| Home | E-Submission | Sitemap | Contact Us |  
Korean J Med > Volume 90(6); 2016 > Article
새로운 경구용 항응고제 사용 중 발생한 하대정맥 필터의 혈전성 폐쇄


A 68-year-old woman presented with chest pain and dyspnea and was diagnosed with a massive pulmonary embolism. Bleeding colon cancer was detected incidentally during anticoagulation therapy. After stabilization, she underwent surgical resection of the cancer with insertion of an inferior vena cava filter and was treated with rivaroxaban as antithrombotic therapy thereafter. Unexpectedly, thrombotic obstruction of the filter was revealed on a computed tomography scan taken in preparation for removing the device. After switching to warfarin, the obstruction had resolved at the 4-week follow-up examination. We discuss what to consider when performing antithrombotic therapy in patients with an inferior vena cava filter.


An inferior vena cava (IVC) filter can be adopted as a preventive measure for pulmonary thromboembolism in patients at high risk for venous thromboembolism and bleeding. Anticoagulation therapy usually must be maintained after introducing these filters [1]. A novel oral anticoagulant can be used depending on the patient’s condition; however, an IVC filter can become occluded by thrombosis even under anticoagulation therapy. The exact causes of or risk factors for this complication are not fully understood. In this case report, we describe the case of a 68-year-old female patient who had an acute pulmonary embolism and bleeding colon cancer. An IVC filter was implanted but totally obstructed the vessel during anticoagulation therapy after cancer resection. The possible mechanism and clinical implications of this event are discussed.


A 68-year-old woman presented to our outpatient cardiology department complaining of episodes of chest pain and dyspnea over the past 10 days. She had experienced severe exercise-induced chest pain and dyspnea while under mental stress traveling across Korea. She had a history of hypercholesterolemia but was not taking a lipid-lowering medication. Although her vital signs were stable, she showed deep T wave inversion on the electrocardiography inferolateral leads and severe right ventricular hypokinesia on echocardiography. She underwent coronary angiography after hospitalization, but no significant coronary artery stenosis was noted. A subsequent computed tomography (CT) scan revealed an extensive bilateral pulmonary embolism and deep vein thrombosis in the right calf vein, and she was started on intravenous heparin (Fig. 1). Laboratory results reported later did not show any hematological or immunological disease predisposing her to thrombosis.
She began to complain of anal bleeding on hospital day 3. A colonoscopy revealed a 5 cm ulcero-fungating, bleeding mass in the sigmoid colon that was ultimately diagnosed as adenocarcinoma (Fig. 2). Accordingly, heparin treatment was stopped. After a staging work-up and discussion with the surgical team, operative resection of the cancer was planned. To reduce the risk of thromboembolism during the period without anticoagulation, an IVC filter (Celect, Cook Medical Inc., Bloomington, IN, USA) was introduced into the infrarenal IVC on hospital day 8. She underwent laparoscopic resection of the sigmoid colon on hospital day 12, and 40 mg subcutaneous enoxaparin b.i.d. was started after achieving hemostasis. She was discharged after a gradual recovery and has maintained self-administration of subcutaneous heparin.
Her condition was good at the 2-week follow-up after discharge, and enoxaparin was switched to 20 mg rivaroxaban daily. A venous CT scan taken 10 days later and prior to removing the IVC filter showed a large thrombus within the filter occluding the IVC (Fig. 3A). This filter thrombus was likely an in situ thrombosis because it was clearly larger than the residual thrombus in the right calf vein. However, it was round, and the possibility of migration of the deep vein thrombus could not be completely ruled out. She did not appear to be in any discomfort or show signs of the occlusion. We changed the rivaroxaban to warfarin and adjusted the dose to 3 mg daily. A follow-up venous CT scan 4 weeks later showed resolution of the thrombus, and the filter was removed uneventfully (Fig. 3B).


IVC filters are usually inserted when anticoagulation therapy is contraindicated or as an adjunct to anticoagulation. Thrombotic occlusion of these filters is reported in 2-30% of cases [2]. Anticoagulation after inserting an IVC filter is reportedly associated with a lower incidence of thrombosis but no quality studies have been published on filter thrombosis [3]. Cancer is a well-known risk factor for thrombosis [4]. In addition, filter design and the resulting flow dynamics contribute to thombotic occlusion [5]. Because the thrombosis in the present case developed during rivaroxaban therapy and resolved after administration of warfarin, drug-related factors such as poor compliance or a lower response to rivaroxaban may have contributed to the thrombosis in this specific patient. However, we could not accurately determine which factors contributed to the thrombotic occlusion in this case.
Although many patients at risk for bleeding are ineligible for systemic anticoagulation therapy, our patient stably recovered after the cancer was resected and underwent anticoagulation therapy. Low molecular weight heparin (LMWH) is recommended in the current guidelines for patients with cancer undergoing abdominal surgery or secondary prophylaxis for a venous thromboembolism [6]. Moreover, a meta-analysis showed that LMWH has better efficacy than vitamin K antagonists during long-term treatment of patients with cancer and an established venous thromboembolism.
Rivaroxaban is an oral factor Xa inhibitor with similar efficacy to that of vitamin K antagonists during long-term treatment of pulmonary embolism with an improved benefit-risk profile [7]. It has similar efficacy to that of conventional anticoagulation therapy but a lower rate of major bleeding in patients with venous thromboembolism [8]. In addition, it does not require injections or regular dose adjustments. Nevertheless, it is not equally recommended in the treatment guidelines, as there is a lack of sufficient data on the efficacy of this anticoagulant in patients with cancer and thromboembolism. Although rivaroxaban is usually prescribed at a dose of 15 mg b.i.d. in patients with an acute stage pulmonary embolism, we prescribed 20 mg daily in the present case. We used heparin in the early stages and switched to the novel anticoagulant 30 days after starting anticoagulation therapy, which was 40 days after the development of symptoms associated with the pulmonary embolism. At that time, we decided to use 20 mg daily as the maintenance dose after the acute stage. The best treatment for an IVC filter thrombosis has not been determined but possible options include thrombolytic therapy, dose escalation, or switching to another anticoagulant, adding an antiplatelet agent [9], or mechanical thrombectomy [10]. In our case, we switched to warfarin, which was effective.
We presented a case of thrombotic occlusion of an IVC filter during maintenance with rivaroxaban. Multiple factors can contribute to an occluded filter, and it was difficult to determine the major cause in our case. More studies are needed to further clarify if anticoagulants have different effects. Until then, drugs must be chosen cautiously when treating patients at high risk for thromboembolism.


1. Becker DM, Philbrick JT, Selby J. Inferior vena cava filters: Indications, safety, effectiveness. Arch Intern Med 1992; 152:1985–1994.
crossref pmid

2. Caplin DM, Nikolic B, Kalva SP, et al. Quality improvement guidelines for the performance of inferior vena cava filter placement for the prevention of pulmonary embolism. J Vasc Interv Radiol 2011; 22:1499–1506.
crossref pmid

3. Lee AY, Levine MN. Venous thromboembolism and cancer: risks and outcomes. Circulation 2003; 107(23 Suppl 1):I17–I21.

4. Corriere MA, Sauve KJ, Ayerdi J, et al. Vena cava filters and inferior vena cava thrombosis. J Vasc Surg 2007; 45:789–794.
crossref pmid

5. Tardy B, Mismetti P, Page Y, et al. Symptomatic inferior vena cava filter thrombosis: clinical study of 30 consecutive cases. Eur Respir J 1996; 9:2012–2016.
crossref pmid

6. Farge D, Debourdeau P, Beckers M, et al. International clinical practice guidelines for the treatment and prophylaxis of venous thromboembolism in patients with cancer. J Thromb Haemost 2013; 11:56–70.
crossref pmid

7. EINSTEIN–PE Investigators, Büller HR, Prins MH, et al. Oral Rivaroxaban for the treatment of symptomatic pulmonary embolism. N Engl J Med 2012; 366:1287–1297.

8. Prins MH, Lensing AW, Bauersachs R, et al. Oral rivaroxaban versus standard therapy for the treatment of symptomatic venous thromboembolism: a pooled analysis of the EINSTEIN-DVT and PE randomized studies. Thromb J 2013; 11:21.
crossref pmid pmc

9. Tardy B, Mismetti P, Page Y, et al. Symptomatic inferior vena cava filter thrombosis: clinical study of 30 consecutive cases. Eur Respir J 1996; 9:2012–2016.
crossref pmid

10. Myers JL, Mukherjee D, Karnaze MG, Joseph AE. Treatment of inferior vena cava filter thrombosis by mechanical thrombectomy and temporary vena cava filter protection: a case report. Vas Endovascular Surg 2000; 34:175–181.

Chest computed tomography scan reveals an extensive bilateral pulmonary embolism (arrow).
Figure 1.
Colonoscopy reveals a 5 cm ulcero-fungating, bleeding mass in the sigmoid colon.
Figure 2.
Venous computed tomography scan shows large thrombi (arrow) within the filter occluding the inferior vena cava (A). Follow-up imaging after warfarin therapy reveals complete resolution of the thrombi (arrow) (B).
Figure 3.
PDF Links  PDF Links
PubReader  PubReader
ePub Link  ePub Link
Full text via DOI  Full text via DOI
Download Citation  Download Citation
CrossRef TDM  CrossRef TDM
Supplementary Material  Supplementary Material
Editorial Office
101-2501, Lotte Castle President, 109 Mapo-daero, Mapo-gu, Seoul 04146, Korea
Tel: +82-2-2271-6791   Fax: +82-2-790-0993    E-mail: kaim@kams.or.kr
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © The Korean Association of Internal Medicine. All rights reserved.                powerd by m2community