA) is FDA approved for the treatment of DVT. The AngioJet system (Possis Medical Inc., Minneapolis, MN), has the broadest FDA-approved uses, including uses in the coronary and peripheral arteries and in obtaining arteriovenous access; this is one of the most effective devices.

Reports have described use of the Arrow-Trerotola, AngioJet (Possis Medical), and Helix percutaneous thrombectomy devices for iliofemoral DVT, combined therapy (often with adjunctive thrombolysis, angioplasty and stenting, and placement of an IVC filter with the Arrow-Trerotola). These devices had 74-100% initial technical and 24-hour clinical success rates. Complete thrombus removal was variable (23-100%). The remainder improved with lytic infusion, with a mean infusion time of 6 hours. Only 1 study had a 6% incidence of major bleeding complications. The primary patency rate at 1 year was 85%, and clinical success was obtained in 92%. At 9- to 12-month follow-up, 2 studies demonstrated an 8% rate of venous insufficiency, whereas 2 others showed repeat DVT in 15-23%.

Although the literature lacks conclusive evidence, some data support the argument that DVT treated with anticoagulation results in a high risk of PTS 5-10 years later. Active removal of the thrombus with surgery or catheter-directed lysis clears the thrombus relatively quickly and improves preservation of valvular function while reducing the incidence and severity of PTS. However, systemic or catheter-directed pharmacologic lysis entails a high risk of bleeding complications. Initial data suggest that combination therapy that includes percutaneous mechanical thrombectomy to reduce the dose and duration of lysis may achieve a level of thrombus clearance that reduces the incidence of PTS without elevating the bleeding risk.

IVC filters

In most patients with DVT, prophylaxis against the potentially fatal passage of thrombus from the lower extremity or pelvic vein to the pulmonary circulation is adequately accomplished with anticoagulation. An IVC filter is a mechanical barrier to the flow of emboli larger than 4 mm. Indications for filter placement include DVT with a contraindication to anticoagulation, major bleeding due to anticoagulation therapy, or failed anticoagulation (manifest by progressive DVT or new PE during adequate anticoagulation).

In the past, IVC filters were placed in 4.4% of patients. Recent use was documented in 14% of patients with DVT; this rate was perhaps due to broadened indications with the introduction of removable filters. Temporary or removable filters, all of which may also be left as permanent, permit transient mechanical PE prophylaxis. This option may be useful in the setting of polytrauma, head injury, hemorrhagic stroke, known VTE, or major surgery when PE prophylaxis must be maintained during a short-term contraindication to anticoagulation.

In a randomized trial, the addition of an IVC filter to anticoagulation for DVT increased the risk of recurrent DVT (11.6% to 20.8%), and it did not improve the 2-year survival rate. However, the filter group had significantly fewer PEs (1.1% vs 4.8%). Of note was the risk of major bleeding at 3 months (10.5%). This result agrees with other reports and highlights the usual trade-off of prophylaxis with a filter versus anticoagulation and the respective complication risks of new DVT (peripheral to the filter) versus major hemorrhage. In the elderly patient with an increased risk of bleeding, and particularly if the patient is at risk for trauma, the risk and benefits may favor use of a filter.

CDT does not add to the risk of PE to warrant routine filter placement. However, for patients with contraindications to pharmacologic lysis in whom a PMT device is to be used, a filter may be a useful adjunct.60,61

Valve replacement

Percutaneously placed bioprosthetic venous valves are under development and may provide a minimally invasive therapy to the long-term complication of PTS due to valve destruction. If successful, this approach may provide a percutaneous therapeutic alternative for patients with primarily palliative options to manage their venous reflux symptoms. An effective therapy should diminish one of the primary indications for aggressive thrombolytic therapy for acute DVT.

Medicolegal Pitfalls

  • False-negative misdiagnosis with embolic sequelae (eg, PE) can result in litigation. For this reason, the threshold for workup and attention to any abnormality on an otherwise normal image should be low.
  • Use of thrombolytic medications to lyse DVT can cause intracranial bleeding, though this is infrequent, and death or impairment can result.
    • Careful assessment of the bleeding risk is needed before this therapy is attempted. Indications for lysis should be balanced against the possibility of bleeding before pharmacologic thrombolysis is attempted.
    • The need should be compelling when thrombolysis is considered in a setting of known contraindications. Factors such as recent surgery, stroke, GI or other bleeding, and underlying coagulopathy increase the bleeding risk when the thrombolytic medication is administered. The process of obtaining informed consent should include a discussion of these risks.
  • Mechanical thrombectomy or potentially any manipulation of catheters within thrombus can cause clot migration and/or PE.
    • If a nonrecirculating device is used, the threshold for temporary filter placement is low.
    • The operator should be capable of treating massive PE if mechanical DVT thrombectomy is being performed.

Special Concerns

  • The incidence of DVT is increased in women who are pregnant compared with the general population
  • Diagnostic confirmation is usually performed by using ultrasonography or MRI.
  • Limited radiographs with appropriate shielding can be obtained after the first trimester.
  • If major DVT occurs, usual treatment is anticoagulation therapy. Treatment more aggressive than this is usually considered only after the baby is delivered.
 


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References
Further Reading

References

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Keywords

deep vein thrombosis, venous thrombosis, thrombophlebitis, May-Thurner syndrome, Cockett syndrome, iliofemoral thrombosis, DVT, lower extremity thrombosis, lower-extremity thrombosis, leg thrombosis, lower extremity deep venous thrombosis, occlusions of the deep veins, below-knee thrombosis, venous thromboembolism, VTE, pulmonary embolus, pulmonary embolism, PE, post-thrombotic syndrome, postthrombotic syndrome, PTE

Contributor Information and Disclosures

Author

Eric K Hoffer, MD, Director, Vascular and Interventional Radiology, Associate Professor of Radiology, Section of Angiography and Interventional Radiology, Dartmouth-Hitchcock Medical Center
Eric K Hoffer, MD is a member of the following medical societies: American Heart Association, Radiological Society of North America, Society for Cardiac Angiography and Interventions, and Society of Interventional Radiology
Disclosure: Nothing to disclose.

Coauthor(s)

John J Borsa, MD, Consulting Staff, Department of Radiology, St Joseph Medical Center
John J Borsa, MD is a member of the following medical societies: American College of Radiology, American Society of Neuroradiology, Cardiovascular and Interventional Radiological Society of Europe, Radiological Society of North America, Royal College of Physicians and Surgeons of Canada, and Society of Interventional Radiology
Disclosure: Nothing to disclose.

Medical Editor

Anthony Watkinson, MD, Professor of Interventional Radiology, The Peninsula Medical School; Consultant and Senior Lecturer, Department of Radiology, The Royal Devon and Exeter Hospital, UK
Anthony Watkinson, MD is a member of the following medical societies: Radiological Society of North America, Royal College of Radiologists, and Royal College of Surgeons of England
Disclosure: Nothing to disclose.

Pharmacy Editor

Bernard D Coombs, MB, ChB, PhD, Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand
Disclosure: Nothing to disclose.

Managing Editor

Douglas M Coldwell, MD, PhD,, Interventional Radiologist, Jane Phillips Medical Center, Bartlesville, Oklahoma
Douglas M Coldwell, MD, PhD, is a member of the following medical societies: American Association for Cancer Research, American College of Radiology, American Heart Association, American Physical Society, American Roentgen Ray Society, Society of Cardiovascular and Interventional Radiology, Southwest Oncology Group, and Special Operations Medical Association
Disclosure: Sirtex, Inc. Consulting fee Speaking and teaching

CME Editor

Robert M Krasny, MD, Resolution Imaging Medical Corporation
Robert M Krasny, MD is a member of the following medical societies: American Roentgen Ray Society and Radiological Society of North America
Disclosure: Nothing to disclose.

Chief Editor

Kyung J Cho, MD, FACR, William Martel Professor of Radiology, Interventional Radiology Fellowship Director, University of Michigan Health System
Kyung J Cho, MD, FACR is a member of the following medical societies: American College of Radiology, American Heart Association, American Medical Association, American Roentgen Ray Society, Association of University Radiologists, and Radiological Society of North America
Disclosure: Nothing to disclose.

 
 
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