Long-Term Safety and Efficacy of Durable Polymer Cobalt-Chromium Everolimus-Eluting Stents in Patients at High Bleeding Risk

Author:

Sorrentino Sabato1,Claessen Bimmer E.1,Chandiramani Rishi1,Guedeney Paul1,Vogel Birgit1,Baber Usman1,Rau Vinuta2,Wang Jin2,Krucoff Mitchell3,Kozuma Ken4,Ge Junbo5,Seth Ashok6,Makkar Raj7,Liu Yuqi1,Bangalore Sripal8,Bhatt Deepak L.9,Angiolillo Dominick J.10,Saito Shigeru11,Neumann Franz-Josef12,Hermiller James13,Valgimigli Marco14,Mehran Roxana1

Affiliation:

1. Mount Sinai Medical Center, New York (S.S., B.E.C., R.C., P.G., B.V., U.B., Y.L., R. Mehran).

2. Abbott Vascular, Santa Clara, CA (V.R., J.W.).

3. Duke University Medical Center, Durham, NC (M.K.).

4. Teikyo University, Tokyo, Japan (K.K.).

5. Zhongshan Hospital, Fudan University, Shanghai, People’s Republic of China (J.G.).

6. Fortis Escorts Heart Institute, New Delhi, India (A.S.).

7. Cedars-Sinai Medical Center, Los Angeles, CA (R. Makkar).

8. New York University Langone Medical Center (S.B.).

9. Brigham and Women’s Hospital Heart & Vascular Center, Harvard Medical School, Boston, MA (D.L.B.).

10. University of Florida College of Medicine-Jacksonville (D.J.A.).

11. Shonan Kamakura General Hospital, Japan (S.S.).

12. University of Freiburg, Germany (F.-J.N.).

13. St Vincent’s Medical Center of Indiana, Indianapolis (J.H.).

14. Bern University Hospital, Switzerland (M.V.).

Abstract

Background: Long-term outcomes in patients at high bleeding risk (HBR) undergoing percutaneous coronary intervention with a drug-eluting stent are unclear. Therefore, we aimed to evaluate long-term adverse events in HBR patients undergoing percutaneous coronary intervention with cobalt-chromium everolimus-eluting stent implantation. Methods: We analyzed stratified data from 4 all-comers postapproval registries. Patients with at least 1 of the following criteria were categorized as HBR: age ≥75 years, history of major bleeding (MB), history of stroke, chronic oral anticoagulant use, chronic kidney disease, anemia, or thrombocytopenia. Additionally, in a separate analysis, patients were categorized according to the recently published Academic Research Consortium HBR criteria. The Kaplan-Meier method was used for time-to-event analyses. Coronary thrombotic events (CTE) included myocardial infarction or definite/probable stent thrombosis. MB was defined according to the TIMI (Thrombolysis in Myocardial Infarction) or GUSTO (Global Use of Strategies to Open Occluded Coronary Arteries) scales. Impact of CTE and MB on subsequent risk of mortality was assessed using multivariable Cox regression with MB and CTE included as time-updated covariates. Results: Of the total 10 502 patients included, 3507 (33%) were identified as HBR. Compared with non-HBR patients, those at HBR had more comorbidities, higher lesion complexity, and a higher risk of 4-year mortality (Hazard Ratio [HR] 4.38 [95% CI, 3.76–5.11]). Results were qualitatively similar when using Academic Research Consortium criteria to define HBR. Risk of mortality was increased after CTE (HR 5.02 [95% CI, 3.93–6.41]), as well as after MB (HR 4.92 [95% CI, 3.82–6.35]). Of note, this effect was consistent across the spectrum of bleeding risk ( P -interaction test 0.97 and 0.06, respectively). Conclusions: Compared with the non-HBR population, HBR patients experienced worse 4-year outcomes after percutaneous coronary intervention with cobalt-chromium everolimus-eluting stent. Both CTE and MB had a significant impact on subsequent risk of mortality irrespective of bleeding risk.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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