Cost-Effectiveness of Left Atrial Appendage Closure and the New Anticoagulants vs. Warfarin in Atrial Fibrillation

Original Title: Time to Cost-Effectiveness Following Stroke Reduction Strategies in AF Warfarin vs. NOACs vs. LAA Closure. Reference: Vivek Y. Reddy et al. J Am Coll Cardiol. 2015;66(24):2728-2739.

Left atrial appendage closure and the new anticoagulants (NOACs) have emerged as safe and effective alternatives to warfarin for stroke in patients with non-valvular atrial fibrillation.

This analysis assessed the cost/effectiveness of warfarin, NOACs and left atrial appendage closure with the Watchman device (Boston Scientific, Marlborough) at multiple points over a time horizon.

The Markov model was used to project the life time cost (20 years) in 70 year old patients with a moderate risk of stroke and bleeding.

The clinical events rate, post stroke evolution and quality of life were obtained mainly from the PROTECT AF study (Watchman Left Atrial Appendage System for Embolic Protection in Patients with Atrial Fibrillation) and the meta-analysis comparing warfarin to NOACs.

As regards warfarin, the left atrial appendage closure was cost effective at 7 years and the NOACs, at 16 years.

At sensitivity analysis, the left appendage closure device was cost effective compared to warfarin, even though procedure costs were doubled.

Conclusion
Both the NOACs and the left atrial appendage closure device Watchmanwere cost effective compared to warfarin. These outcomes should be considered in drafting the guidelines for stroke prevention in atrial fibrillation patients.

Editorial Comment
All calculations in this study were made in US dollars in 2015,in the US. In other countries, costs vary and this could modify the cost effectiveness ratio.

More articles by this author

TAVR in Small Annuli: What Valve Should We Use?

One of the major challenges of severe aortic stenosis are patients with small aortic annuli, defined as ≤430 mm² aortic valve area. This condition...

Patients at High Risk of Bleeding After Coronary Angioplasty: Are Risk Assessment Tools ARC-HBR and PRECISE-DAPT Useful?

Patients undergoing coronary stenting typically receive dual antiplatelet therapy (DAPT) for 6 to 12 months, consisting of a P2Y12 receptor inhibitor and aspirin. While DAPT...

ACC 2025 | TAVI in Low-Risk Patients: 5-Year Outcomes of EVOLUTE LOW RISK

Transcatheter aortic valve implantation (TAVI) is a valid alternative to surgery in low-risk patients with severe aortic stenosis. However, one of its main limitations...

ACC 2025 | BHF PROTECT-TAVI: Are Cerebral Protection Systems Necessary in TAVI?

TAVI has seen a steady increase in use, though stroke continues to be one of its unwanted complications, mostly ischemic and, less frequently, hemorrhagic. The...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

iFR- vs. FFR-Guided Coronary Revascularization: 5-Year Clinical Outcomes

The assessment of coronary stenosis using coronary physiology has become a key tool in guiding revascularization. The two most widely used techniques are fractional...

TAVR in Small Annuli: What Valve Should We Use?

One of the major challenges of severe aortic stenosis are patients with small aortic annuli, defined as ≤430 mm² aortic valve area. This condition...

Patients at High Risk of Bleeding After Coronary Angioplasty: Are Risk Assessment Tools ARC-HBR and PRECISE-DAPT Useful?

Patients undergoing coronary stenting typically receive dual antiplatelet therapy (DAPT) for 6 to 12 months, consisting of a P2Y12 receptor inhibitor and aspirin. While DAPT...