In people with atrial fibrillation needing anticoagulant treatment, deaths were fewer in those who had direct acting oral anticoagulants compared with warfarin. The picture is less clear for the risk of stroke and complications such as bleeding in the brain or gut. Apixaban had the best efficacy and safety profile and was cost-effective compared with warfarin.
This study pooled the data in all trials reporting efficacy, safety and cost of anticoagulant prevention of stroke events in people with atrial fibrillation. Researchers used a technique called network meta-analysis to compare the different drugs used.
There is still a need for a trial directly comparing these drugs, to add to this evidence and to identify whether certain people might benefit more from one or other of the available agents.
Why was this study needed?
Atrial fibrillation is a common irregular heart rhythm estimated to affect almost 1.4 million people in England. It carries a risk of blood clots within the heart which may dislodge into the bloodstream and block smaller blood vessels. More than one in five strokes in England and Wales is attributed to atrial fibrillation.
People with atrial fibrillation are commonly given drugs to reduce blood clotting. Warfarin was traditionally used; it is cheap but requires monitoring and has several interactions with other drugs which make it awkward for patients. The cost of warfarin and its monitoring is estimated at £90 million per year in England, Wales and Northern Ireland. Newer direct acting oral anticoagulants (DOACs) are more expensive but do not require monitoring. There is so far no trial directly comparing DOACs against one another.
This network meta-analysis compares oral anticoagulants regarding efficacy, safety and cost for prevention of stroke in patients with atrial fibrillation.
What did this study do?
This study compared four DOACs at various doses, warfarin and an antiplatelet agent for prevention of strokes in people with atrial fibrillation. It included 23 randomised trials reporting on 27 interventions and 94,656 patients. Thirteen studies included DOACs, and treatment duration ranged from three to 30 months.
The main outcomes were the number of events of stroke or systemic embolism, myocardial infarction, bleeding and mortality. The authors conducted a network meta-analysis combining results of standard meta-analyses for direct comparison. Reference treatment was warfarin to maintain an international normalised ratio 2.0-3.0.
For the cost-effectiveness analysis, the authors estimated expected total lifetime costs, quality-adjusted life years and net monetary benefit for each treatment.
The main source of bias was that in most studies participants and health professionals were aware of the treatment being given, but outcomes are objective, and this limitation is unlikely to have affected confidence in the results.
What did it find?
- All DOACs reduced deaths from any cause compared with warfarin, although results have different levels of certainty. Apixaban 5mg twice daily, for example, reduced deaths by about 30% (odds ratio [OR] 0.71, 95% confidence interval [CI] 0.61 to 0.81).
- Apixaban 5mg twice daily reduced the risk of stroke or systemic embolism compared with warfarin (OR 0.79, 95% CI 0.66 to 0.94) and dabigatran 150mg twice daily did too (OR 0.65, 95% CI 0.52 to 0.81). Edoxaban 60mg daily did not significantly reduce the risk of stroke or systemic embolism compared with warfarin. Risk of clinically relevant bleeding is lower with apixaban 5mg twice daily (OR 0.67, 95% CI 0.60 to 0.75), edoxaban 30mg daily (OR 0.59, 95%CI 0.54 to 0.64) and edoxaban 60mg twice daily (OR 0.84, 95%CI 0.77 to 0.90) than with warfarin.
- Apixaban 5mg twice daily was ranked in the indirect analysis as the most effective and safest intervention for several outcomes.
- Despite the uncertainty around the cost estimates, all DOACs show a positive expected incremental net benefit, and apixaban 5mg twice daily is cost-effective when compared with warfarin.
What does current guidance say on this issue?
The NICE 2014 guideline on management of atrial fibrillation recommends using apixaban, dabigatran, rivaroxaban or a vitamin K antagonist (warfarin) as anticoagulant treatment. The NICE 2016 Clinical Summary Knowledge also mentions edoxaban as an option for prevention of stroke and systemic embolism.
The Technology Appraisal guidance on the use of apixaban for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation recommends considering the potential risks and benefits of all anticoagulation treatments. No guidance recommends the use of one drug over another as individual patient characteristics and preferences should be taken into consideration.
What are the implications?
The findings of this study support the use of DOACs for prevention of stroke and systemic embolism in atrial fibrillation patients. They suggest the current front runner on a range of outcomes may be apixaban 5mg twice daily.
It is hoped that the ease of taking these newer medications might improve compliance outside of clinical trials. If so, this makes them good alternatives to warfarin.
Citation and Funding
Lopez-Lopez JA, Sterne JAC, Thom HHZ, et al. Oral anticoagulants for prevention of stroke in atrial fibrillation: systematic review, network meta-analysis, and cost effectiveness analysis. BMJ. 2017;359:j5058.
This project was funded by the National Institute for Health Research.
Public Health England. Atrial fibrillation prevalence estimates in England: Application of recent population estimates of AF in Sweden. London: Public Health England; 2017.
NHS website. Atrial fibrillation. London: Department of Health and Social Care; 2018.
NICE. Apixaban for preventing stroke and systemic embolism in people with nonvalvular atrial fibrillation. London: National Institute for Health and Clinical Excellence; 2017.
NICE. Atrial fibrillation: management. CG180. London: National Institute for Health and Clinical Excellence; 2014.
NICE. Clinical Knowledge Summaries: Anticoagulation - oral. London: National Institute for Health and Clinical Excellence; 2016.
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