Related Experiment Video
Updated: Jan 26, 2026

Transesophageal Atrial Burst Pacing for Atrial Fibrillation Induction in Rats
Published on: February 14, 2022
Direct oral anticoagulation and mortality in moderate to high-risk atrial fibrillation
Ronen Arbel1, Ruslan Sergienko2, Ariel Hammerman3
1Maximizing Health Outcomes Research Lab, Sapir College, Sderot, Israel.
Insights
Direct oral anticoagulants (DOAC) significantly reduce mortality in non-valvular atrial fibrillation (NVAF) patients. This study shows DOAC therapy is linked to a lower risk of death compared to no anticoagulation, emphasizing its importance for NVAF survival.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Direct oral anticoagulants (DOAC) are recommended for non-valvular atrial fibrillation (NVAF) patients.
- Anticoagulation management in NVAF patients remains suboptimal.
- The impact of withholding DOAC therapy on NVAF patient survival is not well-established.
Purpose of the Study:
- To compare all-cause mortality rates between NVAF patients treated with DOACs and those receiving no anticoagulation.
- To evaluate the survival benefit of DOAC therapy in a real-world NVAF cohort.
Main Methods:
- Retrospective cohort study utilizing an extensive electronic health database.
- Inclusion of newly diagnosed, anticoagulant-naïve NVAF patients eligible for DOAC therapy (2011-2016).
- Propensity score matching was used to compare DOAC-treated patients with a similar group receiving no anticoagulation.
- Primary outcome: all-cause mortality, with follow-up until May 2017.
Main Results:
- 18,901 eligible patients were identified; 8,298 received DOACs and 10,603 received no anticoagulation.
- After matching, 5,657 patients in each group were analyzed.
- DOAC therapy was associated with a significantly lower annual mortality rate (7.6%) compared to no anticoagulation (11.1%).
- Hazard ratio for all-cause mortality with DOAC therapy was 0.69 (95% CI 0.63-0.75, p<0.001).
- Benefits of DOAC therapy were consistent across all analyzed subgroups.
Conclusions:
- DOAC therapy significantly reduces the risk of death in newly diagnosed NVAF patients compared to no oral anticoagulation.
- These findings reinforce the critical importance of initiating and maintaining DOAC therapy for NVAF patients.
- The study provides robust evidence supporting the use of DOACs for improving survival in the NVAF population.
Objective:
Although direct oral anticoagulants (DOAC) are the recommended antithrombotic therapy for patients with non-valvular atrial fibrillation (NVAF), anticoagulation in patients with NVAF is still inadequate. The effect of withholding DOAC therapy on patient survival is unknown. Therefore, our objective was to compare all-cause mortality rates between DOAC-treated patients with NVAF and similar patients receiving no anticoagulation.
Methods:
We performed a retrospective cohort study analysing Clalit Health Services' extensive electronic database, regarding all newly diagnosed, anticoagulant-naïve patients with NVAF who were eligible for DOAC therapy from 1 January 2011 to 31 December 2016. Patients who received DOAC therapy were matched by propensity scoring to patients receiving no anticoagulation. The primary outcome was all-cause mortality. Final patient follow-up date was 15 May 2017.
Results:
18 901 eligible patients were identified. 8298 received treatment with a DOAC and 10 603 received no anticoagulation therapy. Of those, 5657 patients who received DOAC therapy were matched with 5657 patients who did not receive any anticoagulant. Death occurred in 715 patients in the DOAC-treated group (7.6% per year) and in 2075 patients in the non-anticoagulated patient group (11.1% per year). DOAC therapy was associated with significantly lower risk for all-cause mortality (HR=0.69, 95% CI 0.63 to 0.75, p<0.001). The benefit of DOAC therapy was demonstrated across all subgroups analysed.
Conclusions:
In this cohort of newly diagnosed patients with NVAF, DOAC therapy was associated with a significantly lower risk of death compared with no oral anticoagulation. Our findings provide further evidence for the importance of providing DOAC anticoagulation in patients with NVAF.
Related Concept Videos
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Amyloid Fibrils
Fibril-associated Collagen
For example, the type II collagen fibrils in cartilage have covalently bound type IX fibril-associated collagens at regular intervals. Other types of fibril-associated collagens are...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Relative Risk

