This is a cohort study that will assess a new diagnostic management strategy for suspected Deep Vein Thrombosis in outpatients.The new diagnostic strategy is designed to reduce the use of ultrasound testing on the day of presentation, and reduce repeat ultrasound testing a week after an initial normal test.
This is a prospective, multicentre, cohort study that will assess a new diagnostic management strategy for suspected Deep Vein Thrombosis in outpatients. The new diagnostic strategy is designed to reduce the use of ultrasound testing on the day of presentation, and reduce repeat ultrasound testing a week after an initial normal test. Less ultrasound testing will be performed because: i) more patients will have deep vein thrombosis excluded by combinations of Clinical Pretest Probability and D-dimer results on the day of presentation; and, ii) in those who still need an ultrasound, a repeat ultrasound a week after a normal result will only be performed if the D-dimer result is markedly abnormal at initial presentation. The safety of this management strategy will be established by demonstrating a very low rate of proximal Deep Vein Thrombosis or Pulmonary Embolism during 90 days follow-up in patients who had anticoagulant therapy withheld in response to negative diagnostic testing. Diagnostic test utilization will be assessed. All clinical outcomes will be adjudicated by a central independent adjudication committee that will be blind to initial D-dimer measurements and patient management.
Study Type
OBSERVATIONAL
Enrollment
1,513
University of Alberta Hospital
Edmonton, Alberta, Canada
Nova Scotia Cancer Centre
Halifax, Nova Scotia, Canada
Hamilton Health Sciences - Hamilton General
Hamilton, Ontario, Canada
Confirmed symptomatic proximal Deep Vein Thrombosis
The primary outcome is confirmed symptomatic proximal Deep Vein Thrombosis (including involvement of the calf vein trifurcation but not isolated more distal Deep Vein Thrombosis; or pulmonary embolism (not including isolated sub-segmental abnormalities on Computed Tomography Pulmonary Angiogram; within 90 days (± 7 days for follow-up assessment) that is not diagnosed by scheduled diagnostic testing (includes events that occur between initial and scheduled follow-up proximal ultrasound examinations).
Time frame: within 90 days
Clinical Pretest Probability/ D-dimer/ Compression Ultrasound subgroups
The primary outcome in the following subgroups: * Low Clinical Pretest Probability and D-dimer \<1000 ug/L * Moderate Clinical Pretest Probability and D-dimer \<500 ug/L * Moderate Clinical Pretest Probability and D-dimer 500 -999 ug/L * High Clinical Pretest Probability and D-dimer \<500 ug/L * Low Clinical Pretest Probability and D-dimer 1000-2999 ug/L and negative initial ultrasound * Moderate Clinical Pretest Probability and D-dimer 1000-2999 ug/L and negative initial ultrasound * High Clinical Pretest Probability and D-dimer 500-1499 ug/L and negative initial ultrasound
Time frame: within 90 days
Death
Death within 90 days (± 7 days for follow-up assessment).
Time frame: within 90 days
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