2007
DOI: 10.1111/j.1538-7836.2007.02581.x
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Quality of oral anticoagulant treatment and risk of subsequent recurrent thromboembolism in patients with deep vein thrombosis

Abstract: To cite this article: Prandoni P, Hutten BA, van Dongen CJJ, Pesavento R, Prins MH. Quality of oral anticoagulant treatment and risk of subsequent recurrent thromboembolism in patients with deep vein thrombosis. J Thromb Haemost 2007; 5: 1555.While poor quality of oral anticoagulant therapy has been reported to be consistently associated with a higher incidence of later post-thrombotic syndrome in patients with deep vein thrombosis (DVT) of the lower extremities [1,2], whether poor anticoagulation quality may … Show more

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Cited by 8 publications
(8 citation statements)
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“…Conflicting data exist regarding the association between poor-quality oral anticoagulation and the risk of VTE recurrence (30). In view of our results, it seems plausible that the insertion of an inferior vena cava filter might improve outcomes.…”
Section: Discussionmentioning
confidence: 61%
“…Conflicting data exist regarding the association between poor-quality oral anticoagulation and the risk of VTE recurrence (30). In view of our results, it seems plausible that the insertion of an inferior vena cava filter might improve outcomes.…”
Section: Discussionmentioning
confidence: 61%
“…Analysis excluding patients kept on anticoagulation following RVO assessment (G. A. Wells, B. Shea, D. O’Connell, J. Peterson, V. Welch, M. Losos, P. Tugwell, unpublished data) [3–8,13,14,16,18] showed an OR of 1.35 (95% CI 1.01–1.8; I 2 40%) (Fig. 2).…”
Section: Resultsmentioning
confidence: 99%
“…transient risk factor), this annual risk off anticoagulation is 3%, but the annual risk of major bleeding is also in the order of 3%, negating any benefit of continuing anticoagulation [2,3]. In patients with unprovoked VTE, the risk of a recurrent event in the first year following discontinuation of anticoagulation varies from 5% to 15%, and such duration of therapy is controversial [4–7]. In these patients, the American College of Chest Physicians recommends a duration of at least 3 months (Grade 1A), with consideration of long‐term treatment in patients with a low bleeding risk leading to a favorable risk/benefit ratio (Grade 1C) [1].…”
Section: Introductionmentioning
confidence: 99%
“…All individuals who experienced a symptomatic DVT in previous modules (prophylaxis or post-prophylaxis) are at risk of developing PTS. This includes the approximate 37% of patients who have suffered a PE after a DVT (8,27,28). In this extrapolation it was assumed that the risk of an asymptomatic event becoming symptomatic is the same regardless of the prophylaxis used -any differences are driven by the different proportion of patients with an asymptomatic event during the prophylaxis phase of the model.…”
Section: Extrapolation For Ltc Modulementioning
confidence: 99%