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D-dimer testing to determine the duration of anticoagulant therapy

Articolo
Data di Pubblicazione:
2006
Abstract:
Background The optimal duration of oral anticoagulation in patients with idiopathic venous thromboembolism is uncertain. Testing of d-dimer levels may play a role in the assessment of the need for prolonged anticoagulation. Methods We performed d-dimer testing 1 month after the discontinuation of anticoagulation in patients with a first unprovoked proximal deep-vein thrombosis or pulmonary embolism who had received a vitamin K antagonist for at least 3 months. Patients with a normal d-dimer level did not resume anticoagulation, whereas those with an abnormal d-dimer level were randomly assigned either to resume or to discontinue treatment. The study outcome was the composite of recurrent venous thromboembolism and major bleeding during an average follow-up of 1.4 years. Results The d-dimer assay was abnormal in 223 of 608 patients (36.7%). A total of 18 events occurred among the 120 patients who stopped anticoagulation (15.0%), as compared with 3 events among the 103 patients who resumed anticoagulation (2.9%), for an adjusted hazard ratio of 4.26 (95% confidence interval [CI], 1.23 to 14.6; P = 0.02). Thromboembolism recurred in 24 of 385 patients with a normal d-dimer level (6.2%). Among patients who stopped anticoagulation, the adjusted hazard ratio for recurrent thromboembolism among those with an abnormal d-dimer level, as compared with those with a normal d-dimer level, was 2.27 (95% CI, 1.15 to 4.46; P = 0.02). Conclusions Patients with an abnormal d-dimer level 1 month after the discontinuation of anticoagulation have a significant incidence of recurrent venous thromboembolism, which is reduced by the resumption of anticoagulation. The optimal course of anticoagulation in patients with a normal d-dimer level has not been clearly established.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
DEEP-VEIN THROMBOSIS,; RECURRENT VENOUS THROMBOEMBOLISM; NEGATIVE PREDICTIVE VALUE,; PULMONARY-EMBOLISM,; ORAL ANTICOAGULATION,; LABORATORY DIAGNOSIS,; FIRST EPISODE,; RISK; COHORT
Elenco autori:
Palareti, G.; Cosmi, B.; Legnani, C.; Tosetto, A.; Brusi, C.; Iorio, A.; Pengo, V.; Ghirarduzzi, A.; Pattacini, C.; Testa, S.; Lensing, A. W. A.; Tripodi, A.
Link alla scheda completa:
https://iris.unime.it/handle/11570/1682383
Pubblicato in:
THE NEW ENGLAND JOURNAL OF MEDICINE
Journal
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