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The Warfarin/Aspirin Study in Heart failure (WASH): a randomized trial comparing antithrombotic strategies for
J G F Cleland1, I Findlay, S Jafri
1Academic Unit, Department of Cardiology, Castlehill Hospital, University of Hull, Kingston upon Hull, United Kingdom. J.G.Cleland@hull.ac.uk
Insights
Aspirin did not improve outcomes and increased hospitalizations in heart failure patients. Warfarin benefits remain unproven, indicating antithrombotic therapy in heart failure is not evidence-based.
Area of Science:
- Cardiology
- Vascular Medicine
- Pharmacology
Background:
- Heart failure frequently co-occurs with vascular disease and athero-thrombotic events.
- The role of antithrombotic therapy in heart failure management is not well-defined.
Purpose of the Study:
- To assess the feasibility and inform the design of a larger outcome study on antithrombotic therapy in heart failure.
- To compare the safety and efficacy of no antithrombotic therapy, aspirin, and warfarin in heart failure patients.
Main Methods:
- Open-label, randomized, controlled trial involving 279 patients with heart failure and left ventricular systolic dysfunction.
- Comparison of no antithrombotic therapy, aspirin (300 mg/day), and warfarin (target INR 2.5).
- Primary outcome: composite of death, nonfatal myocardial infarction, or nonfatal stroke.
Main Results:
- No significant difference in the primary outcome among the three groups.
- Aspirin group showed a trend towards worse secondary outcomes.
- Significantly more hospitalizations for cardiovascular reasons, particularly worsening heart failure, in the aspirin group (P=.044).
Conclusions:
- The Warfarin/Aspirin Study in Heart failure (WASH) found no evidence supporting aspirin's effectiveness or safety in heart failure.
- The benefits of warfarin in heart failure patients with sinus rhythm are not established.
- Current antithrombotic therapy for heart failure lacks evidence and contributes to polypharmacy.
Background:
Heart failure is commonly associated with vascular disease and a high rate of athero-thrombotic events, but the risks and benefits of antithrombotic therapy are unknown.
Methods:
The current study was an open-label, randomized, controlled trial comparing no antithrombotic therapy, aspirin (300 mg/day), and warfarin (target international normalized ratio 2.5) in patients with heart failure and left ventricular systolic dysfunction requiring diuretic therapy. The primary objective was to demonstrate the feasibility and inform the design of a larger outcome study. The primary clinical outcome was death, nonfatal myocardial infarction, or nonfatal stroke.
Results:
Two hundred seventy-nine patients were randomized and 627 patient-years exposure were accumulated over a mean follow-up time of 27 +/- 1 months. Twenty-six (26%), 29 (32%), and 23 (26%) patients randomized to no antithrombotic treatment, aspirin, and warfarin, respectively, reached the primary outcome (ns). There were trends to a worse outcome among those randomized to aspirin for a number of secondary outcomes. Significantly (P =.044) more patients randomized to aspirin were hospitalized for cardiovascular reasons, especially worsening heart failure.
Conclusions:
The Warfarin/Aspirin Study in Heart failure (WASH) provides no evidence that aspirin is effective or safe in patients with heart failure. The benefits of warfarin for patients with heart failure in sinus rhythm have not been established. Antithrombotic therapy in patients with heart failure is not evidence based but commonly contributes to polypharmacy.
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