OPTIDUAL: Dual Antiaggregation Not Beneficial after 12 Months.

Extending dual antiaggregation therapy (DAT) from 12 to 48 months appears not to offer extra protection after DES implantation in patients with no adverse ischemic events during the first year, neither does it increase the risk of severe bleeding.

The OPTIDUAL study was carried out in 58 centers and included 1.385 patients one year after DES implantation. During that first year, patients had been treated with aspirin and clopidogrel and had not suffered ischemic or bleeding events. This study randomized patients to the same DAT vs. aspirin only for the next 36 months. 2nd generation DES were used in 2/3 of cases and 1st generation DES in the remaining 1/3.

There were no differences in primary outcomes in net adverse clinical events (NACE; a combination of all-cause death, non-fatal infarction, stroke or severe bleeding) between the extended DAT group (5.8%) and the aspirin group (7.5%; p =0.17). Risk rates of components were also similar. However, the post hoc analysis of ischemic results (mortality, stroke or infarction) revealed a certain benefit, with a 4.2% rate in the extended DAT group and a 6.4% in the aspirin only group.

Outcomes were consistent across several pre specified subgroups including the indication of PCI and kind of stent. The thrombosis rate was very low, lower than 0.5% in both groups.

Helft G

More articles by this author

Retrospective Analysis of DCB vs DES in Side-Branch Treatment

Coronary bifurcations are one of the most challenging scenarios in percutaneous coronary intervention (PCI) due to their anatomical complexity, the risk of carina shift,...

TCT 2025 | TUXEDO-2: Ultra-Thin Struts Versus Xience in Diabetic Patients with Multivessel Disease

It is well known that diabetic patients undergoing PCI often present with more extensive coronary artery disease, multivessel involvement, and complex lesions. This population...

TCT 2025 | INFINITY–SWEDEHEART: Long-Term Outcomes of the Bioadaptive Coronary Implant Versus Drug-Eluting Stent

The bioadaptive coronary implant DynamX (Elixir Medical, California) was developed to restore normal vascular function after angioplasty, combining a cobalt-chromium helical structure with bioresorbable...

TCT 2025 | REC-CAGEFREE I: Three-Year Follow-Up of Drug-Coated Balloon Angioplasty vs Stent in De Novo Coronary Lesions

The REC-CAGEFREE I trial evaluated the safety and efficacy of paclitaxel-coated balloon (DCB) angioplasty versus sirolimus-eluting stent (Firebird2 DES) implantation in patients with de...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

Coronary Perforations and Use of Covered Stents: Safe and Effective Long-Term Strategy?

Coronary perforations remain one of the most serious complications of percutaneous coronary intervention (PCI), especially in cases of Ellis ruptures type III. In these...

Is it really necessary to monitor all patients after TAVR?

Conduction disorders (CD) after transcatheter aortic valve replacement (TAVR) are a frequent complication and may lead to the need for permanent pacemaker implantation (PPI)....

Is it really necessary to monitor all patients after TAVR?

Conduction disorders (CD) after transcatheter aortic valve replacement (TAVR) are a frequent complication and may lead to the need for permanent pacemaker implantation (PPI)....