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Background: Venous thromboembolism (VTE) is the third leading cause of preventable hospital-associated (HA) death. Most HA-VTE, including fatal pulmonary emboli, occur among medically ill patients. The rate of symptomatic VTE more than doubles over the first 21 days after hospital discharge. Trials have demonstrated that the burden of HA-VTE may be reduced with postdischarge thromboprophylaxis; however, few patients receive this therapy. We formerly validated the ability of eVTE (eVTE is the abbreviation for a risk assessment tool constituted by 2 calculations: one predicts 90-day VTE and the other predicts 30-day major bleeding derived from only elements of the complete blood count and basic metabolic panel and age) to identify medical patients being discharged with both an elevated risk of VTE and a low risk of bleeding.
Objectives: Implement a cluster-randomized, stepped wedge, type II hybrid implementation/effectiveness trial generating an alert among select at-risk patients upon discharge for implementation of thrombosis chemoprophylaxis in a 23-hospital not-for-profit healthcare system.
Methods: We use the Reach, Effectiveness, Adoption, Implementation, and Maintenance framework to guide implementation and outcomes reporting.
Results: The primary outcome for aim 1 (implementation) is the prescription of rivaroxaban 10 mg daily for 30 days as postdischarge thromboprophylaxis among at-risk patients. The primary efficacy and safety outcomes (effectiveness) are the 90-day composite of symptomatic VTE, myocardial infartcion, nonhemorrhagic stroke, all-cause mortality, and 30-day major bleeding.
Conclusion: The eVTE trial will provide high-quality, real-world evidence on the effectiveness and safety of a pragmatic intervention to implement targeted postdischarge thromboprophylaxis using decision support embedded in the electronic health record.
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http://dx.doi.org/10.1016/j.rpth.2024.102549 | DOI Listing |
Thromb Res
August 2025
School of Medicine, University of California Riverside, Riverside, CA, United States of America; Department of Orthopaedics, Arrowhead Regional Medical Center, Colton, CA, United States of America. Electronic address:
Background: Venous thromboembolism (VTE) is a considerable source of morbidity, mortality, and economic burden within orthopaedic surgery. Our study aimed to analyze the characteristics and reasons for lawsuits pertaining to VTE levied against orthopaedic surgeons.
Methods: The Westlaw database was queried for cases filed between 1980 and 2023 against orthopaedic surgeons involving VTE, using the search terms "orthopaedic", "blood clot," "deep vein thrombosis," "venous thromboembolism," and "pulmonary embolism.
Can Urol Assoc J
August 2025
Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada.
Introduction: Radical cystectomy (RC) is the standard treatment for muscle-invasive and select high-risk non-muscle-invasive bladder cancer. Venous thromboembolism (VTE) is a common and preventable postoperative complication. Extended thromboprophylaxis with low-molecular-weight heparin, such as enoxaparin, is recommended, but direct-acting oral anticoagulants like apixaban are a possible alternative.
View Article and Find Full Text PDFJ Am Acad Orthop Surg
July 2025
From the Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland (Levy, Frey, and Castillo), the Department of Orthopaedics (O'Toole and O'Hara), and the Department of Surgery (Stein), R Adams Cowley Shock Trauma Center, University of Maryland
Introduction: Clinical guidelines recommend low-molecular-weight heparin (enoxaparin) to prevent venous thromboembolism in orthopaedic trauma patients. However, a large trial recently found aspirin noninferior to enoxaparin in preventing death and pulmonary embolism in this population. We modeled cost implications for the United States healthcare system if aspirin replaced enoxaparin as the standard of care for thromboprophylaxis in orthopaedic trauma patients.
View Article and Find Full Text PDFAm J Med
June 2025
Division of Hematology, Department of Medicine, and Department of Pathology, Duke University Medical Center, Durham, NC.
Background: The long-term effects of COVID-19, known as post-acute sequelae of SARS-CoV-2 infection (PASC), impair quality of life (QoL). This secondary analysis of the ACTIV-4c clinical trial evaluates the specific effects of extended thromboprophylaxis with apixaban on individual QoL domains, assessed by EQ-5D-5L index, in patients discharged after COVID-19 hospitalization.
Methods: ACTIV-4c study was a prospective randomized, placebo-controlled, double-blind clinical trial.
Med Clin North Am
July 2025
Department of Medicine, Anticoagulation and Clinical Thrombosis Services, Northwell, New Hyde Park, NY, USA; Institute of Health System Science, Feinstein Institutes for Medical Research, Manhasset, NY, USA; Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA. Elect
Acutely ill hospitalized medical patients are at a higher risk of venous thromboembolism (VTE) compared to the general population. A universal thromboprophylaxis strategy upon admission is inadequate as it fails to consider individual patient VTE and bleeding risk factors. Validated risk assessment models help identify patients at elevated risk for VTE or bleeding, facilitating appropriate thromboprophylaxis.
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