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Meta-Analysis Comparing Single Versus Dual Antiplatelet Therapy Following Transcatheter Aortic Valve Implantation
Frédéric Maes1, Eugenio Stabile2, Gian Paolo Ussia3
1Department of Cardiology, Quebec Heart & Lung Institute, Laval University, Quebec City, Quebec, Canada.
Insights
Dual antiplatelet therapy (DAPT) after transcatheter aortic valve implantation (TAVI) increases bleeding risk without reducing ischemic events compared to single antiplatelet therapy (SAPT). These findings challenge current DAPT recommendations post-TAVI.
Area of Science:
- Cardiology
- Interventional Cardiology
- Thrombosis Research
Background:
- Transcatheter aortic valve implantation (TAVI) is a growing procedure for aortic stenosis.
- Optimal antithrombotic therapy post-TAVI remains debated, with current guidelines often recommending dual antiplatelet therapy (DAPT).
- Concerns exist regarding the balance between preventing thrombotic events and increasing bleeding risk with DAPT.
Purpose of the Study:
- To compare the efficacy and safety of DAPT versus single antiplatelet therapy (SAPT) following TAVI.
- To evaluate the impact of DAPT versus SAPT on ischemic events, bleeding events, and mortality.
- To inform optimal antithrombotic strategies after TAVI procedures.
Main Methods:
- Patient-level meta-analysis of three randomized controlled trials comparing DAPT and SAPT post-TAVI.
- Inclusion of 421 patients (210 DAPT, 211 SAPT).
- Primary endpoint: composite of death, major/life-threatening bleeding, and major vascular complications at 30 days, adjudicated by Valve Academic Research Consortium 2 criteria.
Main Results:
- The 30-day composite primary endpoint was significantly higher in the DAPT group (17.6%) compared to the SAPT group (10.9%).
- Major or life-threatening bleeding events were significantly increased with DAPT (11.4%) versus SAPT (5.2%).
- No significant differences were observed between DAPT and SAPT for death, global ischemic events, or stroke.
Conclusions:
- DAPT following TAVI is associated with a higher rate of major adverse events, primarily driven by increased bleeding risk.
- DAPT did not demonstrate a significant benefit in reducing ischemic events compared to SAPT after TAVI.
- Current recommendations for DAPT post-TAVI may need reevaluation based on these findings, favoring SAPT in many cases.
Abstract:
To compare dual antiplatelet therapy (DAPT) versus single antiplatelet therapy (SAPT) as antithrombotic treatment after transcatheter aortic valve implantation (TAVI) for the prevention of ischemic events, vascular and bleeding events, and death. Data from the 3 randomized trials comparing DAPT versus SAPT post-TAVI were pooled and analyzed in a patient-level meta-analysis. The primary end point was the occurrence of death, major or life-threatening bleedings, and major vascular complications at 30-day follow-up. Events were adjudicated according to the Valve Academic Research Consortium 2 definitions. A total of 421 patients randomized to DAPT (210 patients) or SAPT (211 patients) post-TAVI were analyzed. There were no differences between groups in baseline clinical and procedural characteristics. The occurrence of the 30-day combined primary end point was higher in the DAPT group (17.6% vs 10.9%, odds ratio 1.73, 95% confidence interval 1.00 to 2.98, p = 0.050), with an increased rate of major or life-threatening bleeding events in the DAPT group (11.4% vs 5.2%, odds ratio 2.24, 95% confidence interval 1.12 to 4.46, p = 0.022). There were no differences between DAPT and SAPT groups in the incidence of death (5.2% vs 3.8%, p = 0.477), global ischemic events (3.8% vs 3.8%, p = 0.999), or stroke (2.4% vs 2.4%, p = 0.996). DAPT (vs SAPT) was associated with a higher rate of major adverse events after TAVI, mainly driven by an increased risk of major or life-threatening bleeding complications along with a lack of beneficial effect on ischemic events. These results do not support the current recommendation of DAPT as antithrombotic therapy after TAVI.
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