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Times up to demonstrate a difference is current DES platforms
Hannah Chaudry1, J Dawn Abbott1
1Division of Cardiology, Department of Medicine, Warren Alpert Medical School of Brown university and the Lifespan Cardiovascular Institute, Providence, Rhode Island, USA.
The Orsiro drug-eluting stent (DES) with a bioresorbable polymer shows comparable 3-year safety and efficacy to durable polymer DES. This suggests potential for improved DES safety in clinical practice.
Area of Science:
- Cardiovascular medicine
- Medical devices
- Interventional cardiology
Background:
- Current durable polymer drug-eluting stents (DES) demonstrate sustained efficacy and safety up to 5 years.
- The Orsiro DES features a bioresorbable polymer and ultra-thin struts, aiming to enhance DES safety.
- An all-comers trial was conducted to evaluate the 3-year outcomes of the Orsiro DES.
Discussion:
- The study compared the 3-year clinical outcomes of the Orsiro DES against a durable polymer zotarolimus-eluting stent.
- Findings indicate similar safety and efficacy profiles between the Orsiro DES and the comparator stent.
- The bioresorbable polymer and ultra-thin strut design of the Orsiro DES warrant further investigation for potential safety benefits.
Key Insights:
- The Orsiro DES, utilizing a bioresorbable polymer, achieved comparable 3-year outcomes to durable polymer DES in an all-comers population.
- No significant differences in safety and efficacy were observed between the Orsiro DES and the zotarolimus-eluting stent at the 3-year follow-up.
- The results support the potential of bioresorbable polymer DES to match the performance of established durable polymer DES.
Outlook:
- Further long-term studies are needed to fully elucidate the safety and efficacy advantages of bioresorbable polymer DES.
- Investigating patient subgroups may reveal specific benefits of the Orsiro DES design.
- Continued evaluation of novel DES technologies is crucial for advancing cardiovascular treatment.
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