One-year clinical outcome of biodegradable polymer sirolimus-eluting stent in patients needing short dual antiplatelet therapy. Insight from the ULISSE registry (ULtimaster Italian multicenter all comerS Stent rEgistry)
Autor: | David Rutigliano, Carlo Briguori, Bernhard Reimers, Valeria Magni, Alberto Benassi, Nicola Locuratolo, Giuseppe Ferrante, Giulia Perfetti, Carlo Andrea Pivato, Antonio L. Bartorelli, Alberto Margonato, Maurizio Tespili, Mauro Chiarito, Stefania Falcone, Alessandro Beneduce, Adele Pierri, Stefano De Martini, Angelo Anzuini, Alfonso Ielasi, Antonio Colombo, Cosmo Godino, Franco Fabbiocchi, Rosario Parisi, Alberto Cappelletti, Matteo Montorfano, Eugenio Prati |
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Přispěvatelé: | Godino, Cosmo, Beneduce, Alessandro, Ferrante, Giuseppe, Ielasi, Alfonso, Pivato, Carlo Andrea, Chiarito, Mauro, Cappelletti, Alberto, Perfetti, Giulia, Magni, Valeria, Prati, Eugenio, Falcone, Stefania, Pierri, Adele, De Martini, Stefano, Montorfano, Matteo, Parisi, Rosario, Rutigliano, David, Locuratolo, Nicola, Anzuini, Angelo, Tespili, Maurizio, Margonato, Alberto, Benassi, Alberto, Briguori, Carlo, Fabbiocchi, Franco, Reimers, Bernhard, Bartorelli, Antonio, Colombo, Antonio |
Rok vydání: | 2019 |
Předmět: |
medicine.medical_specialty
animal structures Time Factors Stent thrombosi Polymers medicine.medical_treatment Thrombogenicity 030204 cardiovascular system & hematology Percutaneous coronary intervention 03 medical and health sciences 0302 clinical medicine Biodegradable polymer sirolimus-eluting stent Absorbable Implants Medicine Humans In patient 030212 general & internal medicine Registries Acute Coronary Syndrome Target lesion revascularization Aged Retrospective Studies Aged 80 and over Sirolimus business.industry Stent Drug-Eluting Stents Middle Aged Discontinuation Surgery Treatment Outcome Italy Dual antiplatelet therapy Conventional PCI High bleeding risk Cardiology and Cardiovascular Medicine business Immunosuppressive Agents Platelet Aggregation Inhibitors medicine.drug Follow-Up Studies |
Zdroj: | International journal of cardiology. 290 |
ISSN: | 1874-1754 |
Popis: | Background This study aimed to evaluate real-world clinical outcome of patients needing short dual antiplatelet therapy (S-DAPT) following PCI with Ultimaster® thin-strut, biodegradable polymer sirolimus-eluting stent (BP-SES), which was supposed to induce faster stent endothelialization and reduce device thrombogenicity. Methods In this sub-group analysis of patients enrolled in the ULISSE registry, two groups were identified: 1) patients discharged with S-DAPT (≤3-month) due to high bleeding risk or need for urgent major non-cardiac surgery and 2) patients discharged with recommended DAPT (R-DAPT) duration (≥6-month). The primary ischemic-safety and bleeding-safety endpoints were TLF (composite of cardiac-death, target vessel MI, and clinically driven target lesion revascularization), and BARC major bleedings (≥type-3a) at 1-year follow-up. To account for events occurring before DAPT discontinuation we performed 3-month landmark analysis. Results 82 patients (5%) were discharged with ≤3-month DAPT (57 ± 27 days), and 1558 patients (94%) were discharged with ≥6-month DAPT (318 ± 75 days). No significant differences between S-DAPT and R-DAPT group were observed in TLF at 1-year (7.9% vs. 4.6%). The rate of BARC major bleeding resulted significantly higher in S-DAPT group (3.9% vs. 0.3%; p = 0.001), with the majority of bleeding events occurring within 3 months. The landmark analysis showed no significant differences in BARC major bleedings between groups (1.4% vs. 0.3%; p = 0.142). Conclusions As compared to those treated with R-DAPT (≥6-month), patients needing -S-DAPT (≤3-month) after PCI with Ultimaster® BP-SES had similar rates of 1-year TLF and BARC major bleedings following early DAPT discontinuation. |
Databáze: | OpenAIRE |
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