Thromb Haemost 1995; 74(02): 606-611
DOI: 10.1055/s-0038-1649783
Original Article
Clinical Studies
Schattauer GmbH Stuttgart

Optimal Duration of Oral Anticoagulant Therapy: A Randomized Trial Comparing Four Weeks with Three Months of Warfarin in Patients with Proximal Deep Vein Thrombosis

Mark N Levine
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Jack Hirsh
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Michael Gent
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Alexander G Turpie
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Jeffrey Weitz
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Jeffrey Ginsberg
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
William Geerts
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Jacques LeClerc
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Jean Neemeh
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Peter Powers
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
,
Franco Piovella
The Departments of Medicine and Clinical Epidemiology & Biostatistics, McMaster University; Hamilton Civic Hospitals’ Research Centre; and the Ontario Cancer Treatment & Research Foundation Hamilton Regional Centre, Hamilton, Ontario, Canada
› Author Affiliations
Further Information

Publication History

Received 20 December 1994

Accepted 03 April 1995

Publication Date:
04 July 2018 (online)

Summary

The optimal duration of oral anticoagulant therapy for patients with acute proximal deep vein thrombosis (DVT) is uncertain. Based on the hypothesis that a normal impedance plethysmogram (IPG) following DVT defines a group of patients at low risk of recurrent venous thromboembolism (VTE), a trial was conducted to evaluate the efficacy of only four weeks of warfarin. Patients with venographically confirmed acute proximal DVT who had received four weeks of warfarin after initial heparin and whose four week IPG was normal were allocated to either continue warfarin (targeted International Normalized Ratio 2.0 to 3.0) for a further eight weeks or receive placebo. Patients with an abnormal four week IPG received warfarin for a further eight weeks. Based on clinical characteristics at the time of the qualifying thrombosis, all patients were classified as having either continuing or transient risk factors for recurrent VTE. During the eight weeks following randomization, nine (8.6%) of the 105 placebo patients developed recurrent VTE compared to one (0.9%) of the 109 warfarin patients, P = 0.009. Over the entire 11 months of follow-up, 12 placebo patients developed recurrence compared to seven warfarin patients, P = 0.3. Nineteen of the 192 patients with an abnormal four week IPG experienced recurrence during the nine months after discontinuing warfarin.

In the 301 patients who received three months of warfarin in the randomized trial or in the cohort study, all 26 recurrent events were in the 212 patients with continuing risk factors.

In conclusion, an IPG four weeks after proximal DVT is not a useful predictor for recurrent VTE; whereas the presence of continuing risk factors is a very strong predictor. Four weeks of oral anticoagulants may be all that is required in patients without continuing risk factors. Patients with continuing risk factors may require more than three months of oral anticoagulants.

 
  • References

  • 1 Hyers TM, Hull RD, Weg JG. Antithrombotic therapy for venous thromboembolic disease. Chest 1992; 104 (suppl): 408-425
  • 2 Coon WW, Willis PW. Recurrence of venous thromboembolism. Surgery 1973; 73: 823-827
  • 3 Hull R, Delmore T, Genton E, Hirsh J, Gent M, Sackett D, McLaughlin D, Armstrong P. Warfarin sodium versus low dose heparin in the long term treatment of venous thrombosis. N Engl J Med 1979; 301: 855-858
  • 4 Hull R, Delmore T, Carter C, Hirsh J, Genton E, Gent M, Turpie G, McLaughlin D. Adjusted subcutaneous heparin versus warfarin sodium in long term treatment of venous thrombosis. N Engl J Med 1982; 306: 189-194
  • 5 Hull R, Hirsh J, Jay R, Carter C, England C, Gent M, Turpie G, McLaughlin D, Dodd P, Thomas M, Raskob G, Ockelford P. Different intensities of oral anticoagulant therapy in the treatment of proximal vein thrombosis. N Engl J Med 1982; 307: 1676-1681
  • 6 O’Sullivan EF. Duration of anticoagulant therapy in venous thromboembolism. Med J Aust 1972; 2: 1104-1107
  • 7 Holmgren K, Andersson G, Fagrell B, Johnsson H, Ljungberg B, Nilsson E, Wilhelmsson S, Zettergquist S. One month versus six-month therapy with oral anticoagulants after symptomatic deep vein thrombosis. Acta Med Scand 1985; 218: 279-284
  • 8 Hirsh J, Genton E, Hull R. Venous thromboembolism. Grune & Stratton; New York: 1981. pgs 13-14
  • 9 Huisman MV, Buller HR, ten Cate JW. Utility of impedance plethysmography in the diagnosis of recurrent deep vein thrombosis. Arch Intern Med 1988; 148: 681-3
  • 10 Wheeler HB. Diagnosis of deep vein thrombosis. Review of clinical evaluation and impedance plethysmography Am J Surg 1985; 150: 7-13
  • 11 Research Committee of the British Thoracic SocietyOptimum duration of anticoagulant for deep-vein thrombosis and pulmonary embolism. Lancet. 1992 340. 873-876
  • 12 Hull R, Carter C, Jay R Ockelford P, Hirsh J, Turpie AG G, Zielinsky A, Gent M, Powers P. The diagnosis of acute recurrent deep vein thrombosis: a diagnostic challenge. Circulation 1983; 67: 901-906
  • 13 Lensing AW, Prandoni P, Brandjes D, Huisman P, Vigo M, Tomasella G, Krekt J, ten Cate JW, Huisman MV, Buller H. Detection of deep vein thrombosis by real time B mode ultrasonography. N Hngl J Med 1989; 320: 342-345
  • 14 Hull R, Hirsh J, Carter C, Jay R, Dodd PE, Oekellbrd P, Coates G, Gill G, Turpie G, Doyle D, Butler II, Raskoh G. Pulmonary angiography, ventilation lung scanning and venography for clinically suspected pulmonary embolism with abnormal perfusion lung scan. Ann Int Med 1983; 98: 891-899
  • 15 Levine MN, Hirsh J, Landcfeld S. Haemorrhagic complications of longterm anticoagulant therapy. Chest 1992; 102 (Suppl) 352-363
  • 16 Kaplan EL, Meier P. Non-parametric estimation of incomplete observations. J Am State Assoc 1958; 53: 457-481
  • 17 Mantel N. Evaluation of survival data and two new rank order statistics arising in its consideration. Cancer Chemother Rep 1966; 50: 163-170
  • 18 Hull RD, Raskob GE, Hirsh J, Jay R, Leclerc J, Geerts W, Rosenbloom D, Sackett D, Anderson C, Harrison L, Gent M. Continuous intravenous heparin compared with intermittent subcutaneous heparin in the initial treatment of proximal-vein thrombosis. N Hngl J Med 1986; 315: 1109-1214
  • 19 Hull RD, Raskob GE, Rosenbloom D, Panju A, Brill-Edwards P, Ginsberg J, Hirsh J, Martin G, Green D. Heparin for 5 days versus for 10 days in the initial treatment of proximal venous thrombosis. N Hngl J Med 1990; 322: 1260-1264
  • 20 Hull RD, Raskob GE, Pineo GH, Green D, Trowbridge A, Elliott G, Lerner RD. Subcutaneous low molecular weight heparin compared with continuous intravenous heparin in the treatment of proximal vein thrombosis. N Hngl J Med 1992; 326: 975-982
  • 21 Simmonneau G, Charbonnicr B, Decousus H, Planchon B, Ninel J, Sie P, Silsiguen M, Combe S. Subcutaneous low molecular weight heparin compared with continuous intravenous unfractionated heparin in the treatment of proximal deep vein thrombosis. Arch Intern Med 1993; 153: 1541-1546
  • 22 Prandoni P, Lensing AW, Butler HR, Carta M, Cogo A, Vigo M, Casara D, Ruol A, Ten Cate J. Comparison of subcutaneous low molecular weight heparin with intravenous standard in proximal deep vein thrombosis. Lancet 1992; 339: 441-445
  • 23 Sarasin HP, Bounameaux H. Duration of oral anticoagulant therapy after proximal deep vein thrombosis: a decision analysis. Thromb Haemost 1994; 71: 286-291