Outcomes of patients treated with a biodegradable-polymer sirolimus-eluting stent versus durable-polymer everolimus-eluting stents after rotational atherectomy of severely calcified bifurcation lesion

https://doi.org/10.1007/s00392-025-02625-4

Mohamed Samy (Bad Segeberg)1, A. Alali (Bad Segeberg)1, K. Elbasha (Bad Segeberg)1, A. Allali (Lübeck)2, A. Elsässer (Oldenburg)3, R. Tölg (Bad Oldesloe)4, S. Fichtlscherer (Bad Segeberg)5, G. Richardt (Bad Oldesloe)6, H. Nef (Bad Segeberg)1, N. Mankerious (Bad Segeberg)1

1Segeberger Kliniken GmbH Herz- und Gefäßzentrum Bad Segeberg, Deutschland; 2Universitätsklinikum Schleswig-Holstein Medizinische Klinik II / Kardiologie, Angiologie, Intensivmedizin Lübeck, Deutschland; 3Klinikum Oldenburg AöR Klinik für Kardiologie Oldenburg, Deutschland; 4Asklepios Klinik Bad Oldesloe Zentrum für Herz-, Gefäß- und Diabetesmedizin Bad Oldesloe, Deutschland; 5Segeberger Kliniken GmbH Kardiologie und Angiologie Bad Segeberg, Deutschland; 6Asklepios Klinik Bad Oldesloe Kardiologie Bad Oldesloe, Deutschland

 

Objective: To compare biodegradable-polymer sirolimus-eluting stent (BP-SES) with durable-polymer everolimus-eluting stent (DP-EES) after rotational atherectomy (RA) of severely calcified bifurcation lesions.

Background: New-generation drug-eluting stents (DES) are superior to early-generation DES in all percutaneous coronary intervention (PCI) settings including RA. Among the newer DES generation, the BP-SES (Orsiro, Biotronik) recently proved to be non-inferior to a DP-EES (Xience, Abbott Vascular; Promus, Boston Scientific)) in an all comers’ population.

Methods: In patients who underwent RA for a severely calcified bifurcation lesion at a single center, 111 were treated with BP-SES and 139 with DP-EES. Patients treated with other stent types, presenting with acute myocardial infarction or had a chronic total occlusion were excluded. Incidence of a composite end point of cardiac death, myocardial infarction (MI) or target lesion revascularization (TLR) was retrospectively assessed after three years.

Results: Patients treated with BP-SES were younger (p= 0.003), had a better left ventricular function (p=0.012), less frequently presented with NSTE-ACS (p= 0.033) compared to those treated with DP-EES. Moreover, intravascular imaging was more frequently applied in the BP-SES group (p= <0.001). True bifurcation rates were comparable between the BP-SES and DP-EES groups respectively (16.2 % vs. 10.8%, p= 0.260).
Procedural complications were comparable between the study groups (p= 0.821). Nevertheless, in-hospital MACE rates were lower in the BP-SES group (2.7% vs 9.4 %, OR 0.27; CI 0.08-0.97, p = 0.045), driven by lower rates of periprocedural MI (1.8% vs. 6.5 %, p= 0.073). After three years, the composite endpoint rates in BP-SES and DP-EES groups were 15% and 25%, respectively. In a multivariate regression analysis, both study groups had comparable long term composite outcome (adjusted HR: 0.57, 95%CI: 0.29-1.12, p=0.104). Nevertheless, Age (p=0.046), total stent length (p=0.001) and LVEF < 40% (p=0.001) and presentation with NSTE-ACS (p= 0.030) was associated with the composite endpoint.

Conclusion: BP-SES has might have a potential to improve in-hospital outcomes when used following RA for severely calcified bifurcation lesions. Additionally, BP-SES and DP-EES demonstrated comparable rates of long-term adverse outcomes following this procedure. These results justify the need for further randomized trials to investigate the hypothesis of whether the stent platform may influence bifurcation techniques.
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