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Optimal antithrombotic therapy in patients with atrial fibrillation following percutaneous coronary intervention: A
Jing-Xiu Li1, Yang Li1, Shu-Jun Yan1
1Department of Cardiology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Insights
For patients with atrial fibrillation and acute coronary syndrome post-stenting, triple oral antithrombotic therapy (TOAT) significantly reduces major adverse cardiac events (MACE) and stroke compared to dual antiplatelet therapy (DAPT). Further trials are needed to confirm optimal antithrombotic strategies.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Managing antithrombotic therapy in patients with atrial fibrillation (AF) and acute coronary syndrome (ACS) undergoing percutaneous coronary intervention with stenting (PCIS) presents a significant clinical challenge.
- Balancing the risks of thrombosis and bleeding is crucial in this high-risk patient population.
Purpose of the Study:
- To compare the efficacy and safety of dual antiplatelet therapy (DAPT; aspirin + clopidogrel) versus triple oral antithrombotic therapy (TOAT; DAPT + warfarin) in patients with AF undergoing PCIS.
- To evaluate the incidence of major adverse cardiac events (MACE), stroke, and bleeding events between the two treatment strategies.
Main Methods:
- A meta-analysis was conducted on nine observational trials published before July 2017, identified through Medline, Cochrane, Embase, and conference proceedings.
- Fixed- or random-effect models were used based on heterogeneity, with subgroup analyses performed for MACE, stroke, and bleeding events.
Main Results:
- No significant difference in primary endpoints was observed between DAPT and TOAT groups overall (OR=0.96, 95% CI=0.73-1.27).
- Subgroup analysis revealed no increased risk of major bleeding or ischemic stroke with either DAPT or TOAT.
- However, DAPT was associated with a significantly increased risk of MACE plus ischemic stroke compared to TOAT (OR=1.62, 95% CI=1.43-1.83).
Conclusions:
- Triple oral antithrombotic therapy (TOAT) significantly reduces the risk of MACE and stroke in patients with AF undergoing PCIS compared to dual antiplatelet therapy (DAPT).
- Further randomized controlled trials are necessary to validate these findings and establish optimal antithrombotic treatment strategies for this patient cohort.
Abstract:
A challenge for antithrombotic treatment is patients who present with atrial fibrillation (AF) and acute coronary syndrome, particularly in patients who have undergone coronary percutaneous intervention with stenting (PCIS). In the present study, a total of nine observational trials published prior to July 2017 that investigated the effects of dual antiplatelet therapy (DAPT; aspirin + clopidogrel) and triple oral antithrombotic therapy (TOAT; DAPT + warfarin) among patients with AF concurrent to PCIS were collected from the Medline, Cochrane and Embase databases and conference proceedings of cardiology, gastroenterology and neurology meetings. A meta-analysis was performed using fixed- or random-effect models according to heterogeneity. The subgroups were also analyzed on the occurrence of major adverse cardiac events (MACE), stroke and bleeding events in the two treatment groups. Analysis of baseline characteristics indicated that there was no significant difference in the history of coexistent disease or conventional therapies between the DAPT and TOAT groups. The primary end point incidence was 2,588 patients in the DAPT group (n=13,773) and 871 patients in the TOAT group (n=5,262) following pooling of all nine trials. There was no statistically significant difference in the incidence of primary end points between the DAPT and TOAT groups. Odds ratio (OR)=0.96, 95% confidence interval (CI)=0.73-1.27, P=0.79, with heterogeneity between trials (I2=82%, P<0.00001). Subsequently, on subgroup analysis, the results indicated no increased risk of major bleeding or ischemic stroke in the DAPT or TOAT group. However, compared with the TOAT group, there was an apparent increased risk of MACE plus ischemic stroke in the DAPT group (OR=1.62, 95% CI=1.43-1.83, P<0.00001) with heterogeneity between trials (I2=70%, P=0.01). In conclusion, the present meta-analysis suggests that TOAT (aspirin + clopidogrel + warfarin) therapy for patients with AF concurrent to PCIS significantly reduced the risk of MACE and stroke compared with DAPT (aspirin + clopidogrel) therapy. Further randomized controlled clinical trials are required to confirm the efficacy of the optimal antithrombotic therapy in patients with AF following PCIS.
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