Diagnosis and management of iliofemoral deep vein thrombosis: clinical practice guideline

Novel oral anticoagulants (rivaroxaban, dabigatran and apixaban) have also been shown to be effective for the treatment of acute DVT (see Appendix 2). Studies comparing these agents with warfarin for management of acute venous thromboembolism have shown that all three are non-inferior to warfarin fo...

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Published in:Canadian Medical Association journal (CMAJ) Vol. 187; no. 17; pp. 1288 - 1296
Main Authors: Liu, David, Peterson, Erica, Dooner, James, Baerlocher, Mark, Zypchen, Leslie, Gagnon, Joel, Delorme, Michael, Sing, Chad Kim, Wong, Jason, Guzman, Randolph, Greenfield, Gavin, Moodley, Otto, Yenson, Paul
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Published: Canada Joule Inc 17-11-2015
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Abstract Novel oral anticoagulants (rivaroxaban, dabigatran and apixaban) have also been shown to be effective for the treatment of acute DVT (see Appendix 2). Studies comparing these agents with warfarin for management of acute venous thromboembolism have shown that all three are non-inferior to warfarin for prevention of recurrent venous thromboembolism (dabigatran, hazard ratio [HR] 1.09, 95% CI 0.76-1.57; rivaroxaban, HR 0.89, 95% CI 0.66-1.19; apixaban, HR 0.84, 95% CI 0.60-1.18).31-35 Both rivaroxaban and apixaban were associated with significantly reduced rates of major bleeding relative to conventional therapy (rivaroxaban, HR 0.54, 95% CI 0.37-0.79; apixaban, HR 0.31, 95% CI 0.17- 0.55), whereas the major bleeding profile of dabigatran was similar to that of warfarin (HR 0.73, 95% CI 0.48-1.11). Novel oral anticoagulants offer several advantages over warfarin, including no requirement for laboratory monitoring, use of fixed doses, lack of interactions with food and limited interactions with other medications. Drawbacks to their use include the lack of a reversal agent, renal excretion and higher cost.32,34,35 Rivaroxaban and apixaban are currently approved in Canada for treatment of acute venous thromboembolism. Initial RCTs of compression therapy for the prevention of post-thrombotic syndrome in patients with proximal DVT (including iliofemoral DVT) yielded conflicting results, but were hindered by lack of a placebo control, small numbers of patients, single-centre recruitment and open-label design.59-62 The recent SOX trial, a multicentre placebo-controlled RCT of external compression stockings for the prevention of post-thrombotic syndrome, randomly assigned patients with a first episode of symptomatic proximal DVT to wear active external compression stockings or placebo stockings (without therapeutic compression) daily for two years.63 There was no difference between the groups in cumulative incidence of postthrombotic syndrome (14.2% with active external compression stockings v. 12.7% with placebo stockings, p = 0.58), post-thrombotic syndrome severity or recurrent venous thromboembolism. These results bring into question whether the use of external compression stockings should be recommended for all patients with acute symptomatic DVT for the prevention of post-thrombotic syndrome. Drawbacks of external compression therapy include discomfort, difficulty applying stockings and the cost of original and replacement stockings. The only major contraindication to their use is symptomatic peripheral arterial disease.60 Relative to femoropopliteal or distal DVT, iliofemoral DVT carries a higher risk of phlegmasia cerulea dolens, recurrent venous thromboembolism and post-thrombotic syndrome. Anticoagulant therapy remains the cornerstone of management, mainly to prevent recurrent venot hromboembolism. However, selected patients with iliofemoral DVT may benefit from alternative clot-management strategies, such as inferior vena cava filters, compression therapy, and clot removal or reduction strategies. Clot removal or reduction strategies are life- and limb-salvaging for patients with phlegmasia cerulea dolens, but they also reduce the risk of postthrombotic syndrome in patients without phlegmasia cerulea dolens, particularly if candidate patients undergo early triage for intervention.
AbstractList Venous thromboembolism, presenting as deep vein thrombosis (DVT) or pulmonary embolism, affects over 35 000 Canadians each year.1 It is associated with substantial morbidity, mortality and burden on the Canadian health care system, with one-month mortality rates estimated at 6% for DVT and 12% for pulmonary embolism. Iliofemoral DVT is defined as thrombus involving the iliac and/or common femoral veins, with or without extension to the inferior vena cava; it represents about one-quarter of all cases of DVT. The natural history of iliofemoral DVT is associated with a higher risk of adverse outcomes relative to femoropopliteal or distal DVT, with examples of such outcomes including severe leg pain and swelling, limb ischemia and increased risk of recurrent venous thromboembolism and post-thrombotic syndrome. The poor outcomes observed in patients with iliofemoral DVT treated with standard anticoagulant therapy have led to exploration of alternative therapeutic options. Trials of strategies to reduce or remove thrombi, such as systemic thrombolysis,6,7 catheter-directed thrombolysis8 and surgical thrombectomy,9-11 have resulted in improved long-term vessel patency and reduced postthrombotic syndrome relative to anticoagulation alone. However, these procedures are not uniformly available, are resource intensive and have their own potential complications. 64 references
Novel oral anticoagulants (rivaroxaban, dabigatran and apixaban) have also been shown to be effective for the treatment of acute DVT (see Appendix 2). Studies comparing these agents with warfarin for management of acute venous thromboembolism have shown that all three are non-inferior to warfarin for prevention of recurrent venous thromboembolism (dabigatran, hazard ratio [HR] 1.09, 95% CI 0.76-1.57; rivaroxaban, HR 0.89, 95% CI 0.66-1.19; apixaban, HR 0.84, 95% CI 0.60-1.18).31-35 Both rivaroxaban and apixaban were associated with significantly reduced rates of major bleeding relative to conventional therapy (rivaroxaban, HR 0.54, 95% CI 0.37-0.79; apixaban, HR 0.31, 95% CI 0.17- 0.55), whereas the major bleeding profile of dabigatran was similar to that of warfarin (HR 0.73, 95% CI 0.48-1.11). Novel oral anticoagulants offer several advantages over warfarin, including no requirement for laboratory monitoring, use of fixed doses, lack of interactions with food and limited interactions with other medications. Drawbacks to their use include the lack of a reversal agent, renal excretion and higher cost.32,34,35 Rivaroxaban and apixaban are currently approved in Canada for treatment of acute venous thromboembolism. Initial RCTs of compression therapy for the prevention of post-thrombotic syndrome in patients with proximal DVT (including iliofemoral DVT) yielded conflicting results, but were hindered by lack of a placebo control, small numbers of patients, single-centre recruitment and open-label design.59-62 The recent SOX trial, a multicentre placebo-controlled RCT of external compression stockings for the prevention of post-thrombotic syndrome, randomly assigned patients with a first episode of symptomatic proximal DVT to wear active external compression stockings or placebo stockings (without therapeutic compression) daily for two years.63 There was no difference between the groups in cumulative incidence of postthrombotic syndrome (14.2% with active external compression stockings v. 12.7% with placebo stockings, p = 0.58), post-thrombotic syndrome severity or recurrent venous thromboembolism. These results bring into question whether the use of external compression stockings should be recommended for all patients with acute symptomatic DVT for the prevention of post-thrombotic syndrome. Drawbacks of external compression therapy include discomfort, difficulty applying stockings and the cost of original and replacement stockings. The only major contraindication to their use is symptomatic peripheral arterial disease.60 Relative to femoropopliteal or distal DVT, iliofemoral DVT carries a higher risk of phlegmasia cerulea dolens, recurrent venous thromboembolism and post-thrombotic syndrome. Anticoagulant therapy remains the cornerstone of management, mainly to prevent recurrent venot hromboembolism. However, selected patients with iliofemoral DVT may benefit from alternative clot-management strategies, such as inferior vena cava filters, compression therapy, and clot removal or reduction strategies. Clot removal or reduction strategies are life- and limb-salvaging for patients with phlegmasia cerulea dolens, but they also reduce the risk of postthrombotic syndrome in patients without phlegmasia cerulea dolens, particularly if candidate patients undergo early triage for intervention.
Audience Professional
Author Sing, Chad Kim
Greenfield, Gavin
Baerlocher, Mark
Liu, David
Wong, Jason
Gagnon, Joel
Delorme, Michael
Moodley, Otto
Peterson, Erica
Dooner, James
Zypchen, Leslie
Yenson, Paul
Guzman, Randolph
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  organization: Department of Radiology (Liu), Division of Hematology, Department of Medicine (Peterson, Zypchen, Yenson), Department of Vascular Surgery (Gagnon), Vancouver General Hospital, Vancouver, BC; Vascular Surgery Victoria (Dooner), Victoria General Hospital, Victoria, BC; Department of Interventional Radiology (Baerlocher), University of Toronto, Toronto, Ont.; Department of Hematology (Delorme), Kelowna General Hospital, Kelowna, BC; Departments of Emergency Medicine (Kim Sing) and Radiology (Wong), Foothills Medical Centre, Calgary, Alta.; Department of Vascular Surgery (Guzman), St. Boniface Hospital, Winnipeg, Man.; Department of Emergency Medicine (Greenfield), University of Calgary, Calgary, Alta.; Department of Hematology (Moodley), Royal University Hospital, Saskatoon, Sask. dave.liu@vch.ca
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– sequence: 9
  givenname: Jason
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  organization: Department of Radiology (Liu), Division of Hematology, Department of Medicine (Peterson, Zypchen, Yenson), Department of Vascular Surgery (Gagnon), Vancouver General Hospital, Vancouver, BC; Vascular Surgery Victoria (Dooner), Victoria General Hospital, Victoria, BC; Department of Interventional Radiology (Baerlocher), University of Toronto, Toronto, Ont.; Department of Hematology (Delorme), Kelowna General Hospital, Kelowna, BC; Departments of Emergency Medicine (Kim Sing) and Radiology (Wong), Foothills Medical Centre, Calgary, Alta.; Department of Vascular Surgery (Guzman), St. Boniface Hospital, Winnipeg, Man.; Department of Emergency Medicine (Greenfield), University of Calgary, Calgary, Alta.; Department of Hematology (Moodley), Royal University Hospital, Saskatoon, Sask
– sequence: 10
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– sequence: 12
  givenname: Otto
  surname: Moodley
  fullname: Moodley, Otto
  organization: Department of Radiology (Liu), Division of Hematology, Department of Medicine (Peterson, Zypchen, Yenson), Department of Vascular Surgery (Gagnon), Vancouver General Hospital, Vancouver, BC; Vascular Surgery Victoria (Dooner), Victoria General Hospital, Victoria, BC; Department of Interventional Radiology (Baerlocher), University of Toronto, Toronto, Ont.; Department of Hematology (Delorme), Kelowna General Hospital, Kelowna, BC; Departments of Emergency Medicine (Kim Sing) and Radiology (Wong), Foothills Medical Centre, Calgary, Alta.; Department of Vascular Surgery (Guzman), St. Boniface Hospital, Winnipeg, Man.; Department of Emergency Medicine (Greenfield), University of Calgary, Calgary, Alta.; Department of Hematology (Moodley), Royal University Hospital, Saskatoon, Sask
– sequence: 13
  givenname: Paul
  surname: Yenson
  fullname: Yenson, Paul
  organization: Department of Radiology (Liu), Division of Hematology, Department of Medicine (Peterson, Zypchen, Yenson), Department of Vascular Surgery (Gagnon), Vancouver General Hospital, Vancouver, BC; Vascular Surgery Victoria (Dooner), Victoria General Hospital, Victoria, BC; Department of Interventional Radiology (Baerlocher), University of Toronto, Toronto, Ont.; Department of Hematology (Delorme), Kelowna General Hospital, Kelowna, BC; Departments of Emergency Medicine (Kim Sing) and Radiology (Wong), Foothills Medical Centre, Calgary, Alta.; Department of Vascular Surgery (Guzman), St. Boniface Hospital, Winnipeg, Man.; Department of Emergency Medicine (Greenfield), University of Calgary, Calgary, Alta.; Department of Hematology (Moodley), Royal University Hospital, Saskatoon, Sask
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ContentType Journal Article
Copyright COPYRIGHT 2015 Joule Inc.
Copyright 8872147 Canada Inc. Nov 17, 2015
1995-2015, Canadian Medical Association 2015
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– notice: Copyright 8872147 Canada Inc. Nov 17, 2015
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Snippet Novel oral anticoagulants (rivaroxaban, dabigatran and apixaban) have also been shown to be effective for the treatment of acute DVT (see Appendix 2). Studies...
Venous thromboembolism, presenting as deep vein thrombosis (DVT) or pulmonary embolism, affects over 35 000 Canadians each year.1 It is associated with...
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StartPage 1288
SubjectTerms Algorithms
Anticoagulants - therapeutic use
Canadians
Care and treatment
Clinical medicine
Diagnosis
Disease management
Femoral Vein
Guidelines
Humans
Ilium - blood supply
Medical diagnosis
Postthrombotic Syndrome - diagnosis
Postthrombotic Syndrome - therapy
Practice Guidelines as Topic
Thrombolytic Therapy
Thrombosis
Treatment Outcome
Ultrasonography
Vena Cava Filters
Venous thrombosis
Venous Thrombosis - diagnosis
Venous Thrombosis - diagnostic imaging
Venous Thrombosis - therapy
Title Diagnosis and management of iliofemoral deep vein thrombosis: clinical practice guideline
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