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Extended-Duration Use of Direct Oral Anticoagulants to Prevent VTE in Acutely III Medical Patients
Insights
Direct oral anticoagulants (DOACs) reduce venous thromboembolism (VTE) events in acutely ill medical patients. However, extended use increases bleeding risk, necessitating individualized treatment approaches for older adults.
Area of Science:
- Pharmacology
- Clinical Medicine
- Evidence-Based Practice
Background:
- Acutely ill medical patients are at high risk for venous thromboembolism (VTE).
- Extended-duration thromboprophylaxis is considered for VTE prevention in this population.
- Direct oral anticoagulants (DOACs) are increasingly used for anticoagulation.
Purpose of the Study:
- To evaluate clinical evidence on DOACs for extended thromboprophylaxis in acutely ill medical patients.
- To assess the efficacy and safety of DOACs regarding VTE and bleeding events.
Main Methods:
- Systematic literature search of MEDLINE/PubMed (2008-2018) for relevant clinical trials.
- Inclusion criteria: acutely ill medical patients, extended VTE prevention, DOACs.
- Analysis of three clinical trials and two subgroup analyses.
Main Results:
- DOACs demonstrated efficacy in preventing VTE events compared to enoxaparin in composite endpoints.
- Rivaroxaban and apixaban trials showed increased major bleeding events versus enoxaparin.
- The betrixaban trial reported no significant difference in bleeding compared to enoxaparin.
Conclusions:
- DOACs effectively reduce VTE events with extended-duration thromboprophylaxis in acutely ill medical patients.
- An increased overall bleeding risk is associated with extended DOAC use.
- Individualized risk assessment is crucial for extended DOAC therapy in older adults post-hospitalization.
Abstract:
OBJECTIVE: To evaluate current clinical evidence for the use of direct oral anticoagulants (DOACs) for extended-duration thromboprophylaxis in the acutely ill medical population for venous thromboembolism (VTE) and bleeding events.
DATA SOURCES: Were obtained through a MEDLINE/PubMed search for clinical trials conducted from March 2008 to 2018 using relevant key words. Limitations of English and human subjects were applied to search results.
STUDY SELECTION AND DATA EXTRACTION: Forty-one articles were identified, and abstracts reviewed by the authors for inclusion of the study population (acutely ill medical patients) and VTE outcomes. Clinical studies evaluating the use of DOACs for extended duration of VTE prevention in acutely ill medical patients were included in the review, resulting in three clinical trials and two subgroup analyses. The participants enrolled had an overall mean age of 71.4 years.
DATA SYNTHESIS: The DOAC trials collectively demonstrated a positive outcome in composite endpoints of VTE prevention with extended-duration thromboprophylaxis in acutely ill medical patients compared with enoxaparin. As for safety, rivaroxaban and apixaban trials reported more major bleeding events compared with enoxaparin. The betrixaban trial demonstrated no difference in bleeding compared with enoxaparin.
CONCLUSION: DOACs reduced the number of VTE events in acutely ill medical patients on extended-duration thromboprophylaxis, but with an overall increased bleeding risk. An individualized patient approach based on risk factors should be utilized for treatment with extended-duration DOAC in the older adult population with recent hospitalization.
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