1546: RETHINKING FACTOR XA LEAD-IN STRATEGIES IN ACUTE VTE: HOW DOES PARENTERAL ANTICOAGULATION FIT IN?

Authors

• Stephanie Edwin, Henry Ford HealthFollow
• Natasha Jolakoski
• Sarah Grazia
• Clare Brewster
• Brehanna Edwards
• Danielle Rosas
• Diana Penev
• Whitney Anderson
• Shannon Carabetta
• Bradley Haan
• Thomas Breedan
• Megan Laux
• Kathaleen Watson
• Andrew Harpenau
• Rachel Bruns
• Josephine Varda
• Kathleen Koopman
• Meagan Paylor
• Christopher Giuliano, Henry Ford HealthFollow

Recommended Citation

Edwin S, Jolakoski N, Grazia S, Brewster C, Edwards B, Rosas D, Penev D, Anderson W, Carabetta S, Haan B, Breedan T, Laux M, Watson K, Harpenau A, Bruns R, Varda J, Koopman K, Paylor M, Giuliano C. 1546: RETHINKING FACTOR XA LEAD-IN STRATEGIES IN ACUTE VTE: HOW DOES PARENTERAL ANTICOAGULATION FIT IN?. Crit Care Med 2026; 54(3S).

Document Type

Conference Proceeding

Publication Date

3-1-2026

Publication Title

Crit Care Med

Abstract

INTRODUCTION: Oral factor Xa inhibitors are guideline-recommended therapies for venous thromboembolism (VTE), however, use in critically ill patients is often preceded by parenteral anticoagulation. While both apixaban and rivaroxaban require an initial lead-in period of higher dosing, clinicians may shorten or omit this phase in patients who have already received parenteral anticoagulation despite limited supporting evidence. The purpose of this study is to evaluate the effectiveness and safety of reducing factor Xa inhibitor lead-in duration in patients who have received prior parenteral anticoagulation. METHODS: This multicenter, retrospective cohort study was conducted across 29 hospitals and included adult patients hospitalized with a new diagnosis of VTE who received at least 24 hours of therapeutic parenteral anticoagulation before starting apixaban or rivaroxaban. Patients with active bleeding on admission, anticoagulation prior to admission, antiphospholipid syndrome, severe liver disease, or contraindicated medications were excluded. The primary outcome was time to VTE recurrence within six months. Cox proportional hazard model was used to control for potential confounding factors and a sensitivity analysis was performed using propensity matching. RESULTS: Among 1,424 patients included, 1,068 received a full lead-in and 356 a reduced lead-in regimen. No significant difference in time to recurrent VTE (HR 0.53; 95% CI, 0.20-1.37;p=0.19) or major bleeding (HR 0.69; 95% CI, 0.31-1.56;p=0.45) was observed after controlling for confounding factors. No difference in recurrent VTE and major bleeding persisted after propensity matching. CONCLUSIONS: Among patients transitioning from parenteral anticoagulation to oral factor Xa inhibitors, a reduced lead-in duration was not associated with increased VTE recurrence or major bleeding.

Volume

54

Issue

3S