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Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real-World Practice Mirrors
Elizabeth Joyce1, Brian Haymart2, Xiaowen Kong2
1University of Michigan Medical School Ann Arbor MI.
Insights
Most patients with provoked venous thromboembolism (VTE) receive anticoagulation longer than the recommended 3 months. This real-world practice deviates from guidelines, suggesting opportunities to improve care and reduce bleeding risks.
Area of Science:
- Cardiology
- Hematology
- Clinical Practice Guidelines
Background:
- Guidelines recommend 3 months of anticoagulation for provoked venous thromboembolism (VTE).
- Real-world adherence to these VTE treatment guidelines is not well-documented.
- Understanding current anticoagulation duration practices is crucial for optimizing patient care.
Purpose of the Study:
- To evaluate anticoagulation duration trends in provoked VTE patients.
- To assess real-world practice against guideline recommendations for VTE treatment.
- To identify factors associated with extended anticoagulation therapy.
Main Methods:
- Multicenter retrospective cohort study using the MAQI2 registry (2008-2020).
- Analysis of 474 warfarin users and 302 direct oral anticoagulant (DOAC) users with provoked VTE.
- Multivariable logistic regression identified predictors of anticoagulation exceeding 120 days.
Main Results:
- The majority of patients received anticoagulation for over 120 days, irrespective of medication.
- Median treatment duration was 142 days for warfarin and 180 days for DOACs.
- Recurrent VTE, myocardial infarction history, and DOAC use predicted prolonged anticoagulation.
Conclusions:
- Most provoked VTE patients in this cohort received longer anticoagulation than guideline-recommended.
- Current practice presents an opportunity to refine care delivery for VTE.
- Reducing prolonged anticoagulation may mitigate associated bleeding risks.
Abstract:
Background For more than a decade, guidelines have recommended a limited 3 months of anticoagulation for the treatment of provoked venous thromboembolism (VTE). How closely real-world practice follows guideline recommendations is not well described. Methods and Results In our multicenter, retrospective cohort study, we evaluated trends in anticoagulation duration for patients enrolled in the MAQI2 (Michigan Anticoagulation Quality Improvement Initiative) registry who were receiving anticoagulation for a provoked VTE. The MAQI2 registry comprises 6 centers in Michigan that manage patients' long-term anticoagulation. We identified 474 patients on warfarin and 302 patients on direct oral anticoagulants who were receiving anticoagulation for a primary indication of provoked VTE between 2008 and 2020. Using a predefined threshold of 120 days (3 months plus a buffer period), predictors of extended anticoagulant use were identified using multivariable logistic regression. Most patients received >120 days of anticoagulation, regardless of which medication was used. The median (25th-75th percentile) length of treatment for patients taking warfarin was 142 (91-234) days and for direct oral anticoagulants was 180 (101-360) days. Recurrent VTE (odds ratio [OR], 2.75 [95% CI, 1.67-4.53]), history of myocardial infarction (OR, 3.92 [95% CI, 1.32-11.7]), and direct oral anticoagulant rather than warfarin use (OR, 2.22 [95% CI, 1.59-3.08]) were independently associated with prolonged anticoagulation. Conclusions In our cohort of patients with provoked VTE, most patients received anticoagulation for longer than the guideline-recommended 3 months. This demonstrates a potential opportunity to improve care delivery and reduce anticoagulant-associated bleeding risk.
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