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Therapeutics |
Clinical impact ratings GP/FP/Primary care






IM/Ambulatory care 





Haematology 





Key Words: fibrin fibrinogen degradation products venous thrombosis
| The first 150 words of the full text of this article appear below. |
METHODS
Design:
randomised controlled trial.
Allocation:
concealed.*
Blinding:
blinded (ultrasonographers, technicians who measured D-dimer concentrations, and outcome assessors).*
Follow up period:
3 months.
Setting:
Thrombosis units and emergency departments of 5 academic health centres in Canada.
Patients:
1096 outpatients (mean age 58 y, 58% women) who had suspected lower extremity DVT. Exclusion criteria included refusal or inability to consent and geographic inaccessibility.
Intervention:
patients were stratified by the application of a clinical model as "likely" or "unlikely" to have DVT and were subsequently allocated to D-dimer testing (n = 566) or VUI alone (n = 530). Patients in the D-dimer group received VUI if they were "likely" to have DVT or if they were "unlikely" to have DVT but the D-dimer test result was positive. Patients who were "unlikely" to have DVT and whose D-dimer test result was negative did not receive VUI. Patients in the VUI alone group who were
Jodi B Segal, MD, MPH
Johns Hopkins University School of Medicine
Baltimore, Maryland, USA
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