A Comparison of Six Weeks with Six Months of Oral Anticoagulant Therapy after a First Episode of Venous Thromboembolism
Sam Schulman, M.D., Ann-Sofie Rhedin, M.D., Per Lindmarker, M.D., Anders Carlsson, M.D., Gerd Lärfars, M.D., Peter Nicol, M.D., Enno Loogna, M.D., Else Svensson, M.D., Bengt Ljungberg, M.D., Hans Walter, M.D., Stanka Viering, M.D., Sune Nordlander, M.D., Barbro Leijd, M.D., Kjell-Åke Jönsson, M.D., Martin Hjorth, M.D., Olle Linder, M.D., Jonas Boberg, M.D., for The Duration of Anticoagulation Trial Study Group
Background The optimal duration of oral anticoagulant therapyafter a first episode of venous thromboembolism is still a matterof debate.
Methods We performed a multicenter trial comparing six weeksof oral anticoagulant treatment with six months of such therapyin patients who had a first episode of venous thromboembolism.Anticoagulant therapy consisted of warfarin or dicumarol. Ofthe 902 patients enrolled, 5 were later excluded because theyhad congenital protein C deficiency; 443 were randomly assignedto receive six weeks of oral anticoagulant therapy with a targetedinternational normalized ratio (INR) of 2.0 to 2.85, and 454were randomly assigned to receive six months of such therapy.The initial diagnoses were confirmed by means of venographyin cases of deep-vein thromboses (n = 790) and with perfusionventilationscanning or angiography in cases of pulmonary embolism (n =107); recurrences were confirmed in the same way.
Results After two years of follow-up, there had been 123 recurrencesof venous thromboembolism that met the diagnostic criteria,80 in the six-week group (18.1 percent; 95 percent confidenceinterval, 14.5 to 21.6) and 43 in the six-month group (9.5 percent;95 percent confidence interval, 6.8 to 12.2). The odds ratiofor recurrence in the six-week group was 2.1 (95 percent confidenceinterval, 1.4 to 3.1). There was no difference in mortalityor the rate of major hemorrhage between the six-week and six-monthgroups.
Conclusions Six months of prophylactic oral anticoagulationafter a first episode of venous thromboembolism led to a lowerrecurrence rate than did treatment lasting for six weeks. Thedifference between the two groups occurred between 6 weeks and6 months after the start of treatment, and the rates of recurrenceremained nearly parallel for 11/2 years thereafter.
Source Information
From the Departments of Internal Medicine at Karolinska Hospital, Stockholm (S.S., P.L.), Huddinge Hospital, Huddinge (A.-S.R.), Danderyd Hospital, Danderyd (A.C.), Södersjukhuset, Stockholm (G.L.), Köping Hospital, Köping (P.N.), Nacka Hospital, Stockholm (E.L.), Södertälje Hospital, Södertälje (E.S.), Nyköping Hospital, Nyköping (B. Ljungberg), Sabbatsberg Hospital, Stockholm (H.W.), Norrtälje Hospital, Norrtälje (S.V.), Central Hospital, Västerås (S.N.), St. Göran Hospital, Stockholm (B. Leijd), Linköping Regional Hospital, Linköping (K.-Å.J.), Lidköping Hospital, Lidköping (M.H.), Örebro Regional Hospital, Örebro (O.L.), and Uppsala Academic Hospital, Uppsala (J.B.) all in Sweden.
Address reprint requests to Dr. Schulman at the National Hemophilia Center, Sheba Medical Center, Tel-Hashomer IL-52621, Israel.
Venous Thromboembolism
Block J. A., White T. M., Fetrow C.W., Schulman S., The Duration of Anticoagulation Trial Study Group , Diuguid D. L.
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N Engl J Med 1997;
337:51-53, Jul 3, 1997.
Correspondence
Venous Thromboembolism and Cancer
Eikelboom J. W., Mehta S. R., Hughes-Davies T.H., Roychowdhury D., Zacharski L. R., Ornstein D. L., Schulman S., Lindmarker P.
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N Engl J Med 2000;
343:1337-1338, Nov 2, 2000.
Correspondence
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