ORAL ANTICOAGULATION PROGRAM REDUCES VENOUS THROMBOEMBOLISM IN PATIENTS RECEIVING FIRST-LINE CHEMOTHERAPY FOR OVARIAN CANCER: A REAL-WORLD OUTCOMES STUDY
Author(s)
Limor Helpman, MD, MPH1, Dana Yaffe, BSc2.
1Sheba Medical Center, Ramat Gan, Israel, 2MDClone, Beer Sheba, Israel.
1Sheba Medical Center, Ramat Gan, Israel, 2MDClone, Beer Sheba, Israel.
OBJECTIVES: Metastatic ovarian cancer (OC) is associated with elevated venous thromboembolism (VTE) risk, yet predictors of VTE in this population remain understudied and evidence supporting oral anticoagulation in first-line chemotherapy settings is limited. This study evaluated whether a structured anticoagulation program could reduce VTE incidence in risk-selected OC patients receiving first-line chemotherapy.
METHODS: Patients receiving first-line chemotherapy for OC at a tertiary cancer center between 2020 and 2025 were included. A quality improvement program launched in July 2023 comprised staff education, EMR-integrated Khorana risk scoring, standardized apixaban prescribing protocols, and targeted chemotherapy suite questionnaires. VTE events were identified from imaging reports using natural language processing-enabled EMR data extraction. Descriptive statistics were used to compare patient cohorts before and after program implementation. Predictors of VTE were assessed using multivariable logistic regression.
RESULTS: Patient characteristics were comparable across the pre- and post-implementation cohorts. VTE rates decreased from 16.9% before program implementation to 12.5% following rollout. No increase in bleeding events or blood product utilization was observed. On multivariable analysis adjusting for established VTE risk factors, program implementation was a significant independent protective factor against VTE (adjusted OR 0.39, 95% CI 0.17 to 0.81; p=0.015).
CONCLUSIONS: A structured oral anticoagulation program incorporating risk stratification, clinical decision support, and standardized prescribing significantly reduced VTE events during first-line chemotherapy for ovarian cancer without increasing bleeding risk. These findings support the broader implementation of systematic thromboprophylaxis programs in high-risk oncology populations and highlight the value of real-world outcomes data in guiding quality improvement.
METHODS: Patients receiving first-line chemotherapy for OC at a tertiary cancer center between 2020 and 2025 were included. A quality improvement program launched in July 2023 comprised staff education, EMR-integrated Khorana risk scoring, standardized apixaban prescribing protocols, and targeted chemotherapy suite questionnaires. VTE events were identified from imaging reports using natural language processing-enabled EMR data extraction. Descriptive statistics were used to compare patient cohorts before and after program implementation. Predictors of VTE were assessed using multivariable logistic regression.
RESULTS: Patient characteristics were comparable across the pre- and post-implementation cohorts. VTE rates decreased from 16.9% before program implementation to 12.5% following rollout. No increase in bleeding events or blood product utilization was observed. On multivariable analysis adjusting for established VTE risk factors, program implementation was a significant independent protective factor against VTE (adjusted OR 0.39, 95% CI 0.17 to 0.81; p=0.015).
CONCLUSIONS: A structured oral anticoagulation program incorporating risk stratification, clinical decision support, and standardized prescribing significantly reduced VTE events during first-line chemotherapy for ovarian cancer without increasing bleeding risk. These findings support the broader implementation of systematic thromboprophylaxis programs in high-risk oncology populations and highlight the value of real-world outcomes data in guiding quality improvement.
Conference/Value in Health Info
2026-11, ISPOR Europe 2026, Vienna, Austria
Value in Health, Volume 29, Issue 12S
Code
CO24
Topic
Clinical Outcomes, Health Service Delivery & Process of Care, Organizational Practices
Topic Subcategory
Clinical Outcomes Assessment
Disease
Oncology